Stéphane Viville

7.7k total citations
119 papers, 5.0k citations indexed

About

Stéphane Viville is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Stéphane Viville has authored 119 papers receiving a total of 5.0k indexed citations (citations by other indexed papers that have themselves been cited), including 62 papers in Molecular Biology, 37 papers in Pediatrics, Perinatology and Child Health and 37 papers in Genetics. Recurrent topics in Stéphane Viville's work include Prenatal Screening and Diagnostics (32 papers), Sperm and Testicular Function (25 papers) and Reproductive Biology and Fertility (22 papers). Stéphane Viville is often cited by papers focused on Prenatal Screening and Diagnostics (32 papers), Sperm and Testicular Function (25 papers) and Reproductive Biology and Fertility (22 papers). Stéphane Viville collaborates with scholars based in France, United Kingdom and Netherlands. Stéphane Viville's co-authors include M. Azim Surani, Fumitoshi Ishino, Sheila C. Barton, Céline Moutou, Diane Mathis, Christophe Benoıst, Louis Lefebvre, E.B. Keverne, Karen Sermon and Philippe Tropel and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Stéphane Viville

116 papers receiving 4.9k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Stéphane Viville France 40 2.6k 1.8k 1.5k 1.2k 1.0k 119 5.0k
I. Liebærs Belgium 35 1.5k 0.6× 1.2k 0.7× 1.7k 1.2× 1.3k 1.1× 1.0k 1.0× 81 3.9k
Joep Geraedts Netherlands 42 1.6k 0.6× 1.5k 0.8× 2.5k 1.7× 1.2k 1.0× 1.4k 1.4× 138 5.4k
Karen Sermon Belgium 49 2.8k 1.1× 1.8k 1.0× 3.3k 2.3× 855 0.7× 1.2k 1.2× 164 6.6k
H. Van de Velde Belgium 44 2.2k 0.9× 657 0.4× 1.6k 1.1× 1.5k 1.3× 2.2k 2.2× 129 5.2k
Minoo Rassoulzadegan France 37 3.8k 1.5× 1.8k 1.0× 588 0.4× 683 0.6× 791 0.8× 113 5.8k
Myriam Hemberger United Kingdom 46 5.3k 2.1× 1.6k 0.9× 2.8k 1.9× 723 0.6× 1.1k 1.0× 110 9.1k
Satoshi Tanaka Japan 42 5.8k 2.2× 1.9k 1.1× 945 0.6× 319 0.3× 1.1k 1.1× 138 8.2k
Urvashi Surti United States 46 2.8k 1.1× 2.8k 1.6× 2.5k 1.7× 771 0.7× 2.1k 2.0× 188 7.8k
Antonino Forabosco Italy 34 2.5k 1.0× 2.1k 1.2× 759 0.5× 908 0.8× 1.3k 1.3× 119 4.5k
Anna Veiga Spain 40 2.1k 0.8× 677 0.4× 1.8k 1.2× 2.0k 1.7× 2.3k 2.3× 156 5.1k

Countries citing papers authored by Stéphane Viville

Since Specialization
Citations

This map shows the geographic impact of Stéphane Viville's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Stéphane Viville with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stéphane Viville more than expected).

Fields of papers citing papers by Stéphane Viville

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stéphane Viville. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Stéphane Viville. The network helps show where Stéphane Viville may publish in the future.

Co-authorship network of co-authors of Stéphane Viville

This figure shows the co-authorship network connecting the top 25 collaborators of Stéphane Viville. A scholar is included among the top collaborators of Stéphane Viville based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Stéphane Viville. Stéphane Viville is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Capalbo, Antonio, G. de Wert, Heidi Mertes, et al.. (2024). Screening embryos for polygenic disease risk: a review of epidemiological, clinical, and ethical considerations. Human Reproduction Update. 30(5). 529–557. 18 indexed citations
2.
Capalbo, Antonio, G. de Wert, Lidewij Henneman, et al.. (2024). An ESHG–ESHRE survey on the current practice of expanded carrier screening in medically assisted reproduction. Human Reproduction. 39(8). 1844–1855. 2 indexed citations
3.
Verpoest, Willem, et al.. (2023). Genetics of infertility: a paradigm shift for medically assisted reproduction. Human Reproduction. 38(12). 2289–2295. 3 indexed citations
4.
Mitchell, Valérie, Anne Loyens, Nathalie Rives, et al.. (2023). Results and perinatal outcomes from 189 ICSI cycles of couples with asthenozoospermic men and flagellar defects assessed by transmission electron microscopy. Reproductive BioMedicine Online. 47(5). 103328–103328. 4 indexed citations
5.
Okutman, Özlem, Münevver Serdarogullari, Ingrid Segers, et al.. (2022). 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). 218–232. 18 indexed citations
6.
Okutman, Özlem, et al.. (2022). A biallelic loss of function variant in HORMAD1 within a large consanguineous Turkish family is associated with spermatogenic arrest. Human Reproduction. 38(2). 306–314. 5 indexed citations
7.
Okutman, Özlem, Julien Tarabeux, Jean Muller, & Stéphane Viville. (2021). Evaluation of a Custom Design Gene Panel as a Diagnostic Tool for Human Non-Syndromic Infertility. Genes. 12(3). 410–410. 7 indexed citations
8.
Okutman, Özlem, et al.. (2020). Homozygous Splice Site Mutation in ZP1 Causes Familial Oocyte Maturation Defect. Genes. 11(4). 382–382. 16 indexed citations
9.
Okutman, Özlem, Jean Muller, Moncef Benkhalifa, et al.. (2018). Aspect génétique de l’infertilité masculine : de la recherche à la clinique. Gynécologie Obstétrique Fertilité & Sénologie . 47(1). 54–62. 4 indexed citations
10.
Zambelli, Filippo, Alexander Keller, Philippe Tropel, et al.. (2018). Random Mutagenesis, Clonal Events, and Embryonic or Somatic Origin Determine the mtDNA Variant Type and Load in Human Pluripotent Stem Cells. Stem Cell Reports. 11(1). 102–114. 23 indexed citations
11.
Tropel, Philippe, et al.. (2017). CpG Island Methylation Correlates with the Use of Alternative Promoters for USP44 Gene Expression in Human Pluripotent Stem Cells and Testes. Stem Cells and Development. 26(15). 1100–1110. 8 indexed citations
12.
Oud, Manon S., Liliana Ramos, Moira K. O’Bryan, et al.. (2017). Validation and application of a novel integrated genetic screening method to a cohort of 1,112 men with idiopathic azoospermia or severe oligozoospermia. Human Mutation. 38(11). 1592–1605. 44 indexed citations
13.
Achour, Mayada, Marius Teletin, Tao Ye, et al.. (2017). Tex19 paralogs are new members of the piRNA pathway controlling retrotransposon suppression. Journal of Cell Science. 130(8). 1463–1474. 9 indexed citations
14.
Tropel, Philippe, Julien Côme, Céline Moutou, et al.. (2010). High-efficiency derivation of human embryonic stem cell lines following pre-implantation genetic diagnosis. In Vitro Cellular & Developmental Biology - Animal. 46(3-4). 376–385. 29 indexed citations
15.
Wittemer, Christiane, et al.. (2006). Le don d’embryon : que nous apprennent les entretiens avec les couples donneurs ?. 8(6). 385–387. 1 indexed citations
16.
Moutou, Céline, et al.. (2006). Strategies and outcomes of PGD of familial adenomatous polyposis. Molecular Human Reproduction. 13(2). 95–101. 22 indexed citations
17.
Moutou, Céline & Stéphane Viville. (2003). [Preimplantation genetic diagnosis of monogenic diseases]. SPIRE - Sciences Po Institutional REpository. 1 indexed citations
18.
Sermon, Karen, Joyce Harper, Joep Geraedts, et al.. (2002). ESHRE preimplantation genetic diagnosis consortium: Data collection III (May 2001). Human Reproduction. 17(1). 233–246. 172 indexed citations
19.
Geraedts, Joep, Alan H. Handyside, Joyce Harper, et al.. (1999). ESHRE Preimplantation Genetic Diagnosis (PGD) Consortium: preliminary assessment of data from January 1997 to September 1998. Human Reproduction. 14(12). 3138–3148. 80 indexed citations
20.
Battegay, Manuel, Martin F. Bachmann, Stéphane Viville, et al.. (1996). Antiviral Immune Responses of Mice Lacking MHC Class II or Its Associated Invariant Chain. Cellular Immunology. 167(1). 115–121. 46 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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