Author

Stéphane Viville

Centre National de la Recherche ScientifiqueORCID 0000-0002-5088-3003Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Organism:human· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

Ahmet ŞalvarcıiD· 1 shared Birgit StallmeyeriD· 1 shared David MacKenzie MacLeod· 1 shared Dónal O’CarrolliD· 1 shared Frank TüttelmanniD· 1 shared Margot Julia WyrwolliD· 1 shared Özlem OkutmaniD· 1 shared Sabine KlieschiD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 28 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Ahmet ŞalvarcıORCID

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1 paper

Recent·Most cited

HSP90AA1 variants may contribute to autosomal dominant human male infertility

Margot Julia Wyrwoll, David MacKenzie MacLeod, Ahmet Şalvarcı, Sabine Kliesch, Özlem Okutman, Stéphane Viville, Birgit Stallmeyer, Frank Tüttelmann, Dónal O’Carroll

This study investigates whether HSP90AA1 variants cause autosomal dominant male infertility in humans and finds that while some variants are associated with infertility, their pathogenicity remains uncertain.

medRxiv · Feb 22, 2026 · PreprintGenetic & Genomic Medicine