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D-Index & Metrics

Biology and Biochemistry

D-Index
55
Citations
14395
World Ranking
14845
National Ranking
579

Overview

Gérard Lefranc is affiliated with the University of Montpellier in France. Their academic profile is characterized by a focus on research activities connected to this institution.

Although no recent papers, co-authors, publication venues, or book publications are listed, Lefranc's ongoing association with a major European university suggests involvement in academic and research environments consistent with higher education and scholarly output.

No specific main fields of study, subfields, or detailed topics of work have been documented in the available data. Similarly, there are no recorded awards or distinctions associated with this scholar.

This profile reflects the current data accessible regarding Lefranc's academic contributions and affiliations.

Best Publications

  • IMGT®, the international ImMunoGeneTics information system®

    Marie-Paule Lefranc;Véronique Giudicelli;Chantal Ginestoux;Joumana Jabado-Michaloud

  • IMGT unique numbering for immunoglobulin and T cell receptor variable domains and Ig superfamily V-like domains.

    Marie-Paule Lefranc;Christelle Pommié;Quentin Kaas;Elodie Duprat

  • Haplotype Diversity and Linkage Disequilibrium at Human G6PD: Recent Origin of Alleles That Confer Malarial Resistance

    Sarah A. Tishkoff;Robert Varkonyi;Nelie Cahinhinan;Salem Abbes

  • IMGT®, the international ImMunoGeneTics information system® 25 years on

    Marie-Paule Lefranc;Véronique Giudicelli;Patrice Duroux;Joumana Jabado-Michaloud

  • The Immunoglobulin FactsBook

    Marie-Paule Lefranc;Gérard Lefranc

  • Deep dermatophytosis and inherited CARD9 deficiency.

    Fanny Lanternier;Saad Pathan;Quentin B. Vincent;Luyan Liu

  • IMGT standardized criteria for statistical analysis of immunoglobulin V-REGION amino acid properties.

    Christelle Pommié;Séverine Levadoux;Robert Sabatier;Gérard Lefranc

  • Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IκBα/NF-κB pathway in limb-girdle muscular dystrophy type 2A

    S. Baghdiguian;M. Martin;I. Richard;F. Pons

  • The T cell receptor factsbook

    Marie-Paule Lefranc;Gérard Lefranc

  • DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activation

    Haifa H. Jabara;Douglas R. McDonald;Erin Janssen;Michel J. Massaad

  • Loss of Calpain 3 Proteolytic Activity Leads to Muscular Dystrophy and to Apoptosis-Associated Iκbα/Nuclear Factor κb Pathway Perturbation in Mice

    Isabelle Richard;Carinne Roudaut;Sylvie Marchand;Stephen Baghdiguian

  • The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency.

    Karin R. Engelhardt;Karin R. Engelhardt;Karin R. Engelhardt;Michael E. Gertz;Sevgi Keles;Sevgi Keles;Alejandro A. Schäffer

  • Update in chronic obstructive pulmonary disease: role of antioxidant and metabolizing gene polymorphisms.

    Ramzi Lakhdar;Sabri Denden;Asma Kassab;Nadia Leban

  • Joining the pillars of Hercules: mtDNA sequences show multidirectional gene flow in the western Mediterranean.

    S. Plaza;F. Calafell;A. Helal;N. Bouzerna

  • Evidence for balancing selection from nucleotide sequence analyses of human G6PD.

    Brian C. Verrelli;John H. McDonald;George Argyropoulos;Giovanni Destro-Bisol

  • Alu insertion polymorphisms in NW Africa and the Iberian Peninsula: evidence for a strong genetic boundary through the Gibraltar Straits.

    David Comas;Francesc Calafell;Noufissa Benchemsi;Ahmed Helal

  • Sequence of a human immunoglobulin gamma 3 heavy chain constant region gene: comparison with the other human C gamma genes.

    S. Huck;P. Fort;D.H. Crawford;M.-P. Lefranc

  • IMGT unique numbering for MHC groove G-DOMAIN and MHC superfamily (MhcSF) G-LIKE-DOMAIN.

    Marie-Paule Lefranc;Elodie Duprat;Quentin Kaas;Madeleine Tranne

  • Human Gm, Km, and Am allotypes and their molecular characterization: a remarkable demonstration of polymorphism.

    Marie-Paule Lefranc;Gérard Lefranc

  • Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins.

    I Richard;L Brenguier;P Dinçer;C Roudaut

Frequent Co-Authors

Marie-Paule Lefranc
Marie-Paule Lefranc University of Montpellier
André Mégarbané
André Mégarbané Lebanese American University
Raif S. Geha
Raif S. Geha Boston Children's Hospital
Talal A. Chatila
Talal A. Chatila Boston Children's Hospital
Waleed Al-Herz
Waleed Al-Herz Kuwait University
Sevgi Keles
Sevgi Keles Necmettin Erbakan University
Isabelle Richard
Isabelle Richard Centre national de la recherche scientifique, CNRS
Jacques S. Beckmann
Jacques S. Beckmann University of Lausanne
Janet Chou
Janet Chou Boston Children's Hospital
Necil Kutukculer
Necil Kutukculer Ege University

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