Re-sequencing expands our understanding of the phenotypic impact of variants at GWAS loci.

TitleRe-sequencing expands our understanding of the phenotypic impact of variants at GWAS loci.
Publication TypeJournal Article
AuthorsService SK, Teslovich TM, Fuchsberger C, Ramensky V, Yajnik P, Koboldt DC, Larson DE, Zhang Q, Lin L, Welch R, Ding L, McLellan MD, O'Laughlin M, Fronick C, Fulton LL, Magrini V, Swift A, Elliott P, Jarvelin M-R, Kaakinen M, McCarthy MI, Peltonen L, Pouta A, Bonnycastle LL, Collins FS, Narisu N, Stringham HM, Tuomilehto J, Ripatti S, Fulton RS, Sabatti C, Wilson RK, Boehnke M, Freimer NB
PubMed ID24497850
PubMed Central IDPMC3907339
Grant List098381 / / Wellcome Trust / United Kingdom
DK062370 / DK / NIDDK NIH HHS / United States
G0500539 / / Medical Research Council / United Kingdom
G0600705 / / Medical Research Council / United Kingdom
HG006695 / HG / NHGRI NIH HHS / United States
HL087679 / HL / NHLBI NIH HHS / United States
HL113315 / HL / NHLBI NIH HHS / United States
MH083268 / MH / NIMH NIH HHS / United States
MH63706 / MH / NIMH NIH HHS / United States
R01 HG006695 / HG / NHGRI NIH HHS / United States
R01 HL113315 / HL / NHLBI NIH HHS / United States
U54HG003079 / HG / NHGRI NIH HHS / United States