Publications Luigi Bouchard


Autres publications :

St-Pierre J, Bouchard L, and Poirier P. The Impact of Obesity on Cardiovascular Structure and Function: From the Very Beginning. Pediatric Health, Medicine and Therapeutics2012 March; 3:1 - 8.

Turcot V, Bouchard L,  Faucher G, Tchernof A, Deshaies Y, Pérusse L, Marceau P, Hould FS, Lebel S and Vohl MC. A polymorphism of the interferon-gamma-inducible protein 30 gene is associated with hyperglycemia in severely obese individuals. Hum Genet. 2012 Jan;131(1):57-66.

Bouchard L., Tchernof A., Deshaies Y., Stéphane Lebel, Fédéric-Simon Hould, Picard Marceau and Vohl MC. CYR61 Polymorphisms are Associated with Blood Pressure and Plasma Lipids in Obese Individuals. Clinical Genetics 2007 72(3) :224-229.

Choquette AC., Bouchard L.,Houde A., Bouchard C., Pérusse L. and Vohl MC. Associations between USF1 gene variants and Metabolic Syndrome-related phenotypes in the Quebec Family Study. Clinical Genetics, 2007 7(3) :245-253.

BouchardL., TremblayA., BouchardC. and Pérusse L. Contribution of several candidate gene polymorphisms in adiposity changes with age in the Québec Family Study. International Journal of Obesity, 2007 31(6) :891-899.

Bossé Y., Bouchard L., Després J-P., Bouchard C., Pérusse L. and Vohl M-C. Haplotypes in the Phospholipid Transfer Protein Gene are Associated with Obesity-Related Phenotypes: The Québec Family Study. International Journal of Obesity 2005, 29(11): 1338-45.

Bouchard L., Weisnagel S.J., Engert J.C., Hudson T.J., Bouchard C., Vohl M-C., and Pérusse L. Human Resistin Gene Polymorphism is Associated with Visceral Obesity and Fasting and Oral Glucose Stimulated C-peptide in the Québec Family Study. The Journal of Endocrinological Investigation 2004, 27(11):1003-1009.

Pérusse L. et Bouchard L.. L’épidémie d’obésité : doit-on blâmer les gènes ou l’environnement ? Actualités de Chimie Thérapeutique 29ème Série, Société de Chimie Thérapeutique 2003, 57-69.

Chagnon Y.C., Rice T., Pérusse L., Borecki I. B., Ho-Kim M-A., Lacaille M., Paré C., Bouchard L., Gagnon J., Leon A. S., Skinner J. S., Wilmore J. H., Rao DC and Bouchard C., Genomic scan for body composition genes in sedentary state and in response to training in caucasians from the Heritage Family Study. The Journal of Applied Physiology 2001, 90(5):1777-87.

Bouchard L., Robert M.-F., Vinarov D., Stanley C. A., Thompson G. N., Morris A., Leonard J., Quant P.,Hsu B. Y. L., Boneh A., Boukaftane Y., Ashmarina L., Miziorko H. and Mitchell G. A. : Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency : Clinical Course and Description of Causal Mutations in Two Patients. Pediatric Research 2001, 49(3): 326-31.

Mitchell G. A., Wang S. P., Ashmarina L., Robert M.-F., Bouchard L., Laurin N., Kassovska-Bratinova S., Boukaftane Y.: Inborn Errors of Ketogenesis. Biochemistry Society Transactions 1998, 26: 136-140.

Bouchard L., Boukaftane Y., Bétard C., Hudson T. J., Mitchell G. A.: The Human Mithochondrial 3-Hydroxy-Methylglutaryl CoA Synthase (HMGCS2) Gene: Characterization of an Intragenic Microsatellite (D1S3752) and Gene Mapping with Radiation Hybrids. Print Citation:Human Mutation 1998, 12 (4): 291. On line Citation: Human Mutation, Mutation and Polymorphism Report #23 1998. Print Citation:Human Mutation 1998, 12 (4): 291.