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Catherine Dodé

Catherine Dodé

D-Index & Metrics

Biology and Biochemistry

D-Index
55
Citations
12594
World Ranking
14930
National Ranking
586

Overview

Catherine Dodé is a researcher affiliated with Inserm in France. Their work focuses primarily on the fields of medicine, particularly reproductive medicine and genetics. The research covers topics related to ovarian cancer diagnosis and treatment, genetic and clinical aspects of sex determination and chromosomal abnormalities, and ovarian function and disorders.

The scientist has contributed to recent publications including:

  • Next Generation Sequencing Should Be Proposed to Every Woman With "Idiopathic" Primary Ovarian Insufficiency, 2021, Journal of the Endocrine Society
  • NEXT GENERATION SEQUENCING SHOULD BE PROPOSED TO EVERY WOMAN WITH "IDIOPATHIC" PREMATURE OVARIAN INSUFFICIENCY, 2021, HAL (Le Centre pour la Communication Scientifique Directe)

Frequent co-authors collaborating with Catherine Dodé include:

  • Sarah Eskenazi
  • Anne Bachelot
  • Justine Hugon-Rodin
  • Anne Gompel
  • Sophie Catteau-Jonard

Their research is also published in venues such as the Journal of the Endocrine Society and HAL (Le Centre pour la Communication Scientifique Directe).

Best Publications

  • Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.

    Catherine Dodé;Jacqueline Levilliers;Jean-Michel Dupont;Anne De Paepe

  • Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism—pathogenesis, diagnosis and treatment

    Ulrich Boehm;Pierre Marc Bouloux;Mehul T. Dattani;Nicolas De Roux

  • Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene

    Françoise Denoyelle;Dominique Weil;Marion A. Maw;Stephen A. Wilcox

  • Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats.

    Rubinsztein Dc;Leggo J;Coles R;Almqvist E

  • Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2.

    Catherine Dodé;Luis Teixeira;Jacqueline Levilliers;Corinne Fouveaut

  • Infevers: an evolving mutation database for auto-inflammatory syndromes.

    Isabelle Touitou;Suzanne Lesage;Michael McDermott;Laurence Cuisset

  • Impaired FGF signaling contributes to cleft lip and palate

    Bridget M. Riley;M. Adela Mansilla;Jinghong Ma;Sandra Daack-Hirsch

  • New Mutations of CIAS1 That Are Responsible for Muckle-Wells Syndrome and Familial Cold Urticaria: A Novel Mutation Underlies Both Syndromes

    Catherine Dodé;Nathalie Le Dû;Laurence Cuisset;Frank Letourneur

  • MEFV-Gene Analysis in Armenian Patients with Familial Mediterranean Fever: Diagnostic Value and Unfavorable Renal Prognosis of the M694V Homozygous Genotype—Genetic and Therapeutic Implications

    Cécile Cazeneuve;Tamara Sarkisian;Christophe Pêcheux;Michel Dervichian

  • Non-Founder Mutations in the MEFV Gene Establish This Gene as the Cause of Familial Mediterranean Fever (FMF)

    Alain Bernot;Corinne da Silva;Jean-Louis Petit;Corinne Cruaud

  • The enlarging clinical, genetic, and population spectrum of tumor necrosis factor receptor-associated periodic syndrome.

    Catherine Dodé;Marc André;Thierry Bienvenu;Pierre Hausfater

  • Rapid analysis of ‐α3.7 thalassaemia and αααanti 3.7 triplication by enzymatic amplification analysis

    Catherine Dodé;Rajagopal Krishnamoorthy;Janette Lamb;Jacques Rochette

  • SEMA3A, a Gene Involved in Axonal Pathfinding, Is Mutated in Patients with Kallmann Syndrome

    Naresh Kumar Hanchate;Paolo Giacobini;Paolo Giacobini;Paolo Giacobini;Pierre Lhuillier;Jyoti Parkash;Jyoti Parkash;Jyoti Parkash

  • Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease

    L. Djoussé;B. Knowlton;M. Hayden;E. W. Almqvist

  • The complex genetics of Kallmann syndrome: KAL1, FGFR1, FGF8, PROKR2, PROK2, et al.

    Jean-Pierre Hardelin;Catherine Dodé

  • Huntington’s disease‐like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes

    Giovanni Stevanin;Hiroto Fujigasaki;Anne-Sophie Lebre;Agnes Camuzat

  • Loss-of-Function Mutations in SOX10 Cause Kallmann Syndrome with Deafness

    Veronique Pingault;Veronique Pingault;Virginie Bodereau;Viviane Baral;Viviane Baral;Severine Marcos

  • A Genome Scan for Modifiers of Age at Onset in Huntington Disease: The HD MAPS Study

    Jian Liang Li;Michael R. Hayden;Elisabeth W. Almqvist;Ryan R. Brinkman

  • Clinical significance of P46L and R92Q substitutions in the tumour necrosis factor superfamily 1A gene

    Nathalie Ravet;Saad Rouaghe;Catherine Dode;Jacques Bienvenu

  • Are cognitive changes the first symptoms of Huntington's disease? A study of gene carriers.

    V Hahn-Barma;B Deweer;A Dürr;C Dodé

Frequent Co-Authors

Jacques Young
Jacques Young University of Paris-Saclay
Alexandra Durr
Alexandra Durr Sorbonne University
Alexis Brice
Alexis Brice Institut du Cerveau
James F. Gusella
James F. Gusella Harvard University
Josué Feingold
Josué Feingold Grenoble Alpes University
Rajagopal Krishnamoorthy
Rajagopal Krishnamoorthy Inserm : Institut national de la santé et de la recherche médicale
Jacques Elion
Jacques Elion Université Paris Cité
Michael R. Hayden
Michael R. Hayden University of British Columbia
Marcy E. MacDonald
Marcy E. MacDonald Harvard University

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