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Tytuł:
Author Correction: Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative.
Autorzy:
Johnson R; Department of Computer Science, University of California, Los Angeles, Los Angeles, CA, 90095, USA. .; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA. .
Ding Y; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Bioinformatics Interdepartmental Program, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Venkateswaran V; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Department of Oral Biology, School of Dentistry, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Bhattacharya A; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Institute for Quantitative and Computational Biosciences, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Boulier K; Bioinformatics Interdepartmental Program, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Department of Medicine, Division of Cardiology, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Chiu A; Bioinformatics Interdepartmental Program, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Knyazev S; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Institute for Quantitative and Computational Biosciences, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Schwarz T; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Bioinformatics Interdepartmental Program, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Freund M; Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Department of Genetics, Stanford School of Medicine, Stanford, CA, 94305, USA.
Zhan L; Molecular Biology Institute, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Burch KS; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Bioinformatics Interdepartmental Program, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Caggiano C; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Hill B; Department of Computer Science, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Rakocz N; Department of Computer Science, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Balliu B; Department of Computational Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Denny CT; Division of Hematology/Oncology, Department of Pediatrics, Gwynne Hazen Cherry Memorial Laboratories, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Molecular Biology Institute, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Jonsson Comprehensive Cancer Center, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Sul JH; Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Zaitlen N; Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Department of Computational Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Arboleda VA; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Department of Computational Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Halperin E; Department of Computer Science, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Department of Computational Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Department of Anesthesiology and Perioperative Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Sankararaman S; Department of Computer Science, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Department of Computational Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Butte MJ; Department of Pediatrics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Lajonchere C; Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Institute of Precision Health, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Geschwind DH; Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Institute of Precision Health, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Pasaniuc B; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA. .; Bioinformatics Interdepartmental Program, University of California, Los Angeles, Los Angeles, CA, 90095, USA. .; Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA. .; Department of Computational Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA. .; Institute of Precision Health, University of California, Los Angeles, Los Angeles, CA, 90095, USA. .
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Corporate Authors:
UCLA Precision Health Data Discovery Repository Working Group, UCLA Precision Health ATLAS Working Group
Źródło:
Genome medicine [Genome Med] 2022 Nov 16; Vol. 14 (1), pp. 128. Date of Electronic Publication: 2022 Nov 16.
Typ publikacji:
Published Erratum
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative.
Autorzy:
Johnson R; Department of Computer Science, University of California, Los Angeles, Los Angeles, CA, 90095, USA. .; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA. .
Ding Y; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Bioinformatics Interdepartmental Program, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Venkateswaran V; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Department of Oral Biology, School of Dentistry, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Bhattacharya A; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Institute for Quantitative and Computational Biosciences, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Boulier K; Bioinformatics Interdepartmental Program, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Department of Medicine, Division of Cardiology, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Chiu A; Bioinformatics Interdepartmental Program, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Knyazev S; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Institute for Quantitative and Computational Biosciences, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Schwarz T; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Bioinformatics Interdepartmental Program, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Freund M; Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Department of Genetics, Stanford School of Medicine, Stanford, CA, 94305, USA.
Zhan L; Molecular Biology Institute, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Burch KS; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Bioinformatics Interdepartmental Program, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Caggiano C; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Hill B; Department of Computer Science, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Rakocz N; Department of Computer Science, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Balliu B; Department of Computational Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Denny CT; Division of Hematology/Oncology, Department of Pediatrics, Gwynne Hazen Cherry Memorial Laboratories, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Molecular Biology Institute, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Jonsson Comprehensive Cancer Center, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Sul JH; Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Zaitlen N; Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Department of Computational Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Arboleda VA; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Department of Computational Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Halperin E; Department of Computer Science, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Department of Computational Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Department of Anesthesiology and Perioperative Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Sankararaman S; Department of Computer Science, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Department of Computational Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Butte MJ; Department of Pediatrics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Lajonchere C; Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Institute of Precision Health, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Geschwind DH; Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.; Institute of Precision Health, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Pasaniuc B; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA. .; Bioinformatics Interdepartmental Program, University of California, Los Angeles, Los Angeles, CA, 90095, USA. .; Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA. .; Department of Computational Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA. .; Institute of Precision Health, University of California, Los Angeles, Los Angeles, CA, 90095, USA. .
Pokaż więcej
Corporate Authors:
UCLA Precision Health Data Discovery Repository Working Group, UCLA Precision Health ATLAS Working Group
Źródło:
Genome medicine [Genome Med] 2022 Sep 09; Vol. 14 (1), pp. 104. Date of Electronic Publication: 2022 Sep 09.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms:
Electronic Health Records*
Public Health*
Asian People ; Biological Specimen Banks ; Genomics ; Humans
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Accurate diagnosis of atopic dermatitis by combining transcriptome and microbiota data with supervised machine learning.
Autorzy:
Jiang Z; Department of Automation, Tsinghua University, Beijing, 100084, China.
Li J; Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Kong N; Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, Daejeon, 34141, Republic of Korea.
Kim JH; Department of Medicine, University of Ulsan College of Medicine, Seoul, 05505, Republic of Korea.
Kim BS; Department of Life Science, Multidisciplinary Genome Institute, Hallym University, Chuncheon, 24252, Republic of Korea.
Lee MJ; Department of Life Science, Multidisciplinary Genome Institute, Hallym University, Chuncheon, 24252, Republic of Korea.
Park YM; Department of Medicine, University of Ulsan College of Medicine, Seoul, 05505, Republic of Korea.
Lee SY; Department of Pediatrics, Asan Medical Center, Childhood Asthma Atopy Center, Humidifier Disinfectant Health Center, University of Ulsan College of Medicine, Seoul, 05505, Republic of Korea.
Hong SJ; Department of Pediatrics, Asan Medical Center, Childhood Asthma Atopy Center, Humidifier Disinfectant Health Center, University of Ulsan College of Medicine, Seoul, 05505, Republic of Korea. .
Sul JH; Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, Los Angeles, CA, 90095, USA. .
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Źródło:
Scientific reports [Sci Rep] 2022 Jan 07; Vol. 12 (1), pp. 290. Date of Electronic Publication: 2022 Jan 07.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms:
Diagnosis, Computer-Assisted*
Gastrointestinal Microbiome*
Gene Expression Profiling*
Supervised Machine Learning*
Transcriptome*
Colon/*metabolism
Colon/*microbiology
Dermatitis, Atopic/*diagnosis
Case-Control Studies ; Dermatitis, Atopic/genetics ; Dermatitis, Atopic/microbiology ; Dysbiosis ; Female ; Host-Pathogen Interactions ; Humans ; Infant ; Male ; Predictive Value of Tests
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Engineered small extracellular vesicles displaying ACE2 variants on the surface protect against SARS-CoV-2 infection.
Autorzy:
Kim HK; School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.
Cho J; Division of Emerging Viral Diseases and Vector Research, Centre for Infectious Diseases Research, Korea National Institute of Health, Korea Centres for Disease Control and Prevention Agency, Cheongju, Republic of Korea.
Kim E; School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.
Kim J; School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.
Yang JS; Division of Emerging Viral Diseases and Vector Research, Centre for Infectious Diseases Research, Korea National Institute of Health, Korea Centres for Disease Control and Prevention Agency, Cheongju, Republic of Korea.
Kim KC; Division of Emerging Viral Diseases and Vector Research, Centre for Infectious Diseases Research, Korea National Institute of Health, Korea Centres for Disease Control and Prevention Agency, Cheongju, Republic of Korea.
Lee JY; Division of Emerging Viral Diseases and Vector Research, Centre for Infectious Diseases Research, Korea National Institute of Health, Korea Centres for Disease Control and Prevention Agency, Cheongju, Republic of Korea.
Shin Y; Division of Emerging Viral Diseases and Vector Research, Centre for Infectious Diseases Research, Korea National Institute of Health, Korea Centres for Disease Control and Prevention Agency, Cheongju, Republic of Korea.
Palomera LF; School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.
Park J; School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.
Baek SH; School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.
Bae HG; School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.
Cho Y; School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.
Han J; School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.
Sul JH; School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.
Lee J; School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.
Park JH; Biomedical Institute for Convergence, Sungkyunkwan University, Suwon, Republic of Korea.; Department of Health Sciences and Technology, Samsung Advanced Institute for Health Sciences & Technology (SAIHST), Sungkyunkwan University, Seoul, Republic of Korea.; School of Chemical Engineering, Sungkyunkwan University, Suwon, Republic of Korea.; ExoStemTech Inc., Ansan, Republic of Korea.
Cho YW; Department of Materials Science and Chemical Engineering, Hanyang University ERICA, Ansan, Republic of Korea.; ExoStemTech Inc., Ansan, Republic of Korea.
Lee W; School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.
Jo DG; School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.; Biomedical Institute for Convergence, Sungkyunkwan University, Suwon, Republic of Korea.; Department of Health Sciences and Technology, Samsung Advanced Institute for Health Sciences & Technology (SAIHST), Sungkyunkwan University, Seoul, Republic of Korea.; ExoStemTech Inc., Ansan, Republic of Korea.
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Źródło:
Journal of extracellular vesicles [J Extracell Vesicles] 2022 Jan; Vol. 11 (1), pp. e12179.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Angiotensin-Converting Enzyme 2/*immunology
COVID-19/*immunology
Extracellular Vesicles/*immunology
Spike Glycoprotein, Coronavirus/*immunology
Animals ; Female ; HEK293 Cells ; Humans ; Mice ; Protein Binding ; Protein Interaction Domains and Motifs
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Extracellular vesicles from adipose tissue-derived stem cells alleviate osteoporosis through osteoprotegerin and miR-21-5p.
Autorzy:
Lee KS; Department of Materials Science and Chemical Engineering, Hanyang University ERICA, Ansan, Korea.; Exostemtech, Inc., Ansan, Korea.
Lee J; School of Pharmacy, Sungkyunkwan University, Suwon, Korea.
Kim HK; School of Pharmacy, Sungkyunkwan University, Suwon, Korea.
Yeom SH; Exostemtech, Inc., Ansan, Korea.
Woo CH; Exostemtech, Inc., Ansan, Korea.
Jung YJ; Exostemtech, Inc., Ansan, Korea.
Yun YE; Department of Materials Science and Chemical Engineering, Hanyang University ERICA, Ansan, Korea.
Park SY; Exostemtech, Inc., Ansan, Korea.
Han J; School of Pharmacy, Sungkyunkwan University, Suwon, Korea.
Kim E; School of Pharmacy, Sungkyunkwan University, Suwon, Korea.
Sul JH; School of Pharmacy, Sungkyunkwan University, Suwon, Korea.
Jung JM; School of Chemical Engineering, College of Engineering, Sungkyunkwan University, Suwon, Korea.
Park JH; Exostemtech, Inc., Ansan, Korea.; School of Chemical Engineering, College of Engineering, Sungkyunkwan University, Suwon, Korea.; Biomedical Institute for Convergence, Sungkyunkwan University, Suwon, Korea.; Department of Health Science and Technology, SAIHST, Sungkyunkwan University, Seoul, Korea.
Choi JS; Exostemtech, Inc., Ansan, Korea.
Cho YW; Department of Materials Science and Chemical Engineering, Hanyang University ERICA, Ansan, Korea.; Exostemtech, Inc., Ansan, Korea.
Jo DG; Exostemtech, Inc., Ansan, Korea.; School of Pharmacy, Sungkyunkwan University, Suwon, Korea.; Biomedical Institute for Convergence, Sungkyunkwan University, Suwon, Korea.; Department of Health Science and Technology, SAIHST, Sungkyunkwan University, Seoul, Korea.
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Źródło:
Journal of extracellular vesicles [J Extracell Vesicles] 2021 Oct; Vol. 10 (12), pp. e12152.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Adipose Tissue/*metabolism
Extracellular Vesicles/*metabolism
Osteoporosis/*therapy
Osteoprotegerin/*genetics
Stem Cells/*metabolism
Animals ; Disease Models, Animal ; Female ; Humans ; Mice ; Osteoporosis/pathology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Rare variants in the endocytic pathway are associated with Alzheimer's disease, its related phenotypes, and functional consequences.
Autorzy:
Zhan L; Molecular Biology Institute, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California, United States of America.
Li J; Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California, United States of America.
Jew B; Interdepartmental Program in Bioinformatics, University of California, Los Angeles, Los Angeles, California, United States of America.
Sul JH; Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, Los Angeles, California, United States of America.
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Źródło:
PLoS genetics [PLoS Genet] 2021 Sep 13; Vol. 17 (9), pp. e1009772. Date of Electronic Publication: 2021 Sep 13 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Endocytosis*
Phenotype*
Alzheimer Disease/*pathology
Alzheimer Disease/genetics ; Genome-Wide Association Study ; Humans ; Polymorphism, Single Nucleotide ; Whole Genome Sequencing
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Rare variants regulate expression of nearby individual genes in multiple tissues.
Autorzy:
Li J; Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California, United States of America.
Kong N; Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea.
Han B; Department of Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
Sul JH; Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, Los Angeles, California, United States of America.
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Źródło:
PLoS genetics [PLoS Genet] 2021 Jun 01; Vol. 17 (6), pp. e1009596. Date of Electronic Publication: 2021 Jun 01 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms:
Gene Expression Regulation*
Quantitative Trait Loci*
Humans ; Multifactorial Inheritance
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
ForestQC: Quality control on genetic variants from next-generation sequencing data using random forest.
Autorzy:
Li J; Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, United States of America.
Jew B; Interdepartmental Program in Bioinformatics, University of California, Los Angeles, Los Angeles, CA, United States of America.
Zhan L; Molecular Biology Institute, University of California, Los Angeles, Los Angeles, CA, United States of America.
Hwang S; Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, Los Angeles, CA, United States of America.
Coppola G; Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, Los Angeles, CA, United States of America.
Freimer NB; Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, United States of America.; Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, Los Angeles, CA, United States of America.
Sul JH; Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, Los Angeles, CA, United States of America.
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Źródło:
PLoS computational biology [PLoS Comput Biol] 2019 Dec 18; Vol. 15 (12), pp. e1007556. Date of Electronic Publication: 2019 Dec 18 (Print Publication: 2019).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms:
Genetic Variation*
Software*
High-Throughput Nucleotide Sequencing/*statistics & numerical data
Algorithms ; Computational Biology ; Databases, Genetic/statistics & numerical data ; High-Throughput Nucleotide Sequencing/standards ; Humans ; Machine Learning ; Polymorphism, Single Nucleotide ; Quality Control ; Whole Genome Sequencing/standards ; Whole Genome Sequencing/statistics & numerical data
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Leveraging allelic imbalance to refine fine-mapping for eQTL studies.
Autorzy:
Zou J; Computer Science Department, University of California Los Angeles, Los Angeles, California, United States of America.
Hormozdiari F; Genetic Epidemiology and Statistical Genetics Program, Harvard University, Cambridge, Massachusetts, United States of America.; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, United States of America.
Jew B; Bioinformatics Interdepartmental Program, University of California Los Angeles, Los Angeles, California, United States of America.
Castel SE; New York Genome Center, New York, New York, United States of America.; Department of Systems Biology, Columbia University, New York, New York, United States of America.
Lappalainen T; New York Genome Center, New York, New York, United States of America.; Department of Systems Biology, Columbia University, New York, New York, United States of America.
Ernst J; Computer Science Department, University of California Los Angeles, Los Angeles, California, United States of America.; Department of Biological Chemistry, University of California Los Angeles, Los Angeles, California, United States of America.
Sul JH; Department of Psychiatry and Biobehavioral Sciences, University of California Los Angeles, Los Angeles, California, United States of America.
Eskin E; Computer Science Department, University of California Los Angeles, Los Angeles, California, United States of America.; Department of Human Genetics, University of California Los Angeles, Los Angeles, California, United States of America.
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Źródło:
PLoS genetics [PLoS Genet] 2019 Dec 13; Vol. 15 (12), pp. e1008481. Date of Electronic Publication: 2019 Dec 13 (Print Publication: 2019).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms:
Allelic Imbalance*
Quantitative Trait Loci*
Chromatin/*genetics
Chromosome Mapping/*methods
Genetic Predisposition to Disease ; Genome-Wide Association Study ; Humans ; Linkage Disequilibrium ; Multifactorial Inheritance ; Polymorphism, Single Nucleotide
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Population structure in genetic studies: Confounding factors and mixed models.
Autorzy:
Sul JH; Department of Psychiatry and Biobehavioral Sciences, University of California Los Angeles, Los Angeles, California, United States of America.
Martin LS; Department of Computer Science, University of California, Los Angeles, California, United States of America.
Eskin E; Department of Computer Science, University of California, Los Angeles, California, United States of America.; Department of Human Genetics, University of California Los Angeles, Los Angeles, California, United States of America.
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Źródło:
PLoS genetics [PLoS Genet] 2018 Dec 27; Vol. 14 (12), pp. e1007309. Date of Electronic Publication: 2018 Dec 27 (Print Publication: 2018).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.; Review
MeSH Terms:
Genetics, Population*
Models, Genetic*
Genome-Wide Association Study/*methods
Animals ; Bias ; Disease/genetics ; Female ; Genome-Wide Association Study/statistics & numerical data ; Humans ; Linear Models ; Male ; Mice ; Models, Statistical ; Pedigree ; Phenotype ; Phylogeny ; Polymorphism, Single Nucleotide
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Negative selection in humans and fruit flies involves synergistic epistasis.
Autorzy:
Sohail M
Vakhrusheva OA
Sul JH
Pulit SL
Francioli LC
van den Berg LH
Veldink JH
de Bakker PIW
Bazykin GA
Kondrashov AS
Sunyaev SR
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Corporate Authors:
Genome of the Netherlands Consortium
Alzheimer’s Disease Neuroimaging Initiative
Źródło:
Science (New York, N.Y.) [Science] 2017 May 05; Vol. 356 (6337), pp. 539-542.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Epistasis, Genetic*
Genome, Human*
Genome, Insect*
Mutation Rate*
Selection, Genetic*
Drosophila melanogaster/*genetics
Alleles ; Animals ; Genetic Fitness ; Humans ; Linkage Disequilibrium ; Mutation, Missense
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Accounting for Population Structure in Gene-by-Environment Interactions in Genome-Wide Association Studies Using Mixed Models.
Autorzy:
Sul JH; Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, Los Angeles, California, United States of America.
Bilow M; Computer Science Department, University of California, Los Angeles, Los Angeles, California, United States of America.
Yang WY; Computer Science Department, University of California, Los Angeles, Los Angeles, California, United States of America.
Kostem E; Computer Science Department, University of California, Los Angeles, Los Angeles, California, United States of America.
Furlotte N; Computer Science Department, University of California, Los Angeles, Los Angeles, California, United States of America.
He D; Computer Science Department, University of California, Los Angeles, Los Angeles, California, United States of America.
Eskin E; Computer Science Department, University of California, Los Angeles, Los Angeles, California, United States of America.; Department of Human Genetics, University of California, Los Angeles, Los Angeles, California, United States of America.
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Źródło:
PLoS genetics [PLoS Genet] 2016 Mar 04; Vol. 12 (3), pp. e1005849. Date of Electronic Publication: 2016 Mar 04 (Print Publication: 2016).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms:
Gene-Environment Interaction*
Genetics, Population*
Genome, Human*
Genome-Wide Association Study/*methods
Computer Simulation ; Humans ; Models, Genetic ; Phenotype ; Polymorphism, Single Nucleotide/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Genome-wide association study of NMDA receptor coagonists in human cerebrospinal fluid and plasma.
Autorzy:
Luykx JJ; Human Neurogenetics Unit, Brain Center Rudolf Magnus, University Medical Center Utrecht (UMCU), Utrecht, The Netherlands.; Department of Psychiatry, ZNA Hospitals, Antwerp, Belgium.; Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht (UMCU), Utrecht, The Netherlands.
Bakker SC; Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht (UMCU), Utrecht, The Netherlands.
Visser WF; Department of Metabolic Diseases, University Medical Center Utrecht/Wilhelmina Children's Hospital, Utrecht, The Netherlands.
Verhoeven-Duif N; Department of Metabolic Diseases, University Medical Center Utrecht/Wilhelmina Children's Hospital, Utrecht, The Netherlands.
Buizer-Voskamp JE; Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht (UMCU), Utrecht, The Netherlands.
den Heijer JM; Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht (UMCU), Utrecht, The Netherlands.
Boks MP; Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht (UMCU), Utrecht, The Netherlands.
Sul JH; Computer Science Department, University of California, Los Angeles, CA, USA.
Eskin E; Computer Science Department, University of California, Los Angeles, CA, USA.; Department of Human Genetics, University of California, Los Angeles, CA, USA.
Ori AP; Center for Neurobehavioral Genetics, Semel Institute for Neuroscience and Human Behavior, University of California Los Angeles, Los Angeles, CA, USA.
Cantor RM; Department of Human Genetics, University of California, Los Angeles, CA, USA.
Vorstman J; Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht (UMCU), Utrecht, The Netherlands.
Strengman E; Department of Human Genetics, University of California, Los Angeles, CA, USA.
DeYoung J; Center for Neurobehavioral Genetics, Semel Institute for Neuroscience and Human Behavior, University of California Los Angeles, Los Angeles, CA, USA.
Kappen TH; Department of Anesthesiology, Intensive Care and Pain Management, University Medical Center Utrecht (UMCU), Utrecht, The Netherlands.
Pariama E; Department of Anesthesiology, Intensive Care and Pain Management, Diakonessenhuis Hospital, Utrecht, The Netherlands.
van Dongen EP; Department of Anesthesiology, Intensive Care & Pain Management, St Antonius Hospital, Nieuwegein, The Netherlands.
Borgdorff P; Department of Anesthesiology, Intensive Care and Pain Management, Diakonessenhuis Hospital, Utrecht, The Netherlands.
Bruins P; Department of Anesthesiology, Intensive Care & Pain Management, St Antonius Hospital, Nieuwegein, The Netherlands.
de Koning TJ; Department of Metabolic Diseases, University Medical Center Utrecht/Wilhelmina Children's Hospital, Utrecht, The Netherlands.; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.
Kahn RS; Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht (UMCU), Utrecht, The Netherlands.
Ophoff RA; Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht (UMCU), Utrecht, The Netherlands.; Department of Human Genetics, University of California, Los Angeles, CA, USA.; Center for Neurobehavioral Genetics, Semel Institute for Neuroscience and Human Behavior, University of California Los Angeles, Los Angeles, CA, USA.
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Źródło:
Molecular psychiatry [Mol Psychiatry] 2015 Dec; Vol. 20 (12), pp. 1557-64. Date of Electronic Publication: 2015 Feb 10.
Typ publikacji:
Journal Article
MeSH Terms:
Alanine/*metabolism
Glycine/*metabolism
Proline/*metabolism
Receptors, N-Methyl-D-Aspartate/*agonists
Serine/*metabolism
Adolescent ; Adult ; Alanine/blood ; Alanine/cerebrospinal fluid ; Chromatography, Liquid ; Female ; Genetic Variation ; Genome-Wide Association Study ; Glycine/blood ; Glycine/cerebrospinal fluid ; Humans ; Male ; Membrane Transport Proteins/genetics ; Middle Aged ; Proline/blood ; Proline/cerebrospinal fluid ; Proline Oxidase/genetics ; Quantitative Trait Loci ; Serine/blood ; Serine/cerebrospinal fluid ; Tandem Mass Spectrometry ; Young Adult
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
A genome-wide association study identifies potential susceptibility loci for Hirschsprung disease.
Autorzy:
Kim JH; Research Institute for Basic Science, Sogang University, Seoul, Republic of Korea; Department of Life Science, Sogang University, Seoul, Republic of Korea.
Cheong HS; Department of Genetic Epidemiology, SNP Genetics, Inc., Seoul, Republic of Korea.
Sul JH; Department of Computer Science, University of California Los Angeles, Los Angeles, California, United States of America.
Seo JM; Division of Pediatric Surgery, Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Kim DY; Department of Pediatric Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Oh JT; Department of Pediatric Surgery, Severance Children's Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
Park KW; Department of Pediatric Surgery, Seoul National University Children's Hospital, Seoul, Republic of Korea.
Kim HY; Department of Pediatric Surgery, Seoul National University Children's Hospital, Seoul, Republic of Korea.
Jung SM; Division of Pediatric Surgery, Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Jung K; Department of Surgery, Seoul National University Bundang Hospital, Seongnam, Gyeonggi, Republic of Korea.
Cho MJ; Department of Surgery, Konkuk University Medical Center, Seoul, Republic of Korea.
Bae JS; Laboratory of Translational Genomics, Samsung Genome Institute, Samsung Medical Center, Seoul, Republic of Korea.
Shin HD; Research Institute for Basic Science, Sogang University, Seoul, Republic of Korea; Department of Life Science, Sogang University, Seoul, Republic of Korea; Department of Genetic Epidemiology, SNP Genetics, Inc., Seoul, Republic of Korea.
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Źródło:
PloS one [PLoS One] 2014 Oct 13; Vol. 9 (10), pp. e110292. Date of Electronic Publication: 2014 Oct 13 (Print Publication: 2014).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Loci*
Genetic Predisposition to Disease*
Genome-Wide Association Study*
Hirschsprung Disease/*genetics
Chromosomes, Human/genetics ; Female ; Humans ; Linkage Disequilibrium/genetics ; Male ; Polymorphism, Single Nucleotide/genetics
SCR Disease Name:
Hirschsprung disease 1
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Characterization of genome-methylome interactions in 22 nuclear pedigrees.
Autorzy:
Plongthongkum N; Department of Bioengineering, University of California San Diego, La Jolla, California, United States of America.
van Eijk KR; Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands.
de Jong S; Center for Neurobehavioral Genetics, Semel Institute for Neuroscience and Behavior, David Geffen School of Medicine at the University of California Los Angeles, Los Angeles, California, United States of America.
Wang T; Center for Neurobehavioral Genetics, Semel Institute for Neuroscience and Behavior, David Geffen School of Medicine at the University of California Los Angeles, Los Angeles, California, United States of America.
Sul JH; Department of Computer Science, University of California Los Angeles, Los Angeles, California, United States of America.
Boks MP; Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands.
Kahn RS; Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands.
Fung HL; Department of Bioengineering, University of California San Diego, La Jolla, California, United States of America.
Ophoff RA; Center for Neurobehavioral Genetics, Semel Institute for Neuroscience and Behavior, David Geffen School of Medicine at the University of California Los Angeles, Los Angeles, California, United States of America; Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands.
Zhang K; Department of Bioengineering, University of California San Diego, La Jolla, California, United States of America.
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Źródło:
PloS one [PLoS One] 2014 Jul 14; Vol. 9 (7), pp. e99313. Date of Electronic Publication: 2014 Jul 14 (Print Publication: 2014).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms:
DNA Methylation*
Nuclear Family*
Pedigree*
Genome, Human/*genetics
CpG Islands/genetics ; Female ; Genomics ; Humans ; Male ; Polymorphism, Single Nucleotide ; Quantitative Trait Loci/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.
Autorzy:
Luykx JJ; 1] Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands [2] Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
Bakker SC; Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands.
Lentjes E; Department of Clinical Chemistry and Hematology, University Medical Center Utrecht, Utrecht, The Netherlands.
Neeleman M; Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands.
Strengman E; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
Mentink L; 1] Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands [2] Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
DeYoung J; Center for Neurobehavioral Genetics, Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, Los Angeles, CA, USA.
de Jong S; Center for Neurobehavioral Genetics, Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, Los Angeles, CA, USA.
Sul JH; Computer Science Department, University of California, Los Angeles, Los Angeles, CA, USA.
Eskin E; 1] Computer Science Department, University of California, Los Angeles, Los Angeles, CA, USA [2] Department of Human Genetics, University of California, Los Angeles, Los Angeles, CA, USA.
van Eijk K; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
van Setten J; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
Buizer-Voskamp JE; Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands.
Cantor RM; Department of Human Genetics, University of California, Los Angeles, Los Angeles, CA, USA.
Lu A; Department of Human Genetics, University of California, Los Angeles, Los Angeles, CA, USA.
van Amerongen M; Department of Anesthesiology, Ter Gooi Hospitals, Hilversum, The Netherlands.
van Dongen EP; Department of Anesthesiology, Intensive Care and Pain Management, St Antonius Hospital, Nieuwegein, The Netherlands.
Keijzers P; Department of Anesthesiology, Central Military Hospital, Utrecht, The Netherlands.
Kappen T; Department of Anesthesiology, Intensive Care and Pain Management, University Medical Center Utrecht, Utrecht, The Netherlands.
Borgdorff P; Department of Anesthesiology, Intensive Care and Pain Management, Diakonessenhuis Hospital, Utrecht, The Netherlands.
Bruins P; Department of Anesthesiology, Intensive Care and Pain Management, St Antonius Hospital, Nieuwegein, The Netherlands.
Derks EM; Academic Medical Center, Department of Psychiatry, Amsterdam, The Netherlands.
Kahn RS; Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands.
Ophoff RA; 1] Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands [2] Center for Neurobehavioral Genetics, Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, Los Angeles, CA, USA [3] Department of Human Genetics, University of California, Los Angeles, Los Angeles, CA, USA.
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Źródło:
Molecular psychiatry [Mol Psychiatry] 2014 Feb; Vol. 19 (2), pp. 228-34. Date of Electronic Publication: 2013 Jan 15.
Typ publikacji:
Journal Article
MeSH Terms:
Gene Expression*
Genome-Wide Association Study*
Biogenic Monoamines/*cerebrospinal fluid
Homovanillic Acid/*cerebrospinal fluid
Hydroxyindoleacetic Acid/*cerebrospinal fluid
Methoxyhydroxyphenylglycol/*cerebrospinal fluid
3',5'-Cyclic-AMP Phosphodiesterases/genetics ; Adult ; Chromosomes, Human, Pair 11 ; Female ; Genetic Loci ; Genetic Variation ; Genotyping Techniques ; Humans ; Linear Models ; Male ; Membrane Proteins/genetics ; Mental Disorders/genetics ; Polymorphism, Single Nucleotide ; Tumor Suppressor Proteins
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.
Autorzy:
Rietveld CA; Department of Applied Economics, Erasmus School of Economics, Erasmus University Rotterdam, Rotterdam, Netherlands.
Medland SE
Derringer J
Yang J
Esko T
Martin NW
Westra HJ
Shakhbazov K
Abdellaoui A
Agrawal A
Albrecht E
Alizadeh BZ
Amin N
Barnard J
Baumeister SE
Benke KS
Bielak LF
Boatman JA
Boyle PA
Davies G
de Leeuw C
Eklund N
Evans DS
Ferhmann R
Fischer K
Gieger C
Gjessing HK
Hägg S
Harris JR
Hayward C
Holzapfel C
Ibrahim-Verbaas CA
Ingelsson E
Jacobsson B
Joshi PK
Jugessur A
Kaakinen M
Kanoni S
Karjalainen J
Kolcic I
Kristiansson K
Kutalik Z
Lahti J
Lee SH
Lin P
Lind PA
Liu Y
Lohman K
Loitfelder M
McMahon G
Vidal PM
Meirelles O
Milani L
Myhre R
Nuotio ML
Oldmeadow CJ
Petrovic KE
Peyrot WJ
Polasek O
Quaye L
Reinmaa E
Rice JP
Rizzi TS
Schmidt H
Schmidt R
Smith AV
Smith JA
Tanaka T
Terracciano A
van der Loos MJ
Vitart V
Völzke H
Wellmann J
Yu L
Zhao W
Allik J
Attia JR
Bandinelli S
Bastardot F
Beauchamp J
Bennett DA
Berger K
Bierut LJ
Boomsma DI
Bültmann U
Campbell H
Chabris CF
Cherkas L
Chung MK
Cucca F
de Andrade M
De Jager PL
De Neve JE
Deary IJ
Dedoussis GV
Deloukas P
Dimitriou M
Eiríksdóttir G
Elderson MF
Eriksson JG
Evans DM
Faul JD
Ferrucci L
Garcia ME
Grönberg H
Guðnason V
Hall P
Harris JM
Harris TB
Hastie ND
Heath AC
Hernandez DG
Hoffmann W
Hofman A
Holle R
Holliday EG
Hottenga JJ
Iacono WG
Illig T
Järvelin MR
Kähönen M
Kaprio J
Kirkpatrick RM
Kowgier M
Latvala A
Launer LJ
Lawlor DA
Lehtimäki T
Li J
Lichtenstein P
Lichtner P
Liewald DC
Madden PA
Magnusson PK
Mäkinen TE
Masala M
McGue M
Metspalu A
Mielck A
Miller MB
Montgomery GW
Mukherjee S
Nyholt DR
Oostra BA
Palmer LJ
Palotie A
Penninx BW
Perola M
Peyser PA
Preisig M
Räikkönen K
Raitakari OT
Realo A
Ring SM
Ripatti S
Rivadeneira F
Rudan I
Rustichini A
Salomaa V
Sarin AP
Schlessinger D
Scott RJ
Snieder H
St Pourcain B
Starr JM
Sul JH
Surakka I
Svento R
Teumer A
Tiemeier H
van Rooij FJ
Van Wagoner DR
Vartiainen E
Viikari J
Vollenweider P
Vonk JM
Waeber G
Weir DR
Wichmann HE
Widen E
Willemsen G
Wilson JF
Wright AF
Conley D
Davey-Smith G
Franke L
Groenen PJ
Hofman A
Johannesson M
Kardia SL
Krueger RF
Laibson D
Martin NG
Meyer MN
Posthuma D
Thurik AR
Timpson NJ
Uitterlinden AG
van Duijn CM
Visscher PM
Benjamin DJ
Cesarini D
Koellinger PD
Pokaż więcej
Corporate Authors:
LifeLines Cohort Study
Źródło:
Science (New York, N.Y.) [Science] 2013 Jun 21; Vol. 340 (6139), pp. 1467-71. Date of Electronic Publication: 2013 May 30.
Typ publikacji:
Journal Article; Meta-Analysis; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms:
Educational Status*
Genome-Wide Association Study*
Polymorphism, Single Nucleotide*
Cognition ; Endophenotypes ; Female ; Genetic Loci ; Humans ; Male ; Multifactorial Inheritance
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Effectively identifying eQTLs from multiple tissues by combining mixed model and meta-analytic approaches.
Autorzy:
Sul JH; Computer Science Department, University of California, Los Angeles, California, USA.
Han B
Ye C
Choi T
Eskin E
Pokaż więcej
Źródło:
PLoS genetics [PLoS Genet] 2013 Jun; Vol. 9 (6), pp. e1003491. Date of Electronic Publication: 2013 Jun 13.
Typ publikacji:
Journal Article; Meta-Analysis; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms:
Gene Expression*
Genome-Wide Association Study*
Quantitative Trait Loci/*genetics
Animals ; Gene Expression Profiling ; Genome ; Mice ; Models, Theoretical ; Organ Specificity
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
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