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Charles Sultan

Affiliation : Université de Montpellier · Centre Hospitalier Universitaire de Montpellier · Hôpital Lapeyronie

• 8Publications (affiliation in France)
• 516Total publications
• 13186Citations
• 64h-index

OpenAlex

Research profile

Charles Sultan has 8 indexed publications (1990–2025). Their work appears mainly in “Fertility and Sterility”, “Annales d Endocrinologie” and “Environmental Sciences Europe”. Their most cited article, “Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2” (2009), has been cited 72 times. Their work is co-authored with at least 12 researchers, including institutions in Tunisia.

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Research areas

• Sexual Differentiation and Disorders
• Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
• Adrenal Hormones and Disorders
• Hypothalamic control of reproductive hormones
• Ovarian function and disorders

Publications (8)

• Scientists’ warning: we must change paradigm for a revolution in toxicology and world food supply
  2025 · Environmental Sciences Europe · cited 1 times
• NR5A1 (SF-1) gene variants in a group of 26 young women with XX primary ovarian insufficiency
  2012 · Fertility and Sterility · cited 39 times
• Mutational screening of SF1 and WNT4 in Tunisian women with premature ovarian failure
  2012 · Gene · cited 19 times
• Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2
  2009 · Journal of Medical Genetics · cited 72 times
• Complete androgen insensitivity syndrome is frequently due to premature stop codons in exon 1 of the androgen receptor gene: an international collaborative report of 13 new mutations
  2009 · Fertility and Sterility · cited 44 times
• Syndrome de résistance complète aux androgènes : nouvelle mutation chez une famille tunisienne
  2008 · Annales d Endocrinologie · cited 6 times
• P2-088 - Diagnostic génétique de syndrome de MC cune-albright sur matériel de cytoponction : implication sur la prise en charge
  2006 · Annales d Endocrinologie
• Defective, deleted or converted CYP21B gene and negative association with a rare restriction fragment length polymorphism allele of the factor B gene in congenital adrenal hyperplasia
  1990 · Human Genetics · cited 6 times

Publication venues

• Fertility and Sterility × 2
• Annales d Endocrinologie × 2
• Environmental Sciences Europe × 1
• Gene × 1
• Journal of Medical Genetics × 1
• Human Genetics × 1

Publications per year

• 20251
• 20122
• 20092
• 20081
• 20061
• 19901

Collaborations

Partner institutions : Centre National de la Recherche Scientifique · Inserm · Université Montpellier 1 · Institut Cochin · Université Paris Descartes

Co-authors’ countries : Tunisia

Co-authors

• Françoise Paris
• Françoise Audran
• Pascal Philibert
• Philippe Bouchard
• Jean-Michel Panoff
• Sophie Gil
• Giuseppe O. Longo
• Marc Fellous
• Gérard Lefranc
• Gilles‐Éric Séralini
• Michel Abbal
• Jean‐Marc A. Lobaccaro

Bibliographic data from OpenAlex (open database).