Negligible impact of rare autoimmune-locus coding-region variants on missing heritability
Karen A. Hunt(Queen Mary University of London), David A. van Heel(Queen Mary University of London), Francesca Capon(King's College London), Monkol Lek(Massachusetts General Hospital), Charles A. Mein(Queen Mary University of London), Yong Kong(W. M. Keck Foundation), Jack Satsangi(Western General Hospital), Christopher G. Mathew(Institute of Cancer Research), Michael A. Simpson(Guy's Hospital), Richard C. Trembath(University Medical Center Groningen), John Mansfield(Newcastle University), Oliver S. Burren(AstraZeneca (United Kingdom)), Jeffrey C. Barrett(Centre for Human Genetics), Maria Ban(University of Cambridge), Matthew J. Simmonds(University of Birmingham), Luke Jostins(Wellcome Sanger Institute), Eva Wozniak(Queen Mary University of London), Stephan Brand(Ludwig-Maximilians-Universität München), Nicholas Bockett(Queen Mary University of London), Sarah Nutland(University of Cambridge), Miles Parkes(University of Cambridge), Vincent Plagnol(University College London), Tariq Ahmad(Peninsula College of Medicine and Dentistry), Stephen S. Rich(Wellcome Sanger Institute), Neil Walker, Alastair Compston(University of Cambridge), Efterpi Papouli(King's College London), Suna Önengüt-Gümüşcü(University of Virginia), James Lee(Rutgers, The State University of New Jersey), Stephen Gough(University of Birmingham), Hannah Blackburn(Wellcome Sanger Institute), Vanisha Mistry(Queen Mary University of London), Steven Sawcer(University of Cambridge), John A. Todd(University of Cambridge), Muddassar M. Mirza(Genomics England), Daniel G. MacArthur(Wellcome Sanger Institute)
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