Systematic localization of common disease-associated variation in regulatory DNA

Science

Volumn 337, Issue 6099, 2012, Pages 1190-1195

  Maurano, Matthew T ^a   Humbert, Richard ^a   Rynes, Eric ^a   Thurman, Robert E ^a   Haugen, Eric ^a   Wang, Hao ^a   Reynolds, Alex P ^a   Sandstrom, Richard ^a   Qu, Hongzhu ^a,b   Brody, Jennifer ^c   Shafer, Anthony ^a   Neri, Fidencio ^a   Lee, Kristen ^a   Kutyavin, Tanya ^a   Stehling Sun, Sandra ^a   Johnson, Audra K ^a   Canfield, Theresa K ^a   Giste, Erika ^a   Diegel, Morgan ^a   Bates, Daniel ^a   Hansen, R Scott ^c   Neph, Shane ^a   Sabo, Peter J ^a   Heimfeld, Shelly ^d   Raubitschek, Antony ^e   Ziegler, Steven ^e   Cotsapas, Chris ^f   Sotoodehnia, Nona ^c   Glass, Ian ^c   Sunyaev, Shamil R ^g   Kaul, Rajinder ^c   Stamatoyannopoulos, John A ^a,c   more..

^a UNIVERSITY OF WASHINGTON   (United States)

^b Chinese Academy of Sciences and China National Center for Bioinformation   (China)

^c UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^d Fred Hutchinson Cancer Research Center   (United States)

^e BENAROYA RESEARCH INSTITUTE   (United States)

^f YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^g BRIGHAM AND WOMEN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

B LYMPHOCYTE INDUCED MATURATION PROTEIN 1; CHEMOKINE RECEPTOR CXCR6; CRYOPYRIN; DEOXYRIBONUCLEASE I; DNA; SODIUM CHANNEL NAV1.8; TRANSCRIPTION FACTOR;

CELL ORGANELLE; DISEASE INCIDENCE; GENOME; MITOCHONDRIAL DNA; PATHOGEN; PHENOTYPE; PHYSIOLOGICAL RESPONSE; PREGNANCY;

ALLELE; ARTICLE; CELL TYPE; CHROMATIN; CROHN DISEASE; DISEASE ASSOCIATION; ELECTROCARDIOGRAM; FETUS DEVELOPMENT; GENE REGULATORY NETWORK; GENE TARGETING; GENETIC VARIABILITY; HUMAN; HYPERSENSITIVITY; MULTIPLE SCLEROSIS; PHENOTYPE; PREGNANCY; PRIORITY JOURNAL;

EID: 84865822182     PISSN: 00368075     EISSN: 10959203     Source Type: Journal    
DOI: 10.1126/science.1222794     Document Type: Article

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