Publications by authors named "Stephane Viville"

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ESHRE's key research priorities in infertility: maximizing impact on science, people and society†.
Johanna Tassot, Aisling Ahlstrom, Antonio Capalbo, Ying Cheong, Giovanni Coticchio, Stephane Viville

Hum Reprod· October 2025

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Correction: Evaluation of an Updated Gene Panel as a Diagnostic Tool for Both Male and Female Infertility.
Özlem Okutman, Ali Sami Gürbüz, Ahmet Salvarci, Umut Büyük, Halil Ruso, Stephane Viville

Reprod Sci· July 2025

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PGT-A: what's it for, what's wrong?
Stéphane Viville, Mohamed Aboulghar

J Assist Reprod Genet· January 2025

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Screening embryos for polygenic disease risk: a review of epidemiological, clinical, and ethical considerations.
Antonio Capalbo, Guido de Wert, Heidi Mertes, Liraz Klausner, Edith Coonen, Stephane Viville

Hum Reprod Update· October 2024

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Evaluation of an Updated Gene Panel as a Diagnostic Tool for Both Male and Female Infertility.
Özlem Okutman, Ali Sami Gürbüz, Ahmet Salvarci, Umut Büyük, Halil Ruso, Stephane Viville

Reprod Sci· August 2024

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An ESHG-ESHRE survey on the current practice of expanded carrier screening in medically assisted reproduction.
Antonio Capalbo, Guido de Wert, Lidewij Henneman, Georgia Kakourou, Saria Mcheik, Stéphane Viville

Hum Reprod· August 2024

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Inherited defects of piRNA biogenesis cause transposon de-repression, impaired spermatogenesis, and human male infertility.
Birgit Stallmeyer, Clara Bühlmann, Rytis Stakaitis, Ann-Kristin Dicke, Farah Ghieh, Stéphane Viville

Nat Commun· August 2024

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Genetics of infertility: a paradigm shift for medically assisted reproduction.
Willem Verpoest, Özlem Okutman, Annelore Van Der Kelen, Karen Sermon, Stéphane Viville

Hum Reprod· December 2023

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Results and perinatal outcomes from 189 ICSI cycles of couples with asthenozoospermic men and flagellar defects assessed by transmission electron microscopy.
Angèle Boursier, Augustin Boudry, Valérie Mitchell, Anne Loyens, Nathalie Rives, Stéphane Viville

Reprod Biomed Online· November 2023

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A systematic review and evidence assessment of monogenic gene-disease relationships in human female infertility and differences in sex development.
Annelore Van Der Kelen, Özlem Okutman, Elodie Javey, Münevver Serdarogullari, Charlotte Janssens, Stéphane Viville

Hum Reprod Update· March 2023

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A biallelic loss of function variant in HORMAD1 within a large consanguineous Turkish family is associated with spermatogenic arrest.
Ozlem Okutman, Manon Boivin, Jean Muller, Nicolas Charlet-Berguerand, Stéphane Viville

Hum Reprod· February 2023

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Evaluation of a Custom Design Gene Panel as a Diagnostic Tool for Human Non-Syndromic Infertility.
Ozlem Okutman, Julien Tarabeux, Jean Muller, Stéphane Viville

Genes (Basel)· March 2021

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Programmed Cell Death 2-Like () Is Required for Mouse Embryonic Development.
Brendan J Houston, Manon S Oud, Daniel M Aguirre, D Jo Merriner, Anne E O'Connor, Stéphane Viville

G3 (Bethesda)· December 2020

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Toxoplasma gondii ROP16 kinase silences the cyclin B1 gene promoter by hijacking host cell UHRF1-dependent epigenetic pathways.
Marcela Sabou, Cécile Doderer-Lang, Caroline Leyer, Ana Konjic, Sophie Kubina, Stéphane Viville

Cell Mol Life Sci· June 2020

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Homozygous Splice Site Mutation in Causes Familial Oocyte Maturation Defect.
Özlem Okutman, Cem Demirel, Firat Tülek, Veronique Pfister, Umut Büyük, Stéphane Viville

Genes (Basel)· April 2020

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Comparison of sperm morphology and nuclear sperm quality in SPATA16- and DPY19L2-mutated globozoospermic patients.
Houda Ghédir, Asma Braham, Stéphane Viville, Ali Saad, Samira Ibala-Romdhane

Andrologia· July 2019

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Genetic evaluation of patients with non-syndromic male infertility.
Ozlem Okutman, Maroua Ben Rhouma, Moncef Benkhalifa, Jean Muller, Stéphane Viville

J Assist Reprod Genet· November 2018

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Random Mutagenesis, Clonal Events, and Embryonic or Somatic Origin Determine the mtDNA Variant Type and Load in Human Pluripotent Stem Cells.
Filippo Zambelli, Joke Mertens, Dominika Dziedzicka, Johan Sterckx, Christina Markouli, Stephane Viville

Stem Cell Reports· July 2018

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Validation and application of a novel integrated genetic screening method to a cohort of 1,112 men with idiopathic azoospermia or severe oligozoospermia.
Manon S Oud, Liliana Ramos, Moira K O'Bryan, Robert I McLachlan, Özlem Okutman, Stephane Viville

Hum Mutat· November 2017

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CpG Island Methylation Correlates with the Use of Alternative Promoters for USP44 Gene Expression in Human Pluripotent Stem Cells and Testes.
Philippe Tropel, Laura Jung, Cécile André, Adeline Ndandougou, Stéphane Viville

Stem Cells Dev· August 2017

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A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family.
Ozlem Okutman, Jean Muller, Valerie Skory, Jean Marie Garnier, Angeline Gaucherot, STéphane Viville

J Assist Reprod Genet· May 2017

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paralogs are new members of the piRNA pathway controlling retrotransposon suppression.
Yara Tarabay, Mayada Achour, Marius Teletin, Tao Ye, Aurélie Teissandier, Stéphane Viville

J Cell Sci· April 2017

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Adjuncts in the IVF laboratory: where is the evidence for 'add-on' interventions?
Joyce Harper, Emily Jackson, Karen Sermon, Robert John Aitken, Stephen Harbottle, Stephane Viville

Hum Reprod· March 2017

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Translation of Expanded CGG Repeats into FMRpolyG Is Pathogenic and May Contribute to Fragile X Tremor Ataxia Syndrome.
Chantal Sellier, Ronald A M Buijsen, Fang He, Sam Natla, Laura Jung, Stéphane Viville

Neuron· January 2017

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A new mutation identified in SPATA16 in two globozoospermic patients.
Elias ElInati, Camille Fossard, Ozlem Okutman, Houda Ghédir, Samira Ibala-Romdhane, Stéphane Viville

J Assist Reprod Genet· June 2016

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