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Stéphane Viville

Observed names: Pr Stéphane Viville, S Viville, S. VIVILLE, S. Viville, STéphane Viville, Stephan Viville, Stephane Viville, Stéphane Viville, Stéphane VIVILLE, VIVILLE, STEPHANE, VIVILLE, Stéphane, Viville St, Viville, S, Viville, S., Viville, Stephane, Viville, Stéphane
Institutions: Centre National de la Recherche Scientifique, Inserm, Institut de génétique et de biologie moléculaire et cellulaire, Hôpitaux Universitaires de Strasbourg, Hôpital Civil, Strasbourg, Université de Strasbourg
Observed institutions: Centre National de la Recherche Scientifique, Université de Sherbrooke, Inserm, Collège de France, Cornell University, Charles University, University of Cambridge, Maastricht University, Institut de génétique et de biologie moléculaire et cellulaire, University Hospital in Motol, Département Physiologie Animale et Systèmes d’Élevage, Istanbul Memorial Hospital, Hôpitaux Universitaires de Strasbourg, Institut Pasteur d'Algérie, Institut de Biologie Moléculaire et Cellulaire, Hôpital Civil, Strasbourg, Weill Cornell Medicine, Laboratoire de Génétique Médicale, McGill University, University of Córdoba, Université de Strasbourg, Wellcome Trust, Université de Caen Normandie
ORCID: 0000-0002-5088-3003
Observed ORCID: 0000-0002-5088-3003
OpenAlex ID: A5044042417
Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest
1998 · Louis Lefebvre, Stéphane Viville, et al. · Nature Genetics · 572
Mice lacking the MHC class II-associated invariant chain
1993 · Stéphane Viville, Jacques Neefjes, et al. · Cell · 376
Homozygous Mutation in SPATA16 Is Associated with Male Infertility in Human Globozoospermia
2007 · Anika H.D.M. Dam, Isabelle Koscinski, et al. · The American Journal of Human Genetics · 318
Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization
1995 · Tomoko Kaneko-Ishino, Yoshimi Kuroiwa, et al. · Nature Genetics · 286
Red blood cell generation from human induced pluripotent stem cells: perspectives for transfusion medicine
2010 · H. Lapillonne, L. Kobari, et al. · Haematologica · 265
Translation of Expanded CGG Repeats into FMRpolyG Is Pathogenic and May Contribute to Fragile X Tremor Ataxia Syndrome
2017 · Chantal Sellier, Ronald A.M. Buijsen, et al. · Neuron · 247
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DPY19L2 Deletion as a Major Cause of Globozoospermia
2011 · Isabelle Koscinski, Elias ElInati, et al. · The American Journal of Human Genetics · 224
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A Recurrent Deletion of DPY19L2 Causes Infertility in Man by Blocking Sperm Head Elongation and Acrosome Formation
2011 · Radu Harbuz, Raoudha Zouari, et al. · The American Journal of Human Genetics · 217
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TRIM28 repression of retrotransposon-based enhancers is necessary to preserve transcriptional dynamics in embryonic stem cells
2012 · Helen M. Rowe, Adamandia Kapopoulou, et al. · Genome Research · 191
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Assisted reproduction treatment and epigenetic inheritance
2012 · A.P.A. van Montfoort, L.L.P. Hanssen, et al. · Human Reproduction Update · 177
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Neurons and cardiomyocytes derived from induced pluripotent stem cells as a model for mitochondrial defects in Friedreich's ataxia
2012 · Aurore Hick, Marie Wattenhofer-Donzé, et al. · Disease Models & Mechanisms · 168
Adjuncts in the IVF laboratory: where is the evidence for ‘add-on’ interventions?
2017 · Joyce Harper, Emily Jackson, et al. · Human Reproduction · 160
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Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish family
2015 · Ozlem Okutman, Jean Muller, et al. · Human Molecular Genetics · 143
RNA Polymerase II Transcription in Murine Cells Lacking the TATA Binding Protein
2002 · Igor Martianov, Stephane Viville, et al. · Science · 140
Do morphological anomalies reflect chromosomal aneuploidies?*: Case Report
2000 · Stéphane Viville, Richard Mollard, et al. · Human Reproduction · 132
Tissue-specific expression of retinoic acid receptor isoform transcripts in the mouse embryo
2000 · Richard Mollard, Stéphane Viville, et al. · Mechanisms of Development · 130
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The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African population
2009 · K. Dieterich, R. Zouari, et al. · Human Molecular Genetics · 127
ESHRE Preimplantation Genetic Diagnosis (PGD) Consortium: data collection II (May 2000)
2000 · J Geraedts, A Handyside, et al. · Human Reproduction · 124
Globozoospermia is mainly due to DPY19L2 deletion via non-allelic homologous recombination involving two recombination hotspots
2012 · Elias ElInati, Paul Kuentz, et al. · Human Molecular Genetics · 120
Diversity of Endogenous Epitopes Bound to MHC Class II Molecules Limited by Invariant Chain
1994 · Helen Bodmer, Stéphane Viville, et al. · Science · 119
Fluorescence in situ hybridization sperm analysis of six translocation carriers provides evidence of an interchromosomal effect
2005 · Nadejda Machev, Philippe Gosset, et al. · Fertility and Sterility · 117
ESHRE PGD Consortium data collection VI: cycles from January to December 2003 with pregnancy follow-up to October 2004
2006 · K.D. Sermon, A. Michiels, et al. · Human Reproduction · 110
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Recent developments in genetics and medically assisted reproduction: from research to clinical applications
2017 · on behalf of the European Society of Human Reproduction and Embryology and European Society of Human Genetics, J. C. Harper, et al. · European Journal of Human Genetics · 108
A dual role of linker histone H1.4 Lys 34 acetylation in transcriptional activation
2012 · Kinga Kamieniarz, Annalisa Izzo, et al. · Genes & Development · 99
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ESHRE PGD Consortium data collection IV: May–December 2001
2004 · K. Sermon, C. Moutou, et al. · Human Reproduction · 98
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Works count: 206
Citation count: 8,025
H-index: 49
I10-index: 103
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