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Nature|June 19, 2009
Copy number variation at 1q21.1 associated with neuroblastomaSharon J Diskin, Cuiping Hou, Joseph T Glessner, et al.Nature|December 3, 2010
Integrative genomics identifies LMO1 as a neuroblastoma oncogeneKai Wang, Sharon J Diskin, Haitao Zhang, et al.Human Molecular Genetics|February 24, 2010
Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effectsKai Wang, Robert Baldassano, Haitao Zhang, et al.Nature Communications|January 16, 2020
Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associationsYun Rose Li, Joseph T Glessner, Bradley P Coe, et al.Plos Genetics|June 27, 2009
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genesMaja Bucan, Brett S Abrahams, Kai Wang, et al.Plos Pathogens|July 10, 2010
Leprosy and the adaptation of human toll-like receptor 1Sunny H Wong, Sailesh Gochhait, Dheeraj Malhotra, et al.Human Genetics|October 15, 2011
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorderJillian P Casey, Tiago Magalhaes, Judith M Conroy, et al.Nature Genetics|December 27, 2011
Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitisLavinia Paternoster, Marie Standl, Chih-Mei Chen, et al.Human Molecular Genetics|July 31, 2012
Individual common variants exert weak effects on the risk for autism spectrum disordersRichard Anney, Lambertus Klei, Dalila Pinto, et al.Human Molecular Genetics|July 29, 2010
A genome-wide scan for common alleles affecting risk for autismRichard Anney, Lambertus Klei, Dalila Pinto, et al.Pageof 6