Stéphane Viville (S Viville, Stephane Viville)

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 23

Top Venues

Journal of assisted reproduction and genetics

Human reproduction (Oxford, England)

Human reproduction update

Nature communications

Université de Strasbourg (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

Université de Strasbourg

France

PHD

Publications

O Okutman, A S Gürbüz, U Büyük, E Real, R Leconte, K Chennen, C Mayer, J Muller, N Le May, Stéphane Viville
Pathogenic missense variation in PABPC1L/EPAB causes female infertility due to oocyte maturation arrest at the germinal vesicle stage. Journal of assisted reproduction and genetics 41 (2) (2024)
O Okutman, A S Gürbüz, U Büyük, E Real, R Leconte, K Chennen, C Mayer, J Muller, N Le May, Stéphane Viville
Pathogenic missense variation in PABPC1L/EPAB causes female infertility due to oocyte maturation arrest at the germinal vesicle stage. Journal of assisted reproduction and genetics 41 (2) (2024)
O Okutman, A S Gürbüz, U Büyük, E Real, R Leconte, K Chennen, C Mayer, J Muller, N Le May, Stéphane Viville
Pathogenic missense variation in PABPC1L/EPAB causes female infertility due to oocyte maturation arrest at the germinal vesicle stage. Journal of assisted reproduction and genetics 41 (2) (2024)
Antonio Capalbo, Guido de Wert, Heidi Mertes, Liraz Klausner, Edith Coonen, Francesca Spinella, Hilde Van de Velde, Stéphane Viville, Karen D Sermon, Nathalie Vermeulen, Todd Lencz, Shai Carmi
Screening embryos for polygenic disease risk: a review of epidemiological, clinical, and ethical considerations. Human reproduction update 30 (5) (2024)
Antonio Capalbo, Guido de Wert, Heidi Mertes, Liraz Klausner, Edith Coonen, Francesca Spinella, Hilde Van de Velde, Stéphane Viville, Karen D Sermon, Nathalie Vermeulen, Todd Lencz, Shai Carmi
Screening embryos for polygenic disease risk: a review of epidemiological, clinical, and ethical considerations. Human reproduction update (2024)
Birgit Stallmeyer, Clara Bühlmann, Rytis Stakaitis, Ann-Kristin Dicke, Farah Ghieh, Luisa Meier, Ansgar Zoch, David MacKenzie MacLeod, Johanna Steingröver, Özlem Okutman, Daniela Fietz, Adrian M E Pilatz, Antoni Riera-Escamilla, Miguel J Xavier, Christian Ruckert, Sara Di Persio, Nina Neuhaus, Ali Sami Gurbuz, Ahmet Şalvarci, Nicolas Le May, Kevin McEleny, Corinna Friedrich, Godfried W van der Heijden, Margot J Wyrwoll, Sabine Kliesch, Joris A Veltman, Csilla Krausz, Stéphane Viville, Donald F Conrad, Dònal O' Carroll, Frank Tüttelmann
Inherited defects of piRNA biogenesis cause transposon de-repression, impaired spermatogenesis, and human male infertility. Nature communications 15 (1) (2024)
O Okutman, A S Gürbüz, U Büyük, E Real, R Leconte, K Chennen, C Mayer, J Muller, N Le May, Stéphane Viville
Pathogenic missense variation in PABPC1L/EPAB causes female infertility due to oocyte maturation arrest at the germinal vesicle stage. Journal of assisted reproduction and genetics 41 (2) (2024)
Birgit Stallmeyer, Clara Bühlmann, Rytis Stakaitis, Ann-Kristin Dicke, Farah Ghieh, Luisa Meier, Ansgar Zoch, David MacKenzie MacLeod, Johanna Steingröver, Özlem Okutman, Daniela Fietz, Adrian M E Pilatz, Antoni Riera-Escamilla, Miguel J Xavier, Christian Ruckert, Sara Di Persio, Nina Neuhaus, Ali Sami Gurbuz, Ahmet Şalvarci, Nicolas Le May, Kevin McEleny, Corinna Friedrich, Godfried W van der Heijden, Margot J Wyrwoll, Sabine Kliesch, Joris A Veltman, Csilla Krausz, Stéphane Viville, Donald F Conrad, Dònal O' Carroll, Frank Tüttelmann
Inherited defects of piRNA biogenesis cause transposon de-repression, impaired spermatogenesis, and human male infertility. Nature communications 15 (1) (2024)
Birgit Stallmeyer, Clara Bühlmann, Rytis Stakaitis, Ann-Kristin Dicke, Farah Ghieh, Luisa Meier, Ansgar Zoch, David MacKenzie MacLeod, Johanna Steingröver, Özlem Okutman, Daniela Fietz, Adrian M E Pilatz, Antoni Riera-Escamilla, Miguel J Xavier, Christian Ruckert, Sara Di Persio, Nina Neuhaus, Ali Sami Gurbuz, Ahmet Şalvarci, Nicolas Le May, Kevin McEleny, Corinna Friedrich, Godfried W van der Heijden, Margot J Wyrwoll, Sabine Kliesch, Joris A Veltman, Csilla Krausz, Stéphane Viville, Donald F Conrad, Dònal O' Carroll, Frank Tüttelmann
Inherited defects of piRNA biogenesis cause transposon de-repression, impaired spermatogenesis, and human male infertility. Nature communications 15 (1) (2024)
Antonio Capalbo, Guido de Wert, Lidewij Henneman, Georgia Kakourou, Saria Mcheik, Borut Peterlin, Carla van El, Rita Vassena, Nathalie Vermeulen, Stéphane Viville, Francesca Forzano
An ESHG-ESHRE survey on the current practice of expanded carrier screening in medically assisted reproduction. Human reproduction (Oxford, England) (2024)
O Okutman, A S Gürbüz, U Büyük, E Real, R Leconte, K Chennen, C Mayer, J Muller, N Le May, Stéphane Viville
Pathogenic missense variation in PABPC1L/EPAB causes female infertility due to oocyte maturation arrest at the germinal vesicle stage. Journal of assisted reproduction and genetics (2024)
Antonio Capalbo, Guido de Wert, Lidewij Henneman, Georgia Kakourou, Saria Mcheik, Borut Peterlin, Carla van El, Rita Vassena, Nathalie Vermeulen, Stéphane Viville, Francesca Forzano
An ESHG-ESHRE survey on the current practice of expanded carrier screening in medically assisted reproduction. Human reproduction (Oxford, England) 39 (8) (2024)
Willem Verpoest, Özlem Okutman, Annelore Van Der Kelen, Karen D Sermon, Stéphane Viville
Genetics of infertility: a paradigm shift for medically assisted reproduction. Human reproduction (Oxford, England) (2023)
Annelore Van Der Kelen, Özlem Okutman, Elodie Javey, Münevver Serdarogullari, Charlotte Janssens, Manjusha S Ghosh, Bart J H Dequeker, Florence Perold, Claire Kastner, Emmanuelle Kieffer, Ingrid Segers, Alexander Gheldof, Frederik J Hes, Karen D Sermon, Willem Verpoest, Stéphane Viville
A systematic review and evidence assessment of monogenic gene-disease relationships in human female infertility and differences in sex development. Human reproduction update 29 (2) (2023)
Özlem Okutman, Manon Boivin, Jean Muller, Nicolas Charlet-Berguerand, Stéphane Viville
A biallelic loss of function variant in HORMAD1 within a large consanguineous Turkish family is associated with spermatogenic arrest. Human reproduction (Oxford, England) 38 (2) (2023)
Annelore Van Der Kelen, Özlem Okutman, Elodie Javey, Münevver Serdarogullari, Charlotte Janssens, Manjusha S Ghosh, Bart J H Dequeker, Florence Perold, Claire Kastner, Emmanuelle Kieffer, Ingrid Segers, Alexander Gheldof, Frederik J Hes, Karen D Sermon, Willem Verpoest, Stéphane Viville
A systematic review and evidence assessment of monogenic gene-disease relationships in human female infertility and differences in sex development. Human reproduction update 29 (2) (2023)
Özlem Okutman, Manon Boivin, Jean Muller, Nicolas Charlet-Berguerand, Stéphane Viville
A biallelic loss of function variant in HORMAD1 within a large consanguineous Turkish family is associated with spermatogenic arrest. Human reproduction (Oxford, England) 38 (2) (2023)
Annelore Van Der Kelen, Özlem Okutman, Elodie Javey, Münevver Serdarogullari, Charlotte Janssens, Manjusha S Ghosh, Bart J H Dequeker, Florence Perold, Claire Kastner, Emmanuelle Kieffer, Ingrid Segers, Alexander Gheldof, Frederik J Hes, Karen D Sermon, Willem Verpoest, Stéphane Viville
A systematic review and evidence assessment of monogenic gene-disease relationships in human female infertility and differences in sex development. Human reproduction update (2022)
Özlem Okutman, Manon Boivin, Jean Muller, Nicolas Charlet-Berguerand, Stéphane Viville
A biallelic loss of function variant in HORMAD1 within a large consanguineous Turkish family is associated with spermatogenic arrest. Human reproduction (Oxford, England) (2022)
Ozlem Okutman, Julien Tarabeux, Jean Muller, Stéphane Viville
Evaluation of a Custom Design Gene Panel as a Diagnostic Tool for Human Non-Syndromic Infertility. Genes 12 (3) (2021)
Brendan J Houston, Manon S Oud, Daniel M Aguirre, D Jo Merriner, Anne E O'Connor, Özlem Okutman, Stéphane Viville, Richard Burke, Joris A Veltman, Brendan J Houston
Programmed Cell Death 2-Like (Pdcd2l) Is Required for Mouse Embryonic Development. G3 (Bethesda, Md.) 10 (12) (2020)
Ozlem Okutman, Maroua Ben Rhouma, Moncef Benkhalifa, Jean Muller, Stéphane Viville
Genetic evaluation of patients with non-syndromic male infertility. Journal of assisted reproduction and genetics 35 (11) (2018)
Yara Tarabay, Mayada Achour, Marius Teletin, Tao Ye, Aurélie Teissandier, Manuel Mark, Déborah Bourc'his, Stéphane Viville
Tex19 paralogs are new members of the piRNA pathway controlling retrotransposon suppression. Journal of cell science 130 (8) (2017)

Stéphane Viville (S Viville, Stephane Viville)

Publication Activity (10 Years)

Top Topics

Top Venues