Genome‐wide association study of N370S homozygous Gaucher disease reveals the candidacy of <i>CLN8</i> gene as a genetic modifier contributing to extreme phenotypic variation
Hu Zhang(Sichuan University), Pramod K. Mistry(Yale University), Gregory M. Pastores(New York University), Philip Stein(Yale University), Zuoheng Wang, Hongyu Zhao(Yale University), Peter K. Gregersen(Northwell Health), Jun Liu(Yale University), Judy H. Cho(Cedars-Sinai Medical Center), Ruhua Yang(Yale University), Johannes M. F. G. Aerts(Leiden University Medical Center)
Cited by 59
Related Papers
Finding the missing heritability of complex diseases
|Nature|2009|8.5k
A Genome-Wide Association Study Identifies <i>IL23R</i> as an Inflammatory Bowel Disease Gene
|Science|2006|3k
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations
|Nature Genetics|2015|2.8k
Inflammatory Bowel Disease
|New England Journal of Medicine|2009|2.7k
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
|Nature Genetics|2008|2.6k