A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC
Paul I. W. de Bakker(Broad Institute), Gil McVean(University of Oxford), Pardis C. Sabeti(Broad Institute), Marcos Miretti(Wellcome Sanger Institute), Todd J. Green(Broad Institute), Jonathan Marchini(University of Oxford), Xiayi Ke(Centre for Human Genetics), Alienke J. Monsuur(University Medical Center Utrecht), Pamela Whittaker(Wellcome Sanger Institute), Marcos Delgado(Wellcome Sanger Institute), Jonathan J. Morrison(Wellcome Sanger Institute), Angela M. Richardson(Broad Institute), Emily C. Walsh(Broad Institute), Xiaojiang Gao(National Cancer Institute), Luana Galver(Illumina (United States)), John Hart(Center for Human Genetics), David A. Hafler(Broad Institute), Margaret A. Pericak‐Vance(Center for Human Genetics), John A. Todd(University of Cambridge), Mark Daly(Broad Institute), John Trowsdale(Addenbrooke's Hospital), Cisca Wijmenga(University Medical Center Utrecht), Tim J. Vyse(Imperial College London), Stephan Beck(Wellcome Sanger Institute), Sarah S. Murray(Illumina (United States)), Mary Carrington(National Cancer Institute), Simon G. Gregory(Center for Human Genetics), Panos Deloukas(Wellcome Sanger Institute), John D. Rioux(Broad Institute)
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