Marie‐Pierre Dubé

18.0k total citations · 1 hit paper
185 papers, 5.6k citations indexed

About

Marie‐Pierre Dubé is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Marie‐Pierre Dubé has authored 185 papers receiving a total of 5.6k indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Molecular Biology, 45 papers in Genetics and 44 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Marie‐Pierre Dubé's work include Genetic Associations and Epidemiology (29 papers), Lipoproteins and Cardiovascular Health (23 papers) and Pharmacogenetics and Drug Metabolism (22 papers). Marie‐Pierre Dubé is often cited by papers focused on Genetic Associations and Epidemiology (29 papers), Lipoproteins and Cardiovascular Health (23 papers) and Pharmacogenetics and Drug Metabolism (22 papers). Marie‐Pierre Dubé collaborates with scholars based in Canada, United States and United Kingdom. Marie‐Pierre Dubé's co-authors include Amina Barhdadi, Sylvie Provost, Guy A. Rouleau, Michael R. Hayden, Jean‐Claude Tardif, Yassamin Feroz Zada, Jean‐Claude Tardif, Lambert Busque, Luigina Mollica and Simon de Denus and has published in prestigious journals such as Science, Nucleic Acids Research and Journal of Clinical Investigation.

In The Last Decade

Marie‐Pierre Dubé

176 papers receiving 5.5k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Long-term trials of colchicine for secondary prevention of vascular events: a meta-analysis

2025 18 citations Marie‐Pierre Dubé, Jean‐Claude Tardif et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Marie‐Pierre Dubé Canada	39	1.7k	1.2k	886	877	479	185	5.6k
Qiong Yang United States	40	1.8k 1.1×	764 0.6×	537 0.6×	1.3k 1.5×	687 1.4×	161	6.0k
Roger A. Johns United States	57	2.1k 1.2×	1.6k 1.3×	1.2k 1.4×	514 0.6×	388 0.8×	187	9.2k
Li Liu China	34	1.8k 1.0×	347 0.3×	512 0.6×	589 0.7×	524 1.1×	264	5.4k
Ian N.M. Day United Kingdom	44	2.9k 1.7×	659 0.6×	989 1.1×	2.4k 2.7×	631 1.3×	162	7.5k
Dieter Rosskopf Germany	38	1.6k 0.9×	628 0.5×	433 0.5×	506 0.6×	359 0.7×	87	4.5k
Jeanette Erdmann Germany	44	2.1k 1.2×	2.0k 1.7×	647 0.7×	1.3k 1.5×	534 1.1×	181	5.8k
Harald H.H. Göring United States	40	2.2k 1.3×	345 0.3×	399 0.5×	2.1k 2.4×	528 1.1×	147	5.9k
Mansoureh Eghbali United States	39	1.9k 1.1×	1.6k 1.4×	549 0.6×	581 0.7×	218 0.5×	114	5.0k
Thomas D. Dyer United States	43	2.3k 1.3×	447 0.4×	607 0.7×	2.4k 2.7×	863 1.8×	186	6.7k
Joab Chapman Israel	48	2.3k 1.3×	382 0.3×	377 0.4×	552 0.6×	639 1.3×	288	7.8k

Countries citing papers authored by Marie‐Pierre Dubé

Since Specialization

Citations

This map shows the geographic impact of Marie‐Pierre Dubé's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Marie‐Pierre Dubé with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marie‐Pierre Dubé more than expected).

Fields of papers citing papers by Marie‐Pierre Dubé

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marie‐Pierre Dubé. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Marie‐Pierre Dubé. The network helps show where Marie‐Pierre Dubé may publish in the future.

Co-authorship network of co-authors of Marie‐Pierre Dubé

This figure shows the co-authorship network connecting the top 25 collaborators of Marie‐Pierre Dubé. A scholar is included among the top collaborators of Marie‐Pierre Dubé based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Marie‐Pierre Dubé. Marie‐Pierre Dubé is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

McKay, Carly, M. Critchley, S. Cowan, et al.. (2025). Dissemination and implementation of injury prevention interventions. A scoping review for the for the Female, woman and girl Athlete Injury pRevention (FAIR) consensus. Journal of science and medicine in sport. 28. S64–S65. 1 indexed citations

Jutras, Martin, Ian Mongrain, Caroline Lagacé, et al.. (2024). A Study Of the effect of Sex on drug dosing, concentrations, and pharmacogenomics in the Montreal Heart Institute Hospital Cohort (SOS-PGx): methodology and research progress. European Journal of Clinical Pharmacology. 81(2). 321–332.

Sun, Maxine, et al.. (2023). Somatic Mosaic Chromosomal Alterations and Death of Cardiovascular Disease Causes among Cancer Survivors. Cancer Epidemiology Biomarkers & Prevention. 32(6). 776–783. 3 indexed citations

Leclair, Grégoire, Martin Jutras, Ian Mongrain, et al.. (2023). Females present higher dose‐adjusted drug concentrations of metoprolol and allopurinol/oxypurinol than males. Clinical and Translational Science. 16(5). 872–885. 1 indexed citations

Perreault, Louis‐Philippe Lemieux, et al.. (2022). ExPheWas: a platform for cis -Mendelian randomization and gene-based association scans. Nucleic Acids Research. 50(W1). W305–W311. 8 indexed citations

Julienne, Hanna, Vincent Laville, Zachary R. McCaw, et al.. (2021). Multitrait GWAS to connect disease variants and biological mechanisms. PLoS Genetics. 17(8). e1009713–e1009713. 19 indexed citations

Grenier, Jean‐Christophe, Rocío Sánchez, Éric Rhéaume, et al.. (2021). A sex-specific evolutionary interaction between ADCY9 and CETP. eLife. 10. 7 indexed citations

Peddu, Vikas, Isabelle Dubuc, Annie Gravel, et al.. (2019). Inherited Chromosomally Integrated Human Herpesvirus 6 Demonstrates Tissue-Specific RNA Expression In Vivo That Correlates with an Increased Antibody Immune Response. Journal of Virology. 94(1). 20 indexed citations

Wünnemann, Florian, et al.. (2019). Validation of Genome-Wide Polygenic Risk Scores for Coronary Artery Disease in French Canadians. Circulation Genomic and Precision Medicine. 12(6). e002481–e002481. 46 indexed citations

10.

Buscarlet, Manuel, Sylvie Provost, Yassamin Feroz Zada, et al.. (2017). DNMT3A and TET2 dominate clonal hematopoiesis and demonstrate benign phenotypes and different genetic predispositions. Blood. 130(6). 753–762. 252 indexed citations

11.

Denus, Simon de, Jean-Lucien Rouleau, Douglas L. Mann, et al.. (2017). CYP3A4 genotype is associated with sildenafil concentrations in patients with heart failure with preserved ejection fraction. The Pharmacogenomics Journal. 18(2). 232–237. 11 indexed citations

12.

Girard, Simon, Patrick A. Dion, Cynthia V. Bourassa, et al.. (2015). Mutation Burden of Rare Variants in Schizophrenia Candidate Genes. PLoS ONE. 10(6). e0128988–e0128988. 14 indexed citations

13.

Kadmiri, Nadia El, Nabil Zaïd, Younes Zaid, et al.. (2014). Novel presenilin mutations within Moroccan patients with Early-Onset Alzheimer’s Disease. Neuroscience. 269. 215–222. 17 indexed citations

14.

Pussegoda, Kusala, Colin J.D. Ross, Henk Visscher, et al.. (2013). Replication of TPMT and ABCC3 Genetic Variants Highly Associated With Cisplatin-Induced Hearing Loss in Children. Clinical Pharmacology & Therapeutics. 94(2). 243–251. 89 indexed citations

15.

Srour, Myriam, Jean‐Baptiste Rivière, Marie‐Pierre Dubé, et al.. (2010). Mutations in DCC Cause Congenital Mirror Movements. Science. 328(5978). 592–592. 128 indexed citations

16.

Barhdadi, Amina & Marie‐Pierre Dubé. (2010). Testing for Gene-Gene Interaction with AMMI Models. Statistical Applications in Genetics and Molecular Biology. 9(1). Article 2–Article 2. 8 indexed citations

17.

McCaffery, Jeanne M., Qing Duan, Nancy Frasure‐Smith, et al.. (2008). Genetic predictors of depressive symptoms in cardiac patients. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 150B(3). 381–388. 42 indexed citations

18.

McCaffery, Jeanne M., Nancy Frasure‐Smith, Marie‐Pierre Dubé, et al.. (2006). 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(2). 187–200. 142 indexed citations

19.

Shink, Éric, Mario Harvey, Monique Tremblay, et al.. (2005). 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. 135B(1). 50–58. 32 indexed citations

20.

Lafrenière, Ronald G., Zoha Kibar, Daniel Rochefort, et al.. (1997). Genomic structure of the human GT334 (EHOC-1) gene mapping to 21q22.3. Gene. 198(1-2). 313–321. 5 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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