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Stéphane Viville

Affiliation : Centre National de la Recherche Scientifique · Inserm · Institut de génétique et de biologie moléculaire et cellulaire · Hôpitaux Universitaires de Strasbourg · Université de Strasbourg

• 8Publications (affiliation in France)
• 222Total publications
• 7679Citations
• 49h-index

ORCIDOpenAlex

Research profile

Stéphane Viville has 8 indexed publications (2009–2026). Their work appears mainly in “Journal of Assisted Reproduction and Genetics”, “Andrologia” and “Gynécologie Obstétrique Fertilité & Sénologie”. Their most cited article, “The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African population” (2009), has been cited 112 times. Their work is co-authored with at least 12 researchers, including institutions in Canada, Tunisia, United Kingdom, Algeria.

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Research areas

• Reproductive Health and Technologies
• Prenatal Screening and Diagnostics
• Sperm and Testicular Function
• Reproductive Biology and Fertility
• Assisted Reproductive Technology and Twin Pregnancy

Publications (8)

• A recurrent North African ZP1 variant and a literature review of genotype–phenotype correlations in ZP-related infertility
  2026 · Journal of Assisted Reproduction and Genetics
• Comparison of sperm morphology and nuclear sperm quality in SPATA16‐ and DPY19L2‐ mutated globozoospermic patients
  2019 · Andrologia · cited 21 times
• Aspect génétique de l’infertilité masculine : de la recherche à la clinique
  2018 · Gynécologie Obstétrique Fertilité & Sénologie  · cited 6 times
• A new mutation identified in SPATA16 in two globozoospermic patients
  2016 · Journal of Assisted Reproduction and Genetics · cited 51 times
• Identification of a newDPY19L2mutation and a better definition ofDPY19L2deletion breakpoints leading to globozoospermia
  2015 · Molecular Human Reproduction · cited 42 times
• Identification of a new recurrent Aurora kinase C mutation in both European and African men with macrozoospermia
  2012 · Human Reproduction · cited 58 times
• The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African population
  2009 · Human Molecular Genetics · cited 112 times
• Genetic diagnosis of embryos: Clear explanation, not rhetoric, is needed
  2009 · Canadian Medical Association Journal · cited 17 times

Publication venues

• Journal of Assisted Reproduction and Genetics × 2
• Andrologia × 1
• Gynécologie Obstétrique Fertilité & Sénologie × 1
• Molecular Human Reproduction × 1
• Human Reproduction × 1
• Human Molecular Genetics × 1

Publications per year

• 20261
• 20191
• 20181
• 20161
• 20151
• 20121
• 20092

Collaborations

Partner institutions : Centre Hospitalier Universitaire de Grenoble · Université Joseph Fourier · Andrology Gerontechnology Inflammation Modelisation · Assistance Publique – Hôpitaux de Paris · Translational Innovation in Medicine and Complexity

Co-authors’ countries : Canada · Tunisia · United Kingdom · Algeria

Co-authors

• Özlem Okutman
• Sylviane Hennebicq
• Pierre F. Ray
• Joël Lunardi
• Isabelle Koscinski
• Pierre‐Simon Jouk
• François Vialard
• Radu Harbuz
• Cécile Lang
• Laura Feyereisen
• Agnès Guichet
• Géraldine Viot

Bibliographic data from OpenAlex (open database).