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Patrick Revy

Patrick Revy

D-Index & Metrics

Genetics

D-Index
55
Citations
13588
World Ranking
3567
National Ranking
183

Overview

Patrick Revy is a researcher affiliated with Inserm in France, specializing in the fields of biochemistry, genetics, molecular biology, and medicine. Their work spans multiple subfields including molecular biology, immunology, physiology, pulmonary and respiratory medicine, and genetics.

The main research topics covered by Patrick Revy include:

  • Telomeres, Telomerase, and Senescence
  • DNA Repair Mechanisms
  • Immunodeficiency and Autoimmune Disorders
  • RNA Modifications and Cancer
  • Blood Disorders and Treatments
  • Epigenetics and DNA Methylation
  • Muscle Physiology and Disorders

Patrick Revy has published extensively in several scientific venues, with frequent publications in the following journals:

  • Blood
  • Nature Structural & Molecular Biology
  • Nature Communications
  • Human Molecular Genetics
  • Journal of Clinical Investigation

Some recent publications authored by Patrick Revy and colleagues include:

  • Genetics of human telomere biology disorders (2022), published in Nature Reviews Genetics
  • SLX4 interacts with RTEL1 to prevent transcription-mediated DNA replication perturbations (2020), published in Nature Structural & Molecular Biology
  • Somatic genetic rescue of a germline ribosome assembly defect (2021), published in Nature Communications
  • Unraveling Ewing Sarcoma Tumorigenesis Originating from Patient-Derived Mesenchymal Stem Cells (2021), published in Cancer Research
  • Gain-of-function mutations in RPA1 cause a syndrome with short telomeres and somatic genetic rescue (2021), published in Blood

The researcher collaborates frequently with the following co-authors:

  • Isabelle Callebaut
  • Jean-Pierre de Villartay
  • Caroline Kannengiesser
  • Laëtitia Kermasson
  • Élodie Lainey

Best Publications

  • Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2).

    Patrick Revy;Taro Muto;Yves Levy;Frédéric Geissmann

  • INTERFERON-GAMMA-RECEPTOR DEFICIENCY IN AN INFANT WITH FATAL BACILLE CALMETTE-GUERIN INFECTION

    Emmanuelle Jouanguy;Frédéric Altare;Salma Lamhamedi;Patrick Revy

  • Cernunnos, a novel nonhomologous end-joining factor, is mutated in human immunodeficiency with microcephaly.

    Dietke Buck;Laurent Malivert;Régina de Chasseval;Anne Barraud

  • XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome

    Stéphanie Rigaud;Marie-Claude Fondanèche;Nathalie Lambert;Nathalie Lambert;Benoit Pasquier

  • Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination.

    Kohsuke Imai;Geir Slupphaug;Wen I. Lee;Wen I. Lee;Patrick Revy

  • Inherited interleukin 12 deficiency in a child with bacille Calmette-Guérin and Salmonella enteritidis disseminated infection.

    F Altare;D Lammas;P Revy;E Jouanguy

  • TGF-beta 1 prevents the noncognate maturation of human dendritic Langerhans cells.

    Frederic Geissmann;Patrick Revy;Armelle Regnault;Yves Lepelletier

  • Functional antigen-independent synapses formed between T cells and dendritic cells.

    Patrick Revy;Mireia Sospedra;Boris Barbour;Alain Trautmann

  • Shared genetic predisposition in rheumatoid arthritis-interstitial lung disease and familial pulmonary fibrosis.

    Pierre-Antoine Juge;Raphaël Borie;Caroline Kannengiesser;Steven Gazal;Steven Gazal

  • Retinoids Regulate Survival and Antigen Presentation by Immature Dendritic Cells

    Frédéric Geissmann;Patrick Revy;Nicole Brousse;Yves Lepelletier

  • Dietary means to better control the environmental impact of copper and zinc by pigs from weaning to slaughter

    C Jondreville;P.S Revy;J.Y Dourmad

  • Human RTEL1 deficiency causes Hoyeraal–Hreidarsson syndrome with short telomeres and genome instability

    Tangui Le Guen;Tangui Le Guen;Laurent Jullien;Laurent Jullien;Fabien Touzot;Fabien Touzot;Michael Schertzer

  • Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly.

    Daniela A. Braun;Jia Rao;Geraldine Mollet;Geraldine Mollet;David Schapiro

  • V(D)J and immunoglobulin class switch recombinations: a paradigm to study the regulation of DNA end-joining.

    P Soulas-Sprauel;P Rivera-Munoz;P Rivera-Munoz;L Malivert;L Malivert;G Le Guyader;G Le Guyader

  • Whole-exome sequencing identifies Coronin-1A deficiency in 3 siblings with immunodeficiency and EBV-associated B-cell lymphoproliferation

    Despina Moshous;Despina Moshous;Despina Moshous;Emmanuel Martin;Emmanuel Martin;Wassila Carpentier;Annick Lim

  • Heterozygous RTEL1 mutations are associated with familial pulmonary fibrosis

    Caroline Kannengiesser;Raphael Borie;Christelle Ménard;Marion Réocreux

  • Hyper-IgM syndrome type 4 with a B lymphocyte–intrinsic selective deficiency in Ig class-switch recombination

    Kohsuke Imai;Nadia Catalan;Alessandro Plebani;László Maródi

  • Prevalence and characteristics of TERT and TERC mutations in suspected genetic pulmonary fibrosis

    Raphael Borie;Laure Tabèze;Gabriel Thabut;Hilario Nunes

  • Structural characterization of filaments formed by human Xrcc4-Cernunnos/XLF complex involved in nonhomologous DNA end-joining

    Virginie Ropars;Pascal Drevet;Pierre Legrand;Sonia Baconnais

  • Cernunnos Interacts with the XRCC4·DNA-ligase IV Complex and Is Homologous to the Yeast Nonhomologous End-joining Factor Nej1 *

    Isabelle Callebaut;Laurent Malivert;Alain Fischer;Alain Fischer;Jean-Paul Mornon

Frequent Co-Authors

Jean-Pierre de Villartay
Jean-Pierre de Villartay Université Paris Cité
Alain Fischer
Alain Fischer Collège de France
Isabelle Callebaut
Isabelle Callebaut Sorbonne University
Catherine Boileau
Catherine Boileau Université Paris Cité
Capucine Picard
Capucine Picard Université Paris Cité
Stéphane Blanche
Stéphane Blanche Université Paris Cité
Vincent Cottin
Vincent Cottin Claude Bernard University Lyon 1
Kohsuke Imai
Kohsuke Imai Tokyo Medical and Dental University
Despina Moshous
Despina Moshous Necker-Enfants Malades Hospital

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