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Wyszukujesz frazę ""Edlund, CK"" wg kryterium: Autor


Wyświetlanie 1-11 z 11
Tytuł:
GWASeq: targeted re-sequencing follow up to GWAS.
Autorzy:
Salomon MP; Department of Preventive Medicine, Keck School of Medicine of the University of Southern California, Los Angeles, CA, USA. .; Department of Molecular Oncology, John Wayne Cancer Institute at Providence Saint John's Health Center, Santa Monica, CA, USA. .
Li WL; Department of Preventive Medicine, Keck School of Medicine of the University of Southern California, Los Angeles, CA, USA. .
Edlund CK; Department of Preventive Medicine, Keck School of Medicine of the University of Southern California, Los Angeles, CA, USA. .
Morrison J; Department of Preventive Medicine, Keck School of Medicine of the University of Southern California, Los Angeles, CA, USA. .
Fortini BK; Department of Preventive Medicine, Keck School of Medicine of the University of Southern California, Los Angeles, CA, USA. .
Win AK; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Parkville, Melbourne, VIC, Australia. .
Conti DV; Department of Preventive Medicine, Keck School of Medicine of the University of Southern California, Los Angeles, CA, USA. .
Thomas DC; Department of Preventive Medicine, Keck School of Medicine of the University of Southern California, Los Angeles, CA, USA. .
Duggan D; Translational Genomics Research Institute, Phoenix, AZ, USA. .
Buchanan DD; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Parkville, Melbourne, VIC, Australia. .; Oncogenomics Group, Genetic Epidemiology Laboratory, Department of Pathology, The University of Melbourne, Parkville, Melbourne, VIC, Australia. .
Jenkins MA; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Parkville, Melbourne, VIC, Australia. .
Hopper JL; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Parkville, Melbourne, VIC, Australia. .
Gallinger S; Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, ON, Canada. .
Le Marchand L; University of Hawaii Cancer Center, Honolulu, HI, USA. .
Newcomb PA; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA. .
Casey G; Department of Preventive Medicine, Keck School of Medicine of the University of Southern California, Los Angeles, CA, USA. .
Marjoram P; Department of Preventive Medicine, Keck School of Medicine of the University of Southern California, Los Angeles, CA, USA. .
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Źródło:
BMC genomics [BMC Genomics] 2016 Mar 03; Vol. 17, pp. 176. Date of Electronic Publication: 2016 Mar 03.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms:
Genome-Wide Association Study*
High-Throughput Nucleotide Sequencing/*methods
Sequence Analysis, DNA/*methods
Chromosome Mapping ; Colonic Neoplasms/genetics ; Computational Biology ; Genetic Variation ; Humans
Czasopismo naukowe
Tytuł:
Smokescreen: a targeted genotyping array for addiction research.
Autorzy:
Baurley JW; BioRealm LLC, 6101 W. Centinela Ave., Suite 270, Culver City, CA, 90230-6359, USA. .
Edlund CK; BioRealm LLC, 6101 W. Centinela Ave., Suite 270, Culver City, CA, 90230-6359, USA. chris.edlund@biorealmresearch.com.
Pardamean CI; BioRealm LLC, 6101 W. Centinela Ave., Suite 270, Culver City, CA, 90230-6359, USA. .
Conti DV; BioRealm LLC, 6101 W. Centinela Ave., Suite 270, Culver City, CA, 90230-6359, USA. .
Bergen AW; BioRealm LLC, 6101 W. Centinela Ave., Suite 270, Culver City, CA, 90230-6359, USA. .
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Źródło:
BMC genomics [BMC Genomics] 2016 Feb 27; Vol. 17, pp. 145. Date of Electronic Publication: 2016 Feb 27.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Genotype*
Oligonucleotide Array Sequence Analysis/*methods
Tobacco Use Disorder/*genetics
Asian People ; Black People ; Chromosome Mapping ; Exons ; Genetic Markers ; Genome-Wide Association Study ; Humans ; Nicotine/metabolism ; Polymorphism, Single Nucleotide ; Smoking/genetics ; White People
Czasopismo naukowe
Tytuł:
Multiple functional risk variants in a SMAD7 enhancer implicate a colorectal cancer risk haplotype.
Autorzy:
Fortini BK; Department of Preventive Medicine, University of Southern California, Los Angeles, California, United States of America.
Tring S; Department of Preventive Medicine, University of Southern California, Los Angeles, California, United States of America.
Plummer SJ; Department of Preventive Medicine, University of Southern California, Los Angeles, California, United States of America.
Edlund CK; Department of Preventive Medicine, University of Southern California, Los Angeles, California, United States of America.
Moreno V; Cancer Prevention and Control Program, Catalan Institute of Oncology, CIBERESP and University of Barcelona, Hospitalet de Llobregat, Barcelona, Spain.
Bresalier RS; Department of Gastroenterology, Hepatology and Nutrition, University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.
Barry EL; Department of Community and Family Medicine, Geisel School of Medicine at Dartmouth, Lebanon, New Hampshire, United States of America.
Church TR; Division of Environmental Health Sciences, University of Minnesota School of Public Health, Minneapolis, Minnesota, United States of America.
Figueiredo JC; Department of Preventive Medicine, University of Southern California, Los Angeles, California, United States of America.
Casey G; Department of Preventive Medicine, University of Southern California, Los Angeles, California, United States of America.
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Źródło:
PloS one [PLoS One] 2014 Nov 06; Vol. 9 (11), pp. e111914. Date of Electronic Publication: 2014 Nov 06 (Print Publication: 2014).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Polymorphism, Single Nucleotide*
Bone Morphogenetic Proteins/*metabolism
Colorectal Neoplasms/*genetics
Smad7 Protein/*genetics
Cell Line, Tumor ; Chromosomes, Human, Pair 18/genetics ; Enhancer Elements, Genetic ; Genetic Variation ; HCT116 Cells ; HEK293 Cells ; Humans ; Linkage Disequilibrium ; Signal Transduction ; Transforming Growth Factor beta/metabolism
Czasopismo naukowe
Tytuł:
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture.
Autorzy:
Davis LK; Section of Genetic Medicine, Department of Medicine, University of Chicago, Chicago, Illinois, United States of America.
Yu D
Keenan CL
Gamazon ER
Konkashbaev AI
Derks EM
Neale BM
Yang J
Lee SH
Evans P
Barr CL
Bellodi L
Benarroch F
Berrio GB
Bienvenu OJ
Bloch MH
Blom RM
Bruun RD
Budman CL
Camarena B
Campbell D
Cappi C
Cardona Silgado JC
Cath DC
Cavallini MC
Chavira DA
Chouinard S
Conti DV
Cook EH
Coric V
Cullen BA
Deforce D
Delorme R
Dion Y
Edlund CK
Egberts K
Falkai P
Fernandez TV
Gallagher PJ
Garrido H
Geller D
Girard SL
Grabe HJ
Grados MA
Greenberg BD
Gross-Tsur V
Haddad S
Heiman GA
Hemmings SM
Hounie AG
Illmann C
Jankovic J
Jenike MA
Kennedy JL
King RA
Kremeyer B
Kurlan R
Lanzagorta N
Leboyer M
Leckman JF
Lennertz L
Liu C
Lochner C
Lowe TL
Macciardi F
McCracken JT
McGrath LM
Mesa Restrepo SC
Moessner R
Morgan J
Muller H
Murphy DL
Naarden AL
Ochoa WC
Ophoff RA
Osiecki L
Pakstis AJ
Pato MT
Pato CN
Piacentini J
Pittenger C
Pollak Y
Rauch SL
Renner TJ
Reus VI
Richter MA
Riddle MA
Robertson MM
Romero R
Rosàrio MC
Rosenberg D
Rouleau GA
Ruhrmann S
Ruiz-Linares A
Sampaio AS
Samuels J
Sandor P
Sheppard B
Singer HS
Smit JH
Stein DJ
Strengman E
Tischfield JA
Valencia Duarte AV
Vallada H
Van Nieuwerburgh F
Veenstra-Vanderweele J
Walitza S
Wang Y
Wendland JR
Westenberg HG
Shugart YY
Miguel EC
McMahon W
Wagner M
Nicolini H
Posthuma D
Hanna GL
Heutink P
Denys D
Arnold PD
Oostra BA
Nestadt G
Freimer NB
Pauls DL
Wray NR
Stewart SE
Mathews CA
Knowles JA
Cox NJ
Scharf JM
Pokaż więcej
Źródło:
PLoS genetics [PLoS Genet] 2013 Oct; Vol. 9 (10), pp. e1003864. Date of Electronic Publication: 2013 Oct 24.
Typ publikacji:
Journal Article; Research Support, American Recovery and Reinvestment Act; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Quantitative Trait, Heritable*
Obsessive-Compulsive Disorder/*genetics
Tourette Syndrome/*genetics
Gene Frequency ; Genome-Wide Association Study ; Humans ; Obsessive-Compulsive Disorder/pathology ; Phenotype ; Polymorphism, Single Nucleotide ; Tourette Syndrome/pathology
Czasopismo naukowe
Tytuł:
Genome-wide association study of obsessive-compulsive disorder.
Autorzy:
Stewart SE; Psychiatric and Neurodevelopmental Genetics Unit, Center for Human Genetics Research, Harvard Medical School, Boston, MA 02114, USA. />Yu D
Scharf JM
Neale BM
Fagerness JA
Mathews CA
Arnold PD
Evans PD
Gamazon ER
Davis LK
Osiecki L
McGrath L
Haddad S
Crane J
Hezel D
Illman C
Mayerfeld C
Konkashbaev A
Liu C
Pluzhnikov A
Tikhomirov A
Edlund CK
Rauch SL
Moessner R
Falkai P
Maier W
Ruhrmann S
Grabe HJ
Lennertz L
Wagner M
Bellodi L
Cavallini MC
Richter MA
Cook EH Jr
Kennedy JL
Rosenberg D
Stein DJ
Hemmings SM
Lochner C
Azzam A
Chavira DA
Fournier E
Garrido H
Sheppard B
Umaña P
Murphy DL
Wendland JR
Veenstra-VanderWeele J
Denys D
Blom R
Deforce D
Van Nieuwerburgh F
Westenberg HG
Walitza S
Egberts K
Renner T
Miguel EC
Cappi C
Hounie AG
Conceição do Rosário M
Sampaio AS
Vallada H
Nicolini H
Lanzagorta N
Camarena B
Delorme R
Leboyer M
Pato CN
Pato MT
Voyiaziakis E
Heutink P
Cath DC
Posthuma D
Smit JH
Samuels J
Bienvenu OJ
Cullen B
Fyer AJ
Grados MA
Greenberg BD
McCracken JT
Riddle MA
Wang Y
Coric V
Leckman JF
Bloch M
Pittenger C
Eapen V
Black DW
Ophoff RA
Strengman E
Cusi D
Turiel M
Frau F
Macciardi F
Gibbs JR
Cookson MR
Singleton A
Hardy J
Crenshaw AT
Parkin MA
Mirel DB
Conti DV
Purcell S
Nestadt G
Hanna GL
Jenike MA
Knowles JA
Cox N
Pauls DL
Pokaż więcej
Corporate Authors:
North American Brain Expression Consortium
UK Brain Expression Database
Źródło:
Molecular psychiatry [Mol Psychiatry] 2013 Jul; Vol. 18 (7), pp. 788-98. Date of Electronic Publication: 2012 Aug 14.
Typ publikacji:
Journal Article; Meta-Analysis; Research Support, American Recovery and Reinvestment Act; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Genome-Wide Association Study*
Genetic Predisposition to Disease/*genetics
Nerve Tissue Proteins/*genetics
Obsessive-Compulsive Disorder/*genetics
Case-Control Studies ; Frontal Lobe/metabolism ; Humans ; Parents ; Polymorphism, Single Nucleotide/genetics ; Quantitative Trait Loci/genetics ; SAP90-PSD95 Associated Proteins ; White People/genetics
Czasopismo naukowe
Tytuł:
Genome-wide association study of Tourette's syndrome.
Autorzy:
Scharf JM; Psychiatric and Neurodevelopmental Genetics Unit, Center for Human Genetics Research, Boston, MA, USA. />Yu D
Mathews CA
Neale BM
Stewart SE
Fagerness JA
Evans P
Gamazon E
Edlund CK
Service SK
Tikhomirov A
Osiecki L
Illmann C
Pluzhnikov A
Konkashbaev A
Davis LK
Han B
Crane J
Moorjani P
Crenshaw AT
Parkin MA
Reus VI
Lowe TL
Rangel-Lugo M
Chouinard S
Dion Y
Girard S
Cath DC
Smit JH
King RA
Fernandez TV
Leckman JF
Kidd KK
Kidd JR
Pakstis AJ
State MW
Herrera LD
Romero R
Fournier E
Sandor P
Barr CL
Phan N
Gross-Tsur V
Benarroch F
Pollak Y
Budman CL
Bruun RD
Erenberg G
Naarden AL
Lee PC
Weiss N
Kremeyer B
Berrío GB
Campbell DD
Cardona Silgado JC
Ochoa WC
Mesa Restrepo SC
Muller H
Valencia Duarte AV
Lyon GJ
Leppert M
Morgan J
Weiss R
Grados MA
Anderson K
Davarya S
Singer H
Walkup J
Jankovic J
Tischfield JA
Heiman GA
Gilbert DL
Hoekstra PJ
Robertson MM
Kurlan R
Liu C
Gibbs JR
Singleton A
Hardy J
Strengman E
Ophoff RA
Wagner M
Moessner R
Mirel DB
Posthuma D
Sabatti C
Eskin E
Conti DV
Knowles JA
Ruiz-Linares A
Rouleau GA
Purcell S
Heutink P
Oostra BA
McMahon WM
Freimer NB
Cox NJ
Pauls DL
Pokaż więcej
Corporate Authors:
North American Brain Expression Consortium
UK Human Brain Expression Database
Źródło:
Molecular psychiatry [Mol Psychiatry] 2013 Jun; Vol. 18 (6), pp. 721-8. Date of Electronic Publication: 2012 Aug 14.
Typ publikacji:
Journal Article; Multicenter Study; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Predisposition to Disease*
Genome-Wide Association Study*
Fibrillar Collagens/*genetics
Polymorphism, Single Nucleotide/*genetics
Tourette Syndrome/*genetics
Adolescent ; Adult ; Attention Deficit Disorder with Hyperactivity/etiology ; Attention Deficit Disorder with Hyperactivity/genetics ; Case-Control Studies ; Chromosomes, Human, Pair 9/genetics ; Female ; Genotype ; Humans ; International Cooperation ; Male ; Meta-Analysis as Topic ; Obsessive-Compulsive Disorder/etiology ; Obsessive-Compulsive Disorder/genetics ; Tourette Syndrome/complications ; White People/genetics ; Young Adult
Czasopismo naukowe
Tytuł:
A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer.
Autorzy:
Haiman CA; Department of Preventive Medicine, Keck School of Medicine, University of Southern California/Norris Comprehensive Cancer Center, Los Angeles, USA. />Chen GK
Vachon CM
Canzian F
Dunning A
Millikan RC
Wang X
Ademuyiwa F
Ahmed S
Ambrosone CB
Baglietto L
Balleine R
Bandera EV
Beckmann MW
Berg CD
Bernstein L
Blomqvist C
Blot WJ
Brauch H
Buring JE
Carey LA
Carpenter JE
Chang-Claude J
Chanock SJ
Chasman DI
Clarke CL
Cox A
Cross SS
Deming SL
Diasio RB
Dimopoulos AM
Driver WR
Dünnebier T
Durcan L
Eccles D
Edlund CK
Ekici AB
Fasching PA
Feigelson HS
Flesch-Janys D
Fostira F
Försti A
Fountzilas G
Gerty SM
Giles GG
Godwin AK
Goodfellow P
Graham N
Greco D
Hamann U
Hankinson SE
Hartmann A
Hein R
Heinz J
Holbrook A
Hoover RN
Hu JJ
Hunter DJ
Ingles SA
Irwanto A
Ivanovich J
John EM
Johnson N
Jukkola-Vuorinen A
Kaaks R
Ko YD
Kolonel LN
Konstantopoulou I
Kosma VM
Kulkarni S
Lambrechts D
Lee AM
Marchand LL
Lesnick T
Liu J
Lindstrom S
Mannermaa A
Margolin S
Martin NG
Miron P
Montgomery GW
Nevanlinna H
Nickels S
Nyante S
Olswold C
Palmer J
Pathak H
Pectasides D
Perou CM
Peto J
Pharoah PD
Pooler LC
Press MF
Pylkäs K
Rebbeck TR
Rodriguez-Gil JL
Rosenberg L
Ross E
Rüdiger T
Silva Idos S
Sawyer E
Schmidt MK
Schulz-Wendtland R
Schumacher F
Severi G
Sheng X
Signorello LB
Sinn HP
Stevens KN
Southey MC
Tapper WJ
Tomlinson I
Hogervorst FB
Wauters E
Weaver J
Wildiers H
Winqvist R
Van Den Berg D
Wan P
Xia LY
Yannoukakos D
Zheng W
Ziegler RG
Siddiq A
Slager SL
Stram DO
Easton D
Kraft P
Henderson BE
Couch FJ
Pokaż więcej
Corporate Authors:
Gene Environment Interaction and Breast Cancer in Germany (GENICA) Consortium
Źródło:
Nature genetics [Nat Genet] 2011 Oct 30; Vol. 43 (12), pp. 1210-4. Date of Electronic Publication: 2011 Oct 30.
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:
Genetic Loci*
Breast Neoplasms/*genetics
Membrane Proteins/*genetics
Neoplasm Proteins/*genetics
Receptors, Estrogen/*metabolism
Telomerase/*genetics
Black or African American ; Aged ; Breast Neoplasms/ethnology ; Breast Neoplasms/metabolism ; Case-Control Studies ; Female ; Genetic Predisposition to Disease ; Genome-Wide Association Study ; Genotype ; Humans ; Middle Aged ; Polymorphism, Single Nucleotide ; Receptors, Estrogen/genetics ; White People
Czasopismo naukowe
Tytuł:
Validating genetic risk associations for ovarian cancer through the international Ovarian Cancer Association Consortium.
Autorzy:
Pearce CL; Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA. />Near AM
Van Den Berg DJ
Ramus SJ
Gentry-Maharaj A
Menon U
Gayther SA
Anderson AR
Edlund CK
Wu AH
Chen X
Beesley J
Webb PM
Holt SK
Chen C
Doherty JA
Rossing MA
Whittemore AS
McGuire V
DiCioccio RA
Goodman MT
Lurie G
Carney ME
Wilkens LR
Ness RB
Moysich KB
Edwards R
Jennison E
Kjaer SK
Hogdall E
Hogdall CK
Goode EL
Sellers TA
Vierkant RA
Cunningham JM
Schildkraut JM
Berchuck A
Moorman PG
Iversen ES
Cramer DW
Terry KL
Vitonis AF
Titus-Ernstoff L
Song H
Pharoah PD
Spurdle AB
Anton-Culver H
Ziogas A
Brewster W
Galitovskiy V
Chenevix-Trench G
Pokaż więcej
Corporate Authors:
Australian Cancer Study
Australian Ovarian Cancer Study Group
Źródło:
British journal of cancer [Br J Cancer] 2009 Jan 27; Vol. 100 (2), pp. 412-20. Date of Electronic Publication: 2009 Jan 06.
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.; Validation Study
MeSH Terms:
Genetic Predisposition to Disease*
Cytochrome P-450 CYP3A/*genetics
DNA Ligases/*genetics
DNA-Binding Proteins/*genetics
Ovarian Neoplasms/*genetics
Polymorphism, Single Nucleotide/*genetics
Adult ; Aged ; Case-Control Studies ; Cohort Studies ; DNA Ligase ATP ; Female ; Genotype ; Heterozygote ; Homozygote ; Humans ; Middle Aged ; Neoplasm Invasiveness ; Ovarian Neoplasms/pathology ; Risk Factors
Czasopismo naukowe
Tytuł:
Snagger: a user-friendly program for incorporating additional information for tagSNP selection.
Autorzy:
Edlund CK; Keck School of Medicine, University of Southern California, Los Angeles, California 90033, USA. />Lee WH
Li D
Van Den Berg DJ
Conti DV
Pokaż więcej
Źródło:
BMC bioinformatics [BMC Bioinformatics] 2008 Mar 27; Vol. 9, pp. 174. Date of Electronic Publication: 2008 Mar 27.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms:
Expressed Sequence Tags*
Software*
Chromosome Mapping/*methods
DNA Mutational Analysis/*methods
Linkage Disequilibrium/*genetics
Polymorphism, Single Nucleotide/*genetics
Sequence Analysis, DNA/*methods
Base Sequence ; Genetic Variation/genetics ; Molecular Sequence Data
Czasopismo naukowe
Tytuł:
Lift/transfer and technical aids for persons with severe acquired brain injury. An inventory of problems.
Autorzy:
Edlund CK; Department of Surgical Sciences, Karolinska Institute, Stockholm, Sweden. @kirurgi.ki.se
Harms-Ringdahl K
Seiger A
Pokaż więcej
Źródło:
Scandinavian journal of caring sciences [Scand J Caring Sci] 1998; Vol. 12 (3), pp. 154-9.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Lifting*
Self-Help Devices*
Wheelchairs*
Brain Injuries/*rehabilitation
Activities of Daily Living ; Adolescent ; Adult ; Brain Injuries/complications ; Brain Injuries/physiopathology ; Female ; Humans ; Male ; Middle Aged ; Surveys and Questionnaires
Czasopismo naukowe
    Wyświetlanie 1-11 z 11

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