1.
Schiff ER, Frampton M, Ben-Yosef N, et al. Rare coding variant analysis in a large cohort of Ashkenazi Jewish families with inflammatory bowel disease. Hum Genet. 2018;137(9):723-734. doi:10.1007/s00439-018-1927-7.
1.
Trinh TT, Rioux JD. The promise and perils of interpreting genetic associations in Crohn’s disease. Gut. 2005;54(10):1354-7. doi:10.1136/gut.2005.070920.
1.
Kleinnijenhuis J, Quintin J, Preijers F, et al. Bacille Calmette-Guerin induces NOD2-dependent nonspecific protection from reinfection via epigenetic reprogramming of monocytes. Proc Natl Acad Sci U S A. 2012;109(43):17537-42. doi:10.1073/pnas.1202870109.
1.
Ananthakrishnan AN, Huang H, Nguyen DD, Sauk J, Yajnik V, Xavier RJ. Differential effect of genetic burden on disease phenotypes in Crohn’s disease and ulcerative colitis: analysis of a North American cohort. Am J Gastroenterol. 2014;109(3):395-400. doi:10.1038/ajg.2013.464.
1.
Westra H-J, Arends D, Esko T, et al. Cell Specific eQTL Analysis without Sorting Cells. PLoS Genet. 2015;11(5):e1005223. doi:10.1371/journal.pgen.1005223.
1.
Cleynen I, Boucher G, Jostins L, et al. Inherited determinants of Crohn’s disease and ulcerative colitis phenotypes: a genetic association study. Lancet. 2016;387(10014):156-67. doi:10.1016/S0140-6736(15)00465-1.