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Jean-Louis Guénet

Jean-Louis Guénet

D-Index & Metrics

Genetics

D-Index
74
Citations
15892
World Ranking
1984
National Ranking
88

Overview

Jean-Louis Guénet is affiliated with the Institut Pasteur in France and conducts research primarily within the fields of biochemistry, genetics, and molecular biology. Their work encompasses subfields such as genetics, molecular biology, and ecology.

The scientist's main topics of research include:

  • Animal Genetics and Reproduction
  • Genetic and phenotypic traits in livestock
  • Environmental DNA in Biodiversity Studies
  • CRISPR and Genetic Engineering
  • Pluripotent Stem Cells Research

Jean-Louis Guénet has published in venues such as:

  • Bulletin de l'Académie vétérinaire de France

Recent papers include:

  • "L'édition génomique des animaux domestiques: quels enjeux et quel avenir?", 2021, Bulletin de l'Académie vétérinaire de France

Their research collaborations include frequent co-authorship with Fernando Benavides.

Best Publications

  • A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse.

    P M Nolan;J Peters;M Strivens;D Rogers

  • Transient and restricted expression during mouse embryogenesis of Dll1, a murine gene closely related to Drosophila Delta

    B. Bettenhausen;M. Hrabe de Angelis;D. Simon;J.L. Guenet

  • Pax8, a murine paired box gene expressed in the developing excretory system and thyroid gland.

    D. Plachov;K. Chowdhury;C. Walther;D. Simon

  • Rat gene mapping using PCR-analyzed microsatellites.

    T Serikawa;T Kuramoto;P Hilbert;M Mori

  • Pax: A murine multigene family of paired box-containing genes

    Claudia Walther;Jean-Louis Guenet;Dominique Simon;Urban Deutsch

  • A nonsense mutation in the gene encoding 2′-5′-oligoadenylate synthetase/L1 isoform is associated with West Nile virus susceptibility in laboratory mice

    Tomoji Mashimo;Marianne Lucas;Dominique Simon-Chazottes;Marie-Pascale Frenkiel

  • A single locus in the mouse encodes both myosin light chains 1 and 3, a second locus corresponds to a related pseudogene

    Benoît Robert;Philippe Daubas;Marie-Andrée Akimenko;Arlette Cohen

  • Number and organization of actin-related sequences in the mouse genome

    Adrian J. Minty;Serge Alonso;Jean-Louis Guénet;Marganet E. Buckingham

  • Cell lines derived from teratocarcinomas.

    Jean Francois Daniel Nicolas;P. Avner;J. Gaillard;J L Guenet

  • Genetic analysis of the mouse using interspecific crosses

    P. Avner;L. Amar;L. Dandolo;J.L. Guénet

  • A mouse gene homologous to the Drosophila gene caudal is expressed in epithelial cells from the embryonic intestine.

    P. Duprey;K. Chowdhury;G. R. Dressler;Rudi Balling

  • The spastic mouse: Aberrant splicing of glycine receptor β subunit mRNA caused by intronic insertion of Ll element

    Cornel Mülhardt;Maria Fischer;Peter Gass;Dominique Simon-Chazottes

  • Association of the H-Y male antigen with beta2-microglobulin on human lymphoid and differentiated mouse teratocarcinoma cell lines.

    M Fellous;E Günther;R Kemler;J Wiels

  • The structural gene coding for myelin-associated proteolipid protein is mutated in jimpy mice.

    A. Dautigny;M.-G. Mattei;D. Morello;P. M. Alliel

  • A missense mutation in Tbce causes progressive motor neuronopathy in mice.

    Natalia Martin;Jean Jaubert;Pierre Gounon;Eduardo Salido

  • Sequence interpretation. Functional annotation of mouse genome sequences.

    J. H. Nadeau;R. Balling;G. Barsh;D. Beier

  • A deletion in the gene encoding sphingomyelin phosphodiesterase 3 (Smpd3) results in osteogenesis and dentinogenesis imperfecta in the mouse

    Isabelle Aubin;Carolyn P Adams;Sibylle Opsahl;Dominique Septier

  • Structural analysis of mouse glycine receptor alpha subunit genes. Identification and chromosomal localization of a novel variant.

    B Matzenbach;Y Maulet;L Sefton;B Courtier

  • Investigation of genetic linkage between myosin and actin genes using an interspecific mouse back-cross.

    Benoît Robert;Paul Barton;Adrian Minty;Philippe Daubas

  • Three New Allelic Mouse Mutations that Cause Skeletal Overgrowth Involve the Natriuretic Peptide Receptor C Gene (Npr3)

    Jean Jaubert;Francis Jaubert;Natalia Martin;Linda L. Washburn

Frequent Co-Authors

François Bonhomme
François Bonhomme University of Montpellier
Tadao Serikawa
Tadao Serikawa Kyoto University
Pierre-André Cazenave
Pierre-André Cazenave Institut Pasteur
François Jacob
François Jacob Institut Pasteur
Karen P. Steel
Karen P. Steel King's College London
Philippe Desprès
Philippe Desprès University of La Réunion
Philip Avner
Philip Avner European Bioinformatics Institute
Margaret Buckingham
Margaret Buckingham Institut Pasteur
Rudi Balling
Rudi Balling University of Bonn
Constantino Sotelo
Constantino Sotelo Sorbonne University

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