Origins and functional impact of copy number variation in the human genome
Donald F. Conrad(Wellcome Sanger Institute), Dalila Pinto(Hospital for Sick Children), Richard Redon(Inserm), Lars Feuk(Uppsala University), Ömer Gökçümen(Brigham and Women's Hospital), Yujun Zhang(Wellcome Sanger Institute), Jan Aerts(Wellcome Sanger Institute), T. Daniel Andrews(Wellcome Sanger Institute), C. Barnes(Wellcome Sanger Institute), Peter J. Campbell(Wellcome Sanger Institute), Tomas Fitzgerald(Wellcome Sanger Institute), Min Hu(Wellcome Sanger Institute), Chun Hwa Ihm(Brigham and Women's Hospital), Kati Kristiansson(Wellcome Sanger Institute), Daniel G. MacArthur(Wellcome Sanger Institute), Jeffrey R. MacDonald(Hospital for Sick Children), Ifejinelo Onyiah(Wellcome Sanger Institute), Andy Wing Chun Pang(Hospital for Sick Children), Samuel C. Robson(Wellcome Sanger Institute), Kathy Stirrups(Wellcome Sanger Institute), Armand Valsesia(Wellcome Sanger Institute), Klaudia Walter(Wellcome Sanger Institute), John Wei(Hospital for Sick Children), Chris Tyler‐Smith(Wellcome Sanger Institute), Nigel P. Carter(Wellcome Sanger Institute), Charles Lee(Brigham and Women's Hospital), Stephen W. Scherer(University of Toronto), Matthew E. Hurles(Wellcome Sanger Institute)
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