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American Journal of Human Genetics|December 9, 2017
Penetrance of Polygenic Obesity Susceptibility Loci across the Body Mass Index DistributionArkan Abadi, Akram Alyass, Sebastien Robiou du Pont, et al.
Diabetes|September 28, 2006
Common polymorphisms in the promoter of the visfatin gene (PBEF1) influence plasma insulin levels in a French-Canadian populationSwneke D Bailey, J C Loredo-Osti, Pierre Lepage, et al.
CJC Open|July 23, 2025
A Multidisciplinary Aortopathy Clinic: The McGill ExperienceMasaki Kodaira, Kevin Lachapelle, Richard L Leask, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Genetic variation at the proprotein convertase subtilisin/kexin type 5 gene modulates high-density lipoprotein cholesterol levelsIulia Iatan, Zari Dastani, Ron Do, et al.
Genomics|December 28, 1999
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): high-resolution physical and transcript map of the candidate region in chromosome region 13q11J C Engert, C Doré, J Mercier, et al.
Circulation. Cardiovascular Genetics|September 23, 2010
Fine mapping of the insulin-induced gene 2 identifies a variant associated with LDL cholesterol and total apolipoprotein B levelsRon Do, Swneke D Bailey, Guillaume Paré, et al.
Clinical Genetics|April 10, 2002
ABCA1 regulatory variants influence coronary artery disease independent of effects on plasma lipid levelsK Y Zwarts, S M Clee, A H Zwinderman, et al.
Nature Genetics|February 2, 2000
ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORFJ C Engert, P Bérubé, J Mercier, et al.
BMC Medical Genetics|July 20, 2012
BRCA2 variants and cardiovascular disease in a multi-ethnic studyKevin Zbuk, Changchun Xie, Robin Young, et al.
European Journal of Human Genetics : EJHG|October 22, 2009
Fine mapping and association studies of a high-density lipoprotein cholesterol linkage region on chromosome 16 in French-Canadian subjectsZari Dastani, Päivi Pajukanta, Michel Marcil, et al.
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