Guillaume Paré

47.2k total citations · 3 hit papers
268 papers, 10.6k citations indexed

About

Guillaume Paré is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Guillaume Paré has authored 268 papers receiving a total of 10.6k indexed citations (citations by other indexed papers that have themselves been cited), including 94 papers in Genetics, 67 papers in Molecular Biology and 59 papers in Surgery. Recurrent topics in Guillaume Paré's work include Genetic Associations and Epidemiology (70 papers), Lipoproteins and Cardiovascular Health (38 papers) and Antiplatelet Therapy and Cardiovascular Diseases (19 papers). Guillaume Paré is often cited by papers focused on Genetic Associations and Epidemiology (70 papers), Lipoproteins and Cardiovascular Health (38 papers) and Antiplatelet Therapy and Cardiovascular Diseases (19 papers). Guillaume Paré collaborates with scholars based in Canada, United States and United Kingdom. Guillaume Paré's co-authors include Daniel I. Chasman, Paul M. Ridker, Sonia S. Anand, David Meyre, Yohan Bossé, Michelle Turcotte, Vivian Tam, Nikunj Patel, Hertzel C. Gerstein and Salim Yusuf and has published in prestigious journals such as New England Journal of Medicine, The Lancet and Journal of Biological Chemistry.

In The Last Decade

Guillaume Paré

257 papers receiving 10.4k citations

Hit Papers

Benefits and limitations of genome-wide association studies 2019 2026 2021 2023 2019 2019 2023 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Guillaume Paré Canada 53 2.8k 2.7k 2.1k 1.8k 1.5k 268 10.6k
Markus Perola Finland 58 3.1k 1.1× 3.1k 1.2× 1.2k 0.6× 1.6k 0.8× 1.5k 1.0× 280 11.3k
Michael V. Holmes United Kingdom 41 2.5k 0.9× 3.5k 1.3× 1.8k 0.8× 1.2k 0.7× 1.6k 1.1× 137 10.9k
Daniel I. Chasman United States 59 4.1k 1.5× 4.3k 1.6× 2.2k 1.1× 1.7k 0.9× 1.6k 1.1× 185 12.5k
Claudia Langenberg United Kingdom 54 2.7k 1.0× 2.8k 1.0× 1.6k 0.8× 1.7k 0.9× 1.9k 1.3× 144 11.8k
Adam S. Butterworth United Kingdom 35 2.7k 1.0× 4.2k 1.6× 1.8k 0.9× 1.4k 0.8× 1.4k 1.0× 78 12.0k
Erik Ingelsson Sweden 63 2.9k 1.1× 2.3k 0.9× 1.5k 0.7× 3.3k 1.8× 1.7k 1.1× 209 12.8k
Barry I. Freedman United States 65 3.3k 1.2× 3.0k 1.1× 1.8k 0.9× 2.6k 1.4× 3.2k 2.2× 420 16.3k
Donald W. Bowden United States 59 4.1k 1.5× 3.7k 1.4× 2.0k 1.0× 2.0k 1.1× 2.7k 1.9× 359 14.7k
Ruth McPherson Canada 52 3.8k 1.4× 2.6k 1.0× 3.8k 1.9× 1.8k 1.0× 2.1k 1.5× 197 11.4k
Alexandre C. Pereira Brazil 50 3.0k 1.1× 1.3k 0.5× 1.8k 0.9× 3.6k 1.9× 1.4k 0.9× 431 10.3k

Countries citing papers authored by Guillaume Paré

Since Specialization
Citations

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

Fields of papers citing papers by Guillaume Paré

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Guillaume Paré

This figure shows the co-authorship network connecting the top 25 collaborators of Guillaume Paré. A scholar is included among the top collaborators of Guillaume Paré 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 Guillaume Paré. Guillaume Paré is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Spence, Jessica, P.J. Devereaux, Shaheena Bashir, et al.. (2025). Protein Alterations in Patients with Delirium after Cardiac Surgery: An Exploratory Case–Control Substudy of the VISION Cardiac Surgery Biobank. Anesthesiology. 142(4). 716–725.
2.
Perrot, Nicolas, Yu Huang, Michael Chong, et al.. (2025). Mendelian randomization study implicates inflammaging biomarkers in retinal vasculature, cardiovascular diseases, and longevity. Science Advances. 11(43). eadu1985–eadu1985.
3.
Barra, Lillian, Guillaume Paré, Halim Maaroufi, et al.. (2025). Identification of autoantibodies targeting citrullinated CLEC12A in rheumatoid arthritis patients. Journal of Translational Autoimmunity. 10. 100287–100287.
4.
Dvorkin‐Gheva, Anna, Jennifer Wattie, Karen Howie, et al.. (2024). Neuromedin-U Mediates Rapid Activation of Airway Group 2 Innate Lymphoid Cells in Mild Asthma. American Journal of Respiratory and Critical Care Medicine. 210(6). 755–765. 18 indexed citations
5.
Wu, Jianhan, Caitlyn Vlasschaert, Ricky Lali, et al.. (2024). Kidney Volume and Risk of Incident Kidney Outcomes. Journal of the American Society of Nephrology. 35(9). 1240–1251. 3 indexed citations
7.
Chikowore, Tinashe, Kristi Läll, Lisa K. Micklesfield, et al.. (2024). Variability of polygenic prediction for body mass index in Africa. Genome Medicine. 16(1). 74–74. 2 indexed citations
8.
Deng, Wei Q., Mohammad Daud Khan, Shihong Mao, et al.. (2024). A method to estimate the contribution of rare coding variants to complex trait heritability. Nature Communications. 15(1). 1245–1245. 5 indexed citations
9.
Chong, Michael, Pedrum Mohammadi‐Shemirani, Robert W. Morton, et al.. (2023). Surrogate Adiposity Markers and Mortality. JAMA Network Open. 6(9). e2334836–e2334836. 74 indexed citations breakdown →
10.
Lanktree, Matthew B., Nicolas Perrot, Andrew Smyth, et al.. (2023). A novel multi-ancestry proteome-wide Mendelian randomization study implicates extracellular proteins, tubular cells, and fibroblasts in estimated glomerular filtration rate regulation. Kidney International. 104(6). 1170–1184. 12 indexed citations
11.
Vlasschaert, Caitlyn, Amy J. M. McNaughton, Michael Chong, et al.. (2022). Association of Clonal Hematopoiesis of Indeterminate Potential with Worse Kidney Function and Anemia in Two Cohorts of Patients with Advanced Chronic Kidney Disease. Journal of the American Society of Nephrology. 33(5). 985–995. 61 indexed citations
12.
Forgetta, Vincenzo, Rui Li, Alexandre Bélisle, et al.. (2022). Cohort profile: genomic data for 26 622 individuals from the Canadian Longitudinal Study on Aging (CLSA). BMJ Open. 12(3). e059021–e059021. 31 indexed citations
13.
Chong, Michael, Pedrum Mohammadi‐Shemirani, Nicolas Perrot, et al.. (2022). GWAS and ExWAS of blood mitochondrial DNA copy number identifies 71 loci and highlights a potential causal role in dementia. eLife. 11. 71 indexed citations
14.
Lamri, Amel, Karleen Schulze, Dipika Desai, et al.. (2022). The genetic risk of gestational diabetes in South Asian women. eLife. 11. 15 indexed citations
15.
Kavsak, Peter A., Lorna Clark, Janet Martin, et al.. (2021). Acute Phase Response and Non-Reproducible Elevated Concentrations with a High-Sensitivity Cardiac Troponin I Assay. Journal of Clinical Medicine. 10(5). 1014–1014. 7 indexed citations
16.
Lebeau, Paul, Hanny Wassef, Jae Hyun Byun, et al.. (2020). The loss-of-function PCSK9Q152H variant increases ER chaperones GRP78 and GRP94 and protects against liver injury. Journal of Clinical Investigation. 131(2). 30 indexed citations
17.
Deng, Wei Q., Shihong Mao, Anette Kalnapenkis, et al.. (2019). Analytical strategies to include the X‐chromosome in variance heterogeneity analyses: Evidence for trait‐specific polygenic variance structure. Genetic Epidemiology. 43(7). 815–830. 8 indexed citations
18.
Paré, Guillaume, et al.. (2014). The pharmacogenetics of carboxylesterases: CES1 and CES2 genetic variants and their clinical effect. Drug metabolism and drug interactions. 29(3). 143–151. 79 indexed citations
19.
Conen, David, et al.. (2012). Genetic and phenotypic determinants of blood pressure and other cardiovascular risk factors. Swiss Medical Weekly. 143(102). w13728–w13728. 29 indexed citations
20.
Lefebvre, Julie, Tania Lévesque, Serge Picard, et al.. (2011). Extra domain A of fibronectin primes leukotriene biosynthesis and stimulates neutrophil migration through activation of Toll-like receptor 4. Arthritis & Rheumatism. 63(6). 1527–1533. 43 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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