Ghislain Rocheleau, Ph.D.

Affiliations: 
2003 Université de Montréal, Montréal, Canada 
Area:
Statistics, Genetics
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"Ghislain Rocheleau"

Parents

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Sabin Lessard grad student 2003 Université de Montréal
 (Effets de la consanguinite dans des modeles de selection pour des populations structurees en familles.)
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Publications

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Liu CT, Merino J, Rybin D, et al. (2019) Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals. Scientific Reports. 9: 9439
Imatoh T, Yengo L, Rocheleau G, et al. (2018) ALDH2 Polymorphism rs671, but Not ADH1B Polymorphism rs1229984, Increases Risk for Hypo-HDL-Cholesterolemia in a/a Carriers Compared to the G/G Carriers. Lipids
Field Y, Boyle EA, Telis N, et al. (2016) Detection of human adaptation during the past 2000 years. Science (New York, N.Y.)
Niel C, Sinoquet C, Dina C, et al. (2015) A survey about methods dedicated to epistasis detection. Frontiers in Genetics. 6: 285
Vaxillaire M, Yengo L, Lobbens S, et al. (2014) Type 2 diabetes-related genetic risk scores associated with variations in fasting plasma glucose and development of impaired glucose homeostasis in the prospective DESIR study. Diabetologia. 57: 1601-10
Dastani Z, Hivert MF, Timpson N, et al. (2012) Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. Plos Genetics. 8: e1002607
Bonnefond A, Clément N, Fawcett K, et al. (2012) Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes. Nature Genetics. 44: 297-301
Palmer ND, McDonough CW, Hicks PJ, et al. (2012) A genome-wide association search for type 2 diabetes genes in African Americans. Plos One. 7: e29202
Soranzo N, Sanna S, Wheeler E, et al. (2010) Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways. Diabetes. 59: 3229-39
Voight BF, Scott LJ, Steinthorsdottir V, et al. (2010) Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nature Genetics. 42: 579-89
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