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Genetics
France
2024

D-Index & Metrics

Genetics

D-Index
66
Citations
13713
World Ranking
2635
National Ranking
123

Research.com Recognitions

  • 2024 - Research.com Genetics in France Leader Award

Overview

Josué Feingold was affiliated with Grenoble Alpes University in France. Their research primarily focused on Medicine, with specific contributions to subfields such as Pediatrics, Perinatology and Child Health, and Reproductive Medicine.

The scientist's main topics of study included:

  • Reproductive Health and Technologies
  • Ethics and Legal Issues in Pediatric Healthcare
  • Assisted Reproductive Technology and Twin Pregnancy

Feingold authored research work published in recognized venues, notably in the journal Fertility and Sterility. The known publication includes:

  • IMPROVING FROZEN EMBRYO TRANSFER CONSENT TIMELY RETURN RATE TO REDUCE ADVERSE EVENTS AND IMPROVE PATIENT AND PROVIDER SATISFACTION, 2024, Fertility and Sterility

The scientist collaborated with several frequent co-authors, including:

  • Erin L. Scott
  • Wendy Vitek
  • Kelly Ward
  • A.C. Collins

Best Publications

  • Interleukin-36–Receptor Antagonist Deficiency and Generalized Pustular Psoriasis

    Slaheddine Marrakchi;Philippe Guigue;Blair R. Renshaw;Anne Puel

  • Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study.

    Anne Philippe;Anne Philippe;Maria Martinez;Michel Guilloud-Bataille;Christopher Gillberg

  • The γ e4 allele of the apolipoprotein E gene as a potential protective factor for exudative age-related macular degeneration

    Eric H. Souied;Pascale Benlian;Philippe Amouyel;Josue Feingold

  • Genetic localization of a locus controlling the intensity of infection by Schistosoma mansoni on chromosome 5q31-q33

    Sandrine Marquet;Laurent Abel;Dominique Hillaire;Hélia Dessein

  • Early energy deficit in Huntington disease: identification of a plasma biomarker traceable during disease progression.

    Fanny Mochel;Perrine Charles;François Seguin;Julie Barritault

  • Association Between the Tryptophan Hydroxylase Gene and Manic-depressive Illness

    Frank Bellivier;Marion Leboyer;Philippe Courtet;Catherine Buresi

  • Genome Screen for Asthma and Related Phenotypes in the French EGEA Study

    Marie-Hélène Dizier;Céline Besse-Schmittler;Michel Guilloud-Bataille;Isabella Annesi-Maesano

  • Estimating prevalence in single-gene kidney diseases progressing to renal failure.

    Micheline Levy;Josué Feingold

  • Genetic heterogeneity of Alport syndrome.

    Josué Feingold;Etienne Bois;Agnès Chompert;Michel Broyer

  • Whole blood serotonin and plasma beta-endorphin in autistic probands and their first-degree relatives.

    Marion Leboyer;Anne Philippe;Manuel Bouvard;Michel Guilloud-Bataille

  • A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage.

    Beckmann Js;Richard I;Hillaire D;Broux O

  • Juvenile limb-girdle muscular dystrophy. Clinical, histopathological and genetic data from a small community living in the Reunion Island.

    M. Fardeau;D. Hillaire;C. Mignard;N. Feingold

  • Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11.

    C Hengstenberg;J S Beckmann;P Guicheney

  • Epidemiological study of the genetics and environment of asthma, bronchial hyperresponsiveness, and atopy: phenotype issues.

    Francine Kauffmann;Marie-Hélène Dizier;Isabelle Pin;Evelyne Paty

  • Intellectual status of working-class children adopted early into upper-middle-class families

    Michel Schiff;Michel Duyme;Annick Dumaret;John Stewart

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

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

  • Agenesis of corpus callosum: prenatal diagnosis and prognosis

    Marie-Laure Moutard;Virginie Kieffer;Josué Feingold;François Kieffer

  • Clinical homogeneity and genetic heterogeneity in Weill-Marchesani syndrome.

    Laurence Faivre;Hélène Dollfus;Stanislas Lyonnet;Yves Alembik

  • Meta-analysis of DRD3 gene and schizophrenia: ethnic heterogeneity and significant association in Caucasians.

    Caroline Dubertret;Philip Gorwood;Jean Ades;Josue Feingold

  • Trinucleotide repeat contraction: a pitfall in prenatal diagnosis of myotonic dystrophy

    Jeanne Amiel;Valérie Raclin;Jean-Marie Jouannic;Nicole Morichon

Frequent Co-Authors

Marion Leboyer
Marion Leboyer Paris-Est Créteil University
Alexandra Durr
Alexandra Durr Sorbonne University
Arnold Munnich
Arnold Munnich Necker-Enfants Malades Hospital
Alexis Brice
Alexis Brice Institut du Cerveau
Florence Demenais
Florence Demenais Université Paris Cité
Stanislas Lyonnet
Stanislas Lyonnet Université Paris Cité
Francine Kauffmann
Francine Kauffmann University of Paris-Saclay
Philip Gorwood
Philip Gorwood Université Paris Cité
Yves Agid
Yves Agid Institut du Cerveau

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