Functional variants in the <i>LRRK2</i> gene confer shared effects on risk for Crohn’s disease and Parkinson’s diseaseKen Hui, Judy H. Cho, Manual Rivas et al.|Science Translational Medicine|2018Cited by 411
Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish populationManuel A. Rivas, Daniel G. MacArthur, Brandon E. Avila et al.|PLoS Genetics|2018Cited by 95
A Frameshift in CSF2RB Predominant Among Ashkenazi Jews Increases Risk for Crohn's Disease and Reduces Monocyte Signaling via GM-CSFLing-Shiang Chuang, Vincent Plagnol, Nicole Villaverde et al.|Gastroenterology|2016Cited by 67
Identifying high-impact variants and genes in exomes of Ashkenazi Jewish inflammatory bowel disease patientsYiming Wu, Yuval Itan, Kyle Gettler et al.|Nature Communications|2023Cited by 18
Substitution of a single non-coding nucleotide upstream of TMEM216 causes non-syndromic retinitis pigmentosa and is associated with reduced TMEM216 expressionSamantha Malka, Radha Ayyagari, Pooja Biswas et al.|The American Journal of Human Genetics|2024Cited by 7