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Philippe Jonveaux

Philippe Jonveaux

D-Index & Metrics

Genetics

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

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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