Filtros de búsqueda

Lista de obras de Marie-Pierre Dubé

A Discrete Event Simulation Model to Assess the Economic Value of a Hypothetical Pharmacogenomics Test for Statin-Induced Myopathy in Patients Initiating a Statin in Secondary Cardiovascular Prevention.

artículo científico publicado en 2018

A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura

artículo científico publicado en 2010

A genetic model of ivabradine recapitulates results from randomized clinical trials

artículo científico publicado en 2020

A model to assess the cost-effectiveness of pharmacogenomics tests in chronic heart failure: the case of ivabradine

artículo científico publicado en 2016

A new locus for autosomal dominant intracranial aneurysm, ANIB4, maps to chromosome 5p15.2-14.3.

artículo científico publicado en 2006

A novel autosomal dominant restless legs syndrome locus maps to chromosome 20p13.

artículo científico publicado en 2006

A novel locus for idiopathic generalized epilepsy in French-Canadian families maps to 10p11

article

A pharmacogenetic investigation of intravenous furosemide in decompensated heart failure: a meta-analysis of three clinical trials

scientific article published on March 2016

A variant in XPNPEP2 is associated with angioedema induced by angiotensin I-converting enzyme inhibitors

artículo científico publicado en 2005

Additive Effects of Obesity and TCF7L2 Variants on Risk for Type 2 Diabetes Among Cardiac Patients

scientific article published on 10 March 2007

An expanded pharmacogenomics warfarin dosing table with utility in generalised dosing guidance.

artículo científico publicado en 2016

AnALS2gene mutation causes hereditary spastic paraplegia in a Pakistani kindred

article

Analysis of microsatellite markers and single nucleotide polymorphisms in candidate genes for susceptibility to bipolar affective disorder in the chromosome 12Q24.31 region

article

Application of homozygosity haplotype analysis to genetic mapping with high-density SNP genotype data

artículo científico publicado en 2009

Application of principal component analysis to pharmacogenomic studies in Canada

article

Association between cervical and intracranial dimensions and syringomyelia in the cavalier King Charles spaniel

artículo científico publicado en 2009

Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events

artículo científico publicado en 2019

Autism spectrum disorders associated with X chromosome markers in French-Canadian males

artículo científico publicado en 2006

Autosomal-dominant locus for Restless Legs Syndrome in French-Canadians on chromosome 16p12.1.

artículo científico publicado en 2009

Avoidance of Vitamin K-Rich Foods Is Common among Warfarin Users and Translates into Lower Usual Vitamin K Intakes

artículo científico publicado en 2016

CETP: Pharmacogenomics-Based Response to the CETP Inhibitor Dalcetrapib

artículo científico publicado en 2017

CKM and LILRB5 are associated with serum levels of creatine kinase

artículo científico publicado en 2014

Calcium Signaling Pathway Genes RUNX2 and CACNA1C Are Associated With Calcific Aortic Valve Disease

artículo científico publicado en 2015

Cardiovascular pharmacogenomics; state of current knowledge and implementation in practice

artículo científico

Chromosome 11-q24 region in Tourette syndrome: Association and linkage disequilibrium study in the French Canadian population

article

Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping

artículo científico publicado en 2000

Common genetic vulnerability to depressive symptoms and coronary artery disease: a review and development of candidate genes related to inflammation and serotonin

artículo científico publicado en 2006

Comparison of genotype clustering tools with rare variants

artículo científico publicado en 2014

Comparison of sequencing based CNV discovery methods using monozygotic twin quartets

artículo científico publicado en 2015

Correction: Rare Copy Number Variants Contribute to Congenital Left-Sided Heart Disease

Cuckoo search epistasis: a new method for exploring significant genetic interactions

artículo científico publicado en 2014

DNA methylation signature of human fetal alcohol spectrum disorder.

artículo científico publicado en 2016

DNMT3A and TET2 dominate clonal hematopoiesis and demonstrate benign phenotypes and different genetic predispositions

artículo científico publicado en 2017

De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia

artículo científico publicado en 2010

Design and rationale of a genetic cohort study on congenital cardiac disease: experiences from a multi-institutional platform in Quebec

Development of a broad-based ADME panel for use in pharmacogenomic studies

artículo científico publicado en 2014

Diagnosis, Prevalence, Awareness, Treatment, Prevention, and Control of Hypertension in Cameroon: Protocol for a Systematic Review and Meta-Analysis of Clinic-Based and Community-Based Studies

artículo científico publicado en 2017

Different models and single-nucleotide polymorphisms signal the simulated weak gene-gene interaction for a quantitative trait using haplotype-based and mixed models testing

artículo científico publicado en 2009

Direct measure of the de novo mutation rate in autism and schizophrenia cohorts

artículo científico publicado en 2010

Effects of AGTR1 A1166C gene polymorphism in patients with heart failure treated with candesartan

artículo científico publicado en 2008

Erratum: Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy

scholarly article published in Nature Genetics

Evaluation of links between high-density lipoprotein genetics, functionality, and aortic valve stenosis risk in humans

artículo científico publicado en 2013

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

artículo científico publicado en 2016

Familial ventricular aneurysms and septal defects map to chromosome 10p15

artículo científico publicado en 2010

Family study of restless legs syndrome in Quebec, Canada: clinical characterization of 671 familial cases

artículo científico publicado en 2010

Fetal alcohol spectrum disorders: gene-environment interactions, predictive biomarkers, and the relationship between structural alterations in the brain and functional outcomes

artículo científico publicado en 2011

Fine mapping the candidate region for peripheral neuropathy with or without agenesis of the corpus callosum in the French Canadian population.

artículo científico publicado en 2002

Genetic Modulation of Brugada Syndrome by a Common Polymorphism

artículo científico publicado en 2009

Genetic control of high density lipoprotein-cholesterol in AcB/BcA recombinant congenic strains of mice

artículo científico publicado en 2012

Genetic determinants of blood pressure reduction following potassium supplementation: and the candidates are…

artículo científico publicado en 2010

Genetic markers associated with cutaneous adverse drug reactions to allopurinol: a systematic review

artículo científico

Genetic markers of cisplatin-induced hearing loss in children

artículo científico publicado en 2014

Genetic predictors of depressive symptoms in cardiac patients

artículo científico publicado en 2009

Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy

artículo científico publicado en 2009

Genetics of bronchopulmonary dysplasia in the age of genomics.

artículo científico publicado en 2010

Genome-wide TDT analysis in French-Canadian families with Tourette syndrome

artículo científico publicado en 2010

Genomic structure of the human GT334 (EHOC-1) gene mapping to 21q22.3.

artículo científico publicado en 1997

Genotype-Dependent Effects of Dalcetrapib on Cholesterol Efflux and Inflammation: Concordance With Clinical Outcomes

artículo científico publicado en 2016

Génome Québec & Montreal Heart Institute Pharmacogenomics Centre: a translational pharmacogenomics platform--from R&D to the clinic

artículo científico publicado en 2008

Human monogenic disorders - a source of novel drug targets

artículo científico publicado en 2006

Identification of the genetic determinants responsible for retinal degeneration in families of Mexican descent

artículo científico publicado en 2017

Impact of regular physical activity on weekly warfarin dose requirement

artículo científico publicado en 2015

Institutional profile: the Beaulieu-Saucier Université de Montréal Pharmacogenomics Centre at the Montreal Heart Institute

artículo científico publicado en 2013

Loss-of-function genetic diseases and the concept of pharmaceutical targets

Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations

artículo científico publicado en 2007

Maximal expected benefits from lowering cholesterol in primary prevention for a high-risk population

artículo científico publicado en 2016

Meta-analysis of genome-wide association studies of HDL cholesterol response to statins

artículo científico publicado en 2016

Methylomic changes in individuals with psychosis, prenatally exposed to endocrine disrupting compounds: Lessons from diethylstilbestrol

artículo científico publicado en 2017

Modifiers of (CAG)(n) instability in Machado-Joseph disease (MJD/SCA3) transmissions: an association study with DNA replication, repair and recombination genes

artículo científico publicado en 2014

Molecular genetic studies of DMT1 on 12q in French-Canadian restless legs syndrome patients and families

artículo científico publicado en 2007

Multistage designs in the genomic era: providing balance in complex disease studies

artículo científico publicado en 2007

Multitrait GWAS to connect disease variants and biological mechanisms

artículo científico publicado en 2021

Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy

artículo científico publicado en 2002

Mutation burden of rare variants in schizophrenia candidate genes

artículo científico publicado en 2015

Mutation in pyrroline-5-carboxylate reductase 1 gene in families with cutis laxa type 2

artículo científico publicado en 2009

Mutations in DCC cause congenital mirror movements.

artículo científico publicado en 2010

Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis

artículo científico publicado en 2003

Mutations in a novel serine protease PRSS56 in families with nanophthalmos.

artículo científico publicado en 2011

Mutations in the UBIAD1 gene, encoding a potential prenyltransferase, are causal for Schnyder crystalline corneal dystrophy

artículo científico publicado en 2007

Mutations in the calcium-related gene IL1RAPL1 are associated with autism

artículo científico publicado en 2008

No evidence that skewing of X chromosome inactivation patterns is transmitted to offspring in humans

artículo científico publicado en 2008

Novel mutations in the amyloid precursor protein gene within Moroccan patients with Alzheimer's disease

artículo científico publicado en 2014

Novel mutations in the sacsin gene in ataxia patients from Maritime Canada

article

Novel presenilin mutations within Moroccan patients with Early-Onset Alzheimer's Disease

artículo científico publicado en 2014

Nuclear receptor gene polymorphisms and warfarin dose requirements in the Quebec Warfarin Cohort.

artículo científico publicado en 2018

Older adults with heart failure treated with carvedilol, bisoprolol, or metoprolol tartrate: risk of mortality

artículo científico publicado en 2016

Oral Anticoagulant Prescription Trends, Profile Use, and Determinants of Adherence in Patients with Atrial Fibrillation

artículo científico publicado en 2019

Oral contraceptives and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2002

PRKCB is associated with calcineurin inhibitor-induced renal dysfunction in heart transplant recipients

scientific article published on 01 May 2012

PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

article

Partitioning of copy-number genotypes in pedigrees

artículo científico publicado en 2010

Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy Individuals

artículo científico publicado en 2016

Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins

artículo científico publicado en 2014

Pharmacogenetics of Lipid-Lowering Agents: an Update Review on Genotype-Dependent Effects of HDL-Targetingand Statin Therapies

artículo científico publicado en 2017

Pharmacogenomic Prediction of Anthracycline-Induced Cardiotoxicity in Children

Pharmacogenomic approaches to lipid-regulating trials

artículo científico publicado en 2016

Pharmacogenomic determinants of the cardiovascular effects of dalcetrapib

artículo científico publicado en 2015

Pharmacogenomics to Revive Drug Development in Cardiovascular Disease

artículo científico publicado en 2016

Pillbox Use and INR Stability in a Prospective Cohort of New Warfarin Users

artículo científico publicado en 2016

Polygenic Versus Monogenic Causes of Hypercholesterolemia Ascertained Clinically

artículo científico publicado en 2016

Polygenic determinants in extremes of high-density lipoprotein cholesterol

artículo científico publicado en 2017

Pooled DNA Resequencing of 68 Myocardial Infarction Candidate Genes in French Canadians

article

Positional cloning of a quantitative trait locus contributing to pain sensitivity: possible mediation by Tyrp1.

artículo científico publicado en 2010

Progesterone receptor variant increases ovarian cancer risk in BRCA1 and BRCA2 mutation carriers who were never exposed to oral contraceptives

artículo científico publicado en 2001

Protein-altering and regulatory genetic variants near GATA4 implicated in bicuspid aortic valve

artículo científico publicado en 2017

Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

article

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2019

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.

artículo científico publicado en 2018

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.

artículo científico publicado en 2018

Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits

artículo científico publicado en 2014

Rare copy number variants contribute to congenital left-sided heart disease

artículo científico publicado en 2012

Rationale, design and preliminary results of the Quebec Warfarin Cohort Study.

artículo científico publicado en 2018

Reproductive factors and ovarian cancer risk in Jewish BRCA1 and BRCA2 mutation carriers (United States).

artículo científico publicado en 2003

Resting heart rate as a predictor of aortic valve stenosis progression

scientific article published on 26 November 2015

Risk of congenital heart defects is influenced by genetic variation in folate metabolism

artículo científico publicado en 2012

Role of TPMT and COMT genetic variation in cisplatin-induced ototoxicity.

artículo científico publicado en 2013

Segregation of LIPG, CETP, and GALNT2 mutations in Caucasian families with extremely high HDL cholesterol

artículo científico publicado en 2012

Subsequent Event Risk in Individuals With Established Coronary Heart Disease

artículo científico publicado en 2019

Syringomyelia in cavalier King Charles spaniels: the relationship between syrinx dimensions and pain

artículo científico publicado en 2007

Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease ⬇️

artículo científico publicado en 2017

Ten renin-angiotensin system-related gene polymorphisms in maximally treated Canadian Caucasian patients with heart failure

artículo científico publicado en 2008

Testing for Gene-Gene Interaction with AMMI Models

article

Testing the role of predicted gene knockouts in human anthropometric trait variation

artículo científico publicado en 2016

The 14q restless legs syndrome locus in the French Canadian population

artículo científico publicado en 2004

The Impact of Partial and Complete Loss-of-Function Mutations in Endothelial Lipase on High-Density Lipoprotein Levels and Functionality in Humans

article

The challenge of detecting epistasis (G x G interactions): Genetic Analysis Workshop 16

artículo científico publicado en 2009

The genetics of congenital amusia (tone deafness): a family-aggregation study

artículo científico publicado en 2007

Two-stage strategies to detect gene x gene interactions in case-control data

artículo científico publicado en 2007

Validation of patient-reported warfarin dose in a prospective incident cohort study

artículo científico publicado en 2014

Validation of warfarin pharmacogenetic algorithms in clinical practice

artículo científico publicado en 2012

Whole-genome sequencing in French Canadians from Quebec

artículo científico publicado en 2016

Will personalized drugs for cardiovascular disease become an option? - Defining 'Evidence-based personalized medicine' for its implementation and future use.

artículo científico publicado en 2015

genipe: an automated genome-wide imputation pipeline with automatic reporting and statistical tools

artículo científico publicado en 2016

pyGenClean: efficient tool for genetic data clean up before association testing

artículo científico publicado en 2013

Dominio Público Uruguay está sostenido por:

Acerca de Dominio Público Uruguay

Ayuda