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D-Index & Metrics

Biology and Biochemistry

D-Index
59
Citations
16676
World Ranking
12345
National Ranking
452

Overview

Jean Feunteun is affiliated with the Institut Gustave Roussy in France, engaging in research primarily within the fields of Medicine and Biochemistry, Genetics, and Molecular Biology. Their work spans several subfields, notably Oncology, Cancer Research, Reproductive Medicine, Cell Biology, and Genetics.

The primary research topics addressed by Feunteun include Cancer Cells and Metastasis, Cancer Genomics and Diagnostics, Science, Research, and Medicine, Hippo pathway signaling and YAP/TAZ, Cancer Risks and Factors, Mesenchymal stem cell research, and Cancer, Hypoxia, and Metabolism.

Feunteun has contributed to a number of scholarly articles published in several notable venues. Recent publications include:

  • "Tumor cell malignancy: A complex trait built through reciprocal interactions between tumors and tissue-body system" (2022) in iScience
  • "Reuniting philosophy and science to advance cancer research" (2023) in Biological reviews/Biological reviews of the Cambridge Philosophical Society
  • "Adipose Tissue Properties in Tumor-Bearing Breasts" (2020) in Frontiers in Oncology
  • "Genetic Evidence of a Precisely Tuned Dysregulation in the Hypoxia Signaling Pathway during Oncogenesis" (2020) in UNC Libraries
  • "Glossaire" (2022) in Histoire de la recherche contemporaine

Feunteun frequently collaborates with a select group of researchers, including Pauline Ostyn, Suzette Delaloge, Philippe Dessen, Thomas Pradeu, and Bertrand Daignan-Fornier. These collaborations appear across various publications and research projects.

The scientist's work is disseminated through several academic venues, with multiple contributions in each of the following:

  • Biological reviews/Biological reviews of the Cambridge Philosophical Society
  • iScience
  • Frontiers in Oncology
  • UNC Libraries
  • Histoire de la recherche contemporaine

Best Publications

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

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

  • Association of BRCA1 with Rad51 in Mitotic and Meiotic Cells

    Ralph Scully;Junjie Chen;Annemieke Plug;Yonghong Xiao

  • Dynamic Changes of BRCA1 Subnuclear Location and Phosphorylation State Are Initiated by DNA Damage

    Ralph Scully;Junjie Chen;Robert L Ochs;Kathleen Keegan

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

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

  • PML induces a novel caspase-independent death process

    Frédérique Quignon;Frédéric De Bels;Marcel Koken;Jean Feunteun

  • P53 germline mutations in childhood cancers and cancer risk for carrier individuals.

    A Chompret;L Brugières;M Ronsin;M Gardes

  • Mitotic catastrophe constitutes a special case of apoptosis whose suppression entails aneuploidy

    Maria Castedo;Jean-Luc Perfettini;Thomas Roumier;Alexander Valent

  • BRCA1 Supports XIST RNA Concentration on the Inactive X Chromosome

    Shridar Ganesan;Daniel P. Silver;Roger A. Greenberg;Dror Avni

  • PHD2 Mutation and Congenital Erythrocytosis with Paraganglioma

    Charline Ladroue;Romain Carcenac;Michel Leporrier;Sophie Gad

  • Sensitivity and predictive value of criteria for p53 germline mutation screening

    Agnès Chompret;Anne Abel;Dominique Stoppa-Lyonnet;Laurence Brugières

  • Location of BRCA1 in Human Breast and Ovarian Cancer Cells

    Scully R;Ganesan S;Brown M;De Caprio Ja

  • BRCA1 and BRCA2 Are Necessary for the Transcription-Coupled Repair of the Oxidative 8-Oxoguanine Lesion in Human Cells

    Florence Le Page;Voahangy Randrianarison;Didier Marot;Jeannine Cabannes

  • A 1-kb Alu-mediated germ-line deletion removing BRCA1 exon 17.

    Nadine Puget;Nadine Puget;Delphine Torchard;Olga M. Serova-Sinilnikova;Olga M. Serova-Sinilnikova;Henry T. Lynch

  • X-Chromosome Genetics and Human Cancer

    Alain Spatz;Christophe Borg;Jean Feunteun

  • FLI1 monoallelic expression combined with its hemizygous loss underlies Paris-Trousseau/ Jacobsen thrombopenia

    Hana Raslova;Emiko Komura;Jean Pierre Le Couédic;Frederic Larbret

  • High Frequency of TP53 Mutation in BRCA1 and Sporadic Basal-like Carcinomas but not in BRCA1 Luminal Breast Tumors

    Elodie Manié;Anne Vincent-Salomon;Jacqueline Lehmann-Che;Gaelle Pierron

  • Gamma-rays-induced death of human cells carrying mutations of BRCA1 or BRCA2.

    Nicolas Foray;Voahangy Randrianarison;Didier Marot;Michel Perricaudet

  • Radiation and genetic factors in the risk of second malignant neoplasms after a first cancer in childhood

    Sabine J Kony;Florent de Vathaire;Agnès Chompret;Akthar Shamsaldim

  • Localization of gene functions in polyoma virus DNA

    Jean Feunteun;Lauren Sompayrac;Michele Fluck;Thomas Benjamin

  • Oncogenic potential of guanine nucleotide stimulatory factor alpha subunit in thyroid glands of transgenic mice

    Francine-Marie Michiels;Bernard Caillou;Monique Talbot;Francoise Dessarps-Freichey

Frequent Co-Authors

Gilbert M. Lenoir
Gilbert M. Lenoir International Agency For Research On Cancer
Laurence Brugières
Laurence Brugières Institut Gustave Roussy
Steven A. Narod
Steven A. Narod University of Toronto
Henry T. Lynch
Henry T. Lynch Creighton University
Brigitte Bressac-de Paillerets
Brigitte Bressac-de Paillerets Institut Gustave Roussy
David M. Livingston
David M. Livingston Harvard University
Ralph Scully
Ralph Scully Beth Israel Deaconess Medical Center
Patricia N. Tonin
Patricia N. Tonin McGill University
Kenneth Morgan
Kenneth Morgan McGill University

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