World's Best Scientists 2026 revealed!
David-Alexandre Trégouët

David-Alexandre Trégouët

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Genetics
France
2024

D-Index & Metrics

Genetics

D-Index
87
Citations
37830
World Ranking
1196
National Ranking
42

Medicine

D-Index
88
Citations
38873
World Ranking
12956
National Ranking
404

David-Alexandre Trégouët publication distribution in Genetics in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Genetics in 2026. The highlighted bar marks where David-Alexandre Trégouët sits on this spectrum.

45–54 publications: 6 scientists 55–64 publications: 10 scientists 65–74 publications: 35 scientists 75–84 publications: 84 scientists 85–94 publications: 102 scientists 95–104 publications: 151 scientists 105–114 publications: 175 scientists 115–124 publications: 203 scientists 125–134 publications: 217 scientists 135–144 publications: 205 scientists 145–154 publications: 193 scientists 155–164 publications: 188 scientists 165–174 publications: 170 scientists 175–184 publications: 178 scientists 185–194 publications: 164 scientists 195–204 publications: 173 scientists 205–214 publications: 159 scientists 215–224 publications: 134 scientists 225–234 publications: 143 scientists 235–244 publications: 105 scientists 245–254 publications: 114 scientists 255–264 publications: 92 scientists 265–274 publications: 88 scientists 275–284 publications: 87 scientists 285–294 publications: 80 scientists 295–304 publications: 62 scientists 305–314 publications: 75 scientists 315–324 publications: 67 scientists 325–334 publications: 60 scientists 335–344 publications: 52 scientists 345–354 publications: 40 scientists 355–364 publications: 48 scientists 365–374 publications: 47 scientists 375–384 publications: 46 scientists 385–394 publications: 31 scientists 395–404 publications: 27 scientists 405–414 publications: 40 scientists 415–424 publications: 30 scientists 425–434 publications: 43 scientists 435–444 publications: 29 scientists 445–454 publications: 14 scientists 455–464 publications: 28 scientists 465–474 publications: 21 scientists 475–484 publications: 21 scientists 485–494 publications: 22 scientists 495–504 publications: 17 scientists 505–514 publications: 12 scientists 515–524 publications: 11 scientists 525–534 publications: 8 scientists 535–544 publications: 8 scientists 545–554 publications: 14 scientists 555–564 publications: 4 scientists 565–574 publications: 11 scientists 575–584 publications: 5 scientists 585–594 publications: 11 scientists 595–604 publications: 12 scientists 605–614 publications: 7 scientists 615–624 publications: 6 scientists 625–634 publications: 10 scientists 635–644 publications: 9 scientists 645–654 publications: 10 scientists 655–664 publications: 6 scientists 665–674 publications: 6 scientists 675–684 publications: 6 scientists 685–694 publications: 4 scientists 695–702 publications: 6 scientists 703+ publications: 100 scientists
45 publications 703+

This scientist: 289 publications — 74th percentile

74% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 703 publications or more.

David-Alexandre Trégouët D-index placement in Genetics in 2026

The chart shows the D-index (discipline H-index) distribution of Genetics scientists ranked by Research.com in 2026. The highlighted bar marks where David-Alexandre Trégouët sits on this spectrum.

40–41 D-Index: 24 scientists 42–43 D-Index: 52 scientists 44–45 D-Index: 84 scientists 46–47 D-Index: 112 scientists 48–49 D-Index: 118 scientists 50–51 D-Index: 141 scientists 52–53 D-Index: 143 scientists 54–55 D-Index: 145 scientists 56–57 D-Index: 179 scientists 58–59 D-Index: 162 scientists 60–61 D-Index: 175 scientists 62–63 D-Index: 191 scientists 64–65 D-Index: 172 scientists 66–67 D-Index: 184 scientists 68–69 D-Index: 164 scientists 70–71 D-Index: 158 scientists 72–73 D-Index: 150 scientists 74–75 D-Index: 136 scientists 76–77 D-Index: 127 scientists 78–79 D-Index: 127 scientists 80–81 D-Index: 111 scientists 82–83 D-Index: 110 scientists 84–85 D-Index: 110 scientists 86–87 D-Index: 84 scientists 88–89 D-Index: 102 scientists 90–91 D-Index: 66 scientists 92–93 D-Index: 72 scientists 94–95 D-Index: 70 scientists 96–97 D-Index: 54 scientists 98–99 D-Index: 60 scientists 100–101 D-Index: 49 scientists 102–103 D-Index: 55 scientists 104–105 D-Index: 45 scientists 106–107 D-Index: 42 scientists 108–109 D-Index: 28 scientists 110–111 D-Index: 39 scientists 112–113 D-Index: 25 scientists 114–115 D-Index: 31 scientists 116–117 D-Index: 29 scientists 118–119 D-Index: 34 scientists 120–121 D-Index: 29 scientists 122–123 D-Index: 29 scientists 124–125 D-Index: 18 scientists 126–127 D-Index: 27 scientists 128–129 D-Index: 22 scientists 130–131 D-Index: 16 scientists 132–133 D-Index: 11 scientists 134–135 D-Index: 17 scientists 136–137 D-Index: 12 scientists 138–139 D-Index: 21 scientists 140–141 D-Index: 4 scientists 142–143 D-Index: 9 scientists 144–145 D-Index: 14 scientists 146–147 D-Index: 6 scientists 148–149 D-Index: 10 scientists 150–151 D-Index: 7 scientists 152–153 D-Index: 9 scientists 154–155 D-Index: 8 scientists 156–157 D-Index: 8 scientists 158–159 D-Index: 9 scientists 160+ D-Index: 96 scientists
40 D-Index 160+

This scientist: 87 D-Index — 73rd percentile

73% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 160 D-Index or more.

Research.com Recognitions

  • 2024 - Research.com Genetics in France Leader Award

Overview

David-Alexandre Trégouët is affiliated with the University of Bordeaux in France. Their research primarily focuses on Medicine and Biochemistry, Genetics and Molecular Biology, with significant contributions across related subfields.

The scientist's main fields of study encompass Medicine with 214 publications and Biochemistry, Genetics and Molecular Biology totaling 122 publications. Within these broad areas, they have worked extensively in several subfields including Hematology (66 publications), Molecular Biology (61 publications), Genetics (55 publications), Cardiology and Cardiovascular Medicine (32 publications), and Internal Medicine (26 publications).

Research topics covered in their work span Blood Coagulation and Thrombosis Mechanisms, Genetic Associations and Epidemiology, Venous Thromboembolism Diagnosis and Management, Platelet Disorders and Treatments, RNA modifications and cancer, Cancer-related gene regulation, and Myeloproliferative Neoplasms: Diagnosis and Treatment.

Their recent papers illustrate a focus on cardiovascular and cerebral conditions with notable studies such as:

  • Genome-wide analysis identifies novel susceptibility loci for myocardial infarction, 2020, European Heart Journal
  • Cerebral small vessel disease genomics and its implications across the lifespan, 2020, Nature Communications
  • Interleukin-6 Signaling Effects on Ischemic Stroke and Other Cardiovascular Outcomes, 2020, Circulation Genomic and Precision Medicine
  • Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease, 2023, Nature Medicine
  • Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23, 2021, European Heart Journal

The scientist often collaborates with other researchers, with frequent coauthors including Pierre-Emmanuel Morange, Jean-François Deleuze, Pierre Suchon, Anne Boland, and Gaëlle Munsch.

Publication venues where their work appears regularly include bioRxiv (Cold Spring Harbor Laboratory) with 28 publications, Journal of Thrombosis and Haemostasis with 13, Blood with 7, Circulation with 6, and Nature Communications with 5 publications.

Best Publications

  • Genomewide association analysis of coronary artery disease.

    Nilesh J. Samani;Jeanette Erdmann;Alistair S. Hall;Christian Hengstenberg

  • Large-scale association analysis identifies new risk loci for coronary artery disease

    Panos Deloukas;Stavroula Kanoni;Christina Willenborg;Martin Farrall

  • Genetic studies of body mass index yield new insights for obesity biology

    Adam E. Locke;Bratati Kahali;Sonja I. Berndt;Anne E. Justice

  • DNA methylation and body-mass index: a genome-wide analysis

    Katherine J Dick;Katherine J Dick;Christopher P Nelson;Christopher P Nelson;Loukia Tsaprouni;Johanna K Sandling;Johanna K Sandling

  • Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

    Sonja I Berndt;Stefan Gustafsson;Stefan Gustafsson;Reedik Mägi;Reedik Mägi;Andrea Ganna

  • Genetics and Beyond – The Transcriptome of Human Monocytes and Disease Susceptibility

    Tanja Zeller;Philipp Wild;Silke Szymczak;Maxime Rotival

  • New susceptibility locus for coronary artery disease on chromosome 3q22.3

    Jeanette Erdmann;Anika Großhennig;Peter S Braund;Inke R König

  • A novel channelopathy in pulmonary arterial hypertension.

    Lijiang Ma;Danilo Roman-Campos;Eric D. Austin;Mélanie Eyries

  • Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease

    David-Alexandre Trégouët;Inke R König;Jeanette Erdmann;Alexandru Munteanu

  • Cytochrome P450 2C9 (CYP2C9) and vitamin K epoxide reductase (VKORC1) genotypes as determinants of acenocoumarol sensitivity

    Laurent Bodin;Céline Verstuyft;David-Alexandre Tregouet;Annie Robert

  • Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease

    Nathan O. Stitziel;Kathleen E. Stirrups;Nicholas G. D. Masca;Jeanette Erdmann

  • Repeated Replication and a Prospective Meta-Analysis of the Association Between Chromosome 9p21.3 and Coronary Artery Disease

    Heribert Schunkert;Anika Götz;Peter Braund;Ralph McGinnis

  • A new algorithm for haplotype‐based association analysis: the Stochastic‐EM algorithm

    D. A. Tregouet;S. Escolano;L. Tiret;A. Mallet

  • EIF2AK4 mutations cause pulmonary veno-occlusive disease, a recessive form of pulmonary hypertension

    Mélanie Eyries;David Montani;Barbara Girerd;Claire Perret

  • Human herpesvirus 8 transmission from mother to child and between siblings in an endemic population

    Sabine Plancoulaine;Sabine Plancoulaine;Laurent Abel;Laurent Abel;Monique van Beveren;David-Alexandre Trégouët

  • A new JAVA interface implementation of THESIAS

    D. A. Tregouet;V. Garelle

  • Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach

    David-Alexandre Trégouët;Simon Heath;Noémie Saut;Christine Biron-Andreani

  • Clinical outcomes of pulmonary arterial hypertension in patients carrying an ACVRL1 (ALK1) mutation.

    Barbara Girerd;David Montani;Florence Coulet;Benjamin Sztrymf

  • Thymidylate synthase gene polymorphism predicts toxicity in colorectal cancer patients receiving 5-fluorouracil-based chemotherapy

    Thierry Lecomte;Jean-Marc Ferraz;Franck Zinzindohoué;Marie-Anne Loriot

  • Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

    Sonja I. Berndt;Stefan Gustafsson;Reedik Maegi;Andrea Ganna

Frequent Co-Authors

Pierre-Emmanuel Morange
Pierre-Emmanuel Morange Aix-Marseille University
Laurence Tiret
Laurence Tiret Sorbonne University
François Cambien
François Cambien University of Bordeaux
Nilesh J. Samani
Nilesh J. Samani University of Leicester
Marie-Christine Alessi
Marie-Christine Alessi Aix-Marseille University
Daniel I. Chasman
Daniel I. Chasman Brigham and Women's Hospital
Nicholas L. Smith
Nicholas L. Smith University of Washington
Jeanette Erdmann
Jeanette Erdmann University of Lübeck
Michel Marre
Michel Marre Université Paris Cité

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