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Molecular Biology
France
2026
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Genetics
France
2024

D-Index & Metrics

Genetics

D-Index
101
Citations
49046
World Ranking
718
National Ranking
16

Molecular Biology

D-Index
101
Citations
49046
World Ranking
504
National Ranking
8

Medicine

D-Index
103
Citations
52753
World Ranking
7219
National Ranking
220

Research.com Recognitions

  • 2026 - Research.com Molecular Biology in France Leader Award
  • 2025 - Research.com Molecular Biology in France Leader Award
  • 2024 - Research.com Genetics in France Leader Award
  • 2024 - Research.com Genetics and Molecular Biology in France Leader Award

Overview

Gilbert M. Lenoir is affiliated with the International Agency For Research On Cancer in France. Their research primarily focuses on the field of Health Professions, with a specific emphasis on General Health Professions as a subfield of study.

The main topics explored in their work include:

  • Healthcare Systems and Practices
  • Patient-Provider Communication in Healthcare
  • Health, Medicine and Society

Among their recent contributions is a paper titled "Leviers et freins à la prise de décision partagée en France en 2021: enquête nationale auprès des patients atteints de cancer", published in 2023 in the Bulletin du Cancer. This work has been cited four times.

Lenoir has collaborated with multiple frequent co-authors, which include:

  • Léna Milan
  • Sandra Doucène
  • Fadila Farsi
  • Nora Moumjid
  • François Blot

Their publications have appeared primarily in the Bulletin du Cancer, reflecting the publication venue's central role in disseminating their research findings.

Best Publications

  • Identification of the breast cancer susceptibility gene BRCA2

    Wooster R;Bignell G;Lancaster J;Swift S

  • Genetic Heterogeneity and Penetrance Analysis of the BRCA1 and BRCA2 Genes in Breast Cancer Families

    D Ford;D F Easton;M Stratton;S Narod

  • Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13

    Richard Wooster;Susan L. Neuhausen;Jonathan Mangion;Yvette Quirk

  • Translocation of the c-myc gene into the immunoglobulin heavy chain locus in human Burkitt lymphoma and murine plasmacytoma cells

    R Taub;I Kirsch;C Morton;G Lenoir

  • Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2

    Guy A. Rouleau;Philippe Merel;Mohini Lutchman;Marc Sanson;Marc Sanson

  • The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis.

    Charis Eng;Charis Eng;David Clayton;Isabelle Schuffenecker;Gilbert Lenoir

  • The Ewing Family of Tumors -- A Subgroup of Small-Round-Cell Tumors Defined by Specific Chimeric Transcripts

    O Delattre;J Zucman;T Melot;X S Garau

  • BRCA1 testing in families with hereditary breast-ovarian cancer. A prospective study of patient decision making and outcomes.

    Caryn Lerman;Steven Narod;Kevin Schulman;Chanita Hughes

  • Translocations among antibody genes in human cancer

    Philip Leder;Jim Battey;Gilbert Lenoir;Christopher Moulding

  • The human c-myc oncogene : Structural consequences of translocation into the IgH locus in Burkitt lymphoma

    Jim Battey;Christopher Moulding;Rebecca Taub;William Murphy

  • Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene

    Alison J. Coffey;Robert A. Brooksbank;Oliver Brandau;Toshitaka Oohashi

  • Multifactorial Analysis of Differences Between Sporadic Breast Cancers and Cancers Involving BRCA1 and BRCA2 Mutations

    Sunil R. Lakhani;Jocelyne Jacquemier;John P Sloane;Barry A. Gusterson

  • Identification of the Multiple Endocrine Neoplasia Type 1 (MEN1) Gene. The European Consortium on MEN1

    Irma Lemmens;Wim J. M. Van de Ven;Koen Kas;Chang X. Zhang

  • Familial breast-ovarian cancer locus on chromosome 17q12-q23

    Steven A. Narod;Jean Feunteun;Henry T. Lynch;Patrice Watson

  • Hereditary breast cancer : pathobiology, prognosis, and BRCA1 and BRCA2 gene linkage

    Joseph N. Marcus;Patrice Watson;David L. Page;Steven A. Narod

  • Combinatorial generation of variable fusion proteins in the Ewing family of tumours.

    J Zucman;T Melot;C Desmaze;J Ghysdael

  • Chromosomes in Ewing's sarcoma. I. An evaluation of 85 cases and remarkable consistency of t(11;22)(q24;q12)

    Claude Turc-Carel;Alain Aurias;Francine Mugneret;Sarab Lizard

  • A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

    Corine Bertolotto;Fabienne Lesueur;Sandy Giuliano;Thomas Strub

  • Gene Expression Profiling of Primary Cutaneous Melanoma and Clinical Outcome

    Véronique Winnepenninckx;Vladimir Lazar;Stefan Michiels;Philippe Dessen

  • Erratum: Identification of the breast cancer susceptibility gene BRCA2

    Richard Wooster;Graham Bignell;Jonathan Lancaster;Sally Swift

Frequent Co-Authors

Henry T. Lynch
Henry T. Lynch Creighton University
Steven A. Narod
Steven A. Narod University of Toronto
David E. Goldgar
David E. Goldgar University of Utah
Jean Feunteun
Jean Feunteun Institut Gustave Roussy
Patricia N. Tonin
Patricia N. Tonin McGill University
Georg W. Bornkamm
Georg W. Bornkamm Technical University of Munich
Brigitte Bressac-de Paillerets
Brigitte Bressac-de Paillerets Institut Gustave Roussy
Bruce A.J. Ponder
Bruce A.J. Ponder University of Cambridge

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