TY - JOUR
T1 - Fine-mapping and functional studies highlight potential causal variants for rheumatoid arthritis and type 1 diabetes
AU - Westra, Harm-Jan
AU - Martinez-Bonet, Marta
AU - Onengut-Gumuscu, Suna
AU - Lee, Annette
AU - Luol, Yang
AU - Teslovich, Nikola
AU - Worthington, Jane
AU - Martin, Javier
AU - Huizinga, Tom
AU - Klareskog, Lars
AU - Rantapaa-Dahlqvist, Solbritt
AU - Chen, Wei-Min
AU - Quinlan, Aaron
AU - Todd, John A.
AU - Eyre, Steve
AU - Nigrovic, Peter A.
AU - Regersen, Peter K. G.
AU - Rich, Stephen S.
AU - Raychaudhuri, Soumya
PY - 2018/10
Y1 - 2018/10
N2 - To define potentially causal variants for autoimmune disease, we fine-mapped(1,2) 76 rheumatoid arthritis (11,475 cases,15,870 controls)(3) and type 1 diabetes loci (9,334 cases, 11,111 controls)(4). After sequencing 799 1-kilobase regulatory (H3K4me3) regions within these loci in 568 individuals, we observed accurate imputation for 89% of common variants. We defined credible sets of
AB - To define potentially causal variants for autoimmune disease, we fine-mapped(1,2) 76 rheumatoid arthritis (11,475 cases,15,870 controls)(3) and type 1 diabetes loci (9,334 cases, 11,111 controls)(4). After sequencing 799 1-kilobase regulatory (H3K4me3) regions within these loci in 568 individuals, we observed accurate imputation for 89% of common variants. We defined credible sets of
KW - GENOME-WIDE ASSOCIATION
KW - SYSTEMIC-LUPUS-ERYTHEMATOSUS
KW - INFLAMMATORY-BOWEL-DISEASE
KW - BURROWS-WHEELER TRANSFORM
KW - SUSCEPTIBILITY LOCI
KW - CELL-TYPES
KW - TYROSINE-PHOSPHATASE
KW - GENOTYPE IMPUTATION
KW - COMPLEX TRAIT
KW - RISK LOCI
U2 - 10.1038/s41588-018-0216-7
DO - 10.1038/s41588-018-0216-7
M3 - Article
VL - 50
SP - 1366
EP - 1374
JO - Nature Genetics
JF - Nature Genetics
SN - 1061-4036
IS - 10
ER -