Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic BoundariesMichael E. Talkowski, James F. Gusella, Carrie Hanscom et al.|Cell|2012Cited by 598
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarizationDan E. Arking, Jaroslav A. Hubáček, Sara L. Pulit et al.|Nature Genetics|2014Cited by 335
Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencingAndrew Kirby, Mark J. Daly, Andreas Gnirke et al.|Nature Genetics|2013Cited by 317
Pervasive Sharing of Genetic Effects in Autoimmune DiseaseChris Cotsapas, Benjamin F. Voight, Elizabeth J. Rossin et al.|PLoS Genetics|2011Cited by 31