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Familial Cancer|June 30, 2017
Screening of BMPR1a for pathogenic mutations in familial colorectal cancer type X families from NewfoundlandDaniel R Evans, Jane S Green, Michael O WoodsKidney International|May 25, 2002
Clinical and genetic epidemiology of inherited renal disease in NewfoundlandPatrick S Parfrey, William S Davidson, Jane S GreenMolecular Genetics & Genomic Medicine|October 10, 2018
Impact of colonoscopic screening in Familial Colorectal Cancer Type XElizabeth Hatfield, Jane S Green, Michael O Woods, et al.European Journal of Human Genetics : EJHG|December 17, 2015
Genetic structure of the Newfoundland and Labrador population: founder effects modulate variabilityGuangju Zhai, Jiayi Zhou, Michael O Woods, et al.Human Genetics|November 2, 2004
Linkage disequilibrium mapping in the Newfoundland population: a re-evaluation of the refinement of the Bardet-Biedl syndrome 1 critical intervalYanli Fan, Jane S Green, Alison J Ross, et al.Human Mutation|March 31, 2012
Inherited deleterious variants in GALNT12 are associated with CRC susceptibilityErica Clarke, Roger C Green, Jane S Green, et al.Familial Cancer|October 14, 2006
The phenotypic expression of three MSH2 mutations in large Newfoundland families with Lynch syndromeSusan Stuckless, Patrick S Parfrey, Michael O Woods, et al.American Journal of Human Genetics|February 28, 2002
Newfoundland rod-cone dystrophy, an early-onset retinal dystrophy, is caused by splice-junction mutations in RLBP1Erica R Eichers, Jane S Green, David W Stockton, et al.Kidney International|April 16, 2009
Autosomal recessive Bardet-Biedl syndrome: first-degree relatives have no predisposition to metabolic and renal disordersMichael P Webb, Elizabeth L Dicks, Jane S Green, et al.Hereditary Cancer in Clinical Practice|September 9, 2011
Lynch syndrome: barriers to and facilitators of screening and disease managementKathy E Watkins, Christine Y Way, Jacqueline J Fiander, et al.Pageof 3