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Human Molecular Genetics|December 28, 2018
Construction and benchmarking of a multi-ethnic reference panel for the imputation of HLA class I and II allelesFrauke Degenhardt, Mareike Wendorff, Michael Wittig, et al.
Nature Genetics|January 7, 2015
High-density mapping of the MHC identifies a shared role for HLA-DRB1*01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitisPhilippe Goyette, Gabrielle Boucher, Dermot Mallon, et al.
Science Translational Medicine|September 27, 2019
<i>Lrrk2</i> alleles modulate inflammation during microbial infection of mice in a sex-dependent mannerBojan Shutinoski, Mansoureh Hakimi, Irene E Harmsen, et al.
Gastroenterology|November 8, 2006
Genetic variation in myosin IXB is associated with ulcerative colitisAdriaan A van Bodegraven, Christine R Curley, Karen A Hunt, et al.
Gastroenterology|January 9, 2021
Inflamed Ulcerative Colitis Regions Associated With MRGPRX2-Mediated Mast Cell Degranulation and Cell Activation Modules, Defining a New Therapeutic TargetErnie Chen, Ling-Shiang Chuang, Mamta Giri, et al.
Nature Genetics|April 17, 2007
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesisJohn D Rioux, Ramnik J Xavier, Kent D Taylor, et al.
The American Journal of Gastroenterology|May 16, 2006
Inflammatory bowel disease characteristics among African Americans, Hispanics, and non-Hispanic Whites: characterization of a large North American cohortGeoffrey C Nguyen, Esther A Torres, Miguel Regueiro, et al.
EMBO Molecular Medicine|November 19, 2016
TECRL, a new life-threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVTHarsha D Devalla, Roselle Gélinas, Elhadi H Aburawi, et al.
Inflammatory Bowel Diseases|March 14, 2012
Contribution of higher risk genes and European admixture to Crohn's disease in African AmericansMing-Hsi Wang, Toshihiko Okazaki, Subra Kugathasan, et al.
Nature Genetics|September 26, 2006
A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHCPaul I W de Bakker, Gil McVean, Pardis C Sabeti, et al.
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