Marie-Pierre Dube, Ph.D. - Publications

Affiliations: 
2000 McGill University, Montreal, QC, Canada 
Area:
Neurogenetics

112 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
2016 Girard SL, Bourassa CV, Lemieux Perreault LP, Legault MA, Barhdadi A, Ambalavanan A, Brendgen M, Vitaro F, Noreau A, Dionne G, Tremblay RE, Dion PA, Boivin M, Dubé MP, Rouleau GA. Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy Individuals. Plos One. 11: e0164212. PMID 27723766 DOI: 10.1371/journal.pone.0164212  0.32
2016 Low-Kam C, Rhainds D, Lo KS, Provost S, Mongrain I, Dubois A, Perreault S, Robinson JF, Hegele RA, Dubé MP, Tardif JC, Lettre G. Whole-genome sequencing in French Canadians from Quebec. Human Genetics. PMID 27376640 DOI: 10.1007/s00439-016-1702-6  0.36
2016 Dumas S, Rouleau-Mailloux E, Bouchama N, Lahcene H, Talajic M, Tardif JC, Gaulin MJ, Provost S, Dubé MP, Perreault S. Pillbox Use and INR Stability in a Prospective Cohort of New Warfarin Users. Journal of Managed Care & Specialty Pharmacy. 22: 676-684. PMID 27231795 DOI: 10.18553/jmcp.2016.22.6.676  0.36
2016 Leblanc C, Dubé MP, Presse N, Dumas S, Nguyen M, Rouleau-Mailloux É, Perreault S, Ferland G. Avoidance of Vitamin K-Rich Foods Is Common among Warfarin Users and Translates into Lower Usual Vitamin K Intakes. Journal of the Academy of Nutrition and Dietetics. PMID 26922378 DOI: 10.1016/j.jand.2015.12.023  0.36
2016 Stitziel NO, Stirrups KE, Masca NGD, Erdmann J, Ferrario PG, König IR, Weeke PE, Webb TR, Auer PL, Schick UM, Lu Y, Zhang H, Dube MP, Goel A, Farrall M, et al. Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease New England Journal of Medicine. 374: 1134-1144. DOI: 10.1056/NEJMoa1507652  0.36
2015 Guauque-Olarte S, Messika-Zeitoun D, Droit A, Lamontagne M, Tremblay-Marchand J, Lavoie-Charland E, Gaudreault N, Arsenault BJ, Dubé MP, Tardif JC, Body SC, Seidman JG, Boileau C, Mathieu P, Pibarot P, et al. Calcium Signaling Pathway Genes RUNX2 and CACNA1C Are Associated with Calcific Aortic Valve Disease. Circulation. Cardiovascular Genetics. PMID 26553695 DOI: 10.1161/CIRCGENETICS.115.001145  0.36
2015 Girard SL, Dion PA, Bourassa CV, Geoffroy S, Lachance-Touchette P, Barhdadi A, Langlois M, Joober R, Krebs MO, Dubé MP, Rouleau GA. Mutation burden of rare variants in schizophrenia candidate genes. Plos One. 10: e0128988. PMID 26039597 DOI: 10.1371/journal.pone.0128988  0.36
2015 Jarjour S, Barrette M, Normand V, Rouleau JL, Dubé MP, de Denus S. Genetic markers associated with cutaneous adverse drug reactions to allopurinol: a systematic review. Pharmacogenomics. 16: 755-67. PMID 25965122 DOI: 10.2217/pgs.15.21  0.36
2015 Shahabi P, Dubé MP. Cardiovascular pharmacogenomics; state of current knowledge and implementation in practice. International Journal of Cardiology. 184: 772-95. PMID 25838112 DOI: 10.1016/j.ijcard.2015.02.025  0.4
2015 Legault MA, Girard S, Lemieux Perreault LP, Rouleau GA, Dubé MP. Comparison of sequencing based CNV discovery methods using monozygotic twin quartets. Plos One. 10: e0122287. PMID 25812131 DOI: 10.1371/journal.pone.0122287  0.36
2015 Tardif JC, Rhéaume E, Lemieux Perreault LP, Grégoire JC, Feroz Zada Y, Asselin G, Provost S, Barhdadi A, Rhainds D, L'Allier PL, Ibrahim R, Upmanyu R, Niesor EJ, Benghozi R, Suchankova G, et al. Pharmacogenomic determinants of the cardiovascular effects of dalcetrapib. Circulation. Cardiovascular Genetics. 8: 372-82. PMID 25583994 DOI: 10.1161/CIRCGENETICS.114.000663  0.36
2014 Postmus I, Trompet S, Deshmukh HA, Barnes MR, Li X, Warren HR, Chasman DI, Zhou K, Arsenault BJ, Donnelly LA, Wiggins KL, Avery CL, Griffin P, Feng Q, Taylor KD, et al. Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins. Nature Communications. 5: 5068. PMID 25350695 DOI: 10.1038/ncomms6068  0.36
2014 Dubé MP, Zetler R, Barhdadi A, Brown AM, Mongrain I, Normand V, Laplante N, Asselin G, Zada YF, Provost S, Bergeron J, Kouz S, Dufour R, Diaz A, de Denus S, et al. CKM and LILRB5 are associated with serum levels of creatine kinase. Circulation. Cardiovascular Genetics. 7: 880-6. PMID 25214527 DOI: 10.1161/CIRCGENETICS.113.000395  0.36
2014 Carleton BC, Ross CJ, Pussegoda K, Bhavsar AP, Visscher H, Lee JW, Brooks B, Rassekh SR, Dubé MP, Hayden MR. Genetic markers of cisplatin-induced hearing loss in children. Clinical Pharmacology and Therapeutics. 96: 296-8. PMID 25141953 DOI: 10.1038/clpt.2014.92  0.36
2014 Brown AM, Renaud Y, Ross C, Hansen M, Mongrain I, Valois D, Carleton BC, Hayden MR, Dubé MP, Tardif JC, Phillips MS. Development of a broad-based ADME panel for use in pharmacogenomic studies. Pharmacogenomics. 15: 1185-95. PMID 25141894 DOI: 10.2217/pgs.14.81  0.36
2014 Martins S, Pearson CE, Coutinho P, Provost S, Amorim A, Dubé MP, Sequeiros J, Rouleau GA. Modifiers of (CAG)(n) instability in Machado-Joseph disease (MJD/SCA3) transmissions: an association study with DNA replication, repair and recombination genes. Human Genetics. 133: 1311-8. PMID 25026993 DOI: 10.1007/s00439-014-1467-8  0.36
2014 Auer PL, Teumer A, Schick U, O'Shaughnessy A, Lo KS, Chami N, Carlson C, de Denus S, Dubé MP, Haessler J, Jackson RD, Kooperberg C, Perreault LP, Nauck M, Peters U, et al. Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits. Nature Genetics. 46: 629-34. PMID 24777453 DOI: 10.1038/ng.2962  0.36
2014 Arsenault BJ, Boekholdt SM, Dubé MP, Rhéaume E, Wareham NJ, Khaw KT, Sandhu MS, Tardif JC. Lipoprotein(a) levels, genotype, and incident aortic valve stenosis: a prospective mendelian randomization study and replication in a case-control cohort. Circulation. Cardiovascular Genetics. 7: 304-10. PMID 24704946 DOI: 10.1161/CIRCGENETICS.113.000400  0.36
2014 El Kadmiri N, Zaid N, Zaid Y, Tadevosyan A, Hachem A, Dubé MP, Hamzi K, El Moutawakil B, Slassi I, Nadifi S. Novel presenilin mutations within Moroccan patients with Early-Onset Alzheimer's Disease. Neuroscience. 269: 215-22. PMID 24704512 DOI: 10.1016/j.neuroscience.2014.03.052  0.36
2014 El Kadmiri N, Zaid N, Hachem A, Zaid Y, Dubé MP, Hamzi K, El Moutawakil B, Slassi I, Nadifi S. Novel mutations in the amyloid precursor protein gene within Moroccan patients with Alzheimer's disease. Journal of Molecular Neuroscience : Mn. 53: 189-95. PMID 24627227 DOI: 10.1007/s12031-014-0278-7  0.36
2014 Perreault LP, Legault MA, Barhdadi A, Provost S, Normand V, Tardif JC, Dubé MP. Comparison of genotype clustering tools with rare variants. Bmc Bioinformatics. 15: 52. PMID 24559245 DOI: 10.1186/1471-2105-15-52  0.36
2014 Aflakparast M, Salimi H, Gerami A, Dubé MP, Visweswaran S, Masoudi-Nejad A. Cuckoo search epistasis: a new method for exploring significant genetic interactions. Heredity. 112: 666-74. PMID 24549111 DOI: 10.1038/hdy.2014.4  0.4
2014 Dumas S, Rouleau-Mailloux E, Barhdadi A, Talajic M, Tardif JC, Dubé MP, Perreault S. Validation of patient-reported warfarin dose in a prospective incident cohort study. Pharmacoepidemiology and Drug Safety. 23: 285-9. PMID 24458454 DOI: 10.1002/pds.3571  0.36
2014 Dubé MP. Will statins be an effective anti-inflammatory intervention for prevention of cardiovascular disease in patients with HIV? The Journal of Infectious Diseases. 209: 1149-50. PMID 24415787 DOI: 10.1093/infdis/jiu015  0.4
2014 Park SY, Goeken N, Lee HJ, Bolan R, Dubé MP, Lee HY. Developing high-throughput HIV incidence assay with pyrosequencing platform. Journal of Virology. 88: 2977-90. PMID 24371062 DOI: 10.1128/JVI.03128-13  0.4
2014 Arsenault BJ, Dubé MP, Brodeur MR, de Oliveira Moraes AB, Lavoie V, Kernaleguen AE, Guauque-Olarte S, Mathieu P, Pibarot P, Messika-Zeitoun D, Bossé Y, Rhainds D, Rhéaume E, Tardif JC. Evaluation of links between high-density lipoprotein genetics, functionality, and aortic valve stenosis risk in humans. Arteriosclerosis, Thrombosis, and Vascular Biology. 34: 457-62. PMID 24334872 DOI: 10.1161/ATVBAHA.113.302730  0.4
2014 Carleton BC, Ross CJ, Bhavsar AP, Amstutz U, Pussegoda K, Visscher H, Lee JW, Brooks B, Rassekh SR, Dubé MP, Hayden MR. Role of TPMT and COMT genetic variation in cisplatin-induced ototoxicity. Clinical Pharmacology and Therapeutics. 95: 253. PMID 24193170 DOI: 10.1038/clpt.2013.219  0.36
2014 Timmons T, Shen C, Aldrovandi G, Rollie A, Gupta SK, Stein JH, Dubé MP. Microbial translocation and metabolic and body composition measures in treated and untreated HIV infection. Aids Research and Human Retroviruses. 30: 272-7. PMID 24033288 DOI: 10.1089/AID.2013.0162  0.4
2014 Aminkeng F, Ross CJ, Rassekh SR, Brunham LR, Sistonen J, Dube MP, Ibrahim M, Nyambo TB, Omar SA, Froment A, Bodo JM, Tishkoff S, Carleton BC, Hayden MR. Higher frequency of genetic variants conferring increased risk for ADRs for commonly used drugs treating cancer, AIDS and tuberculosis in persons of African descent. The Pharmacogenomics Journal. 14: 160-70. PMID 23588107 DOI: 10.1038/tpj.2013.13  0.36
2013 Gupta SK, Mi D, Moe SM, Dubé MP, Liu Z. Effects of switching from efavirenz to raltegravir on endothelial function, bone mineral metabolism, inflammation, and renal function: a randomized, controlled trial. Journal of Acquired Immune Deficiency Syndromes (1999). 64: 279-83. PMID 24278992  0.4
2013 Lemieux Perreault LP, Provost S, Legault MA, Barhdadi A, Dubé MP. pyGenClean: efficient tool for genetic data clean up before association testing. Bioinformatics (Oxford, England). 29: 1704-5. PMID 23652425 DOI: 10.1093/bioinformatics/btt261  0.36
2013 Pussegoda K, Ross CJ, Visscher H, Yazdanpanah M, Brooks B, Rassekh SR, Zada YF, Dubé MP, Carleton BC, Hayden MR. Replication of TPMT and ABCC3 genetic variants highly associated with cisplatin-induced hearing loss in children. Clinical Pharmacology and Therapeutics. 94: 243-51. PMID 23588304 DOI: 10.1038/clpt.2013.80  0.4
2013 Dubé MP, Tardif JC. Institutional profile: the Beaulieu-Saucier Université de Montréal Pharmacogenomics Centre at the Montreal Heart Institute. Pharmacogenomics. 14: 131-6. PMID 23327574 DOI: 10.2217/pgs.12.204  0.4
2013 Singaraja RR, Sivapalaratnam S, Hovingh K, Dubé MP, Castro-Perez J, Collins HL, Adelman SJ, Riwanto M, Manz J, Hubbard B, Tietjen I, Wong K, Mitnaul LJ, van Heek M, Lin L, et al. The impact of partial and complete loss-of-function mutations in endothelial lipase on high-density lipoprotein levels and functionality in humans. Circulation. Cardiovascular Genetics. 6: 54-62. PMID 23243195 DOI: 10.1161/CIRCGENETICS.111.962613  0.36
2013 Stein JH, Brown TT, Ribaudo HJ, Chen Y, Yan M, Lauer-Brodell E, McComsey GA, Dubé MP, Murphy RL, Hodis HN, Currier JS. Ultrasonographic measures of cardiovascular disease risk in antiretroviral treatment-naive individuals with HIV infection. Aids (London, England). 27: 929-37. PMID 23196938 DOI: 10.1097/QAD.0b013e32835ce27e  0.4
2013 Christensen KE, Zada YF, Rohlicek CV, Andelfinger GU, Michaud JL, Bigras JL, Richter A, Dubé MP, Rozen R. Risk of congenital heart defects is influenced by genetic variation in folate metabolism. Cardiology in the Young. 23: 89-98. PMID 22475273 DOI: 10.1017/S1047951112000431  0.36
2012 Gupta SK, Shen C, Moe SM, Kamendulis LM, Goldman M, Dubé MP. Worsening endothelial function with efavirenz compared to protease inhibitors: a 12-month prospective study. Plos One. 7: e45716. PMID 23029197 DOI: 10.1371/journal.pone.0045716  0.4
2012 Hitz MP, Lemieux-Perreault LP, Marshall C, Feroz-Zada Y, Davies R, Yang SW, Lionel AC, D'Amours G, Lemyre E, Cullum R, Bigras JL, Thibeault M, Chetaille P, Montpetit A, Khairy P, et al. Rare copy number variants contribute to congenital left-sided heart disease. Plos Genetics. 8: e1002903. PMID 22969434 DOI: 10.1371/journal.pgen.1002903  0.36
2012 Blodget E, Shen C, Aldrovandi G, Rollie A, Gupta SK, Stein JH, Dubé MP. Relationship between microbial translocation and endothelial function in HIV infected patients. Plos One. 7: e42624. PMID 22952600 DOI: 10.1371/journal.pone.0042624  0.4
2012 Tietjen I, Hovingh GK, Singaraja RR, Radomski C, Barhdadi A, McEwen J, Chan E, Mattice M, Legendre A, Franchini PL, Dubé MP, Kastelein JJ, Hayden MR. Segregation of LIPG, CETP, and GALNT2 mutations in Caucasian families with extremely high HDL cholesterol. Plos One. 7: e37437. PMID 22952570 DOI: 10.1371/journal.pone.0037437  0.4
2012 Beaudoin M, Lo KS, N'Diaye A, Rivas MA, Dubé MP, Laplante N, Phillips MS, Rioux JD, Tardif JC, Lettre G. Pooled DNA resequencing of 68 myocardial infarction candidate genes in French canadians. Circulation. Cardiovascular Genetics. 5: 547-54. PMID 22923420 DOI: 10.1161/CIRCGENETICS.112.963165  0.36
2012 Wiltshire SA, Diez E, Miao Q, Dubé MP, Gagné M, Paquette O, Lafrenière RG, Ndao M, Castellani LW, Skamene E, Vidal SM, Fortin A. Genetic control of high density lipoprotein-cholesterol in AcB/BcA recombinant congenic strains of mice. Physiological Genomics. 44: 843-52. PMID 22805347 DOI: 10.1152/physiolgenomics.00025.2012  0.36
2012 Hand CK, Bernard G, Dubé MP, Shevell MI, Rouleau GA. A novel PLP1 mutation further expands the clinical heterogeneity at the locus. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 39: 220-4. PMID 22343157  0.36
2012 Lachance K, Barhdadi A, Mongrain I, Normand V, Zakrzewski M, Leblanc MH, Racine N, Carrier M, Ducharme A, Turgeon J, Dubé MP, Phillips MS, White M, de Denus S. PRKCB is associated with calcineurin inhibitor-induced renal dysfunction in heart transplant recipients. Pharmacogenetics and Genomics. 22: 336-43. PMID 22322241 DOI: 10.1097/FPC.0b013e3283510a35  0.36
2012 Marin-Leblanc M, Perreault S, Bahroun I, Lapointe M, Mongrain I, Provost S, Turgeon J, Talajic M, Brugada R, Phillips M, Tardif JC, Dubé MP. Validation of warfarin pharmacogenetic algorithms in clinical practice. Pharmacogenomics. 13: 21-9. PMID 22176621 DOI: 10.2217/pgs.11.120  0.36
2012 Visscher H, Ross CJ, Rassekh SR, Barhdadi A, Dubé MP, Al-Saloos H, Sandor GS, Caron HN, van Dalen EC, Kremer LC, van der Pal HJ, Brown AM, Rogers PC, Phillips MS, Rieder MJ, et al. Pharmacogenomic prediction of anthracycline-induced cardiotoxicity in children. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 30: 1422-8. PMID 21900104 DOI: 10.1200/JCO.2010.34.3467  0.4
2011 Orr A, Dubé MP, Zenteno JC, Jiang H, Asselin G, Evans SC, Caqueret A, Lakosha H, Letourneau L, Marcadier J, Matsuoka M, Macgillivray C, Nightingale M, Papillon-Cavanagh S, Perry S, et al. Mutations in a novel serine protease PRSS56 in families with nanophthalmos. Molecular Vision. 17: 1850-61. PMID 21850159  0.36
2011 Dubé MP, Bigras JL, Thibeault M, Bureau N, Chetaille P, Richter A, Mercier J, Bellavance M, Rohlicek C, Rozen R, Nemer M, Khairy P, Gendron R, Andelfinger G. Design and rationale of a genetic cohort study on congenital cardiac disease: experiences from a multi-institutional platform in Quebec. Cardiology in the Young. 21: 654-64. PMID 21729494 DOI: 10.1017/S1047951111000813  0.4
2011 Dubé MP, Cadden JJ. Lipid metabolism in treated HIV Infection. Best Practice & Research. Clinical Endocrinology & Metabolism. 25: 429-42. PMID 21663837 DOI: 10.1016/j.beem.2011.04.004  0.4
2011 Reynolds JN, Weinberg J, Clarren S, Beaulieu C, Rasmussen C, Kobor M, Dube MP, Goldowitz D. Fetal alcohol spectrum disorders: gene-environment interactions, predictive biomarkers, and the relationship between structural alterations in the brain and functional outcomes. Seminars in Pediatric Neurology. 18: 49-55. PMID 21575841 DOI: 10.1016/j.spen.2011.02.006  0.36
2011 Tremblay N, Yang SW, Hitz MP, Asselin G, Ginns J, Riopel K, Gendron R, Montpetit A, Duhig E, Dubé MP, Radford D, Andelfinger G. Familial ventricular aneurysms and septal defects map to chromosome 10p15. European Heart Journal. 32: 568-73. PMID 21169613 DOI: 10.1093/eurheartj/ehq447  0.4
2011 de Denus S, Zakrzewski M, Barhdadi A, Leblanc MH, Racine N, Bélanger F, Carrier M, Ducharme A, Dubé MP, Turgeon J, White M. Association between renal function and CYP3A5 genotype in heart transplant recipients treated with calcineurin inhibitors. The Journal of Heart and Lung Transplantation : the Official Publication of the International Society For Heart Transplantation. 30: 326-31. PMID 21094057 DOI: 10.1016/j.healun.2010.09.015  0.4
2010 Lafrenière RG, Cader MZ, Poulin JF, Andres-Enguix I, Simoneau M, Gupta N, Boisvert K, Lafrenière F, McLaughlan S, Dubé MP, Marcinkiewicz MM, Ramagopalan S, Ansorge O, Brais B, Sequeiros J, et al. A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura. Nature Medicine. 16: 1157-60. PMID 20871611 DOI: 10.1038/nm.2216  0.36
2010 Awadalla P, Gauthier J, Myers RA, Casals F, Hamdan FF, Griffing AR, Côté M, Henrion E, Spiegelman D, Tarabeux J, Piton A, Yang Y, Boyko A, Bustamante C, Xiong L, et al. Direct measure of the de novo mutation rate in autism and schizophrenia cohorts. American Journal of Human Genetics. 87: 316-24. PMID 20797689 DOI: 10.1016/j.ajhg.2010.07.019  0.36
2010 Fortin A, Diez E, Ritchie J, Sotocinal SG, Dube MP, Gagne M, Paquette O, Skamene E, Mogil JS. Positional cloning of a quantitative trait locus contributing to pain sensitivity: possible mediation by Tyrp1. Genes, Brain, and Behavior. 9: 856-67. PMID 20633051 DOI: 10.1111/j.1601-183X.2010.00618.x  0.36
2010 de Denus S, Dubé MP. Genetic determinants of blood pressure reduction following potassium supplementation: and the candidates are... Journal of Hypertension. 28: 668-70. PMID 20625248 DOI: 10.1097/HJH.0b013e328336edc2  0.4
2010 Xiong L, Montplaisir J, Desautels A, Barhdadi A, Turecki G, Levchenko A, Thibodeau P, Dubé MP, Gaspar C, Rouleau GA. Family study of restless legs syndrome in Quebec, Canada: clinical characterization of 671 familial cases. Archives of Neurology. 67: 617-22. PMID 20457962 DOI: 10.1001/archneurol.2010.67  0.36
2010 Dubé MP, Sattler FR. Inflammation and complications of HIV disease. The Journal of Infectious Diseases. 201: 1783-5. PMID 20446849 DOI: 10.1086/652751  0.4
2010 Perreault LP, Andelfinger GU, Asselin G, Dubé MP. Partitioning of copy-number genotypes in pedigrees. Bmc Bioinformatics. 11: 226. PMID 20438641 DOI: 10.1186/1471-2105-11-226  0.4
2010 Srour M, Rivière JB, Pham JM, Dubé MP, Girard S, Morin S, Dion PA, Asselin G, Rochefort D, Hince P, Diab S, Sharafaddinzadeh N, Chouinard S, Théoret H, Charron F, et al. Mutations in DCC cause congenital mirror movements. Science (New York, N.Y.). 328: 592. PMID 20431009 DOI: 10.1126/science.1186463  0.36
2010 Gauthier J, Champagne N, Lafrenière RG, Xiong L, Spiegelman D, Brustein E, Lapointe M, Peng H, Côté M, Noreau A, Hamdan FF, Addington AM, Rapoport JL, Delisi LE, Krebs MO, et al. De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia. Proceedings of the National Academy of Sciences of the United States of America. 107: 7863-8. PMID 20385823 DOI: 10.1073/pnas.0906232107  0.36
2010 Barhdadi A, Dubé MP. Testing for gene-gene interaction with AMMI models. Statistical Applications in Genetics and Molecular Biology. 9: Article 2. PMID 20196752 DOI: 10.2202/1544-6115.1410  0.4
2010 Rivière JB, St-Onge J, Gaspar C, Diab S, Dion Y, Lespérance P, Tellier G, Richer F, Chouinard S, Dubé MP, Rouleau GA. Genome-wide TDT analysis in French-Canadian families with Tourette syndrome. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 37: 110-2. PMID 20169783 DOI: 10.1017/S0317167100009744  0.36
2010 Lavoie PM, Dubé MP. Genetics of bronchopulmonary dysplasia in the age of genomics. Current Opinion in Pediatrics. 22: 134-8. PMID 20087186 DOI: 10.1097/MOP.0b013e328336eb85  0.4
2010 Guernsey DL, Dubé MP, Jiang H, Asselin G, Blowers S, Evans S, Ferguson M, Macgillivray C, Matsuoka M, Nightingale M, Rideout A, Delatycki M, Orr A, Ludman M, Dooley J, et al. Novel mutations in the sacsin gene in ataxia patients from Maritime Canada. Journal of the Neurological Sciences. 288: 79-87. PMID 19892370 DOI: 10.1016/j.jns.2009.09.034  0.36
2009 Kovac IP, Dubé MP. Different models and single-nucleotide polymorphisms signal the simulated weak gene-gene interaction for a quantitative trait using haplotype-based and mixed models testing. Bmc Proceedings. 3: S77. PMID 20018072  0.4
2009 An P, Mukherjee O, Chanda P, Yao L, Engelman CD, Huang CH, Zheng T, Kovac IP, Dubé MP, Liang X, Li J, de Andrade M, Culverhouse R, Malzahn D, Manning AK, et al. The challenge of detecting epistasis (G x G interactions): Genetic Analysis Workshop 16. Genetic Epidemiology. 33: S58-67. PMID 19924703 DOI: 10.1002/gepi.20474  0.36
2009 Ross CJ, Katzov-Eckert H, Dubé MP, Brooks B, Rassekh SR, Barhdadi A, Feroz-Zada Y, Visscher H, Brown AM, Rieder MJ, Rogers PC, Phillips MS, Carleton BC, Hayden MR. Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy. Nature Genetics. 41: 1345-9. PMID 19898482 DOI: 10.1038/ng.478  0.36
2009 Carruthers H, Rusbridge C, Dubé MP, Holmes M, Jeffery N. Association between cervical and intracranial dimensions and syringomyelia in the cavalier King Charles spaniel. The Journal of Small Animal Practice. 50: 394-8. PMID 19689666 DOI: 10.1111/j.1748-5827.2009.00768.x  0.4
2009 Visscher H, Ross CJ, Dubé MP, Brown AM, Phillips MS, Carleton BC, Hayden MR. Application of principal component analysis to pharmacogenomic studies in Canada. The Pharmacogenomics Journal. 9: 362-72. PMID 19652663 DOI: 10.1038/tpj.2009.36  0.36
2009 Guernsey DL, Jiang H, Evans SC, Ferguson M, Matsuoka M, Nightingale M, Rideout AL, Provost S, Bedard K, Orr A, Dubé MP, Ludman M, Samuels ME. Mutation in pyrroline-5-carboxylate reductase 1 gene in families with cutis laxa type 2. American Journal of Human Genetics. 85: 120-9. PMID 19576563 DOI: 10.1016/j.ajhg.2009.06.008  0.36
2009 Lizotte E, Junttila MJ, Dube MP, Hong K, Benito B, DE Zutter M, Henkens S, Sarkozy A, Huikuri HV, Towbin J, Vatta M, Brugada P, Brugada J, Brugada R. Genetic modulation of brugada syndrome by a common polymorphism. Journal of Cardiovascular Electrophysiology. 20: 1137-41. PMID 19549036 DOI: 10.1111/j.1540-8167.2009.01508.x  0.36
2009 Jiang H, Orr A, Guernsey DL, Robitaille J, Asselin G, Samuels ME, Dubé MP. Application of homozygosity haplotype analysis to genetic mapping with high-density SNP genotype data. Plos One. 4: e5280. PMID 19399176 DOI: 10.1371/journal.pone.0005280  0.36
2009 Levchenko A, Montplaisir JY, Asselin G, Provost S, Girard SL, Xiong L, Lemyre E, St-Onge J, Thibodeau P, Desautels A, Turecki G, Gaspar C, Dubé MP, Rouleau GA. Autosomal-dominant locus for Restless Legs Syndrome in French-Canadians on chromosome 16p12.1. Movement Disorders : Official Journal of the Movement Disorder Society. 24: 40-50. PMID 18946881 DOI: 10.1002/mds.22263  0.36
2009 McCaffery JM, Duan QL, Frasure-Smith N, Barhdadi A, Lespérance F, Théroux P, Rouleau GA, Dubé MP. Genetic predictors of depressive symptoms in cardiac patients. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 381-8. PMID 18618671 DOI: 10.1002/ajmg.b.30824  0.36
2008 Phillips MS, Hihi AK, van Rooij T, Smith AC, James S, Marsh S, Laplante N, Dubé MP, Tardif JC. Génome Québec & Montreal Heart Institute Pharmacogenomics Centre: a translational pharmacogenomics platform--from R&D to the clinic. Pharmacogenomics. 9: 1391-6. PMID 18855527 DOI: 10.2217/14622416.9.10.1391  0.4
2008 Piton A, Michaud JL, Peng H, Aradhya S, Gauthier J, Mottron L, Champagne N, Lafrenière RG, Hamdan FF, Joober R, Fombonne E, Marineau C, Cossette P, Dubé MP, et al. Mutations in the calcium-related gene IL1RAPL1 are associated with autism. Human Molecular Genetics. 17: 3965-74. PMID 18801879 DOI: 10.1093/hmg/ddn300  0.36
2008 de Denus S, Zakrzewski-Jakubiak M, Dubé MP, Bélanger F, Lepage S, Leblanc MH, Gossard D, Ducharme A, Racine N, Whittom L, Lavoie J, Touyz RM, Turgeon J, White M. Effects of AGTR1 A1166C gene polymorphism in patients with heart failure treated with candesartan. The Annals of Pharmacotherapy. 42: 925-32. PMID 18594050 DOI: 10.1345/aph.1K657  0.36
2008 Dubé MP, Lipshultz SE, Fichtenbaum CJ, Greenberg R, Schecter AD, Fisher SD. Effects of HIV infection and antiretroviral therapy on the heart and vasculature. Circulation. 118: e36-40. PMID 18566318 DOI: 10.1161/CIRCULATIONAHA.107.189625  0.4
2008 Zakrzewski-Jakubiak M, de Denus S, Dubé MP, Bélanger F, White M, Turgeon J. Ten renin-angiotensin system-related gene polymorphisms in maximally treated Canadian Caucasian patients with heart failure. British Journal of Clinical Pharmacology. 65: 742-51. PMID 18279468 DOI: 10.1111/j.1365-2125.2007.03091.x  0.36
2008 Kinirons P, Verlaan DJ, Dubé MP, Poirier J, Deacon C, Lortie A, Clément JF, Desbiens R, Carmant L, Cieuta-Walti C, Shevell M, Rouleau GA, Cossette P. A novel locus for idiopathic generalized epilepsy in French-Canadian families maps to 10p11. American Journal of Medical Genetics. Part A. 146: 578-84. PMID 18241056 DOI: 10.1002/ajmg.a.32139  0.36
2008 Dubé MP, Gorski JC, Shen C. Severe impairment of endothelial function with the HIV-1 protease inhibitor indinavir is not mediated by insulin resistance in healthy subjects. Cardiovascular Toxicology. 8: 15-22. PMID 18172783 DOI: 10.1007/s12012-007-9010-y  0.4
2008 Bolduc V, Chagnon P, Provost S, Dubé MP, Belisle C, Gingras M, Mollica L, Busque L. No evidence that skewing of X chromosome inactivation patterns is transmitted to offspring in humans. The Journal of Clinical Investigation. 118: 333-41. PMID 18097474 DOI: 10.1172/JCI33166  0.36
2007 Barhdadi A, Dubé MP. Two-stage strategies to detect gene x gene interactions in case-control data. Bmc Proceedings. 1: S135. PMID 18466478  0.4
2007 Dubé MP, Schmidt S, Hauser E, Darabi H, Li J, Barhdadi A, Wang X, Sha Q, Zhang Z, Wang T, Aschard H, Guedj M, Rohlfs R, Anderson A, Taylor C, et al. Multistage designs in the genomic era: providing balance in complex disease studies. Genetic Epidemiology. 31: S118-23. PMID 18046769 DOI: 10.1002/gepi.20288  0.4
2007 Peretz I, Cummings S, Dubé MP. The genetics of congenital amusia (tone deafness): a family-aggregation study. American Journal of Human Genetics. 81: 582-8. PMID 17701903 DOI: 10.1086/521337  0.36
2007 Orr A, Dubé MP, Marcadier J, Jiang H, Federico A, George S, Seamone C, Andrews D, Dubord P, Holland S, Provost S, Mongrain V, Evans S, Higgins B, Bowman S, et al. Mutations in the UBIAD1 gene, encoding a potential prenyltransferase, are causal for Schnyder crystalline corneal dystrophy. Plos One. 2: e685. PMID 17668063 DOI: 10.1371/journal.pone.0000685  0.4
2007 Xiong L, Dion P, Montplaisir J, Levchenko A, Thibodeau P, Karemera L, Rivière JB, St-Onge J, Gaspar C, Dubé MP, Desautels A, Turecki G, Rouleau GA. Molecular genetic studies of DMT1 on 12q in French-Canadian restless legs syndrome patients and families. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 911-7. PMID 17510944 DOI: 10.1002/ajmg.b.30528  0.36
2007 Goldberg YP, MacFarlane J, MacDonald ML, Thompson J, Dube MP, Mattice M, Fraser R, Young C, Hossain S, Pape T, Payne B, Radomski C, Donaldson G, Ives E, Cox J, et al. Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations. Clinical Genetics. 71: 311-9. PMID 17470132 DOI: 10.1111/j.1399-0004.2007.00790.x  0.36
2007 Duan QL, Dubé MP, Frasure-Smith N, Barhdadi A, Lesperance F, Théroux P, St-Onge J, Rouleau GA, McCaffery JM. Additive effects of obesity and TCF7L2 variants on risk for type 2 diabetes among cardiac patients. Diabetes Care. 30: 1621-3. PMID 17351281 DOI: 10.2337/dc06-2421  0.36
2007 Song K, Dubé MP, Lim J, Hwang I, Lee I, Kim JJ. Lamin A/C mutations associated with familial and sporadic cases of dilated cardiomyopathy in Koreans. Experimental & Molecular Medicine. 39: 114-20. PMID 17334235 DOI: 10.1038/emm.2007.13  0.4
2007 Matchenko-Shimko N, Dube MP. Gene-gene interaction tests using SVM and neural network modeling 2007 Ieee Symposium On Computational Intelligence and Bioinformatics and Computational Biology, Cibcb 2007. 90-97.  0.36
2006 Levchenko A, Provost S, Montplaisir JY, Xiong L, St-Onge J, Thibodeau P, Rivière JB, Desautels A, Turecki G, Dubé MP, Rouleau GA. A novel autosomal dominant restless legs syndrome locus maps to chromosome 20p13. Neurology. 67: 900-1. PMID 16966564 DOI: 10.1212/01.wnl.0000233991.20410.b6  0.36
2006 Verlaan DJ, Dubé MP, St-Onge J, Noreau A, Roussel J, Satgé N, Wallace MC, Rouleau GA. A new locus for autosomal dominant intracranial aneurysm, ANIB4, maps to chromosome 5p15.2-14.3. Journal of Medical Genetics. 43: e31. PMID 16740915 DOI: 10.1136/jmg.2005.033209  0.52
2006 McCaffery JM, Frasure-Smith N, Dubé MP, Théroux P, Rouleau GA, Duan Q, Lespérance F. Common genetic vulnerability to depressive symptoms and coronary artery disease: a review and development of candidate genes related to inflammation and serotonin. Psychosomatic Medicine. 68: 187-200. PMID 16554382 DOI: 10.1097/01.psy.0000208630.79271.a0  0.36
2006 Brinkman RR, Dubé MP, Rouleau GA, Orr AC, Samuels ME. Human monogenic disorders - a source of novel drug targets. Nature Reviews. Genetics. 7: 249-60. PMID 16534513 DOI: 10.1038/nrg1828  0.36
2006 Gauthier J, Joober R, Dubé MP, St-Onge J, Bonnel A, Gariépy D, Laurent S, Najafee R, Lacasse H, St-Charles L, Fombonne E, Mottron L, Rouleau GA. Autism spectrum disorders associated with X chromosome markers in French-Canadian males. Molecular Psychiatry. 11: 206-13. PMID 16261168 DOI: 10.1038/sj.mp.4001756  0.36
2005 Duan QL, Nikpoor B, Dube MP, Molinaro G, Meijer IA, Dion P, Rochefort D, Saint-Onge J, Flury L, Brown NJ, Gainer JV, Rouleau JL, Agostoni A, Cugno M, Simon P, et al. A variant in XPNPEP2 is associated with angioedema induced by angiotensin I-converting enzyme inhibitors. American Journal of Human Genetics. 77: 617-26. PMID 16175507 DOI: 10.1086/496899  0.36
2005 Díaz-Anzaldúa A, Rivière JB, Dubé MP, Joober R, Saint-Onge J, Dion Y, Lespérance P, Richer F, Chouinard S, Rouleau GA. Chromosome 11-q24 region in Tourette syndrome: association and linkage disequilibrium study in the French Canadian population. American Journal of Medical Genetics. Part A. 138: 225-8. PMID 16158425 DOI: 10.1002/ajmg.a.30928  0.36
2005 Shink E, Harvey M, Tremblay M, Gagné B, Belleau P, Raymond C, Labbé M, Dubé MP, Lafrenière RG, Barden N. Analysis of microsatellite markers and single nucleotide polymorphisms in candidate genes for susceptibility to bipolar affective disorder in the chromosome 12Q24.31 region. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 135: 50-8. PMID 15768393 DOI: 10.1002/ajmg.b.30165  0.4
2004 Hovingh GK, Brownlie A, Bisoendial RJ, Dube MP, Levels JH, Petersen W, Dullaart RP, Stroes ES, Zwinderman AH, de Groot E, Hayden MR, Kuivenhoven JA, Kastelein JJ. A novel apoA-I mutation (L178P) leads to endothelial dysfunction, increased arterial wall thickness, and premature coronary artery disease. Journal of the American College of Cardiology. 44: 1429-35. PMID 15464323 DOI: 10.1016/j.jacc.2004.06.070  0.36
2004 Levchenko A, Montplaisir JY, Dubé MP, Riviere JB, St-Onge J, Turecki G, Xiong L, Thibodeau P, Desautels A, Verlaan DJ, Rouleau GA. The 14q restless legs syndrome locus in the French Canadian population. Annals of Neurology. 55: 887-91. PMID 15174026 DOI: 10.1002/ana.20140  0.36
2004 Lafreniere RG, MacDonald ML, Dube MP, MacFarlane J, O'Driscoll M, Brais B, Meilleur S, Brinkman RR, Dadivas O, Pape T, Platon C, Radomski C, Risler J, Thompson J, Guerra-Escobio AM, et al. Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic Isolates. American Journal of Human Genetics. 74: 1064-73. PMID 15060842 DOI: 10.1086/420795  0.36
2004 Papanikolaou G, Samuels ME, Ludwig EH, MacDonald ML, Franchini PL, Dubé MP, Andres L, MacFarlane J, Sakellaropoulos N, Politou M, Nemeth E, Thompson J, Risler JK, Zaborowska C, Babakaiff R, et al. Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis. Nature Genetics. 36: 77-82. PMID 14647275 DOI: 10.1038/ng1274  0.36
2003 Modugno F, Moslehi R, Ness RB, Nelson DB, Belle S, Kant JA, Wheeler JE, Wonderlick A, Fishman D, Karlan B, Risch H, Cramer DW, Dube MP, Narod SA. Reproductive factors and ovarian cancer risk in Jewish BRCA1 and BRCA2 mutation carriers (United States). Cancer Causes & Control : Ccc. 14: 439-46. PMID 12946038 DOI: 10.1023/A:1024932427503  0.36
2003 Gros-Louis F, Meijer IA, Hand CK, Dubé MP, MacGregor DL, Seni MH, Devon RS, Hayden MR, Andermann F, Andermann E, Rouleau GA. An ALS2 gene mutation causes hereditary spastic paraplegia in a Pakistani kindred. Annals of Neurology. 53: 144-5. PMID 12509863 DOI: 10.1002/ana.10422  0.52
2002 Narod SA, Dubé MP, Klijn J, Lubinski J, Lynch HT, Ghadirian P, Provencher D, Heimdal K, Moller P, Robson M, Offit K, Isaacs C, Weber B, Friedman E, Gershoni-Baruch R, et al. Oral contraceptives and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers. Journal of the National Cancer Institute. 94: 1773-9. PMID 12464649  0.4
2002 Robitaille J, MacDonald ML, Kaykas A, Sheldahl LC, Zeisler J, Dubé MP, Zhang LH, Singaraja RR, Guernsey DL, Zheng B, Siebert LF, Hoskin-Mott A, Trese MT, Pimstone SN, Shastry BS, et al. Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy. Nature Genetics. 32: 326-30. PMID 12172548 DOI: 10.1038/ng957  0.36
2002 Howard HC, Dubé MP, Prévost C, Bouchard JP, Mathieu J, Rouleau GA. Fine mapping the candidate region for peripheral neuropathy with or without agenesis of the corpus callosum in the French Canadian population. European Journal of Human Genetics : Ejhg. 10: 406-12. PMID 12107814 DOI: 10.1038/sj.ejhg.5200815  0.36
1997 Lafrenière RG, Kibar Z, Rochefort DL, Han FY, Fon EA, Dubé MP, Kang X, Baird S, Korneluk RG, Rommens JM, Rouleau GA. Genomic structure of the human GT334 (EHOC-1) gene mapping to 21q22.3. Gene. 198: 313-21. PMID 9370297 DOI: 10.1016/S0378-1119(97)00333-8  0.36
1997 Dubé MP, Mlodzienski MA, Kibar Z, Farlow MR, Ebers G, Harper P, Kolodny EH, Rouleau GA, Figlewicz DA. Hereditary spastic paraplegia: LOD-score considerations for confirmation of linkage in a heterogeneous trait. American Journal of Human Genetics. 60: 625-9. PMID 9042923  0.36
1996 Fink JK, Heiman-Patterson T, Bird T, Cambi F, Dubé MP, Figlewicz DA, Fink JK, Haines JL, Heiman-Patterson T, Hentati A, Pericak-Vance MA, Raskind W, Rouleau GA, Siddique T. Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group. Neurology. 46: 1507-14. PMID 8649538 DOI: 10.1212/WNL.46.6.1507  0.36
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