GREGoR: accelerating genomics for rare diseases
Moez Dawood(Baylor College of Medicine), Tugce Bozkurt‐Yozgatli, Sairam Behera(Baylor College of Medicine), Heidi L. Rehm(Unknown), Evan E. Eichler(University of Washington), Hatoon Al Ali(Baylor College of Medicine), Jonathan LoTempio(Medical Technologies (Czechia)), Ben Heavner(University of Washington), Chia‐Lin Wei(Joint Genome Institute), Marsha M. Wheeler(University of Washington), Lisa H. Chadwick, Kaitlin E. Samocha(Broad Institute), Fritz J. Sedlazeck(Baylor College of Medicine), Elizabeth G. Atkinson(Broad Institute), Casey A. Gifford(Stanford Health Care), Laurens Wiel(Radboud University Nijmegen), Emmanuèle C. Délot(Children's National), Danny E. Miller(Seattle Children's Hospital), Michael J. Bamshad(University of Washington), Susanne May(University of Washington), Jessica X. Chong(Brotman Baty Institute), Aimée M. Dudley(Pacific Northwest Diabetes Research Institute), Jill E. Moore(University of Massachusetts Chan Medical School), Seth Berger(Children's National), Claudia M.B. Carvalho(Pacific Northwest Diabetes Research Institute), Anne O’Donnell‐Luria(Broad Institute), Yang Li(University of Chicago), Eric Boerwinkle(Baylor College of Medicine), Jonathan A. Bernstein(Stanford Medicine), Jennifer E. Posey(Baylor College of Medicine), Shaghayegh Beheshti, Rachel A. Ungar(Stanford University)
Cited by 12
Related Papers
Analysis of protein-coding genetic variation in 60,706 humans
|Nature|2016|10.3k
Finding the missing heritability of complex diseases
|Nature|2009|8.5k
A Draft Sequence of the Neandertal Genome
|Science|2010|4.6k