World's Best Scientists 2026 revealed!
Philippe Jonveaux

Philippe Jonveaux

D-Index & Metrics

Genetics

D-Index
59
Citations
11224
World Ranking
3257
National Ranking
159

Philippe Jonveaux 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 Philippe Jonveaux 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: 177 publications — 41st percentile

41% of scientists in this discipline score the same or lower.

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

Philippe Jonveaux 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 Philippe Jonveaux 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: 59 D-Index — 27th percentile

27% of scientists in this discipline score the same or lower.

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

Overview

Philippe Jonveaux is affiliated with the University of Lorraine in France. Their research primarily focuses on medicine, with significant contributions also in biochemistry, genetics, and molecular biology. Their work spans several subfields including pediatrics, perinatology and child health, genetics, reproductive medicine, public health, environmental and occupational health, as well as obstetrics and gynecology.

The scientist's research covers a range of main topics related to reproductive and prenatal health, including:

  • Assisted Reproductive Technology and Twin Pregnancy
  • Prenatal Screening and Diagnostics
  • Genomics and Rare Diseases
  • Ovarian function and disorders
  • Reproductive Health and Technologies
  • Ectopic Pregnancy Diagnosis and Management
  • Reproductive Biology and Fertility

Philippe Jonveaux has collaborated frequently with several co-authors, including:

  • Sylvie Epelboin
  • J. de Mouzon
  • Patricia Fauque
  • Fabienne Pessione
  • M. Boyer

Their publications have appeared in journals such as:

  • Reproductive BioMedicine Online
  • Human Reproduction
  • PLoS Medicine
  • Genome Medicine
  • Clinical Epigenetics

Some notable papers authored or co-authored by Philippe Jonveaux include:

  • Obstetrical outcomes and maternal morbidities associated with COVID-19 in pregnant women in France: A national retrospective cohort study (2021, PLoS Medicine)
  • Endometriosis and assisted reproductive techniques independently related to mother-child morbidities: a French longitudinal national study (2020, Reproductive BioMedicine Online)
  • Reproductive technologies, female infertility, and the risk of imprinting-related disorders (2020, Clinical Epigenetics)
  • Genotype-first in a cohort of 95 fetuses with multiple congenital abnormalities: when exome sequencing reveals unexpected fetal phenotype-genotype correlations (2020, Journal of Medical Genetics)
  • Do in vitro fertilization, intrauterine insemination or female infertility impact the risk of congenital anomalies in singletons? A longitudinal national French study (2020, Human Reproduction)

Best Publications

  • A new highly penetrant form of obesity due to deletions on chromosome 16p11.2

    R. G. Walters;S. Jacquemont;A. Valsesia;A. Valsesia;A. Valsesia;A. J. de Smith

  • High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemia

    SP Romana;H Poirel;M Leconiat;MA Flexor

  • Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

    Sébastien Jacquemont;Alexandre Reymond;Flore Zufferey;Louise Harewood

  • MECP2 mutations account for most cases of typical forms of Rett syndrome

    Thierry Bienvenu;Alain Carrié;Nicolas de Roux;Marie-Claude Vinet

  • A Human Homologue of the Drosophila melanogaster diaphanous Gene Is Disrupted in a Patient with Premature Ovarian Failure: Evidence for Conserved Function in Oogenesis and Implications for Human Sterility

    Silvia Bione;Cinzia Sala;Chiara Manzini;Giulia Arrigo

  • A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders

    Flore Zufferey;Elliott H. Sherr;Noam D. Beckmann;Ellen Hanson

  • Key clinical features to identify girls with CDKL5 mutations

    Nadia Bahi-Buisson;Juliette Nectoux;Juliette Nectoux;Haydeé Rosas-Vargas;Haydeé Rosas-Vargas;Mathieu Milh

  • The Signal Transducer and Activator of Transcription STAT5b Gene Is a New Partner of Retinoic Acid Receptor α in Acute Promyelocytic-Like Leukaemia

    Cécile Arnould;Christophe Philippe;Violaine Bourdon;Marie José Grégoire

  • AF6q21, a novel partner of the MLL gene in t(6;11)(q21;q23), defines a forkhead transcriptional factor subfamily.

    Josette Hillion;Maryvonne Le Coniat;Philippe Jonveaux;Roland Berger

  • The t(6;8)(q27;p11) translocation in a stem cell myeloproliferative disorder fuses a novel gene, FOP, to fibroblast growth factor receptor 1

    Cornel Popovici;Bin Zhang;Marie-José Grégoire;Philippe Jonveaux

  • P53 Gene Mutations in Acute Myeloid Leukemia With 17p Monosomy

    Pierre Fenaux;Philippe Jonveaux;Isabelle Quiquandon;Jean Luc Lai

  • Mutations of the p53 gene in B-cell chronic lymphocytic leukemia: a report on 39 cases with cytogenetic analysis.

    Fenaux P;Preudhomme C;Laï Jl;Quiquandon I

  • Mutations in the p53 gene in myelodysplastic syndromes.

    Jonveaux P;Fenaux P;Quiquandon I;Pignon Jm

  • DNMT3B Mutations and DNA Methylation Defect Define Two Types of ICF Syndrome

    YL Jiang;M Rigolet;D Bourc'his;F Nigon

  • Two site-specific deletions and t(1;14) translocation restricted to human T-cell acute leukemias disrupt the 5' part of the tal-1 gene.

    Bernard O;Lecointe N;Jonveaux P;Souyri M

  • Biomarkers (BM) France: Results of routine EGFR, HER2, KRAS, BRAF, PI3KCA mutations detection and EML4-ALK gene fusion assessment on the first 10,000 non-small cell lung cancer (NSCLC) patients (pts).

    Fabrice Barlesi;Helene Blons;Michele Beau-Faller;Isabelle Rouquette

  • Mutations of the P53 gene in acute myeloid leukaemia.

    Pierre Fenaux;Claude Preudhomme;Isabelle Quiquandon;Philippe Jonveaux

  • Eleven X Chromosome Breakpoints Associated with Premature Ovarian Failure (POF) Map to a 15-Mb YAC Contig Spanning Xq21

    Cinzia Sala;Giulia Arrigo;Giovanna Torri;Francesco Martinazzi

  • Two distinct mechanisms for the SCL gene activation in the t(1;14) translocation of T-cell leukemias.

    Olivier Bernard;Paul Guglielmi;Philippe Jonveaux;Dorra Cherif

  • Molecular basis of the Li-Fraumeni syndrome: an update from the French LFS families

    G. Bougeard;R. Sesboué;S. Desurmont;P. Berthet

Frequent Co-Authors

Roland Berger
Roland Berger Necker-Enfants Malades Hospital
Laurence Faivre
Laurence Faivre University of Burgundy
Christel Thauvin-Robinet
Christel Thauvin-Robinet University of Burgundy
Thierry Bienvenu
Thierry Bienvenu Université Paris Cité
Albert David
Albert David University of Nantes
Jamel Chelly
Jamel Chelly Institute of Genetics and Molecular and Cellular Biology
Delphine Héron
Delphine Héron Sorbonne University
Olivier Bernard
Olivier Bernard University of Paris-Saclay
Thierry Frebourg
Thierry Frebourg Grenoble Alpes University
Laurent Pasquier
Laurent Pasquier University of Rennes

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