Amina Barhdadi

2.2k total citations
33 papers, 1.3k citations indexed

About

Amina Barhdadi is a scholar working on Genetics, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Amina Barhdadi has authored 33 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 9 papers in Molecular Biology and 9 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Amina Barhdadi's work include Genetic Associations and Epidemiology (9 papers), Lipoproteins and Cardiovascular Health (5 papers) and Epigenetics and DNA Methylation (4 papers). Amina Barhdadi is often cited by papers focused on Genetic Associations and Epidemiology (9 papers), Lipoproteins and Cardiovascular Health (5 papers) and Epigenetics and DNA Methylation (4 papers). Amina Barhdadi collaborates with scholars based in Canada, United States and France. Amina Barhdadi's co-authors include Marie‐Pierre Dubé, Sylvie Provost, Andrew Brown, Michael R. Hayden, Michael Phillips, Paul Rogers, Henk Visscher, Bruce Carleton, Shahrad R. Rassekh and Michael Rieder and has published in prestigious journals such as Nature Genetics, Journal of Clinical Oncology and Blood.

In The Last Decade

Amina Barhdadi

32 papers receiving 1.3k citations

Peers

Amina Barhdadi

CCM

PPCH

ONCOL

HEMAT

Vardiella Meiner Israel

Lance A. Bare United States

Matthew B. Lanktree Canada

Joël Oger Canada

Karl‐Uwe Petersen Germany

Katrin Wenzel Germany

Jonathan Manning United Kingdom

Jin Zhu China

Sylvain Loric France

Aris Baras United States

Vardiella Meiner Israel

Amina Barhdadi

1.1k ×2.8

243 ×0.8

CCM

531 ×1.8

PPCH

301 ×1.2

ONCOL

80 ×0.4

HEMAT

Citations per year, relative to Amina Barhdadi Amina Barhdadi (= 1×) peers Vardiella Meiner

Countries citing papers authored by Amina Barhdadi

Since Specialization

Citations

This map shows the geographic impact of Amina Barhdadi'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 Amina Barhdadi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Amina Barhdadi more than expected).

Fields of papers citing papers by Amina Barhdadi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Amina Barhdadi. 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 Amina Barhdadi. The network helps show where Amina Barhdadi may publish in the future.

Co-authorship network of co-authors of Amina Barhdadi

This figure shows the co-authorship network connecting the top 25 collaborators of Amina Barhdadi. A scholar is included among the top collaborators of Amina Barhdadi 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 Amina Barhdadi. Amina Barhdadi 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

Sun, Maxine, Lambert Busque, Louis‐Philippe Lemieux Perreault, et al.. (2025). Impact of clonal hematopoiesis on cardiovascular outcomes in cancer patients of the UK Biobank. ESMO Open. 10(8). 105539–105539.

Gagnon, Daniel, Hadiatou Barry, Amina Barhdadi, et al.. (2023). A dataset of proteomic changes during human heat stress and heat acclimation. Scientific Data. 10(1). 877–877. 2 indexed citations

Barhdadi, Amina, Audrey Lemaçon, Louis‐Philippe Lemieux Perreault, et al.. (2023). Study of effect modifiers of genetically predicted CETP reduction. Genetic Epidemiology. 47(2). 198–212. 1 indexed citations

Dubé, Marie‐Pierre, Olympe Chazara, Audrey Lemaçon, et al.. (2022). Pharmacogenomic Study of Heart Failure and Candesartan Response from the CHARM Programme. ESC Heart Failure. 9(5). 2997–3008. 5 indexed citations

Lemaçon, Audrey, Géraldine Asselin, Sylvie Provost, et al.. (2021). Genetic meta-analysis of cancer diagnosis following statin use identifies new associations and implicates human leukocyte antigen (HLA) in women. The Pharmacogenomics Journal. 21(4). 446–457. 3 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

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

Girard, Simon, Cynthia V. Bourassa, Louis‐Philippe Lemieux Perreault, et al.. (2016). Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy Individuals. PLoS ONE. 11(10). e0164212–e0164212. 32 indexed citations

Portales-Casamar, Élodie, Alexandre A. Lussier, Meaghan J. Jones, et al.. (2016). DNA methylation signature of human fetal alcohol spectrum disorder. Epigenetics & Chromatin. 9(1). 25–25. 106 indexed citations

10.

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

11.

Perreault, Louis‐Philippe Lemieux, et al.. (2013). pyGenClean: efficient tool for genetic data clean up before association testing. Bioinformatics. 29(13). 1704–1705. 9 indexed citations

12.

Barhdadi, Amina, Ian Mongrain, Valérie Normand, et al.. (2012). PRKCB is associated with calcineurin inhibitor-induced renal dysfunction in heart transplant recipients. Pharmacogenetics and Genomics. 22(5). 336–343. 8 indexed citations

13.

Visscher, Henk, Colin J.D. Ross, Shahrad R. Rassekh, et al.. (2011). Pharmacogenomic Prediction of Anthracycline-Induced Cardiotoxicity in Children. Journal of Clinical Oncology. 30(13). 1422–1428. 298 indexed citations

14.

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

15.

Xiong, Lan, Jacques Montplaisir, Alex Désautels, et al.. (2010). Family Study of Restless Legs Syndrome in Quebec, Canada. Archives of Neurology. 67(5). 617–22. 47 indexed citations

16.

Denus, Simon de, Amina Barhdadi, Marie-Hélène Leblanc, et al.. (2010). Association between renal function and CYP3A5 genotype in heart transplant recipients treated with calcineurin inhibitors. The Journal of Heart and Lung Transplantation. 30(3). 326–331. 20 indexed citations

17.

Ross, Colin J.D., Marie‐Pierre Dubé, Beth Brooks, et al.. (2009). Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy. Nature Genetics. 41(12). 1345–1349. 231 indexed citations

18.

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

19.

Barhdadi, Amina & Marie‐Pierre Dubé. (2007). Two-stage strategies to detect gene × gene interactions in case-control data. BMC Proceedings. 1(S1). S135–S135. 2 indexed citations

20.

Mesurolle, Benoı̂t, et al.. (2006). Contribution of Tissue Harmonic Imaging and Frequency Compound Imaging in Interventional Breast Sonography. Journal of Ultrasound in Medicine. 25(7). 845–855. 24 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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