Brisson D - Search Results

1

LRP1B, BRD2 and CACNA1D: new candidate genes in fetal metabolic programming of newborns exposed to maternal hyperglycemia.

Houde AA, Ruchat SM, Allard C, Baillargeon JP, St-Pierre J, Perron P, Gaudet D, Brisson D, Hivert MF, Bouchard L. Houde AA, et al. Among authors: brisson d. Epigenomics. 2015 Oct;7(7):1111-22. doi: 10.2217/epi.15.72. Epub 2015 Nov 20. Epigenomics. 2015. PMID: 26586120

2

A sequence variation in the mitochondrial glycerol-3-phosphate dehydrogenase gene is associated with increased plasma glycerol and free fatty acid concentrations among French Canadians.

St-Pierre J, Vohl MC, Brisson D, Perron P, Després JP, Hudson TJ, Gaudet D. St-Pierre J, et al. Among authors: brisson d. Mol Genet Metab. 2001 Mar;72(3):209-17. doi: 10.1006/mgme.2000.3144. Mol Genet Metab. 2001. PMID: 11243726

3

Glycerol: a neglected variable in metabolic processes?

Brisson D, Vohl MC, St-Pierre J, Hudson TJ, Gaudet D. Brisson D, et al. Bioessays. 2001 Jun;23(6):534-42. doi: 10.1002/bies.1073. Bioessays. 2001. PMID: 11385633 Review.

4

Effect of apolipoprotein E, peroxisome proliferator-activated receptor alpha and lipoprotein lipase gene mutations on the ability of fenofibrate to improve lipid profiles and reach clinical guideline targets among hypertriglyceridemic patients.

Brisson D, Ledoux K, Bossé Y, St-Pierre J, Julien P, Perron P, Hudson TJ, Vohl MC, Gaudet D. Brisson D, et al. Pharmacogenetics. 2002 Jun;12(4):313-20. doi: 10.1097/00008571-200206000-00007. Pharmacogenetics. 2002. PMID: 12042669

5

The pleiotropic expression of the myotonic dystrophy protein kinase gene illustrates the complex relationships between genetic, biological and clinical covariates of male aging.

Brisson D, Houde G, St-Pierre J, Vohl MC, Mathieu J, Gaudet D. Brisson D, et al. Aging Male. 2002 Dec;5(4):223-32. Aging Male. 2002. PMID: 12630069

6

Presence of palmar xanthomas in myotonic dystrophy identifies different patterns of linkage disequilibrium between the apolipoprotein E and myotonic dystrophy protein kinase loci.

Brisson D, Mathieu J, Vohl MC, Gaudet D. Brisson D, et al. Genet Med. 2005 Mar;7(3):213-5. doi: 10.1097/01.gim.0000157130.81975.fe. Genet Med. 2005. PMID: 15775763 No abstract available.

7

Low plasma adiponectin exacerbates the risk of premature coronary artery disease in familial hypercholesterolemia.

Bouhali T, Brisson D, St-Pierre J, Tremblay G, Perron P, Laprise C, Vohl MC, Vissers MN, Hutten BA, Després JP, Kastelein JJP, Gaudet D. Bouhali T, et al. Among authors: brisson d. Atherosclerosis. 2008 Jan;196(1):262-269. doi: 10.1016/j.atherosclerosis.2006.10.035. Epub 2006 Nov 22. Atherosclerosis. 2008. PMID: 17123536

8

Relation of the "hypertriglyceridemic waist" phenotype to earlier manifestations of coronary artery disease in patients with glucose intolerance and type 2 diabetes mellitus.

St-Pierre J, Lemieux I, Perron P, Brisson D, Santuré M, Vohl MC, Després JP, Gaudet D. St-Pierre J, et al. Among authors: brisson d. Am J Cardiol. 2007 Feb 1;99(3):369-73. doi: 10.1016/j.amjcard.2006.08.041. Epub 2006 Dec 8. Am J Cardiol. 2007. PMID: 17261400

9

Genetic epistasis in the VLDL catabolic pathway is associated with deleterious variations on triglyceridemia in obese subjects.

Brisson D, St-Pierre J, Santuré M, Hudson TJ, Després JP, Vohl MC, Gaudet D. Brisson D, et al. Int J Obes (Lond). 2007 Aug;31(8):1325-33. doi: 10.1038/sj.ijo.0803586. Epub 2007 Mar 6. Int J Obes (Lond). 2007. PMID: 17342071

10

Genetic analysis of 103 candidate genes for coronary artery disease and associated phenotypes in a founder population reveals a new association between endothelin-1 and high-density lipoprotein cholesterol.

Pare G, Serre D, Brisson D, Anand SS, Montpetit A, Tremblay G, Engert JC, Hudson TJ, Gaudet D. Pare G, et al. Among authors: brisson d. Am J Hum Genet. 2007 Apr;80(4):673-82. doi: 10.1086/513286. Epub 2007 Feb 21. Am J Hum Genet. 2007. PMID: 17357073 Free PMC article.

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