Diane Brisson, Ph.D. - Publications

2005 Universite Laval (Canada) 

82 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Khoury E, Brisson D, Roy N, Tremblay G, Gaudet D. Identifying Markers of Cardiovascular Event-Free Survival in Familial Hypercholesterolemia. Journal of Clinical Medicine. 10. PMID 33375401 DOI: 10.3390/jcm10010064  1
2020 Sun CJ, Brisson D, Gaudet D, Ooi TC. Relative effect of hypertriglyceridemia on non-HDLC and apolipoprotein B as cardiovascular disease risk markers. Journal of Clinical Lipidology. PMID 33032940 DOI: 10.1016/j.jacl.2020.09.006  1
2020 Aljenedil S, Alothman L, Bélanger AM, Brown L, Lahijanian Z, Bergeron J, Couture P, Baass A, Ruel I, Brisson D, Khoury E, Gaudet D, Genest J. Lomitapide for treatment of homozygous familial hypercholesterolemia: The Québec experience. Atherosclerosis. 310: 54-63. PMID 32906018 DOI: 10.1016/j.atherosclerosis.2020.07.028  1
2020 Tremblay K, Brisson D, Gaudet D. Gene expression profiles of recurrent acute pancreatitis risk in patients with sustained chylomicronemia. Endocrine Journal. PMID 32727960 DOI: 10.1507/endocrj.EJ20-0123  1
2020 Tremblay K, Gaudet D, Khoury E, Brisson D. Dissection of Clinical and Gene Expression Signatures of Familial versus Multifactorial Chylomicronemia. Journal of the Endocrine Society. 4: bvaa056. PMID 32537545 DOI: 10.1210/jendso/bvaa056  1
2020 Roy N, Gaudet D, Tremblay G, Brisson D. Association of common gene-smoking interactions with elevated plasma apolipoprotein B concentration. Lipids in Health and Disease. 19: 98. PMID 32430061 DOI: 10.1186/s12944-020-01287-7  1
2020 Sun CJ, McCudden C, Brisson D, Shaw J, Gaudet D, Ooi TC. Calculated Non-HDL Cholesterol Includes Cholesterol in Larger Triglyceride-Rich Lipoproteins in Hypertriglyceridemia. Journal of the Endocrine Society. 4: bvz010. PMID 32010872 DOI: 10.1210/jendso/bvz010  1
2020 Khoury E, Brisson D, Gaudet D. Preclinical discovery and development of evolocumab for the treatment of hypercholesterolemia. Expert Opinion On Drug Discovery. 1-12. PMID 31973581 DOI: 10.1080/17460441.2020.1704728  1
2019 Guay SP, Houde AA, Breton E, Baillargeon JP, Perron P, Gaudet D, Hivert MF, Brisson D, Bouchard L. DNA methylation at gene locus mediates the association between maternal total cholesterol changes in pregnancy and cord blood leptin levels. Journal of Developmental Origins of Health and Disease. 1-10. PMID 31753053 DOI: 10.1017/S204017441900076X  1
2019 Floyd JS, Bloch KM, Brody JA, Maroteau C, Siddiqui MK, Gregory R, Carr DF, Molokhia M, Liu X, Bis JC, Ahmed A, Liu X, Hallberg P, Yue QY, Magnusson PKE, ... Brisson D, et al. Pharmacogenomics of statin-related myopathy: Meta-analysis of rare variants from whole-exome sequencing. Plos One. 14: e0218115. PMID 31242253 DOI: 10.1371/journal.pone.0218115  1
2019 Khoury E, Brisson D, Roy N, Tremblay G, Gaudet D. Review of the long-term safety of lomitapide: a microsomal triglycerides transfer protein inhibitor for treating homozygous familial hypercholesterolemia. Expert Opinion On Drug Safety. PMID 30945578 DOI: 10.1080/14740338.2019.1602606  1
2018 Tremblay M, Brisson D, Gaudet D. Association study between a polymorphic poly-T repeat sequence in the promoter of the somatostatin gene and metabolic syndrome. Bmc Medical Genetics. 19: 130. PMID 30053852 DOI: 10.1186/s12881-018-0641-6  1
2018 Dron JS, Wang J, Berberich AJ, Iacocca MA, Cao H, Yang P, Knoll J, Tremblay K, Brisson D, Netzer C, Gouni-Berthold I, Gaudet D, Hegele RA. Large-scale deletions of the ABCA1 gene in patients with hypoalphalipoproteinemia. Journal of Lipid Research. PMID 29866657 DOI: 10.1194/jlr.P086280  1
2018 Cardenas A, Gagné-Ouellet V, Allard C, Brisson D, Perron P, Bouchard L, Hivert MF. Placenta DNA Methylation Adaptation to Maternal Glycemic Response in Pregnancy. Diabetes. PMID 29752424 DOI: 10.2337/db18-0123  0.52
2017 Tremblay K, Brisson D, Gaudet D. Natural history and gene expression signature of platelet count in lipoprotein lipase deficiency. Atherosclerosis. 263: e100. PMID 29365429 DOI: 10.1016/j.atherosclerosis.2017.06.325  1
2017 Ruel I, Aljenedil S, Sadri I, de Varennes É, Hegele RA, Couture P, Bergeron J, Wanneh E, Baass A, Dufour R, Gaudet D, Brisson D, Brunham LR, Francis GA, Cermakova L, et al. Imputation of Baseline LDL Cholesterol Concentration in Patients with Familial Hypercholesterolemia on Statins or Ezetimibe. Clinical Chemistry. PMID 29038147 DOI: 10.1373/clinchem.2017.279422  1
2017 Paquette M, Brisson D, Dufour R, Khoury É, Gaudet D, Baass A. Cardiovascular disease in familial hypercholesterolemia: Validation and refinement of the Montreal-FH-SCORE. Journal of Clinical Lipidology. PMID 28801029 DOI: 10.1016/j.jacl.2017.07.008  1
2017 Gaudet D, Gipe DA, Pordy R, Ahmad Z, Cuchel M, Shah PK, Chyu KY, Sasiela WJ, Chan KC, Brisson D, Khoury E, Banerjee P, Gusarova V, Gromada J, Stahl N, et al. ANGPTL3 Inhibition in Homozygous Familial Hypercholesterolemia. The New England Journal of Medicine. 377: 296-297. PMID 28723334 DOI: 10.1056/NEJMc1705994  1
2017 Gagné-Ouellet V, Houde AA, Guay SP, Perron P, Gaudet D, Guérin R, Baillargeon JP, Hivert MF, Brisson D, Bouchard L. Placental lipoprotein lipase DNA methylation alterations are associated with gestational diabetes and body composition at 5 years of age. Epigenetics. 0. PMID 28486003 DOI: 10.1080/15592294.2017.1322254  1
2017 Hivert MF, Scholtens DM, Allard C, Nodzenski M, Bouchard L, Brisson D, Lowe LP, McDowell I, Reddy T, Dastani Z, Richards JB, Hayes MG, Lowe WL. Genetic determinants of adiponectin regulation revealed by pregnancy. Obesity (Silver Spring, Md.). PMID 28317342 DOI: 10.1002/oby.21805  0.48
2016 Gaudet D, Stroes ES, Methot J, Brisson D, Tremblay K, Bernelot Moens SJ, Iotti G, Rastelletti I, Ardigo D, Corzo D, Meyer C, Andersen M, Ruszniewski P, Deakin M, Bruno MJ. A Long-Term (up to 6 years) Retrospective Analysis of Gene Therapy with Alipogene Tiparvovec and its Effect on Lipoprotein Lipase Deficiency (LPLD)-Induced Pancreatitis. Human Gene Therapy. PMID 27412455 DOI: 10.1089/hum.2015.158  1
2016 Côté S, Gagné-Ouellet V, Guay SP, Allard C, Houde AA, Perron P, Baillargeon JP, Gaudet D, Guérin R, Brisson D, Hivert MF, Bouchard L. PPARGC1α gene DNA methylation variations in human placenta mediate the link between maternal hyperglycemia and leptin levels in newborns. Clinical Epigenetics. 8: 72. PMID 27340502 DOI: 10.1186/s13148-016-0239-9  1
2016 Besseling J, Reitsma JB, Gaudet D, Brisson D, Kastelein JJ, Hovingh GK, Hutten BA. Selection of individuals for genetic testing for familial hypercholesterolaemia: development and external validation of a prediction model for the presence of a mutation causing familial hypercholesterolaemia. European Heart Journal. PMID 27044878 DOI: 10.1093/eurheartj/ehw135  1
2016 Guay SP, Légaré C, Brisson D, Mathieu P, Bossé Y, Gaudet D, Bouchard L. Epigenetic and genetic variations at the TNNT1 gene locus are associated with HDL-C levels and coronary artery disease. Epigenomics. 8: 359-71. PMID 26950807 DOI: 10.2217/epi.15.120  1
2016 Tremblay M, Brisson D, Gaudet D. Association between a polymorphic poly-T repeat sequence in the promoter of the somatostatin gene and hypertension. Hypertension Research : Official Journal of the Japanese Society of Hypertension. 39: 467-74. PMID 26818653 DOI: 10.1038/hr.2016.4  1
2015 Gaudet D, Brisson D. Gene-based therapies in lipidology: current status and future challenges. Current Opinion in Lipidology. 26: 553-65. PMID 26780008 DOI: 10.1097/MOL.0000000000000240  1
2015 Villeneuve S, Brisson D, Gaudet D. Influence of Abdominal Obesity on the Lipid-Lipoprotein Profile in Apoprotein E2/4 Carriers: The Effect of an Apparent Duality. Journal of Lipids. 2015: 742408. PMID 26605088 DOI: 10.1155/2015/742408  1
2015 Houde AA, Ruchat SM, Allard C, Baillargeon JP, St-Pierre J, Perron P, Gaudet D, Brisson D, Hivert MF, Bouchard L. LRP1B, BRD2 and CACNA1D: new candidate genes in fetal metabolic programming of newborns exposed to maternal hyperglycemia. Epigenomics. PMID 26586120 DOI: 10.2217/epi.15.72  1
2015 Gaudet D, Alexander VJ, Baker BF, Brisson D, Tremblay K, Singleton W, Geary RS, Hughes SG, Viney NJ, Graham MJ, Crooke RM, Witztum JL, Brunzell JD, Kastelein JJ. Antisense Inhibition of Apolipoprotein C-III in Patients with Hypertriglyceridemia. The New England Journal of Medicine. 373: 438-47. PMID 26222559 DOI: 10.1056/NEJMoa1400283  1
2015 Guay SP, Brisson D, Mathieu P, Bossé Y, Gaudet D, Bouchard L. A study in familial hypercholesterolemia suggests reduced methylomic plasticity in men with coronary artery disease. Epigenomics. 7: 17-34. PMID 25687463 DOI: 10.2217/epi.14.64  1
2015 Gaudet D, Brisson D. Gene-based therapies in lipidology: Current status and future challenges Current Opinion in Lipidology. 26: 553-565. DOI: 10.1097/MOL.0000000000000240  1
2014 Gaudet D, Brisson D, Tremblay K, Alexander VJ, Singleton W, Hughes SG, Geary RS, Baker BF, Graham MJ, Crooke RM, Witztum JL. Targeting APOC3 in the familial chylomicronemia syndrome. The New England Journal of Medicine. 371: 2200-6. PMID 25470695 DOI: 10.1056/NEJMoa1400284  1
2014 Villeneuve S, Brisson D, Marchant NL, Gaudet D. The potential applications of Apolipoprotein E in personalized medicine. Frontiers in Aging Neuroscience. 6: 154. PMID 25071563 DOI: 10.3389/fnagi.2014.00154  1
2014 Houde AA, St-Pierre J, Hivert MF, Baillargeon JP, Perron P, Gaudet D, Brisson D, Bouchard L. Placental lipoprotein lipase DNA methylation levels are associated with gestational diabetes mellitus and maternal and cord blood lipid profiles. Journal of Developmental Origins of Health and Disease. 5: 132-41. PMID 24847699 DOI: 10.1017/S2040174414000038  1
2014 Desgagné V, Hivert MF, St-Pierre J, Guay SP, Baillargeon JP, Perron P, Gaudet D, Brisson D, Bouchard L. Epigenetic dysregulation of the IGF system in placenta of newborns exposed to maternal impaired glucose tolerance. Epigenomics. 6: 193-207. PMID 24811788 DOI: 10.2217/epi.14.3  1
2014 Tremblay K, Dubois-Bouchard C, Brisson D, Gaudet D. Association of CTRC and SPINK1 gene variants with recurrent hospitalizations for pancreatitis or acute abdominal pain in lipoprotein lipase deficiency. Frontiers in Genetics. 5: 90. PMID 24795752 DOI: 10.3389/fgene.2014.00090  1
2014 Guay SP, Brisson D, Lamarche B, Biron S, Lescelleur O, Biertho L, Marceau S, Vohl MC, Gaudet D, Bouchard L. ADRB3 gene promoter DNA methylation in blood and visceral adipose tissue is associated with metabolic disturbances in men. Epigenomics. 6: 33-43. PMID 24579945 DOI: 10.2217/epi.13.82  1
2014 Guay SP, Brisson D, Lamarche B, Gaudet D, Bouchard L. Epipolymorphisms within lipoprotein genes contribute independently to plasma lipid levels in familial hypercholesterolemia. Epigenetics : Official Journal of the Dna Methylation Society. 9: 718-29. PMID 24504152 DOI: 10.4161/epi.27981  1
2014 Ferreira V, Twisk J, Kwikkers K, Aronica E, Brisson D, Methot J, Petry H, Gaudet D. Immune responses to intramuscular administration of alipogene tiparvovec (AAV1-LPL(S447X)) in a phase II clinical trial of lipoprotein lipase deficiency gene therapy. Human Gene Therapy. 25: 180-8. PMID 24299335 DOI: 10.1089/hum.2013.169  1
2014 Tremblay M, Bouhali T, Gaudet D, Brisson D. Genealogical analysis as a new approach for the investigation of drug intolerance heritability. European Journal of Human Genetics : Ejhg. 22: 916-22. PMID 24281370 DOI: 10.1038/ejhg.2013.270  1
2013 Houde AA, Guay SP, Desgagné V, Hivert MF, Baillargeon JP, St-Pierre J, Perron P, Gaudet D, Brisson D, Bouchard L. Adaptations of placental and cord blood ABCA1 DNA methylation profile to maternal metabolic status. Epigenetics : Official Journal of the Dna Methylation Society. 8: 1289-302. PMID 24113149 DOI: 10.4161/epi.26554  1
2013 Ruchat SM, Houde AA, Voisin G, St-Pierre J, Perron P, Baillargeon JP, Gaudet D, Hivert MF, Brisson D, Bouchard L. Gestational diabetes mellitus epigenetically affects genes predominantly involved in metabolic diseases. Epigenetics : Official Journal of the Dna Methylation Society. 8: 935-43. PMID 23975224 DOI: 10.4161/epi.25578  1
2013 Hayes MG, Urbanek M, Hivert MF, Armstrong LL, Morrison J, Guo C, Lowe LP, Scheftner DA, Pluzhnikov A, Levine DM, McHugh CP, Ackerman CM, Bouchard L, Brisson D, Layden BT, et al. Identification of HKDC1 and BACE2 as genes influencing glycemic traits during pregnancy through genome-wide association studies. Diabetes. 62: 3282-91. PMID 23903356 DOI: 10.2337/db12-1692  1
2013 Brisson D, Perron P, Kahn HS, Gaudet D, Bouchard L. The lipid accumulation product for the early prediction of gestational insulin resistance and glucose dysregulation. Journal of Women's Health (2002). 22: 362-7. PMID 23717842 DOI: 10.1089/jwh.2012.3807  1
2013 Guay SP, Brisson D, Lamarche B, Marceau P, Vohl MC, Gaudet D, Bouchard L. DNA methylation variations at CETP and LPL gene promoter loci: new molecular biomarkers associated with blood lipid profile variability. Atherosclerosis. 228: 413-20. PMID 23623643 DOI: 10.1016/j.atherosclerosis.2013.03.033  1
2013 Gaudet D, Signorovitch J, Swallow E, Fan L, Tremblay K, Brisson D, Meyers C, Gruenberger JB. Medical resource use and costs associated with chylomicronemia. Journal of Medical Economics. 16: 657-66. PMID 23428107 DOI: 10.3111/13696998.2013.779277  1
2013 Gagnon C, Chouinard MC, Laberge L, Brisson D, Gaudet D, Lavoie M, Leclerc N, Mathieu J. Prevalence of lifestyle risk factors in myotonic dystrophy type 1. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 40: 42-7. PMID 23250126  1
2013 Gaudet D, Méthot J, Déry S, Brisson D, Essiembre C, Tremblay G, Tremblay K, de Wal J, Twisk J, van den Bulk N, Sier-Ferreira V, van Deventer S. Efficacy and long-term safety of alipogene tiparvovec (AAV1-LPLS447X) gene therapy for lipoprotein lipase deficiency: an open-label trial. Gene Therapy. 20: 361-9. PMID 22717743 DOI: 10.1038/gt.2012.43  1
2013 Guay SP, Gaudet D, Brisson D. The g.-469G>A polymorphism in the GPIHBP1 gene promoter is associated with hypertriglyceridemia and has an additive effect on the risk conferred by LPL defective alleles. Nutrition, Metabolism, and Cardiovascular Diseases : Nmcd. 23: 358-65. PMID 21978733 DOI: 10.1016/j.numecd.2011.08.005  1
2012 Guay SP, Voisin G, Brisson D, Munger J, Lamarche B, Gaudet D, Bouchard L. Epigenome-wide analysis in familial hypercholesterolemia identified new loci associated with high-density lipoprotein cholesterol concentration. Epigenomics. 4: 623-39. PMID 23244308 DOI: 10.2217/epi.12.62  1
2012 Tremblay M, Brisson D, Gaudet D. Association between salivary pH and metabolic syndrome in women: a cross-sectional study. Bmc Oral Health. 12: 40. PMID 22958748 DOI: 10.1186/1472-6831-12-40  1
2012 St-Pierre J, Hivert MF, Perron P, Poirier P, Guay SP, Brisson D, Bouchard L. IGF2 DNA methylation is a modulator of newborn's fetal growth and development. Epigenetics : Official Journal of the Dna Methylation Society. 7: 1125-32. PMID 22907587 DOI: 10.4161/epi.21855  1
2012 Carpentier AC, Frisch F, Labbé SM, Gagnon R, de Wal J, Greentree S, Petry H, Twisk J, Brisson D, Gaudet D. Effect of alipogene tiparvovec (AAV1-LPL(S447X)) on postprandial chylomicron metabolism in lipoprotein lipase-deficient patients. The Journal of Clinical Endocrinology and Metabolism. 97: 1635-44. PMID 22438229 DOI: 10.1210/jc.2011-3002  1
2012 Mammen AL, Gaudet D, Brisson D, Christopher-Stine L, Lloyd TE, Leffell MS, Zachary AA. Increased frequency of DRB1*11:01 in anti-hydroxymethylglutaryl-coenzyme A reductase-associated autoimmune myopathy. Arthritis Care & Research. 64: 1233-7. PMID 22422616 DOI: 10.1002/acr.21671  1
2012 Guay SP, Brisson D, Munger J, Lamarche B, Gaudet D, Bouchard L. ABCA1 gene promoter DNA methylation is associated with HDL particle profile and coronary artery disease in familial hypercholesterolemia. Epigenetics : Official Journal of the Dna Methylation Society. 7: 464-72. PMID 22419126 DOI: 10.4161/epi.19633  1
2012 Bouchard L, Hivert MF, Guay SP, St-Pierre J, Perron P, Brisson D. Placental adiponectin gene DNA methylation levels are associated with mothers' blood glucose concentration. Diabetes. 61: 1272-80. PMID 22396200 DOI: 10.2337/db11-1160  1
2012 Tremblay M, Loucif Y, Methot J, Brisson D, Gaudet D. Salivary pH as a marker of plasma adiponectin concentrations in Women. Diabetology & Metabolic Syndrome. 4: 4. PMID 22304893 DOI: 10.1186/1758-5996-4-4  1
2012 Méthot J, Brisson D, Gaudet D. On-site management of investigational products and drug delivery systems in conformity with Good Clinical Practices (GCPs). Clinical Trials (London, England). 9: 265-71. PMID 22222352 DOI: 10.1177/1740774511431280  1
2012 Mammen AL, Pak K, Williams EK, Brisson D, Coresh J, Selvin E, Gaudet D. Rarity of anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase antibodies in statin users, including those with self-limited musculoskeletal side effects. Arthritis Care & Research. 64: 269-72. PMID 21972203 DOI: 10.1002/acr.20662  1
2011 Tremblay M, Gaudet D, Brisson D. Metabolic syndrome and oral markers of cardiometabolic risk. Journal (Canadian Dental Association). 77: b125. PMID 21975074  1
2011 Tremblay K, Méthot J, Brisson D, Gaudet D. Etiology and risk of lactescent plasma and severe hypertriglyceridemia. Journal of Clinical Lipidology. 5: 37-44. PMID 21262505 DOI: 10.1016/j.jacl.2010.11.004  1
2011 Loucif Y, Méthot J, Tremblay K, Brisson D, Gaudet D. Contribution of adiponectin to the cardiometabolic risk of postmenopausal women with loss-of-function lipoprotein lipase gene mutations. Menopause (New York, N.Y.). 18: 558-62. PMID 21252727 DOI: 10.1097/gme.0b013e3181fca1d4  1
2011 Sirois-Gagnon D, Chamberland A, Perron S, Brisson D, Gaudet D, Laprise C. Association of common polymorphisms in the fractalkine receptor (CX3CR1) with obesity. Obesity (Silver Spring, Md.). 19: 222-7. PMID 20523302 DOI: 10.1038/oby.2010.125  1
2010 Brisson D, Méthot J, Tremblay K, Tremblay M, Perron P, Gaudet D. Comparison of the efficacy of fibrates on hypertriglyceridemic phenotypes with different genetic and clinical characteristics. Pharmacogenetics and Genomics. 20: 742-7. PMID 21217359 DOI: 10.1097/FPC.0b013e328340095e  1
2010 van der Graaf A, Vissers MN, Gaudet D, Brisson D, Sivapalaratnam S, Roseboom TJ, Jansen AC, Kastelein JJ, Hutten BA. Dyslipidemia of mothers with familial hypercholesterolemia deteriorates lipids in adult offspring. Arteriosclerosis, Thrombosis, and Vascular Biology. 30: 2673-7. PMID 20864670 DOI: 10.1161/ATVBAHA.110.209064  1
2010 Brisson D, Perron P, Guay SP, Gaudet D, Bouchard L. The "hypertriglyceridemic waist" phenotype and glucose intolerance in pregnancy. Cmaj : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne. 182: E722-5. PMID 20855478 DOI: 10.1503/cmaj.100378  1
2010 Bouchard L, Thibault S, Guay SP, Santure M, Monpetit A, St-Pierre J, Perron P, Brisson D. Leptin gene epigenetic adaptation to impaired glucose metabolism during pregnancy. Diabetes Care. 33: 2436-41. PMID 20724651 DOI: 10.2337/dc10-1024  1
2010 Gaudet D, de Wal J, Tremblay K, Déry S, van Deventer S, Freidig A, Brisson D, Méthot J. Review of the clinical development of alipogene tiparvovec gene therapy for lipoprotein lipase deficiency. Atherosclerosis. Supplements. 11: 55-60. PMID 20427244 DOI: 10.1016/j.atherosclerosissup.2010.03.004  1
2008 Engert JC, Lemire M, Faith J, Brisson D, Fujiwara TM, Roslin NM, Brewer CG, Montpetit A, Darmond-Zwaig C, Renaud Y, Doré C, Bailey SD, Verner A, Tremblay G, St-Pierre J, et al. Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population. European Journal of Human Genetics : Ejhg. 16: 105-14. PMID 17805225 DOI: 10.1038/sj.ejhg.5201920  1
2008 Bouhali T, Brisson D, St-Pierre J, Tremblay G, Perron P, Laprise C, Vohl MC, Vissers MN, Hutten BA, Després JP, Kastelein JJ, Gaudet D. Low plasma adiponectin exacerbates the risk of premature coronary artery disease in familial hypercholesterolemia. Atherosclerosis. 196: 262-9. PMID 17123536 DOI: 10.1016/j.atherosclerosis.2006.10.035  1
2007 Perron P, Brisson D, Santuré M, Blackburn P, Bergeron J, Vohl MC, Després JP, Gaudet D. Apolipoprotein E and lipoprotein lipase gene polymorphisms interaction on the atherogenic combined expression of hypertriglyceridemia and hyperapobetalipoproteinemia phenotypes. Journal of Endocrinological Investigation. 30: 551-7. PMID 17848837 DOI: 10.1007/BF03346348  1
2007 Pare G, Serre D, Brisson D, Anand SS, Montpetit A, Tremblay G, Engert JC, Hudson TJ, Gaudet D. 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. American Journal of Human Genetics. 80: 673-82. PMID 17357073 DOI: 10.1086/513286  1
2007 Brisson D, St-Pierre J, Santuré M, Hudson TJ, Després JP, Vohl MC, Gaudet D. Genetic epistasis in the VLDL catabolic pathway is associated with deleterious variations on triglyceridemia in obese subjects. International Journal of Obesity (2005). 31: 1325-33. PMID 17342071 DOI: 10.1038/sj.ijo.0803586  1
2007 St-Pierre J, Lemieux I, Perron P, Brisson D, Santuré M, Vohl MC, Després JP, Gaudet D. Relation of the "hypertriglyceridemic waist" phenotype to earlier manifestations of coronary artery disease in patients with glucose intolerance and type 2 diabetes mellitus. The American Journal of Cardiology. 99: 369-73. PMID 17261400 DOI: 10.1016/j.amjcard.2006.08.041  1
2005 Carroll G, Brisson DP, Ross MM, Labbé R. The French version of the palliative care quiz for nursing (PCQN-F): development and evaluation. Journal of Palliative Care. 21: 27-34. PMID 15895547  1
2005 Brisson D, Mathieu J, Vohl MC, Gaudet D. Presence of palmar xanthomas in myotonic dystrophy identifies different patterns of linkage disequilibrium between the apolipoprotein E and myotonic dystrophy protein kinase loci. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 7: 213-5. PMID 15775763 DOI: 10.1097/01.GIM.0000157130.81975.FE  1
2002 Brisson D, Tremblay M, Prévost C, Laberge C, Puymirat J, Mathieu J. Sibship stability of genotype and phenotype in myotonic dystrophy. Clinical Genetics. 62: 220-5. PMID 12220437 DOI: 10.1034/j.1399-0004.2002.620306.x  1
2002 Brisson D, Ledoux K, Bossé Y, St-Pierre J, Julien P, Perron P, Hudson TJ, Vohl MC, Gaudet D. 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. Pharmacogenetics. 12: 313-20. PMID 12042669 DOI: 10.1097/00008571-200206000-00007  1
2001 Brisson D, Vohl MC, St-Pierre J, Hudson TJ, Gaudet D. Glycerol: a neglected variable in metabolic processes? Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. 23: 534-42. PMID 11385633 DOI: 10.1002/bies.1073  1
2001 St-Pierre J, Vohl MC, Brisson D, Perron P, Després JP, Hudson TJ, Gaudet D. 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. Molecular Genetics and Metabolism. 72: 209-17. PMID 11243726 DOI: 10.1006/mgme.2000.3144  1
2000 Vigneault A, Brisson D, Bélanger C, Gaudet D. Community genetics in Eastern Québec: The experience of the Corporation for Research and Action on Hereditary Diseases Community Genetics. 3: 151-155. DOI: 10.1159/000051128  1
2000 Brisson D. Analysis and integration of definitions of community genetics Community Genetics. 3: 99-101. DOI: 10.1159/000051114  1
Show low-probability matches.