Skocz do pozycji: 1.

Tytuł:

A homozygous CAP2 pathogenic variant in a neonate presenting with rapidly progressive cardiomyopathy and nemaline rods.

Autorzy:

Gurunathan S; Department of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Sebastian J; Department of Pediatrics, Division of Medical Genetics and Genomic Medicine, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Baker J; Department of Pediatrics, Division of Medical Genetics and Genomic Medicine, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Abdel-Hamid HZ; Department of Pediatrics, Division of Child Neurology, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.
West SC; Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Feingold B; Department of Pediatrics and Clinical and Translational Science, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Peche V; Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Reyes-Múgica M; Department of Pathology, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Madan-Khetarpal S; Department of Pediatrics, Division of Medical Genetics and Genomic Medicine, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Field J; Department of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

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Źródło:

American journal of medical genetics. Part A [Am J Med Genet A] 2022 Mar; Vol. 188 (3), pp. 970-977. Date of Electronic Publication: 2021 Dec 04.

Typ publikacji:

Case Reports; Research Support, N.I.H., Extramural

MeSH Terms:

Cardiomyopathy, Dilated*/complications
Cardiomyopathy, Dilated*/diagnosis
Cardiomyopathy, Dilated*/genetics
Myopathies, Nemaline*/diagnosis
Myopathies, Nemaline*/genetics
Myopathies, Nemaline*/pathology
Adaptor Proteins, Signal Transducing/genetics ; Homozygote ; Humans ; Infant, Newborn ; Male ; Membrane Proteins/genetics ; Muscle, Skeletal/pathology ; Mutation

Raport

• na półce

Szczegóły

Skocz do pozycji: 2.

Tytuł:

De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities.

Autorzy:

Okur V; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.; Baylor Genetics Laboratories, Houston, TX, 77021, USA.
Chen Z; Department of Orthopedic Surgery, Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Key Laboratory of Big Data for Spinal Deformities, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, 100730, Beijing, China.; Graduate School of Peking Union Medical College, 100005, Beijing, China.
Vossaert L; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.; Baylor Genetics Laboratories, Houston, TX, 77021, USA.
Peacock S; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.; Baylor Genetics Laboratories, Houston, TX, 77021, USA.
Rosenfeld J; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Zhao L; Department of Orthopedic Surgery, Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Key Laboratory of Big Data for Spinal Deformities, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, 100730, Beijing, China.; Medical Research Center, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, 100730, Beijing, China.
Du H; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Calamaro E; Department of Pediatrics, University of Rochester School of Medicine and Dentistry, Rochester, NY, 14642, USA.
Gerard A; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.; Texas Children's Hospital, Houston, TX, 77030, USA.
Zhao S; Department of Orthopedic Surgery, Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Key Laboratory of Big Data for Spinal Deformities, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, 100730, Beijing, China.; Medical Research Center, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, 100730, Beijing, China.
Kelsay J; Section of Genetics and Metabolism, University of Arkansas for Medical Sciences, Little Rock, AR, 72701, USA.
Lahr A; Department of Medical Genetics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, 15224, USA.
Mighton C; Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, ON, M5T 3M6, Canada.; Li Ka Shing Knowledge Institute, St. Michael's Hospital, Unity Health Toronto, Toronto, ON, M5B 1A6, Canada.; Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, Sinai Health, Toronto, ON, M5G 1X5, Canada.; Lunenfeld-Tanenbaum Research Institute, Sinai Health, Toronto, ON, M5G 1X5, Canada.
Porter HM; Rare Disease Institute, Children's National Hospital, Washington, DC, 20010, USA.
Siemon A; Nationwide Children's Hospital (NCH) and The Ohio State University College of Medicine Section of Genetic and Genomic Medicine, Columbus, OH, 43205, USA.
Silver J; The Fred A. Litwin Family Centre in Genetic Medicine, University Health Network and Mount Sinai Hospital, Toronto, ON, M5T 3L9, Canada.; Department of Molecular Genetics, University of Toronto, Toronto, ON, M5S 1A8, Canada.
Svihovec S; Department of Pediatrics, University of Colorado Anschutz Medical Campus, and Children's Hospital Colorado, Aurora, CO, 80045, USA.
Fong CT; Department of Pediatrics, University of Rochester School of Medicine and Dentistry, Rochester, NY, 14642, USA.
Grant CL; Rare Disease Institute, Children's National Hospital, Washington, DC, 20010, USA.
Lerner-Ellis J; Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, Sinai Health, Toronto, ON, M5G 1X5, Canada.; Lunenfeld-Tanenbaum Research Institute, Sinai Health, Toronto, ON, M5G 1X5, Canada.; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, M5S 1A8, Canada.
Manickam K; Nationwide Children's Hospital (NCH) and The Ohio State University College of Medicine Section of Genetic and Genomic Medicine, Columbus, OH, 43205, USA.
Madan-Khetarpal S; Department of Medical Genetics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, 15224, USA.
McCandless SE; Department of Pediatrics, University of Colorado Anschutz Medical Campus, and Children's Hospital Colorado, Aurora, CO, 80045, USA.
Morel CF; The Fred A. Litwin Family Centre in Genetic Medicine, University Health Network and Mount Sinai Hospital, Toronto, ON, M5T 3L9, Canada.; Department of Medicine, University of Toronto, Toronto, ON, M5S 1A8, Canada.
Schaefer GB; Section of Genetics and Metabolism, University of Arkansas for Medical Sciences, Little Rock, AR, 72701, USA.
Berry-Kravis EM; Departments of Pediatrics, Neurological Sciences, and Biochemistry, Rush University Medical Center, Chicago, IL, 60612, USA.
Gates R; Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Gomez-Ospina N; Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Qiu G; Department of Orthopedic Surgery, Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Key Laboratory of Big Data for Spinal Deformities, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, 100730, Beijing, China.
Zhang TJ; Department of Orthopedic Surgery, Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Key Laboratory of Big Data for Spinal Deformities, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, 100730, Beijing, China.
Wu Z; Department of Orthopedic Surgery, Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Key Laboratory of Big Data for Spinal Deformities, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, 100730, Beijing, China.; Medical Research Center, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, 100730, Beijing, China.
Meng L; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.; Baylor Genetics Laboratories, Houston, TX, 77021, USA.
Liu P; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.; Baylor Genetics Laboratories, Houston, TX, 77021, USA.
Scott DA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.; Texas Children's Hospital, Houston, TX, 77030, USA.
Lupski JR; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.; Texas Children's Hospital, Houston, TX, 77030, USA.; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, 77030, USA.; Department of Pediatrics, Baylor College of Medicine, Houston, TX, 77030, USA.
Eng CM; Baylor Genetics Laboratories, Houston, TX, 77021, USA.
Wu N; Department of Orthopedic Surgery, Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Key Laboratory of Big Data for Spinal Deformities, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, 100730, Beijing, China. .
Yuan B; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA. .; Baylor Genetics Laboratories, Houston, TX, 77021, USA. .; Seattle Children's Hospital, Seattle, WA, 98105, USA. .; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, UW, 98105, USA. .

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Źródło:

NPJ genomic medicine [NPJ Genom Med] 2021 Dec 07; Vol. 6 (1), pp. 104. Date of Electronic Publication: 2021 Dec 07.

Typ publikacji:

Journal Article

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 3.

Tytuł:

CSNK2B: A broad spectrum of neurodevelopmental disability and epilepsy severity.

Autorzy:

Ernst ME; Institute for Genomic Medicine, Columbia University Irving Medical Center, New York, NY, USA.; Department of Genetics and Development, Columbia University Irving Medical Center, New York, NY, USA.
Baugh EH; Institute for Genomic Medicine, Columbia University Irving Medical Center, New York, NY, USA.
Thomas A; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY, USA.
Bier L; Institute for Genomic Medicine, Columbia University Irving Medical Center, New York, NY, USA.
Lippa N; Institute for Genomic Medicine, Columbia University Irving Medical Center, New York, NY, USA.
Stong N; Institute for Genomic Medicine, Columbia University Irving Medical Center, New York, NY, USA.
Mulhern MS; Institute for Genomic Medicine, Columbia University Irving Medical Center, New York, NY, USA.
Kushary S; Institute for Genomic Medicine, Columbia University Irving Medical Center, New York, NY, USA.
Akman CI; Department of Neurology, The Neurological Institute of New York, Columbia University Irving Medical Center, New York, NY, USA.
Heinzen EL; Institute for Genomic Medicine, Columbia University Irving Medical Center, New York, NY, USA.; Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Yeh R; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY, USA.
Bi W; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Hanchard NA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Burrage LC; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Leduc MS; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Chong JSC; Joint CUHK-Baylor Center of Medical Genetics, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR, China.
Bend R; Greenwood Genetic Center, Greenwood, SC, USA.
Lyons MJ; Greenwood Genetic Center, Greenwood, SC, USA.
Lee JA; Greenwood Genetic Center, Greenwood, SC, USA.
Suwannarat P; Mid-Atlantic Permanente Medical Group, Rockville, MD, USA.
Brilstra E; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
Simon M; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
Koopmans M; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
van Binsbergen E; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
Groepper D; Department of Pediatrics, Southern Illinois University School of Medicine, Springfield, IL, USA.
Fleischer J; Department of Pediatrics, Southern Illinois University School of Medicine, Springfield, IL, USA.
Nava C; Department of Genetics, APHP Sorbonne University, Paris, France.
Keren B; Department of Genetics, APHP Sorbonne University, Paris, France.
Mignot C; Department of Genetics, APHP Sorbonne University, Paris, France.; Reference Center for Intellectual Disabilities of Rare Causes, Paris, France.
Mathieu S; Department of Neuropediatrics, APHP Sorbonne University, Trousseau Hospital, Paris, France.
Mancini GMS; Department of Clinical Genetics, ErasmusMC University Medical Center, Rotterdam, The Netherlands.
Madan-Khetarpal S; Department of Medical Genetics, UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA, USA.
Infante EM; Department of Medical Genetics, UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA, USA.
Bluvstein J; School of Medicine, New York University, New York, NY, USA.
Seeley A; Geisinger Medical Center, Danville, PA, USA.
Bachman K; Geisinger Medical Center, Danville, PA, USA.
Klee EW; Center for Individualized Medicine, Mayo Clinic, Rochester, MN, USA.; Department of Health Sciences, Mayo Clinic, Rochester, MN, USA.
Schultz-Rogers LE; Center for Individualized Medicine, Mayo Clinic, Rochester, MN, USA.; Department of Health Sciences, Mayo Clinic, Rochester, MN, USA.
Hasadsri L; Division of Laboratory Genetics and Genomics, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Barnett S; Division of Laboratory Genetics and Genomics, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Ellingson MS; Division of Laboratory Genetics and Genomics, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Ferber MJ; Clinical Genome Sequencing Laboratory, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Narayanan V; Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, AZ, USA.
Ramsey K; Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, AZ, USA.
Rauch A; Institute of Medical Genetics, University of Zürich, Schlieren, Zürich, Switzerland.
Joset P; Institute of Medical Genetics, University of Zürich, Schlieren, Zürich, Switzerland.
Steindl K; Institute of Medical Genetics, University of Zürich, Schlieren, Zürich, Switzerland.
Sheehan T; Department of Neurology, Boston Children's Hospital, Boston, MA, USA.
Poduri A; Department of Neurology, Boston Children's Hospital, Boston, MA, USA.
Vasquez A; Department of Neurology, Boston Children's Hospital, Boston, MA, USA.; Division of Child and Adolescent Neurology, Department of Neurology, Mayo Clinic, Rochester, MN, USA.
Ruivenkamp C; Department of Clinical Genetics, Leiden University Medical Center (LUMC), Leiden, the Netherlands.
White SM; Victorian Clinical Genetics Service, Murdoch Children's Research Institute, Melbourne, Australia.; Department of Paediatrics, University of Melbourne, Melbourne, Australia.
Pais L; Center for Mendelian Genomics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Monaghan KG; GeneDx, Gaithersburg, MD, USA.
Goldstein DB; Institute for Genomic Medicine, Columbia University Irving Medical Center, New York, NY, USA.
Sands TT; Institute for Genomic Medicine, Columbia University Irving Medical Center, New York, NY, USA.; Department of Neurology, The Neurological Institute of New York, Columbia University Irving Medical Center, New York, NY, USA.
Aggarwal V; Institute for Genomic Medicine, Columbia University Irving Medical Center, New York, NY, USA.; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY, USA.

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Źródło:

Epilepsia [Epilepsia] 2021 Jul; Vol. 62 (7), pp. e103-e109. Date of Electronic Publication: 2021 May 26.

Typ publikacji:

Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

MeSH Terms:

Developmental Disabilities/*genetics
Epilepsy, Generalized/*genetics
Adolescent ; Adult ; Age of Onset ; Child ; Child, Preschool ; Developmental Disabilities/physiopathology ; Epilepsies, Myoclonic/diagnosis ; Epilepsies, Myoclonic/etiology ; Epilepsies, Myoclonic/genetics ; Epilepsy, Generalized/diagnosis ; Epilepsy, Generalized/etiology ; Exome/genetics ; Female ; Genetic Variation ; Humans ; Infant ; Intellectual Disability/etiology ; Intellectual Disability/genetics ; Male ; Mutation/genetics ; Phenotype ; Status Epilepticus/diagnosis ; Status Epilepticus/etiology ; Status Epilepticus/genetics ; Young Adult

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 4.

Tytuł:

Clinical presentation of a complex neurodevelopmental disorder caused by mutations in ADNP

Autorzy:

Dijck, A. van
Vulto-van Silfhout, A.T.
Cappuyns, E.
Werf, I.M. van der
Mancini, G.M.
Tzschach, A.
Bernier, R.
Gozes, I.
Eichler, E.E.
Romano, C.
Lindstrand, A.
Nordgren, A.
Kvarnung, M.
Kleefstra, T.
Vries, B.B.A. de
Kury, S.
Rosenfeld, J.A.
Meuwissen, M.E.
Vandeweyer, G.
Kooy, R.F.
Bakshi, M.
Wilson, M.
Berman, Y.
Dickson, R.
Fransen, E.
Helsmoortel, C.
Ende, J. van den
Aa, N. van der
Wijdeven, M.J. van de
Rosenblum, J.
Monteiro, F.
Kok, F.
Quercia, N.
Bowdin, S.
Dyment, D.
Chitayat, D.
Alkhunaizi, E.
Boonen, S.E.
Keren, B.
Jacquette, A.
Faivre, L.
Bezieau, S.
Isidor, B.
Riess, A.
Moog, U.
Lynch, S.A.
McVeigh, T.
Elpeleg, O.
Smeland, M.F.
Fannemel, M.
Haeringen, A. van
Maas, S.M.
Veenstra-Knol, H.E.
Schouten, M.
Willemsen, M.H.
Marcelis, C.L.
Ockeloen, C.
Burgt, I. van der
Feenstra, I.
Smagt, J. van der
Jezela-Stanek, A.
Krajewska-Walasek, M.
Gonzalez-Lamuno, D.
Anderlid, B.M.
Malmgren, H.
Nordenskjold, M.
Clement, E.
Hurst, J.
Metcalfe, K.
Mansour, S.
Lachlan, K.
Clayton-Smith, J.
Hendon, L.G.
Abdulrahman, O.A.
Morrow, E.
McMillan, C.
Gerdts, J.
Peeden, J.
Vergano, S.A.S.
Valentino, C.
Chung, W.K.
Ozmore, J.R.
Bedrosian-Sermone, S.
Dennis, A.
Treat, K.
Hughes, S.S.
Safina, N.
Pichon, J.B. le
McGuire, M.
Infante, E.
Madan-Khetarpal, S.
Desai, S.
Benke, P.
Krokosky, A.
Cristian, I.
Baker, L.
Gripp, K.
Stessman, H.A.
Eichenberger, J.
Jayakar, P.
Pizzino, A.
Manning, M.A.
Slattery, L.
ADNP Consortium

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Temat:

Biology
Human medicine
ADNP
Autism
Genetics
Helsmoortel-Van der Aa syndrome
Intellectual disability
Neurodevelopmental disorder
Biological Psychiatry
Cohort
Pediatrics
medicine.medical_specialty
medicine
Hypotonia
medicine.symptom
business.industry
business
medicine.disease
Genotype-phenotype distinction
Autism spectrum disorder
Epilepsy
Article
Helsmoortel-Van der Aa Síndrome
Intellectual Disability
Neurodevelopmental Disorder

Źródło:

Biological psychiatry
Biological Psychiatry, 85(4), 287-297. ELSEVIER SCIENCE INC
Biological Psychiatry, 85, 287-297
Biological Psychiatry, 85(4), 287. Elsevier USA
Biological Psychiatry Volume 85, Issue 4, 15 February 2019, Pages 287-297
Biological psychiatry, 85(4), 287-297. Elsevier USA

Opis pliku:

pdf; application/pdf; text/plain

Dostępność:

https://explore.openaire.eu/search/publication?articleId=doi_dedup___::517869385daa59216cda03fc628eb520

• na półce

Szczegóły

Skocz do pozycji: 5.

Tytuł:

Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.

Autorzy:

Gillentine MA; Department of Genome Sciences, University of Washington School of Medicine, 3720 15th Ave NE S413A, Box 355065, Seattle, WA, 981095-5065, USA.
Wang T; Department of Genome Sciences, University of Washington School of Medicine, 3720 15th Ave NE S413A, Box 355065, Seattle, WA, 981095-5065, USA.
Hoekzema K; Department of Genome Sciences, University of Washington School of Medicine, 3720 15th Ave NE S413A, Box 355065, Seattle, WA, 981095-5065, USA.
Rosenfeld J; Baylor Genetics Laboratories, Houston, TX, USA.; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Liu P; Baylor Genetics Laboratories, Houston, TX, USA.
Guo H; Department of Genome Sciences, University of Washington School of Medicine, 3720 15th Ave NE S413A, Box 355065, Seattle, WA, 981095-5065, USA.; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Kim CN; Department of Anatomy, University of California, San Francisco, CA, USA.; Department of Psychiatry, University of California, San Francisco, CA, USA.; Weill Institute for Neurosciences, University of California at San Francisco, San Francisco, CA, USA.; The Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, CA, USA.
De Vries BBA; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Vissers LELM; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Nordenskjold M; Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.; Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden.
Kvarnung M; Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.; Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden.
Lindstrand A; Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.; Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden.
Nordgren A; Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.; Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden.
Gecz J; School of Medicine and the Robinson Research Institute, the University of Adelaide at the Women's and Children's Hospital, Adelaide, South Australia, Australia.; Genetics and Molecular Pathology, SA Pathology, Adelaide, South Australia, Australia.; South Australian Health and Medical Research Institute, Adelaide, South Australia, Australia.
Iascone M; Laboratorio di Genetica Medica - ASST Papa Giovanni XXIII, Bergamo, Italy.
Cereda A; Department of Pediatrics, ASST Papa Giovanni XXIII, Bergamo, Italy.
Scatigno A; Department of Pediatrics, ASST Papa Giovanni XXIII, Bergamo, Italy.
Maitz S; Genetic Unit, Department of Pediatrics, Fondazione MBBM S. Gerardo Hospital, Monza, Italy.
Zanni G; Unit of Neuromuscular and Neurodegenerative Disorders, Department Neurosciences, Bambino Gesù Children's Hospital, IRCCS, 00146, Rome, Italy.
Bertini E; Unit of Neuromuscular and Neurodegenerative Disorders, Department Neurosciences, Bambino Gesù Children's Hospital, IRCCS, 00146, Rome, Italy.
Zweier C; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.
Schuhmann S; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.
Wiesener A; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.
Pepper M; Center on Human Development and Disability, University of Washington, Seattle, WA, USA.; Seattle Children's Autism Center, Seattle, WA, USA.
Panjwani H; Center on Human Development and Disability, University of Washington, Seattle, WA, USA.; Seattle Children's Autism Center, Seattle, WA, USA.
Torti E; GeneDX, Gaithersburg, MD, USA.
Abid F; Department of Pediatrics-Neurology, Baylor College of Medicine, Houston, TX, USA.; Texas Children's Hospital, Houston, TX, USA.
Anselm I; Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Srivastava S; Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Atwal P; The Atwal Clinic: Genomic & Personalized Medicine, Jacksonville, FL, USA.
Bacino CA; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Bhat G; Department of Pediatrics, Section of Genetics, University of Illinois at Chicago, Chicago, IL, USA.
Cobian K; Department of Pediatrics, Section of Genetics, University of Illinois at Chicago, Chicago, IL, USA.
Bird LM; Department of Pediatrics, University of California San Diego, San Diego, CA, USA.; Genetics/Dysmorphology, Rady Children's Hospital San Diego, San Diego, CA, USA.
Friedman J; Department of Pediatrics, University of California San Diego, San Diego, CA, USA.; Rady Children's Institute for Genomic Medicine, San Diego, CA, USA.; Department of Neurosciences, University of California San Diego, San Diego, CA, USA.
Wright MS; Department of Pediatrics, University of California San Diego, San Diego, CA, USA.; Rady Children's Institute for Genomic Medicine, San Diego, CA, USA.
Callewaert B; Department of Biomolecular Medicine, Ghent University Hospital, Ghent, Belgium.
Petit F; Clinique de Génétique, Hôpital Jeanne de Flandre, Bâtiment Modulaire, CHU, 59037, Lille Cedex, France.
Mathieu S; Sorbonne Universités, Centre de Référence déficiences intellectuelles de causes rares, département de génétique et embryologie médicale, Hôpital Trousseau, AP-HP, Paris, France.
Afenjar A; Sorbonne Universités, Centre de Référence déficiences intellectuelles de causes rares, département de génétique et embryologie médicale, Hôpital Trousseau, AP-HP, Paris, France.
Christensen CK; Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.
White KM; Department of Medical and Molecular Genetics, IU Health, Indianapolis, IN, USA.
Elpeleg O; Department of Genetics, Hadassah, Hebrew University Medical Center, Jerusalem, Israel.
Berger I; Pediatric Neurology, Assuta-Ashdod University Hospital, Ashdod, Israel.; Health Sciences, Ben-Gurion University of the Negev, Beersheba, Israel.
Espineli EJ; Department of Pediatrics-Neurology, Baylor College of Medicine, Houston, TX, USA.; Texas Children's Hospital, Houston, TX, USA.
Fagerberg C; Department of Clinical Genetics, Odense University Hospital, Odense, Denmark.
Brasch-Andersen C; Department of Clinical Genetics, Odense University Hospital, Odense, Denmark.
Hansen LK; H C Andersen Chilldrens Hospital, Odense University Hospital, Odense, Denmark.
Feyma T; Gillette Children's Specialty Healthcare, Saint Paul, MN, USA.
Hughes S; Division of Clinical Genetics, Children's Mercy Kansas City, Kansas City, MO, USA.; The University of Missouri-Kansas City, School of Medicine, Kansas City, MO, USA.
Thiffault I; The University of Missouri-Kansas City, School of Medicine, Kansas City, MO, USA.; Children's Mercy Kansas City, Center for Pediatric Genomic Medicine, Kansas City, MO, USA.
Sullivan B; Division of Clinical Genetics, Children's Mercy Kansas City, Kansas City, MO, USA.
Yan S; Division of Clinical Genetics, Children's Mercy Kansas City, Kansas City, MO, USA.
Keller K; Oregon Health & Science University, Corvallis, OR, USA.
Keren B; Department of Genetics, Hópital Pitié-Salpêtrière, Paris, France.
Mignot C; Department of Genetics, Hópital Pitié-Salpêtrière, Paris, France.
Kooy F; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.
Meuwissen M; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.
Basinger A; Genetics Department, Cook Children's Hospital, Fort Worth, TX, USA.
Kukolich M; Genetics Department, Cook Children's Hospital, Fort Worth, TX, USA.
Philips M; Genetics Department, Cook Children's Hospital, Fort Worth, TX, USA.
Ortega L; Genetics Department, Cook Children's Hospital, Fort Worth, TX, USA.
Drummond-Borg M; Genetics Department, Cook Children's Hospital, Fort Worth, TX, USA.
Lauridsen M; Department of Clinical Genetics, Odense University Hospital, Odense, Denmark.
Sorensen K; Department of Clinical Genetics, Odense University Hospital, Odense, Denmark.
Lehman A; Department of Medical Genetics, University of British Columbia, Vancouver, Canada.; BC Children's Hospital and BC Women's Hospital, Vancouver, BC, Canada.
Lopez-Rangel E; Department of Medical Genetics, University of British Columbia, Vancouver, Canada.; Division of Developmental Pediatrics, Department of Pediatrics, BC Children's Hospital, University of British Columbia, Vancouver, BC, Canada.; Sunny Hill Health Centre for Children, Vancouver, BC, Canada.
Levy P; Department of Pediatrics, The Children's Hospital at Montefiore, Bronx, NY, USA.
Lessel D; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Lotze T; Department of Pediatrics-Neurology, Baylor College of Medicine, Houston, TX, USA.
Madan-Khetarpal S; Department of Human Genetics, University of Pittsburgh, Pittsburgh, PA, USA.; UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA, USA.
Sebastian J; Department of Human Genetics, University of Pittsburgh, Pittsburgh, PA, USA.
Vento J; Department of Human Genetics, University of Pittsburgh, Pittsburgh, PA, USA.
Vats D; Kaiser Permanente Southern California, Los Angeles, CA, USA.
Benman LM; The Permanente Medical Group, Oakland, CA, USA.
Mckee S; Northern Ireland Regional Genetics Service, Belfast City Hospital, Belfast, UK.
Mirzaa GM; Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, WA, USA.; Department of Pediatrics, University of Washington, Seattle, WA, USA.; Brotman Baty Institute for Precision Medicine, Seattle, WA, USA.
Muss C; Al Dupont Hospital for Children, Wilmington, DE, USA.
Pappas J; NYU Grossman School of Medicine, Department of Pediatrics, Clinical Genetic Services, New York, NY, USA.
Peeters H; Center for Human Genetics, KU Leuven and Leuven Autism Research (LAuRes), Leuven, Belgium.
Romano C; Oasi Research Institute-IRCCS, Troina, Italy.
Elia M; Oasi Research Institute-IRCCS, Troina, Italy.
Galesi O; Oasi Research Institute-IRCCS, Troina, Italy.
Simon MEH; Department of Genetics, University Medical Center, Utrecht University, Utrecht, The Netherlands.
van Gassen KLI; Department of Genetics, University Medical Center, Utrecht University, Utrecht, The Netherlands.
Simpson K; Rare Disease Institute, Children's National Health System, Washington, DC, USA.
Stratton R; Department of Genetics, Driscoll Children's Hospital, Corpus Christi, TX, USA.
Syed S; Department of Pediatric Gastroenterology, Driscoll Children's Hospital, Corpus Christi, TX, USA.
Thevenon J; Àrea de Genètica Clínica i Molecular, Hospital Vall d'Hebrón, Barcelona, Spain.
Palafoll IV; Centre de référence Anomalies du développement, CHU Grenoble-Alpes, Grenoble, France.
Vitobello A; UF Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne and INSERM UMR1231 GAD, Université de Bourgogne Franche-Comté, F-21000, Dijon, France.; INSERM UMR 1231 Génétique des Anomalies du Développement, Université Bourgogne Franche-Comté, Dijon, France.
Bournez M; Centre de Référence Maladies Rares « déficience intellectuelle », Centre de Génétique, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Centre de Référence Maladies Rares « Anomalies du Développement et Syndromes malformatifs »​ Université Bourgogne Franche-Comté, Dijon, France.
Faivre L; INSERM UMR 1231 Génétique des Anomalies du Développement, Université Bourgogne Franche-Comté, Dijon, France.; Centre de Référence Maladies Rares « Anomalies du Développement et Syndromes malformatifs »​ Université Bourgogne Franche-Comté, Dijon, France.
Xia K; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Earl RK; Center on Human Development and Disability, University of Washington, Seattle, WA, USA.; Seattle Children's Autism Center, Seattle, WA, USA.; Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, USA.
Nowakowski T; Department of Anatomy, University of California, San Francisco, CA, USA.; Department of Psychiatry, University of California, San Francisco, CA, USA.; Weill Institute for Neurosciences, University of California at San Francisco, San Francisco, CA, USA.; The Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, CA, USA.
Bernier RA; Center on Human Development and Disability, University of Washington, Seattle, WA, USA.; Seattle Children's Autism Center, Seattle, WA, USA.; Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, USA.
Eichler EE; Department of Genome Sciences, University of Washington School of Medicine, 3720 15th Ave NE S413A, Box 355065, Seattle, WA, 981095-5065, USA. .; Howard Hughes Medical Institute, University of Washington, Seattle, WA, USA. .

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Corporate Authors:

CAUSES Study
SPARK Consortium

Źródło:

Genome medicine [Genome Med] 2021 Apr 19; Vol. 13 (1), pp. 63. Date of Electronic Publication: 2021 Apr 19.

Typ publikacji:

Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

MeSH Terms:

Genetic Predisposition to Disease*
Heterogeneous-Nuclear Ribonucleoproteins/*genetics
Mutation/*genetics
Neurodevelopmental Disorders/*genetics
Brain/metabolism ; DNA Copy Number Variations/genetics ; Gene Expression Regulation ; Genetic Association Studies ; Genetic Variation ; Heterogeneous-Nuclear Ribonucleoproteins/metabolism ; Humans ; Inheritance Patterns/genetics ; Mutation, Missense/genetics ; Phenotype ; RNA Processing, Post-Transcriptional/genetics ; Single-Cell Analysis

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 6.

Tytuł:

Deletion of conserved non-coding sequences downstream from NKX2-1: A novel disease-causing mechanism for benign hereditary chorea.

Autorzy:

Liao J; Pittsburgh Cytogenetics Laboratory, Magee-Womens Hospital of UPMC, Pittsburgh, PA, USA.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
Coffman KA; Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Locker J; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Padiath QS; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
Nmezi B; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
Filipink RA; Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Hu J; Pittsburgh Cytogenetics Laboratory, Magee-Womens Hospital of UPMC, Pittsburgh, PA, USA.; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, PA, USA.
Sathanoori M; Pittsburgh Cytogenetics Laboratory, Magee-Womens Hospital of UPMC, Pittsburgh, PA, USA.; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, PA, USA.
Madan-Khetarpal S; Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
McGuire M; Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Schreiber A; Genomic Medicine Institute, Cleveland Clinic, Cleveland, OH, USA.
Moran R; Genomic Medicine Institute, Cleveland Clinic, Cleveland, OH, USA.
Friedman N; Center for Pediatric Neurology, Cleveland Clinic, Cleveland, OH, USA.
Hoffner L; Magee Womens Research Institute, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
Rajkovic A; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, PA, USA.; Magee Womens Research Institute, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
Yatsenko SA; Pittsburgh Cytogenetics Laboratory, Magee-Womens Hospital of UPMC, Pittsburgh, PA, USA.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, PA, USA.; Magee Womens Research Institute, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
Surti U; Pittsburgh Cytogenetics Laboratory, Magee-Womens Hospital of UPMC, Pittsburgh, PA, USA.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, PA, USA.; Magee Womens Research Institute, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.

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Źródło:

Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2021 Apr; Vol. 9 (4), pp. e1647. Date of Electronic Publication: 2021 Mar 05.

Typ publikacji:

Case Reports; Journal Article

MeSH Terms:

Regulatory Sequences, Nucleic Acid*
Chorea/*genetics
Thyroid Nuclear Factor 1/*genetics
Adolescent ; Child ; Chorea/pathology ; Chromosomes, Human, Pair 14/genetics ; Conserved Sequence ; Female ; Humans ; Male ; Pedigree ; Sequence Deletion

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknieSzczegóły

Skocz do pozycji: 7.

Tytuł:

SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females.

Autorzy:

Radio FC; Genetics and Rare Disease Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.
Pang K; Division of Neurology and Developmental Neuroscience, Baylor College of Medicine, Houston, TX 77030, USA.
Ciolfi A; Genetics and Rare Disease Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.
Levy MA; Molecular Genetics Laboratory, Molecular Diagnostics Division, London Health Sciences Centre, London, ON N6A5W9, Canada.
Hernández-García A; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Pedace L; Oncohaematology Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.
Pantaleoni F; Genetics and Rare Disease Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.
Liu Z; Division of Neurology and Developmental Neuroscience, Baylor College of Medicine, Houston, TX 77030, USA.
de Boer E; Department of Human Genetics, Radboudumc, 6525 GA Nijmegen, the Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud University, 6525 GA Nijmegen, the Netherlands.
Jackson A; Division of Evolution & Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, M13 9 WL Manchester, UK; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, M13 9WL Manchester, UK.
Bruselles A; Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, 00161 Rome, Italy.
McConkey H; Molecular Genetics Laboratory, Molecular Diagnostics Division, London Health Sciences Centre, London, ON N6A5W9, Canada.
Stellacci E; Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, 00161 Rome, Italy.
Lo Cicero S; Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, 00161 Rome, Italy.
Motta M; Genetics and Rare Disease Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.
Carrozzo R; Genetics and Rare Disease Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.
Dentici ML; Genetics and Rare Disease Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.
McWalter K; GeneDx, Gaithersburg, MD 20877, USA.
Desai M; GeneDx, Gaithersburg, MD 20877, USA.
Monaghan KG; GeneDx, Gaithersburg, MD 20877, USA.
Telegrafi A; GeneDx, Gaithersburg, MD 20877, USA.
Philippe C; Inserm UMR 1231 GAD (Génétique des Anomalies du Développement), Université de Bourgogne, 21070 Dijon, France; UF Innovation en Diagnostic Génomique des Maladies Rares, CHU, Dijon Bourgogne, 21079 Dijon, France.
Vitobello A; Inserm UMR 1231 GAD (Génétique des Anomalies du Développement), Université de Bourgogne, 21070 Dijon, France; UF Innovation en Diagnostic Génomique des Maladies Rares, CHU, Dijon Bourgogne, 21079 Dijon, France.
Au M; Division of Medical Genetics, Department of Pediatrics, Cedars Sinai Medical Center, David Geffen School of Medicine at UCLA, Los Angeles, CA 90048, USA.
Grand K; Division of Medical Genetics, Department of Pediatrics, Cedars Sinai Medical Center, David Geffen School of Medicine at UCLA, Los Angeles, CA 90048, USA.
Sanchez-Lara PA; Division of Medical Genetics, Department of Pediatrics, Cedars Sinai Medical Center, David Geffen School of Medicine at UCLA, Los Angeles, CA 90048, USA.
Baez J; Division of Medical Genetics, Department of Pediatrics, Cedars Sinai Medical Center, David Geffen School of Medicine at UCLA, Los Angeles, CA 90048, USA.
Lindstrom K; Phoenix Children's Hospital, Phoenix, AZ 85016, USA.
Kulch P; Phoenix Children's Hospital, Phoenix, AZ 85016, USA.
Sebastian J; Division of Medical Genetics, Department of Pediatrics, UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA 15224, USA.
Madan-Khetarpal S; Division of Medical Genetics, Department of Pediatrics, UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA 15224, USA.
Roadhouse C; McMaster Children's Hospital, Hamilton, ON L8N 3Z5, Canada.
MacKenzie JJ; McMaster Children's Hospital, Hamilton, ON L8N 3Z5, Canada.
Monteleone B; Clinical genetics, NYU Langone Long Island School of Medicine, Mineola, NY 11501, USA.
Saunders CJ; Center for Pediatric Genomic Medicine, Children's Mercy Hospital, Kansas City, MO 64108, USA.
Jean Cuevas JK; Center for Pediatric Genomic Medicine, Children's Mercy Hospital, Kansas City, MO 64108, USA.
Cross L; Center for Pediatric Genomic Medicine, Children's Mercy Hospital, Kansas City, MO 64108, USA.
Zhou D; Center for Pediatric Genomic Medicine, Children's Mercy Hospital, Kansas City, MO 64108, USA.
Hartley T; Children's Hospital of Eastern Ontario, Ottawa, ON K1H 8L1, Canada.
Sawyer SL; Children's Hospital of Eastern Ontario, Ottawa, ON K1H 8L1, Canada.
Monteiro FP; Mendelics Genomic Analysis, Campo Belo - São Paulo 04013-000, Brazil.
Secches TV; Mendelics Genomic Analysis, Campo Belo - São Paulo 04013-000, Brazil.
Kok F; Mendelics Genomic Analysis, Campo Belo - São Paulo 04013-000, Brazil.
Schultz-Rogers LE; Center for Individualized Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Macke EL; Center for Individualized Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Morava E; Center for Individualized Medicine, Mayo Clinic, Rochester, MN 55905, USA; Department of Clinical Genomics, Mayo Clinic, Rochester, MN 55905, USA.
Klee EW; Center for Individualized Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Kemppainen J; Center for Individualized Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Iascone M; Ospedale Papa Giovanni XXIII, 24127 Bergamo, Italy.
Selicorni A; Azienda Socio Sanitaria Territoriale Lariana, 22100 Como, Italy.
Tenconi R; Dipartimento di Pediatria, Università di Padova, 35137 Padua, Italy.
Amor DJ; Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, VIC 3052, Australia; Department of Paediatrics, University of Melbourne, Royal Children's Hospital, Melbourne, VIC 3052, Australia.
Pais L; Medical and Populations Genetics Program, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Gallacher L; Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, VIC 3052, Australia; Department of Paediatrics, University of Melbourne, Royal Children's Hospital, Melbourne, VIC 3052, Australia.
Turnpenny PD; Royal Devon & Exeter NHS Foundation Trust, Exeter EX2 5DW, UK.
Stals K; Royal Devon & Exeter NHS Foundation Trust, Exeter EX2 5DW, UK.
Ellard S; Royal Devon & Exeter NHS Foundation Trust, Exeter EX2 5DW, UK.
Cabet S; Department of Genetics, Hospices Civils de Lyon, Groupement Hospitalier Est, Claude Bernard Lyon 1 University, 69002 Lyon, France.
Lesca G; Department of Genetics, Hospices Civils de Lyon, Groupement Hospitalier Est, Claude Bernard Lyon 1 University, 69002 Lyon, France.
Pascal J; Institute of Medical Genetics, University of Zurich, 8952 Schlieren, Zurich, Switzerland.
Steindl K; Institute of Medical Genetics, University of Zurich, 8952 Schlieren, Zurich, Switzerland.
Ravid S; Pediatric Neurology Unit, Ruth Children's Hospital, Rambam Health Care Campus, Haifa 3109601, Israel.
Weiss K; Genetics Institute, Rambam Health Care Campus, Rappaport Faculty of Medicine, Israel Institute of Technology, Haifa 3109601, Israel.
Castle AMR; Department of Genetics, CHEO, University of Ottawa, Ottawa, ON K1N 6N5, Canada.
Carter MT; Department of Genetics, CHEO, University of Ottawa, Ottawa, ON K1N 6N5, Canada.
Kalsner L; Connecticut Children's Medical Center, University of Connecticut School of Medicine, Farmington, CT 06032, USA.
de Vries BBA; Department of Human Genetics, Radboudumc, 6525 GA Nijmegen, the Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud University, 6525 GA Nijmegen, the Netherlands.
van Bon BW; Department of Human Genetics, Radboudumc, 6525 GA Nijmegen, the Netherlands.
Wevers MR; Department of Human Genetics, Radboudumc, 6525 GA Nijmegen, the Netherlands.
Pfundt R; Department of Human Genetics, Radboudumc, 6525 GA Nijmegen, the Netherlands.
Stegmann APA; Department of Human Genetics, Radboudumc, 6525 GA Nijmegen, the Netherlands; Department of Clinical Genetics, Maastricht University Medical Center+, 6229 HX Maastricht, the Netherlands.
Kerr B; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, M13 9WL Manchester, UK.
Kingston HM; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, M13 9WL Manchester, UK.
Chandler KE; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, M13 9WL Manchester, UK.
Sheehan W; Department of Medical Genetics, Shodair Children's Hospital, Helena, MT 59601, USA.
Elias AF; Department of Medical Genetics, Shodair Children's Hospital, Helena, MT 59601, USA.
Shinde DN; Ambry Genetics, Aliso Viejo, CA 92656, USA.
Towne MC; Ambry Genetics, Aliso Viejo, CA 92656, USA.
Robin NH; Department of Genetics, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Goodloe D; Department of Genetics, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Vanderver A; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA; Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Sherbini O; Department of Genetics, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Bluske K; Illumina Clinical Services Laboratory, San Diego, CA 92122, USA.
Hagelstrom RT; Illumina Clinical Services Laboratory, San Diego, CA 92122, USA.
Zanus C; Institute for Maternal and Child Health, IRCCS 'Burlo Garofolo,' 34137 Trieste, Italy.
Faletra F; Institute for Maternal and Child Health, IRCCS 'Burlo Garofolo,' 34137 Trieste, Italy.
Musante L; Institute for Maternal and Child Health, IRCCS 'Burlo Garofolo,' 34137 Trieste, Italy.
Kurtz-Nelson EC; Department of Psychiatry & Behavioral Sciences, University of Washington, Seattle, WA 98195, USA.
Earl RK; Department of Psychiatry & Behavioral Sciences, University of Washington, Seattle, WA 98195, USA.
Anderlid BM; Department of Molecular Medicine and Surgery, Karolinska Institutet and Department of Clinical Genetics, Karolinska University Hospital, 17176 Stockholm, Sweden.
Morin G; CA de Génétique Clinique & Oncogénétique, CHU Amiens-Picardie, 80054 Amiens, France.
van Slegtenhorst M; Department of Clinical Genetics, Erasmus MC University Medical Center, 3015 GD Rotterdam, the Netherlands.
Diderich KEM; Department of Clinical Genetics, Erasmus MC University Medical Center, 3015 GD Rotterdam, the Netherlands.
Brooks AS; Department of Clinical Genetics, Erasmus MC University Medical Center, 3015 GD Rotterdam, the Netherlands.
Gribnau J; Department of Developmental Biology, Oncode Institute, Erasmus MC, University Medical Center, 3015 GD Rotterdam, the Netherlands.
Boers RG; Department of Developmental Biology, Oncode Institute, Erasmus MC, University Medical Center, 3015 GD Rotterdam, the Netherlands.
Finestra TR; Department of Developmental Biology, Oncode Institute, Erasmus MC, University Medical Center, 3015 GD Rotterdam, the Netherlands.
Carter LB; Department of Pediatrics, Division of Medical Genetics, Levine Children's Hospital Atrium Health, Charlotte, NC 28203, USA.
Rauch A; Institute of Medical Genetics, University of Zurich, 8952 Schlieren, Zurich, Switzerland.
Gasparini P; Institute for Maternal and Child Health, IRCCS 'Burlo Garofolo,' 34137 Trieste, Italy; Department of Medicine, Surgery & Health Science, University of Trieste, 34143 Trieste, Italy.
Boycott KM; Children's Hospital of Eastern Ontario, Ottawa, ON K1H 8L1, Canada.
Barakat TS; Department of Clinical Genetics, Erasmus MC University Medical Center, 3015 GD Rotterdam, the Netherlands.
Graham JM Jr; Division of Medical Genetics, Department of Pediatrics, Cedars Sinai Medical Center, David Geffen School of Medicine at UCLA, Los Angeles, CA 90048, USA.
Faivre L; Centre de Référence Maladies Rares « Anomalies du Développement et Syndromes Malformatifs », Centre de Génétique, FHU-TRANSLAD et Institut GIMI, 77908 Dijon, France; UMR 1231 GAD, Inserm - Université Bourgogne-Franche Comté, 77908 Dijon, France.
Banka S; Division of Evolution & Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, M13 9 WL Manchester, UK; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, M13 9WL Manchester, UK.
Wang T; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195, USA.
Eichler EE; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195, USA; Howard Hughes Medical Institute, University of Washington, Seattle, WA 98195, USA.
Priolo M; UOSD Genetica Medica del Grande Ospedale Metropolitano 'Bianchi Melacrino Morelli' di Reggio Calabria, 89124 Reggio Calabria, Italy.
Dallapiccola B; Genetics and Rare Disease Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.
Vissers LELM; Department of Human Genetics, Radboudumc, 6525 GA Nijmegen, the Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud University, 6525 GA Nijmegen, the Netherlands.
Sadikovic B; Molecular Genetics Laboratory, Molecular Diagnostics Division, London Health Sciences Centre, London, ON N6A5W9, Canada.
Scott DA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX 77030, USA.
Holder JL Jr; Division of Neurology and Developmental Neuroscience, Baylor College of Medicine, Houston, TX 77030, USA.
Tartaglia M; Genetics and Rare Disease Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy. Electronic address: .

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Źródło:

American journal of human genetics [Am J Hum Genet] 2021 Mar 04; Vol. 108 (3), pp. 502-516. Date of Electronic Publication: 2021 Feb 16.

Typ publikacji:

Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

MeSH Terms:

Chromosome Disorders/*genetics
Chromosomes, Human, Pair 1/*genetics
Chromosomes, Human, X/*genetics
DNA-Binding Proteins/*genetics
RNA-Binding Proteins/*genetics
Adolescent ; Autism Spectrum Disorder/genetics ; Autism Spectrum Disorder/pathology ; Child ; Child, Preschool ; Chromosome Deletion ; Chromosome Disorders/physiopathology ; DNA Methylation/genetics ; Epigenesis, Genetic/genetics ; Female ; Haploinsufficiency/genetics ; Humans ; Intellectual Disability/genetics ; Intellectual Disability/physiopathology ; Male ; Neurodevelopmental Disorders/genetics ; Neurodevelopmental Disorders/physiopathology ; Phenotype ; Young Adult

SCR Disease Name:

Chromosome 1p36 Deletion Syndrome

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 8.

Tytuł:

Ocular findings of albinism in DYRK1A- related intellectual disability syndrome.

Autorzy:

Ernst J; UPMC Eye Center , Pittsburgh, PA, USA.; Ophthalmology Departement, UPMC Children's Hospital of Pittsburgh , Pittsburgh, PA, USA.; Medical University of Warsaw , Warsaw, Poland.
Alabek ML; UPMC Eye Center , Pittsburgh, PA, USA.; Ophthalmology Departement, UPMC Children's Hospital of Pittsburgh , Pittsburgh, PA, USA.
Eldib A; UPMC Eye Center , Pittsburgh, PA, USA.; Ophthalmology Departement, UPMC Children's Hospital of Pittsburgh , Pittsburgh, PA, USA.
Madan-Khetarpal S; Ophthalmology Departement, UPMC Children's Hospital of Pittsburgh , Pittsburgh, PA, USA.; School of Medicine, University of Pittsburgh , Pittsburgh, PA, USA.
Sebastian J; Ophthalmology Departement, UPMC Children's Hospital of Pittsburgh , Pittsburgh, PA, USA.
Bhatia A; Ophthalmology Departement, UPMC Children's Hospital of Pittsburgh , Pittsburgh, PA, USA.; School of Medicine, University of Pittsburgh , Pittsburgh, PA, USA.; UPMC Radiology Department at Children's Hospital of Pittsburgh , Pittsburgh, PA, USA.
Liasis A; UPMC Eye Center , Pittsburgh, PA, USA.; Ophthalmology Departement, UPMC Children's Hospital of Pittsburgh , Pittsburgh, PA, USA.
Nischal KK; UPMC Eye Center , Pittsburgh, PA, USA.; Ophthalmology Departement, UPMC Children's Hospital of Pittsburgh , Pittsburgh, PA, USA.; School of Medicine, University of Pittsburgh , Pittsburgh, PA, USA.

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Źródło:

Ophthalmic genetics [Ophthalmic Genet] 2020 Dec; Vol. 41 (6), pp. 650-655. Date of Electronic Publication: 2020 Aug 24.

Typ publikacji:

Case Reports; Journal Article

MeSH Terms:

Haploinsufficiency*
Albinism/*pathology
Intellectual Disability/*pathology
Protein Serine-Threonine Kinases/*genetics
Protein-Tyrosine Kinases/*genetics
Albinism/complications ; Albinism/genetics ; Evoked Potentials, Visual ; Female ; Humans ; Infant ; Intellectual Disability/complications ; Intellectual Disability/genetics ; Retrospective Studies ; Syndrome

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 9.

Tytuł:

Copy number alterations involving 59 ACMG-recommended secondary findings genes.

Autorzy:

Yatsenko SA; Department of Pathology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.; Magee-Womens Research Institute, Pittsburgh, Pennsylvania, USA.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Aarabi M; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Hu J; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Surti U; Department of Pathology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Ortiz D; Department of Medical Genetics, Childrens Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania, USA.
Madan-Khetarpal S; Department of Medical Genetics, Childrens Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania, USA.
Saller DN; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Bellissimo D; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Rajkovic A; Department of Pathology, University of California San Francisco, San Francisco, California, USA.; Department of Obstetrics, Gynecology and Reproductive Sciences, University of California San Francisco, San Francisco, California, USA.

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Źródło:

Clinical genetics [Clin Genet] 2020 Dec; Vol. 98 (6), pp. 577-588. Date of Electronic Publication: 2020 Oct 10.

Typ publikacji:

Journal Article

MeSH Terms:

Cytogenetic Analysis*
Genomics*
DNA Copy Number Variations/*genetics
Whole Exome Sequencing/*trends
Adolescent ; Adult ; Child ; Child, Preschool ; Exome/genetics ; Female ; Genetic Testing/trends ; Genetics, Medical/trends ; Genome, Human ; Humans ; Infant ; Male ; Microarray Analysis/trends ; Polymorphism, Single Nucleotide/genetics ; Young Adult

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 10.

Tytuł:

Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases.

Autorzy:

Montenegro-Garreaud X; Servicio de Genética y Errores Innatos del Metabolismo, Instituto Nacional de Salud del Niño, Lima, Perú.; División de Investigación, Instituto de Medicina Genética, Lima, Perú.; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.
Hansen AW; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Khayat MM; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Chander V; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Grochowski CM; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Jiang Y; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.
Li H; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.
Mitani T; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Kessler E; Division of Medical Genetics, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Jayaseelan J; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.
Shen H; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.
Gezdirici A; Department of Medical Genetics, Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey.
Pehlivan D; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Section of Neurology, Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
Meng Q; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.
Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Jhangiani SN; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.
Madan-Khetarpal S; Division of Medical Genetics, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Scott DA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, Texas, USA.
Abarca-Barriga H; Servicio de Genética y Errores Innatos del Metabolismo, Instituto Nacional de Salud del Niño, Lima, Perú.; Facultad de Ciencias de la Salud, Medicina Humana, Universidad Científica del Sur, Lima, Perú.
Trubnykova M; Servicio de Genética y Errores Innatos del Metabolismo, Instituto Nacional de Salud del Niño, Lima, Perú.; Area Preclínica, Facultad de Ciencias de la Salud, Universidad Peruana de Ciencias Aplicadas, Lima, Perú.
Gingras MC; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, Texas, USA.
Muzny DM; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Posey JE; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Liu P; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Baylor Genetics, Houston, Texas, USA.
Lupski JR; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Department of Pediatrics, Texas Children's Hospital, Houston, Texas, USA.; Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
Gibbs RA; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.

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Źródło:

Human mutation [Hum Mutat] 2020 Dec; Vol. 41 (12), pp. 2094-2104. Date of Electronic Publication: 2020 Oct 08.

Typ publikacji:

Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Review

MeSH Terms:

Genes, Dominant*
Genetic Predisposition to Disease*
Kinesins/*genetics
Mutation/*genetics
Child ; Child, Preschool ; Family ; Female ; Humans ; Male ; Pedigree ; Peru ; Phenotype

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 11.

Tytuł:

Phenotypic expansion of Bosch-Boonstra-Schaaf optic atrophy syndrome and further evidence for genotype-phenotype correlations.

Autorzy:

Rech ME; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, Texas, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
McCarthy JM; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, Texas, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Chen CA; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, Texas, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Edmond JC; Department of Ophthalmology, Dell Medical School, University of Texas at Austin, Austin, Texas, USA.; Division of Ophthalmology, Texas Children's Hospital, Houston, Texas, USA.; Department of Ophthalmology, Baylor College of Medicine, Houston, Texas, USA.
Shah VS; Division of Ophthalmology, Texas Children's Hospital, Houston, Texas, USA.; Department of Ophthalmology, Baylor College of Medicine, Houston, Texas, USA.
Bosch DGM; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
Berry GT; Division of Genetics and Genomics, Manton Center for Orphan Disease Research Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Williams L; Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania, USA.
Madan-Khetarpal S; Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania, USA.
Niyazov D; Department of Pediatrics, Ochsner Health System and University of Queensland, New Orleans, Louisiana, USA.
Shaw-Smith C; Department of Clinical Genetics, Royal Devon and Exeter NHS Foundation Trust, Exeter, UK.
Kovar EM; Section of Hematology and Oncology, Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
Lupo PJ; Section of Hematology and Oncology, Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
Schaaf CP; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, Texas, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Heidelberg University, Institute of Human Genetics, Heidelberg, Germany.

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Źródło:

American journal of medical genetics. Part A [Am J Med Genet A] 2020 Jun; Vol. 182 (6), pp. 1426-1437. Date of Electronic Publication: 2020 Apr 10.

Typ publikacji:

Journal Article

MeSH Terms:

COUP Transcription Factor I/*genetics
Intellectual Disability/*genetics
Optic Atrophies, Hereditary/*genetics
Seizures/*genetics
Codon, Nonsense/genetics ; DNA-Binding Proteins ; Female ; Frameshift Mutation/genetics ; Genetic Association Studies ; Humans ; Intellectual Disability/complications ; Intellectual Disability/physiopathology ; Male ; Mutation/genetics ; Optic Atrophies, Hereditary/complications ; Optic Atrophies, Hereditary/physiopathology ; Point Mutation/genetics ; Seizures/complications ; Seizures/physiopathology

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 12.

Tytuł:

Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veins

Autorzy:

Szafranski, P.
Gambin, T.
Dharmadhikari, A.V.
Akdemir, K.C.
Jhangiani, S.N.
Schuette, J.
Godiwala, N.
Yatsenko, S.A.
Sebastian, J.
Madan-Khetarpal, S.
Surti, U.
Abellar, R.G.
Bateman, D.A.
Wilson, A.L.
Markham, M.H.
Slamon, J.
Santos-Simarro, F.
Palomares, M.
Nevado, J.
Lapunzina, P.
Chung, B.H.
Wong, W.L.
Chu, Y.W.
Mok, G.T.
Kerem, E.
Reiter, J.
Ambalavanan, N.
Anderson, S.A.
Kelly, D.R.
Shieh, J.
Rosenthal, T.C.
Scheible, K.
Steiner, L.
Iqbal, M.A.
McKinnon, M.L.
Hamilton, S.J.
Schlade-Bartusiak, K.
English, D.
Hendson, G.
Roeder, E.R.
DeNapoli, T.S.
Littlejohn, R.O.
Wolff, D.J.
Wagner, C.L.
Yeung, A.
Francis, D.
Fiorino, E.K.
Edelman, M.
Fox, J.
Hayes, D.A.
Janssens, S.
De Baere, E.
Menten, B.
Loccufier, A.
Vanwalleghem, L.
Moerman, P.
Sznajer, Y.
Lay, A.S.
Kussmann, J.L.
Chawla, J.
Payton, D.J.
Phillips, G.E.
Brosens, E.
Tibboel, D.
Klein, A.
Maystadt, I.
Fisher, R.
Sebire, N.
Male, A.
Chopra, M.
Pinner, J.
Malcolm, G.
Peters, G.
Arbuckle, S.
Lees, M.
Mead, Z.
Quarrell, O.
Sayers, R.
Owens, M.
Shaw-Smith, C.
Lioy, J.
McKay, E.
de Leeuw, N.
Feenstra, I.
Spruijt, L.
Elmslie, F.
Thiruchelvam, T.
Bacino, C.A.
Langston, C.
Lupski, J.R.
Sen, P.
Popek, E.
Stankiewicz, P.

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Temat:

Chromosomes, Human, Pair 16
Comparative Genomic Hybridization
Female
Forkhead Transcription Factors
Genes, Lethal
High-Throughput Nucleotide Sequencing
Humans
Infant, Newborn
Male
Pedigree
Persistent Fetal Circulation Syndrome
Pulmonary Alveoli
Pulmonary Veins
Sequence Deletion
Genome, Human
Genomic Imprinting
Article
Genetics(clinical)
Genetics
Chromosome 16
Alveolar capillary dysplasia
medicine.disease
medicine
Uniparental disomy
Exome sequencing
Genomic imprinting
Locus (genetics)
Molecular biology
Copy-number variation
Biology
Sanger sequencing
symbols.namesake
symbols

Źródło:

Human Genetics, 135, 569-586

Opis pliku:

application/pdf

Dostępność:

https://explore.openaire.eu/search/publication?articleId=doi_dedup___::940199cff9fdefb150d9d6b25e41e0da
https://repositoriosaludmadrid.es/handle/20.500.12530/26871

• na półce

Szczegóły

Skocz do pozycji: 13.

Tytuł:

Four children with postnatally diagnosed mosaic trisomy 12: Clinical features, literature review, and current diagnostic capabilities of genetic testing.

Autorzy:

Hu J; Pittsburgh Cytogenetics Laboratory, UPMC Magee-Womens Hospital, Pittsburgh, Pennsylvania.; Department of Obstetrics, Gynecology & Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Ou Z; Pittsburgh Cytogenetics Laboratory, UPMC Magee-Womens Hospital, Pittsburgh, Pennsylvania.
Surti U; Pittsburgh Cytogenetics Laboratory, UPMC Magee-Womens Hospital, Pittsburgh, Pennsylvania.; Department of Obstetrics, Gynecology & Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.; Department of Pathology, University of Pittsburgh, UPMC Magee-Womens Hospital, Pittsburgh, Pennsylvania.
Kochmar S; Pittsburgh Cytogenetics Laboratory, UPMC Magee-Womens Hospital, Pittsburgh, Pennsylvania.
Hoffner L; Department of Pathology, University of Pittsburgh, UPMC Magee-Womens Hospital, Pittsburgh, Pennsylvania.
Madan-Khetarpal S; Department of Medical Genetics, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.
Arnold GL; Department of Medical Genetics, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.
Walsh L; Department of Medical Genetics, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.
Acquaro R; Department of Medical Genetics, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.
Sebastian J; Department of Medical Genetics, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.
Yatsenko SA; Pittsburgh Cytogenetics Laboratory, UPMC Magee-Womens Hospital, Pittsburgh, Pennsylvania.; Department of Obstetrics, Gynecology & Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.; Department of Pathology, University of Pittsburgh, UPMC Magee-Womens Hospital, Pittsburgh, Pennsylvania.

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Źródło:

American journal of medical genetics. Part A [Am J Med Genet A] 2020 Apr; Vol. 182 (4), pp. 813-822. Date of Electronic Publication: 2020 Jan 08.

Typ publikacji:

Case Reports; Journal Article; Review

MeSH Terms:

Abnormalities, Multiple/*diagnosis
Chromosome Disorders/*diagnosis
Congenital Abnormalities/*diagnosis
Developmental Disabilities/*diagnosis
Trisomy/*genetics
Abnormalities, Multiple/genetics ; Child ; Child, Preschool ; Chromosome Disorders/genetics ; Chromosomes, Human, Pair 12/genetics ; Congenital Abnormalities/genetics ; Developmental Disabilities/genetics ; Female ; Genetic Testing ; Humans ; Infant ; Infant, Newborn ; Male ; Mosaicism ; Phenotype ; Prenatal Diagnosis

SCR Disease Name:

Chromosome 12, 12p trisomy; Chromosome 12, trisomy 12q

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 14.

Tytuł:

Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling.

Autorzy:

Johnson BV; University of Adelaide and Robinson Research Institute, Adelaide, Australia.
Kumar R; University of Adelaide and Robinson Research Institute, Adelaide, Australia.
Oishi S; School of Biomedical Sciences, The University of Queensland, Brisbane, Australia.
Alexander S; Queensland Brain Institute, The University of Queensland, Brisbane, Australia; Queensland Centre for Mental Health Research, Wacol, Queensland, Australia.
Kasherman M; School of Biomedical Sciences, The University of Queensland, Brisbane, Australia; Griffith Institute for Drug Discovery, Griffith University, Brisbane, Australia.
Vega MS; Queensland Brain Institute, The University of Queensland, Brisbane, Australia.
Ivancevic A; University of Adelaide and Robinson Research Institute, Adelaide, Australia; BioFrontiers Institute, University of Colorado Boulder, Boulder, Colorado.
Gardner A; University of Adelaide and Robinson Research Institute, Adelaide, Australia.
Domingo D; University of Adelaide and Robinson Research Institute, Adelaide, Australia.
Corbett M; University of Adelaide and Robinson Research Institute, Adelaide, Australia.
Parnell E; Department of Physiology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Yoon S; Department of Physiology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Oh T; Department of Medical Genetics, British Columbia Women's Hospital and University of British Columbia, Vancouver, British Columbia, Canada.
Lines M; Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
Lefroy H; Oxford Centre for Genomic Medicine, Oxford University Hospitals National Health Services Foundation Trust, Oxford, United Kingdom.
Kini U; Oxford Centre for Genomic Medicine, Oxford University Hospitals National Health Services Foundation Trust, Oxford, United Kingdom.
Van Allen M; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
Grønborg S; Center for Rare Diseases, Department of Pediatrics and Department of Clinical Genetics, University Hospital Copenhagen, Copenhagen, Denmark.
Mercier S; Service de Génétique Médicale, Centre Hospitalier Universitaire Nantes and l'Institut du Thorax, Institut National de la Santé et de la Recherche Médicale, Centre National de la Recherche Scientifique, Université de Nantes, Nantes, France.
Küry S; Service de Génétique Médicale, Centre Hospitalier Universitaire Nantes and l'Institut du Thorax, Institut National de la Santé et de la Recherche Médicale, Centre National de la Recherche Scientifique, Université de Nantes, Nantes, France.
Bézieau S; Service de Génétique Médicale, Centre Hospitalier Universitaire Nantes and l'Institut du Thorax, Institut National de la Santé et de la Recherche Médicale, Centre National de la Recherche Scientifique, Université de Nantes, Nantes, France.
Pasquier L; Service de Génétique Clinique, Centre de Référence Déficiences Intellectuelles de Causes Rares, Centre Hospitalier Universitaire Hôpital Sud, Rennes, France.
Raynaud M; Centre Hospitalier Régional Universitaire de Tours, Service de Génétique, Unité Nixte de Recherche 1253, iBrain, Université de Tours, Institut National de la Santé et de la Recherche Médicale, Tours, France.
Afenjar A; Groupe de Recherche Clinique No. 19, ConCer-LD, Département de Génétique, Assistance Publique-Hôpitaux de Paris, Hôpital Armand Trousseau, Centres de Référence Maladies Rares des Déficits Intellectuels de Causes Rares, Paris, France.
Billette de Villemeur T; Sorbonne Université, Groupe de Recherche Clinique No. 19, ConCer-LD, Neuropédiatrie, Centres de Référence Maladies Rares Neurogénétique, Institut National de la Santé et de la Recherche Médicale, Assistance Publique-Hôpitaux de Paris, Hôpital Armand Trousseau, Paris, France.
Keren B; Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, France.
Désir J; Erasme University Hospital, Université Libre de Bruxelles, Brussels, Belgium.
Van Maldergem L; Centre de Génétique Humaine, Université de Franche-Comté, Besançon, France.
Marangoni M; Erasme University Hospital, Université Libre de Bruxelles, Brussels, Belgium.
Dikow N; Institute of Human Genetics, Heidelberg University, Heidelberg, Germany.
Koolen DA; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
VanHasselt PM; Department of Metabolic Diseases, University Medical Center Utrecht, Utrecht, The Netherlands.
Weiss M; Department of Clinical Genetics, Vrije Universiteit University Medical Center, Amsterdam, The Netherlands.
Zwijnenburg P; Medical Genetics Unit, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.
Sa J; Medical Genetics Unit, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.
Reis CF; Medical Genetics Unit, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.
López-Otín C; Departamento de Bioquímica y Biología Molecular, Instituto Universitário de Oncología del Principado de Asturias, Universidad de Oviedo, Oviedo, Spain; Centro de Investigación Biomédica en Red de Cáncer, Spain.
Santiago-Fernández O; Departamento de Bioquímica y Biología Molecular, Instituto Universitário de Oncología del Principado de Asturias, Universidad de Oviedo, Oviedo, Spain.
Fernández-Jaén A; Unidad de Neurología Infantil, Hospital Universitário Quirón Madrid, Madrid, Spain.
Rauch A; Institute of Medical Genetics, University of Zurich, Schlieren, Switzerland.
Steindl K; Institute of Medical Genetics, University of Zurich, Schlieren, Switzerland.
Joset P; Institute of Medical Genetics, University of Zurich, Schlieren, Switzerland.
Goldstein A; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Madan-Khetarpal S; Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.
Infante E; Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.
Zackai E; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Mcdougall C; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Narayanan V; Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, Arizona.
Ramsey K; Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, Arizona.
Mercimek-Andrews S; Division of Clinical and Metabolic Genetics, Department of Pediatrics, University of Toronto, The Hospital for Sick Children, Toronto, Ontario, Canada.
Pena L; Division of Human Genetics, Cincinnati Children's Hospital; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Shashi V; Department of Pediatrics, Division of Medical Genetics, Duke University Medical Center, Durham, North Carolina.
Schoch K; Department of Pediatrics, Division of Medical Genetics, Duke University Medical Center, Durham, North Carolina.
Sullivan JA; Department of Pediatrics, Division of Medical Genetics, Duke University Medical Center, Durham, North Carolina.
Pinto E Vairo F; Department of Clinical Genomics, Mayo Clinic, Rochester, Minnesota; Center for Individualized Medicine, Mayo Clinic, Rochester, Minnesota.
Pichurin PN; Department of Clinical Genomics, Mayo Clinic, Rochester, Minnesota.
Ewing SA; Department of Clinical Genomics, Mayo Clinic, Rochester, Minnesota.
Barnett SS; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.
Klee EW; Department of Clinical Genomics, Mayo Clinic, Rochester, Minnesota.
Perry MS; Jane and John Justin Neuroscience Center, Cook Children's Medical Center, Fort Worth, Texas.
Koenig MK; Department of Pediatrics, University of Texas Medical School at Houston, Houston, Texas.
Keegan CE; Division of Genetics, Department of Pediatrics, University of Michigan, Ann Arbor, Michigan.
Schuette JL; Division of Genetics, Department of Pediatrics, University of Michigan, Ann Arbor, Michigan.
Asher S; Translational Medicine & Human Genetics, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania.
Perilla-Young Y; Division of Pediatric Genetics and Metabolism, University of North Carolina, Chapel Hill, North Carolina.
Smith LD; Division of Pediatric Genetics and Metabolism, University of North Carolina, Chapel Hill, North Carolina.
Rosenfeld JA; Baylor College of Medicine, Houston, Texas.
Bhoj E; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Kaplan P; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Li D; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Oegema R; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
van Binsbergen E; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
van der Zwaag B; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
Smeland MF; Department of Medical Genetics, University Hospital of North Norway, Tromsø, Norway.
Cutcutache I; Translational Medicine, UCB Pharma, Slough, United Kingdom.
Page M; Translational Medicine, UCB Pharma, Braine-l'Alleud, Belgium.
Armstrong M; Translational Medicine, UCB Pharma, Braine-l'Alleud, Belgium.
Lin AE; Medical Genetics Unit, Mass General Hospital for Children, Boston, Massachusetts.
Steeves MA; Medical Genetics Unit, Mass General Hospital for Children, Boston, Massachusetts.
Hollander ND; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Hoffer MJV; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Reijnders MRF; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.
Demirdas S; Department of Clinical Genetics, Erasmus University Medical Center, Rotterdam, The Netherlands.
Koboldt DC; Nationwide Children's Hospital, Columbus, Ohio.
Bartholomew D; Nationwide Children's Hospital, Columbus, Ohio.
Mosher TM; Nationwide Children's Hospital, Columbus, Ohio.
Hickey SE; Department of Pediatrics, The Ohio State University College of Medicine, Columbus, Ohio.
Shieh C; David Geffen School of Medicine, University of California-Los Angeles, California.
Sanchez-Lara PA; Department of Pediatrics, Cedars-Sinai Medical Center, Los Angeles, California.
Graham JM Jr; Department of Pediatrics, Cedars-Sinai Medical Center, Los Angeles, California.
Tezcan K; Department of Genetics, Kaiser Permanente, Sacramento, California.
Schaefer GB; Section of Genetics and Metabolism, University of Arkansas for Medical Sciences, Little Rock, Arkansas.
Danylchuk NR; Department of Genetic Counseling, University of Arkansas for Medical Sciences, Little Rock, Arkansas.
Asamoah A; Department of Pediatrics, University of Louisville School of Medicine, Louisville, Kentucky.
Jackson KE; Department of Pediatrics, University of Louisville School of Medicine, Louisville, Kentucky.
Yachelevich N; Clinical Genetics Services, Department of Pediatrics, New York University School of Medicine, New York, New York.
Au M; Department of Pediatrics, Cedars-Sinai Medical Center, Los Angeles, California.
Pérez-Jurado LA; University of Adelaide and Robinson Research Institute, Adelaide, Australia; Women's and Children's Hospital, Adelaide, Australia; South Australian Health and Medical Research Institute, Adelaide, South Australia; Hospital del Mar Research Institute, Network Research Centre for Rare Diseases and Universitat Pompeu Fabra, Barcelona, Spain.
Kleefstra T; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Penzes P; Department of Physiology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Wood SA; Griffith Institute for Drug Discovery, Griffith University, Brisbane, Australia.
Burne T; Queensland Brain Institute, The University of Queensland, Brisbane, Australia; Queensland Centre for Mental Health Research, Wacol, Queensland, Australia.
Pierson TM; Department of Pediatrics, Cedars-Sinai Medical Center, Los Angeles, California; Department of Neurology and the Board of Governors Regenerative Medicine Institute, Cedars-Sinai Medical Center, Los Angeles, California.
Piper M; School of Biomedical Sciences, The University of Queensland, Brisbane, Australia; Queensland Brain Institute, The University of Queensland, Brisbane, Australia.
Gécz J; University of Adelaide and Robinson Research Institute, Adelaide, Australia; South Australian Health and Medical Research Institute, Adelaide, South Australia. Electronic address: .
Jolly LA; University of Adelaide and Robinson Research Institute, Adelaide, Australia. Electronic address: .

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Corporate Authors:

Undiagnosed Diseases Network

Źródło:

Biological psychiatry [Biol Psychiatry] 2020 Jan 15; Vol. 87 (2), pp. 100-112. Date of Electronic Publication: 2019 Jun 29.

Typ publikacji:

Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

MeSH Terms:

Developmental Disabilities*/genetics
Intellectual Disability*/genetics
Transforming Growth Factor beta*
Animals ; Female ; Haploinsufficiency ; Humans ; Male ; Mice ; Phenotype ; Signal Transduction ; Ubiquitin Thiolesterase/genetics ; Ubiquitin Thiolesterase/metabolism

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 15.

Tytuł:

Syndromic and Systemic Diagnoses Associated With Isolated Sagittal Synostosis.

Autorzy:

Davis AA; Department of Ophthalmology, UPMC Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, Pittsburgh, Pa.
Haredy MM; Department of Plastic Surgery, UPMC Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, Pittsburgh Pa.; Plastic Surgery Department, Cleft and Craniofacial Unit, Sohag University Hospital, Sohag, Egypt.
Huey J; Department of Ophthalmology, UPMC Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, Pittsburgh, Pa.
Scanga H; Department of Ophthalmology, UPMC Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, Pittsburgh, Pa.
Zuccoli G; Department of Radiology, UPMC Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, Pittsburgh, Pa.; Department of Radiology, Children's Hospital of Philadelphia, Philadelphia, Pa.
Pollack IF; Department of Neurosurgery, UPMC Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, Pittsburgh, Pa.
Tamber MS; Department of Neurosurgery, UPMC Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, Pittsburgh, Pa.; †Department of Medical Genetics, UPMC Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, Pittsburgh, Pa.
Goldstein J; Department of Plastic Surgery, UPMC Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, Pittsburgh Pa.
Madan-Khetarpal S; UBC Department of Surgery, Division of Neurosurgery, BC Children's Hospital, Vancouver, British Columbia.
Nischal KK; Department of Ophthalmology, UPMC Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, Pittsburgh, Pa.; ‡UPMC Eye center, University of Pittsburgh Medical Center, Pittsburgh, Pa.

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Źródło:

Plastic and reconstructive surgery. Global open [Plast Reconstr Surg Glob Open] 2019 Dec 30; Vol. 7 (12), pp. e2540. Date of Electronic Publication: 2019 Dec 30 (Print Publication: 2019).

Typ publikacji:

Journal Article

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 16.

Tytuł:

Reticular Dysgenesis and Mitochondriopathy Induced by Adenylate Kinase 2 Deficiency with Atypical Presentation.

Autorzy:

Ghaloul-Gonzalez L; Division of Medical Genetics, Department of Pediatrics, University of Pittsburgh, Pittsburgh, PA, USA. .; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA. .
Mohsen AW; Division of Medical Genetics, Department of Pediatrics, University of Pittsburgh, Pittsburgh, PA, USA.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
Karunanidhi A; Division of Medical Genetics, Department of Pediatrics, University of Pittsburgh, Pittsburgh, PA, USA.
Seminotti B; Division of Medical Genetics, Department of Pediatrics, University of Pittsburgh, Pittsburgh, PA, USA.
Chong H; Division of Pulmonology, Allergy and Immunology, Department of Pediatrics, University of Pittsburgh, Pittsburgh, PA, USA.
Madan-Khetarpal S; Division of Medical Genetics, Department of Pediatrics, University of Pittsburgh, Pittsburgh, PA, USA.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
Sebastian J; Division of Medical Genetics, Department of Pediatrics, University of Pittsburgh, Pittsburgh, PA, USA.
Vockley CW; Division of Medical Genetics, Department of Pediatrics, University of Pittsburgh, Pittsburgh, PA, USA.
Reyes-Múgica M; Division of Pediatric Pathology, Department of Pathology, University of Pittsburgh, Pittsburgh, PA, USA.
Vander Lugt MT; Division of Blood and Marrow Transplantation and Cellular Therapies, Department of Pediatrics, University of Pittsburgh, Pittsburgh, PA, USA.
Vockley J; Division of Medical Genetics, Department of Pediatrics, University of Pittsburgh, Pittsburgh, PA, USA.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.

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Źródło:

Scientific reports [Sci Rep] 2019 Oct 31; Vol. 9 (1), pp. 15739. Date of Electronic Publication: 2019 Oct 31.

Typ publikacji:

Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

MeSH Terms:

Adenylate Kinase/*genetics
Leukopenia/*diagnosis
Mitochondria/*metabolism
Severe Combined Immunodeficiency/*diagnosis
Adenylate Kinase/deficiency ; Bone Marrow/pathology ; Cell Membrane Permeability ; Child, Preschool ; Energy Metabolism ; Fibroblasts/cytology ; Fibroblasts/metabolism ; Homozygote ; Humans ; Leukopenia/genetics ; Male ; Mitochondrial Membranes/metabolism ; Oxygen Consumption ; Pedigree ; Polymorphism, Single Nucleotide ; Reactive Oxygen Species/metabolism ; Severe Combined Immunodeficiency/genetics ; Whole Exome Sequencing

SCR Disease Name:

Reticular dysgenesis

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 17.

Tytuł:

Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism.

Autorzy:

Kim HG; 1Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar.
Rosenfeld JA; 2Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX USA.
Scott DA; 2Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX USA.; 3Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX USA.
Bénédicte G; 4Laboratoires de Diagnostic Génétique, Unité de génétique moléculaire, Nouvel Hôpital Civil, Strasbourg Cedex, France.
Labonne JD; 5Section of Reproductive Endocrinology, Infertility & Genetics, Department of Obstetrics & Gynecology, Augusta University, Augusta, GA USA.
Brown J; 5Section of Reproductive Endocrinology, Infertility & Genetics, Department of Obstetrics & Gynecology, Augusta University, Augusta, GA USA.
McGuire M; Baylor Genetic Laboratories, Houston, TX USA.
Mahida S; 7Kennedy Krieger Institute, Baltimore, MD USA.
Naidu S; 7Kennedy Krieger Institute, Baltimore, MD USA.
Gutierrez J; 3Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX USA.
Lesca G; 8Department of Medical Genetics, Lyon University Hospital, Lyon, France.
des Portes V; 9Department of Pediatric Neurology, Lyon University Hospital, Lyon, France.
Bruel AL; 10Équipe Génétique des Anomalies du Développement (GAD), INSERM, Dijon, France.
Sorlin A; Centre de Génétique, CHU Dijon Bourgogne, Dijon, France.
Xia F; 2Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX USA.
Capri Y; Service de Génétique Clinique, CHU Robert Debré, Paris, France.
Muller E; 13Clinical Genetics, Stanford Children's Health at CPMC, San Francisco, CA USA.
McKnight D; 14GeneDx, Gaithersburg, MD USA.
Torti E; 14GeneDx, Gaithersburg, MD USA.
Rüschendorf F; 15Max Delbrück Center (MDC) for Molecular Medicine, Berlin, Germany.
Hummel O; 15Max Delbrück Center (MDC) for Molecular Medicine, Berlin, Germany.
Islam Z; 16Diabetes Center, Qatar Biomedical Research Institute (QBRI), Hamad Bin Khalifa University, Doha, Qatar.
Kolatkar PR; 16Diabetes Center, Qatar Biomedical Research Institute (QBRI), Hamad Bin Khalifa University, Doha, Qatar.
Layman LC; 5Section of Reproductive Endocrinology, Infertility & Genetics, Department of Obstetrics & Gynecology, Augusta University, Augusta, GA USA.; 17Department of Neuroscience and Regenerative Medicine, Augusta University, Augusta, GA USA.
Ryu D; 18Department of Statistics and Actuarial Science, Northern Illinois University, DeKalb, IL USA.
Kong IK; 19Department of Animal Science, Division of Applied Life Science (BK21plus), Gyeongsang National University, Jinju, Korea.
Madan-Khetarpal S; 20Pediatric Medical Genetics, Children's Hospital of Pittsburgh, Pittsburgh, PA USA.
Kim CH; 21Department of Biology, Chungnam National University, Daejeon, Korea.

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Źródło:

Molecular autism [Mol Autism] 2019 Oct 22; Vol. 10, pp. 35. Date of Electronic Publication: 2019 Oct 22 (Print Publication: 2019).

Typ publikacji:

Case Reports; Journal Article; Research Support, Non-U.S. Gov't

MeSH Terms:

Behavior*
Autistic Disorder/*genetics
Craniofacial Abnormalities/*genetics
Epilepsy/*genetics
Histone Deacetylases/*genetics
Intellectual Disability/*genetics
Muscle Hypotonia/*genetics
Adolescent ; Amino Acid Sequence ; Autistic Disorder/complications ; Brain/metabolism ; Child ; Child, Preschool ; Craniofacial Abnormalities/complications ; Epilepsy/complications ; Female ; Histone Deacetylases/chemistry ; Histone Deacetylases/metabolism ; Humans ; Infant ; Infant, Newborn ; Intellectual Disability/complications ; Male ; Muscle Hypotonia/complications ; Mutation/genetics ; Protein Domains ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; Syndrome

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 18.

Tytuł:

Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmission.

Autorzy:

Guo H; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
Li Y; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Shen L; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Wang T; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
Jia X; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Liu L; Institute of Life Sciences, Key Laboratory of Developmental Genes and Human Disease, Southeast University, Nanjing, Jiangsu, China.
Xu T; Department of Neurobiology, Beijing Key Laboratory of Neural Regeneration and Repair, Beijing Laboratory of Brain Disorders (Ministry of Science and Technology), Beijing Institute of Brain Disorders, Capital Medical University, Beijing, China.
Ou M; Institute of Life Sciences, Key Laboratory of Developmental Genes and Human Disease, Southeast University, Nanjing, Jiangsu, China.
Hoekzema K; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
Wu H; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Gillentine MA; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
Liu C; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Ni H; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Peng P; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Zhao R; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Zhang Y; Key Laboratory of Developmental Disorders in Children, Liuzhou Maternity and Child Healthcare Hospital, Liuzhou, Guangxi, China.
Phornphutkul C; Division of Human Genetics, Warren Alpert Medical School of Brown University, Hasbro Children's Hospital/Rhode Island Hospital, Providence, RI, USA.
Stegmann APA; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, Netherlands.
Prada CE; Department of Pediatrics, University of Cincinnati College of Medicine, Division of Human Genetics, Cincinnati Children's Hospital, Cincinnati, OH, USA.
Hopkin RJ; Department of Pediatrics, University of Cincinnati College of Medicine, Division of Human Genetics, Cincinnati Children's Hospital, Cincinnati, OH, USA.
Shieh JT; Institute for Human Genetics and Department of Pediatrics, University of California, San Francisco, San Francisco, CA, USA.
McWalter K; GeneDx, Gaithersburg, MD, USA.
Monaghan KG; GeneDx, Gaithersburg, MD, USA.
van Hasselt PM; University Medical Center Utrecht, Utrecht, Netherlands.
van Gassen K; University Medical Center Utrecht, Utrecht, Netherlands.
Bai T; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Long M; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Han L; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Quan Y; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Chen M; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Zhang Y; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Li K; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Zhang Q; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Tan J; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Zhu T; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Liu Y; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Pang N; Department of Pediatrics, Xiangya Hospital, Central South University, Changsha, China.
Peng J; Department of Pediatrics, Xiangya Hospital, Central South University, Changsha, China.
Scott DA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX, USA.
Lalani SR; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Azamian M; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Mancini GMS; Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, Netherlands.
Adams DJ; Goryeb Children's Hospital, Atlantic Health System, Morristown, NJ, USA.
Kvarnung M; Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden.; Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden.
Lindstrand A; Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden.; Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden.
Nordgren A; Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden.; Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden.
Pevsner J; Department of Neurology, Kennedy Krieger Institute, Baltimore, MD, USA.; Program in Human Genetics, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Osei-Owusu IA; Department of Neurology, Kennedy Krieger Institute, Baltimore, MD, USA.; Program in Human Genetics, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Romano C; Oasi Research Institute-IRCCS, Troina, Italy.
Calabrese G; Oasi Research Institute-IRCCS, Troina, Italy.
Galesi O; Oasi Research Institute-IRCCS, Troina, Italy.
Gecz J; School of Medicine and the Robinson Research Institute, University of Adelaide at the Women's and Children's Hospital, Adelaide, South Australia, Australia.
Haan E; Adult Genetics Unit, Royal Adelaide Hospital, and School of Medicine, University of Adelaide, Adelaide, South Australia, Australia.
Ranells J; Department of Pediatrics, University of South Florida, Tampa, FL, USA.
Racobaldo M; Department of Pediatrics, University of South Florida, Tampa, FL, USA.
Nordenskjold M; Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden.; Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden.
Madan-Khetarpal S; Division of Medical Genetics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, USA.
Sebastian J; Division of Medical Genetics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, USA.
Ball S; Central Washington Genetics Program, Virginia Mason Memorial, Yakima, WA, USA.
Zou X; Children Development Behavior Center of the Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China.
Zhao J; Mental Health Institute of the Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Hu Z; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Xia F; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Baylor Genetics, Houston, TX, USA.
Liu P; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Baylor Genetics, Houston, TX, USA.
Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
de Vries BBA; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, Netherlands.
Bernier RA; Department of Psychiatry, University of Washington, Seattle, WA, USA.
Xu ZD; Department of Neurobiology, Beijing Key Laboratory of Neural Regeneration and Repair, Beijing Laboratory of Brain Disorders (Ministry of Science and Technology), Beijing Institute of Brain Disorders, Capital Medical University, Beijing, China.
Li H; Key Laboratory of Developmental Disorders in Children, Liuzhou Maternity and Child Healthcare Hospital, Liuzhou, Guangxi, China.
Xie W; Institute of Life Sciences, Key Laboratory of Developmental Genes and Human Disease, Southeast University, Nanjing, Jiangsu, China.
Hufnagel RB; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, NIH, Bethesda, MD, USA.
Eichler EE; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.; Howard Hughes Medical Institute, University of Washington, Seattle, WA, USA.
Xia K; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.; Key Laboratory of Medical Information Research, Central South University, Changsha, Hunan, China.; CAS Center for Excellence in Brain Science and Intelligences Technology (CEBSIT), Chinese Academy of Sciences, Shanghai 200030, China.; Hunan Key Laboratory of Animal Models for Human Diseases, Central South University, Changsha, Hunan 410078, China.

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Źródło:

Science advances [Sci Adv] 2019 Sep 25; Vol. 5 (9), pp. eaax2166. Date of Electronic Publication: 2019 Sep 25 (Print Publication: 2019).

Typ publikacji:

Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

MeSH Terms:

Genetic Predisposition to Disease*
Genetic Variation*
Autistic Disorder/*diagnosis
Autistic Disorder/*genetics
DNA-Binding Proteins/*genetics
Neurogenesis/*genetics
RNA-Binding Proteins/*genetics
Synaptic Transmission/*genetics
Adolescent ; Animals ; Autistic Disorder/psychology ; Child ; Child, Preschool ; DNA-Binding Proteins/metabolism ; Disease Models, Animal ; Female ; Genetic Association Studies ; Genetic Loci ; Humans ; Male ; Mice ; Neurons/metabolism ; Pedigree ; Phenotype ; RNA-Binding Proteins/metabolism ; Synapses/genetics ; Synapses/metabolism ; Young Adult

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 19.

Tytuł:

RASopathy in Patients With Isolated Sagittal Synostosis.

Autorzy:

Davis AA; Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, USA.
Zuccoli G; Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, USA.
Haredy MM; Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, USA.
Losee J; Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, USA.
Pollack IF; Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, USA.
Madan-Khetarpal S; Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, USA.
Goldstein JA; Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, USA.
Nischal KK; Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, USA.

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Źródło:

Global pediatric health [Glob Pediatr Health] 2019 May 12; Vol. 6, pp. 2333794X19846774. Date of Electronic Publication: 2019 May 12 (Print Publication: 2019).

Typ publikacji:

Journal Article

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 20.

Tytuł:

Autism spectrum disorder in females with ARHGEF9 alterations and a random pattern of X chromosome inactivation.

Autorzy:

Aarabi M; Medical Genetics & Genomics Laboratories, Magee-Womens Hospital of UPMC, Pittsburgh, PA, Unitetd States; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, PA, Unitetd States.
Kessler E; Medical Genetics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, Unitetd States.
Madan-Khetarpal S; Medical Genetics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, Unitetd States.
Surti U; Medical Genetics & Genomics Laboratories, Magee-Womens Hospital of UPMC, Pittsburgh, PA, Unitetd States; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, PA, Unitetd States; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA, Unitetd States; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, Unitetd States.
Bellissimo D; Medical Genetics & Genomics Laboratories, Magee-Womens Hospital of UPMC, Pittsburgh, PA, Unitetd States; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, PA, Unitetd States.
Rajkovic A; Medical Genetics & Genomics Laboratories, Magee-Womens Hospital of UPMC, Pittsburgh, PA, Unitetd States; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, PA, Unitetd States; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA, Unitetd States; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, Unitetd States; Magee-Womens Research Institute, Pittsburgh, PA, Unitetd States.
Yatsenko SA; Medical Genetics & Genomics Laboratories, Magee-Womens Hospital of UPMC, Pittsburgh, PA, Unitetd States; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, PA, Unitetd States; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA, Unitetd States; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, Unitetd States; Magee-Womens Research Institute, Pittsburgh, PA, Unitetd States. Electronic address: .

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Źródło:

European journal of medical genetics [Eur J Med Genet] 2019 Apr; Vol. 62 (4), pp. 239-242. Date of Electronic Publication: 2018 Jul 23.

Typ publikacji:

Case Reports; Journal Article

MeSH Terms:

Phenotype*
X Chromosome Inactivation*
Autism Spectrum Disorder/*genetics
Rho Guanine Nucleotide Exchange Factors/*genetics
Adolescent ; Autism Spectrum Disorder/pathology ; Child ; Female ; Humans ; Rho Guanine Nucleotide Exchange Factors/metabolism

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 21.

Tytuł:

Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay.

Autorzy:

Machol K; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Rousseau J; Department of Pediatrics, CHU Sainte-Justine Research Center and University of Montreal, Montreal, QC H3T 1C5, Canada.
Ehresmann S; Department of Pediatrics, CHU Sainte-Justine Research Center and University of Montreal, Montreal, QC H3T 1C5, Canada.
Garcia T; Department of Pediatrics, CHU Sainte-Justine Research Center and University of Montreal, Montreal, QC H3T 1C5, Canada.
Nguyen TTM; Department of Pediatrics, CHU Sainte-Justine Research Center and University of Montreal, Montreal, QC H3T 1C5, Canada.
Spillmann RC; Department of Pediatrics, Duke University School of Medicine, Durham, NC 27710, USA.
Sullivan JA; Department of Pediatrics, Duke University School of Medicine, Durham, NC 27710, USA.
Shashi V; Department of Pediatrics, Duke University School of Medicine, Durham, NC 27710, USA.
Jiang YH; Department of Pediatrics and Neurobiology, Program in Genetics and Genomics, Duke University School of Medicine, Durham, NC 27710, USA.
Stong N; Institute for Genomic Medicine, Columbia University, New York, NY 10032, USA.
Fiala E; Department of Pediatrics, Washington University School of Medicine, St. Louis, MO 63110, USA.
Willing M; Department of Pediatrics, Washington University School of Medicine, St. Louis, MO 63110, USA.
Pfundt R; Human Genetics Department, Radboud University Medical Center, 6500 HB Nijmegen, the Netherlands.
Kleefstra T; Human Genetics Department, Radboud University Medical Center, 6500 HB Nijmegen, the Netherlands.
Cho MT; GeneDx, Gaithersburg, MD 20877, USA.
McLaughlin H; GeneDx, Gaithersburg, MD 20877, USA.
Rosello Piera M; Unidad de Genética, Hospital Universitario i Politècnic La Fe, 106, 46026 Valencia, Spain.
Orellana C; Unidad de Genética, Hospital Universitario i Politècnic La Fe, 106, 46026 Valencia, Spain.
Martínez F; Unidad de Genética, Hospital Universitario i Politècnic La Fe, 106, 46026 Valencia, Spain.
Caro-Llopis A; Unidad de Genética, Hospital Universitario i Politècnic La Fe, 106, 46026 Valencia, Spain.
Monfort S; Unidad de Genética, Hospital Universitario i Politècnic La Fe, 106, 46026 Valencia, Spain.
Roscioli T; Neuroscience Research Australia (NeuRA), University of New South Wales, Sydney, NSW 2031, Australia; New South Wales Health Pathology, Randwick, NSW 2217, Australia; Centre for Clinical Genetics, Sydney Children's Hospital, Sydney, NSW 2031, Australia.
Nixon CY; Neuroscience Research Australia (NeuRA), University of New South Wales, Sydney, NSW 2031, Australia.
Buckley MF; New South Wales Health Pathology, Randwick, NSW 2217, Australia.
Turner A; Centre for Clinical Genetics, Sydney Children's Hospital, Sydney, NSW 2031, Australia.
Jones WD; North East Thames Regional Genetics service, Great Ormond Street Hospital for Children NHS Foundation Trust, London WC1N 3JH, UK.
van Hasselt PM; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center, 3584 EA Utrecht, the Netherlands.
Hofstede FC; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center, 3584 EA Utrecht, the Netherlands.
van Gassen KLI; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center, 3584 EA Utrecht, the Netherlands.
Brooks AS; Department of Clinical Genetics, Erasmus Medical Center, 3015 GD Rotterdam, the Netherlands.
van Slegtenhorst MA; Department of Clinical Genetics, Erasmus Medical Center, 3015 GD Rotterdam, the Netherlands.
Lachlan K; Wessex Clinical Genetics Service, University Hospital Southampton NHS Foundation Trust, Southampton SO16 5YA, UK; Human Genetics and Genomic Medicine, Faculty of Medicine, University of Southampton, Southampton SO17 1BJ, UK.
Sebastian J; Department of Medical Genetics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA 15224, USA.
Madan-Khetarpal S; Department of Medical Genetics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA 15224, USA.
Sonal D; Department of Neurogenetics, Kennedy Krieger Institute, Baltimore, MD 21205, USA.
Sakkubai N; Department of Neurogenetics, Kennedy Krieger Institute, Baltimore, MD 21205, USA.
Thevenon J; Centre de Génétique, Centre de Référence Anomalies du Développement et Syndromes Malformatifs de l'Interrégion Est et FHU TRANSLAD, CHU Dijon, 21079 Dijon, France.
Faivre L; Centre de Génétique, Centre de Référence Anomalies du Développement et Syndromes Malformatifs de l'Interrégion Est et FHU TRANSLAD, CHU Dijon, 21079 Dijon, France.
Maurel A; Centre de Génétique, Centre de Référence Anomalies du Développement et Syndromes Malformatifs de l'Interrégion Est et FHU TRANSLAD, CHU Dijon, 21079 Dijon, France.
Petrovski S; AstraZeneca Centre for Genomics Research, Precision Medicine and Genomics, IMED Biotech Unit, AstraZeneca, Cambridge CB2 0AA, UK.
Krantz ID; Department of Pediatrics and Division of Human Genetics, The Children's Hospital of Philadelphia and the Perelman School of Medicine at The University of Pennsylvania, Philadelphia, PA 19104, USA.
Tarpinian JM; Department of Pediatrics and Division of Human Genetics, The Children's Hospital of Philadelphia and the Perelman School of Medicine at The University of Pennsylvania, Philadelphia, PA 19104, USA.
Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Lee BH; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Campeau PM; Department of Pediatrics, CHU Sainte-Justine Research Center and University of Montreal, Montreal, QC H3T 1C5, Canada. Electronic address: .

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Corporate Authors:

Undiagnosed Diseases Network

Źródło:

American journal of human genetics [Am J Hum Genet] 2019 Jan 03; Vol. 104 (1), pp. 164-178. Date of Electronic Publication: 2018 Dec 20.

Typ publikacji:

Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

MeSH Terms:

Mutation*
Developmental Disabilities/*complications
Developmental Disabilities/*genetics
Intellectual Disability/*complications
Intellectual Disability/*genetics
Transcription Factors/*genetics
Abnormalities, Multiple/genetics ; Adolescent ; Child ; Child, Preschool ; DNA-Binding Proteins ; Face/abnormalities ; Female ; Hand Deformities, Congenital/genetics ; Humans ; Male ; Micrognathism/genetics ; Neck/abnormalities ; Reelin Protein ; Syndrome

SCR Disease Name:

Coffin-Siris syndrome

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 22.

Tytuł:

ARHGEF9 gene variant leads to developmental and epileptic encephalopathy: Genotypic phenotype analysis and treatment exploration.

Autorzy:

Yang, Haiyan (AUTHOR)
Liao, Hongmei (AUTHOR)
Gan, Siyi (AUTHOR)
Xiao, Ting (AUTHOR)
Wu, Liwen (AUTHOR)

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Źródło:

Molecular Genetics & Genomic Medicine. Jul2022, Vol. 10 Issue 7, p1-9. 9p.

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 23.

Tytuł:

De novo apparent loss-of-function mutations in PRR12 in three patients with intellectual disability and iris abnormalities.

Autorzy:

Leduc MS; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Houston, TX, 77030-3411, USA.; Baylor Genetics Laboratories, Houston, TX, USA.
Mcguire M; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Houston, TX, 77030-3411, USA.
Madan-Khetarpal S; Children's Hospital of Pittsburgh of UPMC, University of Pittsburgh, Pittsburgh, PA, USA.
Ortiz D; Children's Hospital of Pittsburgh of UPMC, University of Pittsburgh, Pittsburgh, PA, USA.
Hayflick S; Department of Molecular and Medical Genetics, Oregon Health and Sciences University, Portland, OR, USA.
Keller K; Department of Molecular and Medical Genetics, Oregon Health and Sciences University, Portland, OR, USA.
Eng CM; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Houston, TX, 77030-3411, USA.; Baylor Genetics Laboratories, Houston, TX, USA.
Yang Y; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Houston, TX, 77030-3411, USA.; Baylor Genetics Laboratories, Houston, TX, USA.
Bi W; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Houston, TX, 77030-3411, USA. .; Baylor Genetics Laboratories, Houston, TX, USA. .

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Źródło:

Human genetics [Hum Genet] 2018 Mar; Vol. 137 (3), pp. 257-264. Date of Electronic Publication: 2018 Mar 19.

Typ publikacji:

Journal Article

MeSH Terms:

Eye Abnormalities/*genetics
Intellectual Disability/*genetics
Iris Diseases/*genetics
Membrane Proteins/*genetics
Proline-Rich Protein Domains/*genetics
Child ; Child, Preschool ; Exome/genetics ; Eye Abnormalities/physiopathology ; Female ; Haploinsufficiency/genetics ; Heterozygote ; Humans ; Intellectual Disability/physiopathology ; Iris Diseases/physiopathology ; Loss of Function Mutation/genetics ; Male ; Phenotype ; Translocation, Genetic/genetics ; Whole Exome Sequencing

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 24.

Tytuł:

Kaufman oculocerebrofacial syndrome: Novel UBE3B mutations and clinical features in four unrelated patients.

Autorzy:

Yilmaz R; Institute of Human Genetics, University of Ulm, Ulm, Germany.; International Graduate School in Molecular Medicine Ulm, University of Ulm, Ulm, Germany.
Szakszon K; Faculty of Medicine, Institute of Pediatrics, University of Debrecen, Debrecen, Hungary.
Altmann A; St. John Hospital Buda Children's Hospital, Epilepsy Center, Budapest, Hungary.
Altunoglu U; Medical Genetics Department, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey.
Senturk L; Medical Genetics Department, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey.
McGuire M; Baylor Miraca Genetic Laboratories, Houston, Texas.
Calabrese O; Medical Genetic Service, ASL di Imola, Imola, Italy.
Madan-Khetarpal S; University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.
Basel-Vanagaite L; The Raphael Recanati Genetic Institute, Rabin Medical Center, Petach Tikva, Israel.; Pediatric Genetics Unit, Schneider Children's Medical Center of Israel, Petach Tikva, Israel.; Felsenstein Medical Research Center, Rabin Medical Center, Petach Tikva, Israel.; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Borck G; Institute of Human Genetics, University of Ulm, Ulm, Germany.

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Źródło:

American journal of medical genetics. Part A [Am J Med Genet A] 2018 Jan; Vol. 176 (1), pp. 187-193. Date of Electronic Publication: 2017 Nov 21.

Typ publikacji:

Case Reports; Journal Article

MeSH Terms:

Genetic Association Studies*
Mutation*
Phenotype*
Eye Abnormalities/*diagnosis
Eye Abnormalities/*genetics
Intellectual Disability/*diagnosis
Intellectual Disability/*genetics
Limb Deformities, Congenital/*diagnosis
Limb Deformities, Congenital/*genetics
Microcephaly/*diagnosis
Microcephaly/*genetics
Ubiquitin-Protein Ligases/*genetics
Biomarkers ; Child ; DNA Mutational Analysis ; Diagnostic Imaging ; Eye Abnormalities/therapy ; Facies ; Female ; Genetic Heterogeneity ; High-Throughput Nucleotide Sequencing ; Humans ; Infant ; Intellectual Disability/therapy ; Limb Deformities, Congenital/therapy ; Microcephaly/therapy ; Sequence Analysis, DNA

SCR Disease Name:

Kaufman oculocerebrofacial syndrome

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 25.

Tytuł:

Phenotypic and molecular characterisation of CDK13-related congenital heart defects, dysmorphic facial features and intellectual developmental disorders.

Autorzy:

Bostwick BL; Department of Molecular and Human Genetics, Baylor College of Medicine, 6701 Fannin St, Suite 1560, Houston, TX, 77030, USA. .
McLean S; Department of Molecular and Human Genetics, Baylor College of Medicine, 6701 Fannin St, Suite 1560, Houston, TX, 77030, USA.; Department of Pediatrics, Baylor College of Medicine, San Antonio, TX, 78207, USA.
Posey JE; Department of Molecular and Human Genetics, Baylor College of Medicine, 6701 Fannin St, Suite 1560, Houston, TX, 77030, USA.
Streff HE; Department of Molecular and Human Genetics, Baylor College of Medicine, 6701 Fannin St, Suite 1560, Houston, TX, 77030, USA.
Gripp KW; Division of Medical Genetics, A.I. duPont Hospital for Children/Nemours, Wilmington, DE, USA.
Blesson A; Division of Medical Genetics, A.I. duPont Hospital for Children/Nemours, Wilmington, DE, USA.
Powell-Hamilton N; Division of Medical Genetics, A.I. duPont Hospital for Children/Nemours, Wilmington, DE, USA.
Tusi J; Division of Medical Genetics, A.I. duPont Hospital for Children/Nemours, Wilmington, DE, USA.
Stevenson DA; Division of Medical Genetics, Stanford University School of Medicine, Stanford, CA, USA.
Farrelly E; Division of Medical Genetics, Stanford University School of Medicine, Stanford, CA, USA.
Hudgins L; Division of Medical Genetics, Stanford University School of Medicine, Stanford, CA, USA.
Yang Y; Department of Molecular and Human Genetics, Baylor College of Medicine, 6701 Fannin St, Suite 1560, Houston, TX, 77030, USA.; Baylor Genetics, Baylor College of Medicine, Houston, TX, USA.
Xia F; Department of Molecular and Human Genetics, Baylor College of Medicine, 6701 Fannin St, Suite 1560, Houston, TX, 77030, USA.; Baylor Genetics, Baylor College of Medicine, Houston, TX, USA.
Wang X; Department of Molecular and Human Genetics, Baylor College of Medicine, 6701 Fannin St, Suite 1560, Houston, TX, 77030, USA.; Baylor Genetics, Baylor College of Medicine, Houston, TX, USA.
Liu P; Department of Molecular and Human Genetics, Baylor College of Medicine, 6701 Fannin St, Suite 1560, Houston, TX, 77030, USA.; Baylor Genetics, Baylor College of Medicine, Houston, TX, USA.
Walkiewicz M; Department of Molecular and Human Genetics, Baylor College of Medicine, 6701 Fannin St, Suite 1560, Houston, TX, 77030, USA.; Baylor Genetics, Baylor College of Medicine, Houston, TX, USA.
McGuire M; Department of Molecular and Human Genetics, Baylor College of Medicine, 6701 Fannin St, Suite 1560, Houston, TX, 77030, USA.
Grange DK; Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, USA.
Andrews MV; Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, USA.
Hummel M; Department of Pediatrics, Section of Medical Genetics, West Virginia University Health Sciences Center, Morgantown, WV, USA.
Madan-Khetarpal S; Children's Hospital of Pittsburgh of UPMC, University of Pittsburgh, Pittsburgh, PA, USA.
Infante E; Children's Hospital of Pittsburgh of UPMC, University of Pittsburgh, Pittsburgh, PA, USA.
Coban-Akdemir Z; Department of Molecular and Human Genetics, Baylor College of Medicine, 6701 Fannin St, Suite 1560, Houston, TX, 77030, USA.
Miszalski-Jamka K; Division of Magnetic Resonance Imaging, Silesian Center for Heart Disease, Zabrze, Poland.
Jefferies JL; The Heart Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, 6701 Fannin St, Suite 1560, Houston, TX, 77030, USA.
Emrick L; Department of Molecular and Human Genetics, Baylor College of Medicine, 6701 Fannin St, Suite 1560, Houston, TX, 77030, USA.
Nugent KM; Department of Molecular and Human Genetics, Baylor College of Medicine, 6701 Fannin St, Suite 1560, Houston, TX, 77030, USA.; Department of Pediatrics, Baylor College of Medicine, San Antonio, TX, 78207, USA.
Lupski JR; Department of Molecular and Human Genetics, Baylor College of Medicine, 6701 Fannin St, Suite 1560, Houston, TX, 77030, USA.; Texas Children's Hospital, Houston, TX, 77030, USA.; Department of Pediatrics, Baylor College of Medicine, Houston, TX, 77030, USA.; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, 77030, USA.
Belmont JW; Department of Molecular and Human Genetics, Baylor College of Medicine, 6701 Fannin St, Suite 1560, Houston, TX, 77030, USA.
Lee B; Department of Molecular and Human Genetics, Baylor College of Medicine, 6701 Fannin St, Suite 1560, Houston, TX, 77030, USA.
Lalani SR; Department of Molecular and Human Genetics, Baylor College of Medicine, 6701 Fannin St, Suite 1560, Houston, TX, 77030, USA.

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Corporate Authors:

Members of the Undiagnosed Diseases Network

Źródło:

Genome medicine [Genome Med] 2017 Aug 14; Vol. 9 (1), pp. 73. Date of Electronic Publication: 2017 Aug 14.

Typ publikacji:

Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural

MeSH Terms:

Mutation*
Phenotype*
CDC2 Protein Kinase/*genetics
Face/*abnormalities
Heart Defects, Congenital/*metabolism
Intellectual Disability/*metabolism
Adolescent ; Adult ; Child ; Child, Preschool ; Female ; Heart Defects, Congenital/genetics ; Humans ; Infant ; Intellectual Disability/genetics ; Male ; Syndrome

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknieSzczegóły

Skocz do pozycji: 26.

Tytuł:

Infant Botulism in the Very Young Neonate: A Case Series.

Autorzy:

Jackson L; Division of Newborn Medicine, Department of Pediatrics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania.
Madan-Khetarpal S; Division of Medical Genetics, Department of Pediatrics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania.
Naik M; Division of Neurology, Department of Pediatrics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania.
Michaels MG; Division of Infectious Disease, Department of Pediatrics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania.
Riley M; Division of Newborn Medicine, Department of Pediatrics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania.

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Źródło:

AJP reports [AJP Rep] 2017 Jul; Vol. 7 (3), pp. e163-e166. Date of Electronic Publication: 2017 Jul 31.

Typ publikacji:

Case Reports

Raport

• na półce

Szczegóły

Skocz do pozycji: 27.

Tytuł:

6q25.1 (TAB2) microdeletion syndrome: Congenital heart defects and cardiomyopathy.

Autorzy:

Cheng A; Department of Cardiology, University of Washington School of Medicine, Seattle, Washington.
Dinulos MBP; Departments of Pediatrics and Pathology, Section of Medical Genetics, Dartmouth-Hitchcock Medical Center, One Medical Center Drive, Lebanon, New Hampshire.
Neufeld-Kaiser W; Department of Pathology, University of Washington School of Medicine, Seattle, Washington.
Rosenfeld J; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
Kyriss M; Prevention Genetics, Marshfield, Wisconsin.
Madan-Khetarpal S; Department of Medical Genetics, Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.
Risheg H; Laboratory Corporation of America/Dynacare, Seattle, Washington.
Byers PH; Department of Pathology, University of Washington School of Medicine, Seattle, Washington.
Liu YJ; Department of Pathology, University of Washington School of Medicine, Seattle, Washington.

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Źródło:

American journal of medical genetics. Part A [Am J Med Genet A] 2017 Jul; Vol. 173 (7), pp. 1848-1857. Date of Electronic Publication: 2017 May 02.

Typ publikacji:

Journal Article

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 28.

Tytuł:

Chromosome 12q13.13q13.13 microduplication and microdeletion: a case report and literature review.

Autorzy:

Hu J; Center for Clinical Genetics and Genomics, Pittsburgh Cytogenetics Laboratory, Magee-Womens Hospital of UPMC, Pittsburgh, PA 15213 USA.; Department of Obstetrics, Gynecology & Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213 USA.
Ou Z; Center for Clinical Genetics and Genomics, Pittsburgh Cytogenetics Laboratory, Magee-Womens Hospital of UPMC, Pittsburgh, PA 15213 USA.
Infante E; Department of Genetics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA 15224 USA.
Kochmar SJ; Center for Clinical Genetics and Genomics, Pittsburgh Cytogenetics Laboratory, Magee-Womens Hospital of UPMC, Pittsburgh, PA 15213 USA.
Madan-Khetarpal S; Department of Genetics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA 15224 USA.
Hoffner L; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213 USA.
Parsazad S; Center for Clinical Genetics and Genomics, Pittsburgh Cytogenetics Laboratory, Magee-Womens Hospital of UPMC, Pittsburgh, PA 15213 USA.
Surti U; Center for Clinical Genetics and Genomics, Pittsburgh Cytogenetics Laboratory, Magee-Womens Hospital of UPMC, Pittsburgh, PA 15213 USA.; Department of Obstetrics, Gynecology & Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213 USA.; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213 USA.

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Źródło:

Molecular cytogenetics [Mol Cytogenet] 2017 Jun 19; Vol. 10, pp. 24. Date of Electronic Publication: 2017 Jun 19 (Print Publication: 2017).

Typ publikacji:

Case Reports

Raport

• na półce

Pełny tekst  Link otwiera się w nowym oknieSzczegóły

Skocz do pozycji: 29.

Tytuł:

Familial deletion of the HOXA gene cluster associated with Hand-Foot-Genital syndrome and phenotypic variability.

Autorzy:

Tas E; Pediatric Endocrinology, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania.
Sebastian J; Medical Genetics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania.
Madan-Khetarpal S; Medical Genetics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania.
Sweet P; Kenneth P. Dietrich School of Arts and Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania.
Yatsenko AN; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania.; Magee-Womens Research Institute, Pittsburgh, Pennsylvania.; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Pollock N; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania.; Magee-Womens Research Institute, Pittsburgh, Pennsylvania.
Rajkovic A; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania.; Magee-Womens Research Institute, Pittsburgh, Pennsylvania.; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
Schneck FX; Pediatric Urology, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania.
Yatsenko SA; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
Witchel SF; Pediatric Endocrinology, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania.

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Źródło:

American journal of medical genetics. Part A [Am J Med Genet A] 2017 Jan; Vol. 173 (1), pp. 221-224. Date of Electronic Publication: 2016 Sep 20.

Typ publikacji:

Case Reports; Journal Article

MeSH Terms:

Genetic Association Studies*
Phenotype*
Sequence Deletion*
Abnormalities, Multiple/*diagnosis
Abnormalities, Multiple/*genetics
Foot Deformities, Congenital/*diagnosis
Foot Deformities, Congenital/*genetics
Hand Deformities, Congenital/*diagnosis
Hand Deformities, Congenital/*genetics
Homeodomain Proteins/*genetics
Urogenital Abnormalities/*diagnosis
Urogenital Abnormalities/*genetics
Chromosomes, Human, Pair 7 ; Comparative Genomic Hybridization ; Humans ; Infant ; Male ; Oligonucleotide Array Sequence Analysis ; Pedigree ; Polymorphism, Single Nucleotide

SCR Disease Name:

Hand foot uterus syndrome

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 30.

Tytuł:

Scribble Controls Social Motivation Behavior through the Regulation of the ERK/Mnk1 Pathway.

Autorzy:

Moreau, Maïté M. (AUTHOR)
Pietropaolo, Susanna (AUTHOR)
Ezan, Jérôme (AUTHOR)
Robert, Benjamin J. A. (AUTHOR)
Miraux, Sylvain (AUTHOR)
Maître, Marlène (AUTHOR)
Cho, Yoon (AUTHOR)
Crusio, Wim E. (AUTHOR)
Montcouquiol, Mireille (AUTHOR)
Sans, Nathalie (AUTHOR)

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Źródło:

Cells (2073-4409). May2022, Vol. 11 Issue 10, p1601-N.PAG. 21p.

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 31.

Tytuł:

Pathophysiological Heterogeneity of the BBSOA Neurodevelopmental Syndrome.

Autorzy:

Bertacchi, Michele (AUTHOR)
Tocco, Chiara (AUTHOR)
Schaaf, Christian P. (AUTHOR)
Studer, Michèle (AUTHOR)

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Źródło:

Cells (2073-4409). Apr2022, Vol. 11 Issue 8, p1260. 47p.

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 32.

Tytuł:

Elastic Fibre Proteins in Elastogenesis and Wound Healing.

Autorzy:

Zhang, Xinyang (AUTHOR)
Alanazi, Yasmene F. (AUTHOR)
Jowitt, Thomas A. (AUTHOR)
Roseman, Alan M. (AUTHOR)
Baldock, Clair (AUTHOR)

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Źródło:

International Journal of Molecular Sciences. Apr2022, Vol. 23 Issue 8, p4087-4087. 14p.

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 33.

Tytuł:

Small Vessel Disease: Ancient Description, Novel Biomarkers.

Autorzy:

Moretti, Rita (AUTHOR)
Caruso, Paola (AUTHOR)

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Źródło:

International Journal of Molecular Sciences. Apr2022, Vol. 23 Issue 7, p3508-N.PAG. 22p.

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknieSzczegóły

Skocz do pozycji: 34.

Tytuł:

ЕСТЕСТВЕННОЕ ТЕЧЕНИЕ АЛЛЕРГИИ И РАЗВИТИЕ ТОЛЕРАНТНОСТИ К БЕЛКАМ КОРОВЬЕГО МОЛОКА .

Autorzy:

Галимова, А. А.
Вязанкина, С. С.
Макарова, С. Г.
Фисенко, А. П.
Ерешко, О. А.
Мурашкин, Н. Н.

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Alternatywny tytuł:

THE NATURAL COURSE OF ALLERGY AND THE DEVELOPMENT OF TOLERANCE TO COW’S MILK PROTEINS.

Źródło:

Pediatriya named after G. N. Speransky. Mar/Apr2022, Issue 2, p64-73. 10p.

Czasopismo naukowe

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Skocz do pozycji: 35.

Tytuł:

СИНДРОМ ИММУННОЙ ДИСРЕГУЛЯЦИИ С ГАПЛОНЕДОСТАТОЧНОСТЬЮ CTLA4: ОСОБЕННОСТИ КЛИНИЧЕСКОГО И ИММУНОЛОГИЧЕСКОГО ФЕНОТИПА, ПОДХОДЫ К ЛЕЧЕНИЮ .

Autorzy:

Богданова, Д. В.
Родина, Ю. А.
Щербина, А. Ю.

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Alternatywny tytuł:

IMMUNE DYSREGULATION SYNDROME WITH CTLA4 HAPLOINSUFFICIENCY: CLINICAL AND IMMUNOLOGICAL PHENOTYPE AND THERAPEUTIC APPROACHES .

Źródło:

Pediatriya named after G. N. Speransky. Mar/Apr2022, Issue 2, p56-64. 9p.

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknieSzczegóły

Skocz do pozycji: 36.

Informacja:

Dostęp do tej pozycji wymaga zalogowania się.

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 37.

Tytuł:

Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veins.

Autorzy:

Szafranski P; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Rm. R809, Houston, TX, 77030, USA.
Gambin T; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Rm. R809, Houston, TX, 77030, USA.
Dharmadhikari AV; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Rm. R809, Houston, TX, 77030, USA.; Interdepartmental Program in Translational Biology and Molecular Medicine, Baylor College of Medicine, Houston, TX, USA.
Akdemir KC; Genomic Medicine Department, MD Anderson Cancer Center, Houston, TX, USA.
Jhangiani SN; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Rm. R809, Houston, TX, 77030, USA.; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.
Schuette J; Division of Pediatric Anesthesia and Critical Care Medicine, Johns Hopkins Medical Institutions, Baltimore, MD, USA.
Godiwala N; Division of Critical Care Medicine, Children's National Health System, Washington, DC, USA.
Yatsenko SA; Department of Obstetrics, Gynecology, and Reproductive Sciences, Center for Medical Genetics and Genomics, Magee-Womens Hospital of UPMC, Pittsburgh, PA, USA.; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Sebastian J; Division of Medical Genetics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, USA.
Madan-Khetarpal S; Division of Medical Genetics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, USA.
Surti U; Department of Obstetrics, Gynecology, and Reproductive Sciences, Center for Medical Genetics and Genomics, Magee-Womens Hospital of UPMC, Pittsburgh, PA, USA.; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
Abellar RG; Department of Pathology, Columbia University Medical Center, New York, NY, USA.
Bateman DA; Department of Pediatrics, Columbia University Medical Center, New York, NY, USA.
Wilson AL; Children's Hospital of New York-Presbyterian, New York, NY, USA.
Markham MH; Division of Neonatology, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN, USA.
Slamon J; Division of Maternal Fetal Medicine, Department of Obstetrics and Gynecology, Vanderbilt University Medical Center, Nashville, TN, USA.
Santos-Simarro F; INGEMM, Instituto de Genética Médica y Molecular, IdiPAZ, Madrid, Spain.; CIBERER, ISCIII, Madrid, Spain.
Palomares M; INGEMM, Instituto de Genética Médica y Molecular, IdiPAZ, Madrid, Spain.; CIBERER, ISCIII, Madrid, Spain.
Nevado J; INGEMM, Instituto de Genética Médica y Molecular, IdiPAZ, Madrid, Spain.; CIBERER, ISCIII, Madrid, Spain.
Lapunzina P; INGEMM, Instituto de Genética Médica y Molecular, IdiPAZ, Madrid, Spain.; CIBERER, ISCIII, Madrid, Spain.
Chung BH; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong, China.; Department of Obstetrics and Gynaecology, and Centre for Genomic Sciences, The University of Hong Kong, Hong Kong, China.
Wong WL; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong, China.
Chu YWY; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong, China.
Mok GTK; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong, China.
Kerem E; Pediatric Pulmonary Unit, Department of Pediatrics, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
Reiter J; Pediatric Pulmonary Unit, Department of Pediatrics, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
Ambalavanan N; Department of Pediatrics, University of Alabama at Birmingham, Birmingham, AL, USA.; Department of Cell Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL, USA.
Anderson SA; Division of Pediatric Surgery, Department of Surgery, University of Alabama at Birmingham and Children's of Alabama, Birmingham, AL, USA.
Kelly DR; Department of Pathology, University of Alabama at Birmingham and Pathology and Laboratory Medicine Service, Children's of Alabama, Birmingham, AL, USA.
Shieh J; Division of Medical Genetics, Department of Pediatrics, and Institute for Human Genetics, University of California San Francisco, San Francisco, CA, USA.
Rosenthal TC; Genetics Department, Kaiser Permanente San Jose Medical Center, San Jose, CA, USA.
Scheible K; Division of Neonatology, Department of Pediatrics, University of Rochester, Rochester, NY, USA.
Steiner L; Division of Neonatology, Department of Pediatrics, University of Rochester, Rochester, NY, USA.
Iqbal MA; Pathology and Laboratory Medicine, University of Rochester Medical Center, Rochester, NY, USA.
McKinnon ML; Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
Hamilton SJ; Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
Schlade-Bartusiak K; Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
English D; Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
Hendson G; Department of Pathology, University of British Columbia, Vancouver, Canada.
Roeder ER; Department of Pediatrics, Baylor College of Medicine, San Antonio, TX, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, San Antonio, TX, USA.
DeNapoli TS; Department of Pathology, Children's Hospital of San Antonio, San Antonio, TX, USA.
Littlejohn RO; Department of Pediatrics, Baylor College of Medicine, San Antonio, TX, USA.
Wolff DJ; Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, SC, USA.
Wagner CL; Department of Pediatrics, Medical University of South Carolina, Charleston, SC, USA.
Yeung A; Victorian Clinical Genetics Services, Murdoch Childrens Research Institute, Parkville, VIC, Australia.
Francis D; Victorian Clinical Genetics Services, Murdoch Childrens Research Institute, Parkville, VIC, Australia.
Fiorino EK; Division of Pediatric Pulmonary Medicine, The Children's Heart Center Steven and Alexandra Cohen Children's Medical Center of New York, New Hyde Park, NY, USA.
Edelman M; Division of Pediatric Pathology, The Children's Heart Center Steven and Alexandra Cohen Children's Medical Center of New York, New Hyde Park, NY, USA.
Fox J; Division of Medical Genetics, Steven and Alexandra Cohen Children's Medical Center of New York, New Hyde Park, NY, USA.
Hayes DA; Pediatric Cardiology, The Children's Heart Center Steven and Alexandra Cohen Children's Medical Center of New York, New Hyde Park, NY, USA.
Janssens S; Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
De Baere E; Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
Menten B; Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
Loccufier A; Department of Obstetrics, Gynaecology, and Fertility, AZ St Jan Brugge, Brugge, Belgium.
Vanwalleghem L; Department of Anatomopathology, AZ St Jan Brugge, Brugge, Belgium.
Moerman P; Department of Pathology, UZ Leuven, Louvain, Belgium.
Sznajer Y; Center for Human Genetics, Cliniques Universitaires St-Luc, Universite Catholique de Louvain, Brussels, Belgium.
Lay AS; Division of Pediatric Cardiology, Children's Mercy Hospital, Kansas City, MS, USA.
Kussmann JL; Division of Clinical Genetics, Children's Mercy Hospital, Kansas City, MS, USA.
Chawla J; Division of Paediatric Respiratory and Sleep Medicine, Lady Cilento Children's Hospital, Children's Health Queensland Hospital and Health Service, Brisbane, QLD, Australia.; The University of Queensland, Brisbane, QLD, Australia.
Payton DJ; Division of Anatomical Pathology, Lady Cilento Children's Hospital, Children's Health Queensland Hospital and Health Service, Brisbane, QLD, Australia.; Pathology Queensland, Brisbane, QLD, Australia.
Phillips GE; Division of Anatomical Pathology, Lady Cilento Children's Hospital, Children's Health Queensland Hospital and Health Service, Brisbane, QLD, Australia.; Pathology Queensland, Brisbane, QLD, Australia.
Brosens E; Clinical Genetics Department, Erasmus MC-Sophia, Rotterdam, The Netherlands.; Paediatric Surgery, Erasmus MC-Sophia, Rotterdam, The Netherlands.
Tibboel D; Paediatric Surgery, Erasmus MC-Sophia, Rotterdam, The Netherlands.
de Klein A; Clinical Genetics Department, Erasmus MC-Sophia, Rotterdam, The Netherlands.
Maystadt I; Centre de Génétique Humaine, Institut de Pathologie et de Génétique, Gosselies, Belgium.
Fisher R; James Cook University Hospital, Middlesborough, UK.
Sebire N; Department of Paediatric Histopathology, Great Ormond Street Hospital for Children and UCL Institute of Child Health, London, UK.
Male A; Clinical Genetics Unit, Great Ormond Street Hospital for Children and UCL Institute of Child Health, London, UK.
Chopra M; Department of Medical Genomics, Royal Prince Alfred Hospital, Sydney, NSW, Australia.
Pinner J; Department of Medical Genomics, Royal Prince Alfred Hospital, Sydney, NSW, Australia.
Malcolm G; Department of Newborn Care, Royal Prince Alfred Hospital, Sydney, NSW, Australia.
Peters G; Cytogenetics Department, The Children's Hospital at Westmead, Westmead, NSW, Australia.
Arbuckle S; Histopathology Department, The Children's Hospital at Westmead, Westmead, NSW, Australia.
Lees M; Clinical Genetics Unit, Great Ormond Street Hospital for Children and UCL Institute of Child Health, London, UK.
Mead Z; Department of Histopathology, Addenbrooke's NHS Trust Pathology Department, Addenbrooke's Hospital, Cambridge, UK.
Quarrell O; Department of Clinical Genetics, Sheffield Children's Hospital, Sheffield, UK.
Sayers R; Department of Clinical Genetics, Sheffield Children's Hospital, Sheffield, UK.
Owens M; Molecular Genetics Department, Royal Devon and Exeter NHS Foundation Trust, Exeter, UK.
Shaw-Smith C; Molecular Genetics Department, Royal Devon and Exeter NHS Foundation Trust, Exeter, UK.
Lioy J; Division of Neonatology, The Children's Hospital of Philadelphia, The University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA, USA.
McKay E; Department of Pathology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
de Leeuw N; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Feenstra I; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Spruijt L; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Elmslie F; South West Thames Regional Genetics Service, St George's University Hospital, London, UK.
Thiruchelvam T; Critical Care and Cardiorespiratory Unit, Great Ormond Street Hospital NHS Trust, London, UK.
Bacino CA; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Rm. R809, Houston, TX, 77030, USA.; Texas Children's Hospital, Houston, TX, USA.
Langston C; Department of Pathology and Immunology, Baylor College of Medicine, Houston, TX, USA.
Lupski JR; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Rm. R809, Houston, TX, 77030, USA.; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.; Texas Children's Hospital, Houston, TX, USA.; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
Sen P; Department of Pediatrics, Northwestern University, Chicago, IL, USA.
Popek E; Department of Pathology and Immunology, Baylor College of Medicine, Houston, TX, USA.
Stankiewicz P; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Rm. R809, Houston, TX, 77030, USA. .; Interdepartmental Program in Translational Biology and Molecular Medicine, Baylor College of Medicine, Houston, TX, USA. .; Institute of Mother and Child, Warsaw, Poland. .

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Źródło:

Human genetics [Hum Genet] 2016 May; Vol. 135 (5), pp. 569-586. Date of Electronic Publication: 2016 Apr 12.

Typ publikacji:

Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

MeSH Terms:

Genome, Human*
Genomic Imprinting*
Persistent Fetal Circulation Syndrome/*pathology
Pulmonary Alveoli/*abnormalities
Pulmonary Veins/*pathology
Chromosomes, Human, Pair 16/genetics ; Comparative Genomic Hybridization ; Female ; Forkhead Transcription Factors/genetics ; Genes, Lethal ; High-Throughput Nucleotide Sequencing ; Humans ; Infant, Newborn ; Male ; Pedigree ; Persistent Fetal Circulation Syndrome/genetics ; Pulmonary Alveoli/pathology ; Sequence Deletion

SCR Disease Name:

Alveolar capillary dysplasia

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 38.

Tytuł:

Respiratory motile cilia dysfunction in a patient with cranioectodermal dysplasia.

Autorzy:

Li Y; Department of Developmental Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Garrod AS; Division of Pulmonary Medicine, Allergy & Immunology, Children's Hospital of Pittsburgh of University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Madan-Khetarpal S; Division of Medical Genetics, Children's Hospital of Pittsburgh of University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Sreedher G; Division of Medical Genetics, Children's Hospital of Pittsburgh of University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
McGuire M; Division of Medical Genetics, Children's Hospital of Pittsburgh of University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.; Department of Medical Genetics, Baylor College of Medicine, Houston, Texas.
Yagi H; Department of Developmental Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Klena NT; Department of Developmental Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Gabriel GC; Department of Developmental Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Khalifa O
Zahid M; Department of Developmental Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Panigrahy A; Department of Pediatric Radiology, Children's Hospital of Pittsburgh of University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Weiner DJ; Division of Pulmonary Medicine, Allergy & Immunology, Children's Hospital of Pittsburgh of University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Lo CW; Department of Developmental Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.

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Źródło:

American journal of medical genetics. Part A [Am J Med Genet A] 2015 Sep; Vol. 167A (9), pp. 2188-96. Date of Electronic Publication: 2015 Apr 25.

Typ publikacji:

Case Reports; Journal Article; Research Support, Non-U.S. Gov't

MeSH Terms:

Bone and Bones/*abnormalities
Cilia/*genetics
Craniosynostoses/*genetics
Ectodermal Dysplasia/*genetics
Respiratory Tract Diseases/*genetics
Child ; Cytoskeletal Proteins ; Hedgehog Proteins ; Heterozygote ; Humans ; Intracellular Signaling Peptides and Proteins ; Male ; Mutation/genetics ; Proteins/genetics

SCR Disease Name:

Cranioectodermal Dysplasia

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 39.

Tytuł:

Identification of a novel KAT6A variant in an infant presenting with facial dysmorphism and developmental delay: a case report and literature review.

Autorzy:

Bae, Soyoung (AUTHOR)
Yang, Aram (AUTHOR)
Kim, Jinsup (AUTHOR)
Lee, Hyun Ju (AUTHOR)
Park, Hyun Kyung (AUTHOR)

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Źródło:

BMC Medical Genomics. 12/20/2021, Vol. 14 Issue 1, p1-8. 8p.

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 40.

Tytuł:

A novel maternally inherited 8q24.3 and a rare paternally inherited 14q23.3 CNVs in a family with neurodevelopmental disorders.

Autorzy:

Hu J; Pittsburgh Cytogenetics Laboratory, Magee- Womens Hospital of UPMC, Pittsburgh, Pennsylvania.; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Sathanoori M; Pittsburgh Cytogenetics Laboratory, Magee- Womens Hospital of UPMC, Pittsburgh, Pennsylvania.; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Kochmar S; Pittsburgh Cytogenetics Laboratory, Magee- Womens Hospital of UPMC, Pittsburgh, Pennsylvania.
Azage M; Department of Pediatrics, University of Pittsburgh School of Medicine and Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania.
Mann S; Pittsburgh Cytogenetics Laboratory, Magee- Womens Hospital of UPMC, Pittsburgh, Pennsylvania.
Madan-Khetarpal S; Department of Pediatrics, University of Pittsburgh School of Medicine and Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania.
Goldstein A; Department of Neurology, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania.
Surti U; Pittsburgh Cytogenetics Laboratory, Magee- Womens Hospital of UPMC, Pittsburgh, Pennsylvania.; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.

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Źródło:

American journal of medical genetics. Part A [Am J Med Genet A] 2015 Aug; Vol. 167A (8), pp. 1921-6. Date of Electronic Publication: 2015 Apr 10.

Typ publikacji:

Case Reports; Journal Article

MeSH Terms:

Chromosomes, Human, Pair 14*
Chromosomes, Human, Pair 8*
DNA Copy Number Variations*
Genomic Imprinting*
Neurodevelopmental Disorders/*genetics
Child ; Female ; Humans ; In Situ Hybridization, Fluorescence ; Male ; Pregnancy

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 41.

Tytuł:

Craniofacial abnormalities and developmental delay in two families with overlapping 22q12.1 microdeletions involving the MN1 gene.

Autorzy:

Beck M; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
Peterson JF
McConnell J
McGuire M
Asato M
Losee JE
Surti U
Madan-Khetarpal S
Rajkovic A
Yatsenko SA

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Źródło:

American journal of medical genetics. Part A [Am J Med Genet A] 2015 May; Vol. 167A (5), pp. 1047-53. Date of Electronic Publication: 2015 Mar 21.

Typ publikacji:

Case Reports; Journal Article

MeSH Terms:

Cleft Palate/*genetics
Craniofacial Abnormalities/*genetics
Developmental Disabilities/*genetics
Tumor Suppressor Proteins/*genetics
Adult ; Animals ; Child, Preschool ; Chromosome Deletion ; Chromosomes, Human, Pair 22/genetics ; Cleft Palate/physiopathology ; Craniofacial Abnormalities/physiopathology ; Developmental Disabilities/physiopathology ; Female ; Humans ; Infant ; Male ; Mice ; Neurofibromin 2/genetics ; Pedigree ; Trans-Activators

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 42.

Tytuł:

Biomechanical properties of the skin in cutis laxa.

Autorzy:

Kozel BA; Department of Pediatrics, Washington University School of Medicine, St Louis, Missouri, USA.
Su CT; Department of Human Genetics, University of Pittsburgh Graduate School of Public Health, Pittsburgh, Pennsylvania, USA.
Danback JR; Department of Pediatrics, Washington University School of Medicine, St Louis, Missouri, USA.
Minster RL; Department of Human Genetics, University of Pittsburgh Graduate School of Public Health, Pittsburgh, Pennsylvania, USA.
Madan-Khetarpal S; Division of Medical Genetics, Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.
McConnell JS; Division of Medical Genetics, Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Mac Neal MK; Department of Human Genetics, University of Pittsburgh Graduate School of Public Health, Pittsburgh, Pennsylvania, USA.
Levine KL; Department of Human Genetics, University of Pittsburgh Graduate School of Public Health, Pittsburgh, Pennsylvania, USA.
Wilson RC; Division of Pulmonary and Critical Care Medicine, Department of Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Sciurba FC; Division of Pulmonary and Critical Care Medicine, Department of Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Urban Z; Department of Human Genetics, University of Pittsburgh Graduate School of Public Health, Pittsburgh, Pennsylvania, USA. Electronic address: .

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Źródło:

The Journal of investigative dermatology [J Invest Dermatol] 2014 Nov; Vol. 134 (11), pp. 2836-2838. Date of Electronic Publication: 2014 May 20.

Typ publikacji:

Letter; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

MeSH Terms:

Cutis Laxa/*physiopathology
Skin/*physiopathology
Adult ; Area Under Curve ; Biomechanical Phenomena ; Case-Control Studies ; Cohort Studies ; Elasticity ; Elastin/genetics ; Female ; Humans ; Latent TGF-beta Binding Proteins/genetics ; Male ; Mutation ; Proton-Translocating ATPases/genetics ; ROC Curve ; Sensitivity and Specificity ; Viscosity

Raport

• na półce

Szczegóły

Skocz do pozycji: 43.

Tytuł:

Genetic evaluation of newborns with critical congenital heart defects admitted to the intensive care unit.

Autorzy:

Miletic, Aleksandra (AUTHOR)
Stojanovic, Jelena Ruml (AUTHOR)
Parezanovic, Vojislav (AUTHOR)
Rsovac, Snezana (AUTHOR)
Drakulic, Danijela (AUTHOR)
Soldatovic, Ivan (AUTHOR)
Mijovic, Marija (AUTHOR)
Bosankic, Brankica (AUTHOR)
Petrovic, Hristina (AUTHOR)
Borlja, Nikola (AUTHOR)
Milivojevic, Milena (AUTHOR)
Marjanovic, Ana (AUTHOR)
Brankovic, Marija (AUTHOR)
Cuturilo, Goran (AUTHOR)

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Źródło:

European Journal of Pediatrics. Oct2021, Vol. 180 Issue 10, p3219-3227. 9p. 1 Color Photograph, 6 Charts.

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 44.

Tytuł:

Familial microduplication of 17q23.1–q23.2 involving TBX4 is associated with congenital clubfoot and reduced penetrance in females.

Autorzy:

Peterson JF
Ghaloul-Gonzalez L
Madan-Khetarpal S
Hartman J
Surti U
Rajkovic A
Yatsenko SA

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Źródło:

American journal of medical genetics. Part A [Am J Med Genet A] 2014 Feb; Vol. 164A (2), pp. 364-9.

Typ publikacji:

Case Reports; Journal Article

MeSH Terms:

Chromosome Duplication*
Chromosomes, Human, Pair 17*
Penetrance*
Clubfoot/*genetics
T-Box Domain Proteins/*genetics
Abnormalities, Multiple/diagnosis ; Abnormalities, Multiple/genetics ; Clubfoot/diagnosis ; Comparative Genomic Hybridization ; Female ; Humans ; Infant, Newborn ; Male ; Pedigree ; Phenotype

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 45.

Tytuł:

Comprehensive clinical and molecular analysis of 12 families with type 1 recessive cutis laxa.

Autorzy:

Callewaert B; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
Su CT
Van Damme T
Vlummens P
Malfait F
Vanakker O
Schulz B
Mac Neal M
Davis EC
Lee JG
Salhi A
Unger S
Heimdal K
De Almeida S
Kornak U
Gaspar H
Bresson JL
Prescott K
Gosendi ME
Mansour S
Piérard GE
Madan-Khetarpal S
Sciurba FC
Symoens S
Coucke PJ
Van Maldergem L
Urban Z
De Paepe A

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Źródło:

Human mutation [Hum Mutat] 2013 Jan; Vol. 34 (1), pp. 111-21. Date of Electronic Publication: 2012 Aug 13.

Typ publikacji:

Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

MeSH Terms:

Mutation*
Cutis Laxa/*genetics
Extracellular Matrix Proteins/*genetics
Latent TGF-beta Binding Proteins/*genetics
Adolescent ; Base Sequence ; Blotting, Western ; Child ; Child, Preschool ; Consanguinity ; Cutis Laxa/complications ; Extracellular Matrix Proteins/metabolism ; Family Health ; Female ; Gene Expression ; Humans ; Infant ; Latent TGF-beta Binding Proteins/metabolism ; Male ; Microscopy, Electron ; Pedigree ; Pulmonary Emphysema/complications ; Reverse Transcriptase Polymerase Chain Reaction ; Sequence Analysis, DNA ; Skin/metabolism ; Skin/pathology ; Skin/ultrastructure ; Young Adult

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 46.

Tytuł:

Co-existence of 9p deletion and Silver-Russell syndromes in a patient with maternally inherited cryptic complex chromosome rearrangement involving chromosomes 4, 9, and 11.

Autorzy:

Hu J; Pittsburgh Cytogenetics Laboratory, Magee-Womens Hospital of UPMC, Pittsburgh, PA. />Sathanoori M
Kochmar S
Madan-Khetarpal S
McGuire M
Surti U

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Źródło:

American journal of medical genetics. Part A [Am J Med Genet A] 2013 Jan; Vol. 161A (1), pp. 179-84. Date of Electronic Publication: 2012 Dec 07.

Typ publikacji:

Case Reports; Journal Article

MeSH Terms:

Chromosomes, Human, Pair 11/*genetics
Chromosomes, Human, Pair 4/*genetics
Silver-Russell Syndrome/*genetics
Chromosome Deletion ; Chromosomes, Human, Pair 9/genetics ; Cleft Palate/genetics ; Comparative Genomic Hybridization ; Female ; Gene Duplication ; Gene Rearrangement ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Microarray Analysis ; Phenotype ; Silver-Russell Syndrome/diagnosis ; Translocation, Genetic ; Young Adult

SCR Disease Name:

Chromosome 9p Deletion Syndrome

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 47.

Tytuł:

Clinical significance and mechanisms associated with segmental UPD.

Autorzy:

Papenhausen, Peter R. (AUTHOR)
Kelly, Carla A. (AUTHOR)
Harris, Samuel (AUTHOR)
Caldwell, Samantha (AUTHOR)
Schwartz, Stuart (AUTHOR)
Penton, Andrea (AUTHOR)

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Źródło:

Molecular Cytogenetics (17558166). 7/20/2021, Vol. 14 Issue 1, p1-22. 22p.

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknieSzczegóły

Skocz do pozycji: 48.

Tytuł:

X-chromosome inactivation: implications in human disease.

Autorzy:

Pereira, Guilherme (AUTHOR)
Dória, Sofia (AUTHOR)

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Źródło:

Journal of Genetics. 2021, Vol. 100 Issue 2, p1-7. 7p.

Czasopismo naukowe

• na półce

Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły

Skocz do pozycji: 49.

Tytuł:

Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features.

Autorzy:

Lamb AN; Signature Genomic Laboratories, PerkinElmer, Inc., Spokane, Washington 99207, USA.
Rosenfeld JA
Neill NJ
Talkowski ME
Blumenthal I
Girirajan S
Keelean-Fuller D
Fan Z
Pouncey J
Stevens C
Mackay-Loder L
Terespolsky D
Bader PI
Rosenbaum K
Vallee SE
Moeschler JB
Ladda R
Sell S
Martin J
Ryan S
Jones MC
Moran R
Shealy A
Madan-Khetarpal S
McConnell J
Surti U
Delahaye A
Heron-Longe B
Pipiras E
Benzacken B
Passemard S
Verloes A
Isidor B
Le Caignec C
Glew GM
Opheim KE
Descartes M
Eichler EE
Morton CC
Gusella JF
Schultz RA
Ballif BC
Shaffer LG

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Źródło:

Human mutation [Hum Mutat] 2012 Apr; Vol. 33 (4), pp. 728-40.

Typ publikacji:

Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

MeSH Terms:

Haploinsufficiency*
Body Dysmorphic Disorders/*genetics
Developmental Disabilities/*genetics
Language Development Disorders/*genetics
Mental Disorders/*genetics
SOXD Transcription Factors/*genetics
Adolescent ; Adult ; Case-Control Studies ; Child ; Child, Preschool ; Chromosomes, Human, Pair 12 ; Female ; Humans ; Male

Czasopismo naukowe

• na półce

Szczegóły

Skocz do pozycji: 50.

Tytuł:

Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats.

Autorzy:

Stankiewicz P; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA. />Kulkarni S
Dharmadhikari AV
Sampath S
Bhatt SS
Shaikh TH
Xia Z
Pursley AN
Cooper ML
Shinawi M
Paciorkowski AR
Grange DK
Noetzel MJ
Saunders S
Simons P
Summar M
Lee B
Scaglia F
Fellmann F
Martinet D
Beckmann JS
Asamoah A
Platky K
Sparks S
Martin AS
Madan-Khetarpal S
Hoover J
Medne L
Bonnemann CG
Moeschler JB
Vallee SE
Parikh S
Irwin P
Dalzell VP
Smith WE
Banks VC
Flannery DB
Lovell CM
Bellus GA
Golden-Grant K
Gorski JL
Kussmann JL
McGregor TL
Hamid R
Pfotenhauer J
Ballif BC
Shaw CA
Kang SH
Bacino CA
Patel A
Rosenfeld JA
Cheung SW
Shaffer LG

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Źródło:

Human mutation [Hum Mutat] 2012 Jan; Vol. 33 (1), pp. 165-79. Date of Electronic Publication: 2011 Nov 02.

Typ publikacji:

Journal Article; Research Support, Non-U.S. Gov't

MeSH Terms:

Chromosome Aberrations*
Sequence Deletion*
Abnormalities, Multiple/*genetics
Nerve Growth Factors/*genetics
Segmental Duplications, Genomic/*genetics
Vesicular Acetylcholine Transport Proteins/*genetics
Child ; Child, Preschool ; Chromosome Mapping ; Chromosomes, Human, Pair 10 ; DNA Copy Number Variations ; Developmental Disabilities/complications ; Developmental Disabilities/genetics ; Female ; Genetic Variation ; Homologous Recombination ; Humans ; In Situ Hybridization, Fluorescence ; Infant ; Intellectual Disability/complications ; Intellectual Disability/genetics ; Male ; Oligonucleotide Array Sequence Analysis ; Penetrance

Czasopismo naukowe

• na półce

Szczegóły