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Author Details

Guillaume Paré
1989
313
68
PMIDPaper TitleJournal TitlePublished Year
38052102Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity.Hum Reprod2024
36595202From 'Omics to Multi-omics Technologies: the Discovery of Novel Causal Mediators.2023
36300369Anti-Epileptic Drug Target Perturbation and Intracranial Aneurysm Risk: Mendelian Randomization and Colocalization Study.Stroke2023
36325912Pharmacogenomics in Stroke and Cardiovascular Disease: State of the Art.Stroke2023
37626057A versatile, fast and unbiased method for estimation of gene-by-environment interaction effects on biobank-scale datasets.2023
37034649Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.medRxiv2023
36719157Fibroblast Growth Factor-23 and Risk of Cardiovascular Diseases: A Mendelian Randomization Study.Clin J Am Soc Nephrol2023
36897834Biomarker Changes Associated With Both Dulaglutide and Cardiovascular Events in the REWIND Randomized Controlled Trial: A Nested Case-Control Post Hoc Analysis.2023
36960777Validation of Urinary Thiocyanate as a Robust Biomarker of Active Tobacco Smoking in the Prospective Urban and Rural Epidemiological Study.2023
36894711Identifying individuals at extreme risk of venous thromboembolism using polygenic risk scores.2023
37139638A DNA methylation based measure outperforms circulating CRP as a marker of chronic inflammation and partly reflects the monocytic response to long-term inflammatory exposure: A Canadian Longitudinal Study on Aging analysis.Aging Cell2023
36702047Changes in energy, macronutrient, and food consumption in 47 countries over the last 70 years (1950-2019): a systematic review and meta-analysis.2023
36548480Rationale, Design, and the Baseline Characteristics of the RHDGen (The Genetics of Rheumatic Heart Disease) Network Studyâ¿ .Circ Genom Precis Med2023
37380764GDF15 promotes weight loss by enhancing energy expenditure in muscle.Nature2023
37060189Leveraging related health phenotypes for polygenic prediction of impulsive choice, impulsive action, and impulsive personality traits in 1534 European ancestry community adults.2023
36858924Thyroid Dysfunction and Cardiovascular Events in Patients With Dysglycemia.2023
36854916Identifying blood biomarkers for type 2 diabetes subtyping: a report from the ORIGIN trial.2023
37498601Biomarkers Associated With Severe COVID-19 Among Populations With High Cardiometabolic Risk: A 2-Sample Mendelian Randomization Study.2023
37351707SNP Panel and Genomic Sex Identification in Atlantic Halibut (Hippoglossus hippoglossus).2023
37035923Current State and Future of Polygenic Risk Scores in Cardiometabolic Disease: A Scoping Review.2023
36917778Vascular-Parenchymal Cross-Talk Promotes Lung Fibrosis through BMPR2 Signaling.Am J Respir Crit Care Med2023
35197325Association of Clonal Hematopoiesis of Indeterminate Potential with Worse Kidney Function and Anemia in Two Cohorts of Patients with Advanced Chronic Kidney Disease.J Am Soc Nephrol2022
35393509Identification of genetic effects underlying type 2 diabetes in South Asian and European populations.Commun Biol2022
36240095Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke.Neurology2022
35904973Cost-Effectiveness of Polygenic Risk Scores to Guide Statin Therapy for Cardiovascular Disease Prevention.Circulation. Genomic and precision medicine2022
35513483Author Correction: Identification of genetic effects underlying type 2 diabetes in South Asian and European populations.Commun Biol2022
36360312Evaluation of DNA Methylation Array for Glioma Tumor Profiling and Description of a Novel Epi-Signature to Distinguish IDH1/IDH2 Mutant and Wild-Type Tumors.Genes (Basel)2022
35446786Genome-wide studies reveal factors associated with circulating uromodulin and its relationships to complex diseases.JCI Insight2022
36349701Effects of routine early treatment with PCSK9 inhibitors in patients undergoing primary percutaneous coronary intervention for ST-segment elevation myocardial infarction: a randomised, double-blind, sham-controlled trial.EuroIntervention2022
35953142Reply: Lipoprotein(a) and Atrial Fibrillation.Journal of the American College of Cardiology2022
35812273ACLY and CKD: A Mendelian Randomization Analysis.Kidney International Reports2022
35431237Biomarkers of Prevalent and Incident Cognitive Dysfunction in People with Dysglycemia: Data from the ORIGIN Trial.Journal of Alzheimer's Disease2022
35551307Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.Nat Genet2022
35677977Association of Lipids, Lipoproteins, and Apolipoproteins with Stroke Subtypes in an International Case Control Study (INTERSTROKE).J Stroke2022
35675800Inhibition of ATP-citrate lyase improves NASH, liver fibrosis, and dyslipidemia.Cell Metab2022
36412575The genetic risk of gestational diabetes in South Asian women.Elife2022
36050321Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.Nat Commun2022
34467996Dysbetalipoproteinemia: Differentiating Multifactorial Remnant Cholesterol Disease From Genetic ApoE Deficiency.Journal of Clinical Endocrinology and Metabolism2022
35063112Variations in risks from smoking between high-income, middle-income, and low-income countries: an analysis of data from 179â¿¿000 participants from 63 countries.Lancet Global Health,The2022
35317326Comparison of Neutrophil Function in Granulocyte Concentrates From Prednisone- and G-CSF-Treated Donors: Effect of Stimulant, Leukapheresis and Storage.Frontiers in Medicine2022
35300815Lipoprotein(a) Cholesterol Masquerading as Low-Density Lipoprotein Cholesterol: Catch Me if You Can.Journal of the American College of Cardiology2022
34676424Validation of the classification for type 2 diabetes into five subgroups: a report from the ORIGIN trial.Diabetologia2022
35273064Cohort profile: genomic data for 26 622 individuals from the Canadian Longitudinal Study on Aging (CLSA).BMJ Open2022
35023831GWAS and ExWAS of blood mitochondrial DNA copy number identifies 71 loci and highlights a potential causal role in dementia.eLife2022
35140212Caffeine blocks SREBP2-induced hepatic PCSK9 expression to enhance LDLR-mediated cholesterol clearance.Nat Commun2022
34880091Mitochondrial DNA Copy Number as a Marker and Mediator of Stroke Prognosis: Observational and Mendelian Randomization Analyses.Neurology2022
35305575DNA methylation changes in cord blood and the developmental origins of health and disease - a systematic review and replication study.BMC Genomics2022
34587750Epigenetic Age and the Risk of Incident Atrial Fibrillation.Circulation2021
33752449Testosterone and sex hormone-binding globulin in dysglycemic women at high cardiovascular risk: A report from the Outcome Reduction with an Initial Glargine Intervention trial.2021
34234773The Inhibitory Receptor CLEC12A Regulates PI3K-Akt Signaling to Inhibit Neutrophil Activation and Cytokine Release.Frontiers in Immunology2021
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Erasmus University Medical Center
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University of Michigan School of Public Health ann arbor
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National Institute on Aging
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The University of Manchester
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University of Oxford
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German Research Center for Cardiovascular Disease (DZHK)
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