Éric Vilain
Impact in
- Reproductive Medicine top 0.5%
- Sperm and Testicular Function
- Reproductive Health and Technologies
- Genetics top 0.5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
-
- Sexual Differentiation and Disorders 60
- Epigenetics and DNA Methylation 7
- Genetics 69
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 56
- Genomic variations and chromosomal abnormalities 5
- Genomics and Rare Diseases 5
- Co-authors
- Francisco J. Sánchez (5 shared papers)Steve Horvath (2 shared papers)David E. Sandberg (11 shared papers)Janet S. Sinsheimer (3 shared papers)Sven Bocklandt (2 shared papers)Mary E. Sehl (1 shared paper)Wen Lin (1 shared paper)Ken McElreavey (10 shared papers)
- Journals
- Molecular Genetics and Metabolism (8 papers)Proceedings of the National Academy of Sciences (5 papers)The Journal of Clinical Endocrinology & Metabolism (5 papers)American Journal of Medical Genetics Part C Seminars in Medical Genetics (3 papers)Clinical Genetics (3 papers)
- Partner nations
- United StatesFranceAustralia
In The Last Decade
Éric Vilain
112 papers receiving 6.0k citations
Éric Vilain's Hit Papers
Peers
Comparison fields: 5 of 147
- Reproductive Medicine 969
- Genetics 2.8k
- Urology 566
- Molecular Biology 3.9k
- Aging 94
Countries citing papers authored by Éric Vilain
This map shows the geographic impact of Éric Vilain'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 Éric Vilain with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Éric Vilain more than expected).
Fields of papers citing papers by Éric Vilain
This network shows the impact of papers produced by Éric Vilain. 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 Éric Vilain. The network helps show where Éric Vilain may publish in the future.
Co-authors
The 25 scholars most cited alongside Éric Vilain, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 116 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Global Disorders of Sex Development Update since 2006: Perceptions, Approach and Care Hit paper breakdown → | 2016 | 759 |
| 2 | Epigenetic Predictor of Age Hit paper breakdown → | 2011 | 696 |
| 3 | Sexual Orientation, Controversy, and Science Hit paper breakdown → | 2016 | 326 |
| 4 | 1993 | 280 | |
| 5 | 2003 | 259 | |
| 6 | 2014 | 201 | |
| 7 | 2014 | 158 | |
| 8 | 2003 | 155 | |
| 9 | 1992 | 132 | |
| 10 | 2012 | 124 | |
| 11 | 2008 | 119 | |
| 12 | 2009 | 117 | |
| 13 | 2015 | 96 | |
| 14 | 2014 | 96 | |
| 15 | 2006 | 93 | |
| 16 | 1994 | 92 | |
| 17 | 2014 | 90 | |
| 18 | 1999 | 78 | |
| 19 | 2016 | 75 | |
| 20 | 2009 | 73 |
About Éric Vilain
Éric Vilain is a scholar working on Molecular Biology, Genetics, Reproductive Medicine, Urology and Social Psychology, having authored 116 papers that have together received 6.2k indexed citations. Recurring topics across this work include Sexual Differentiation and Disorders (60 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (56 papers), Sperm and Testicular Function (19 papers), Urological Disorders and Treatments (16 papers), LGBTQ Health, Identity, and Policy (10 papers), Epigenetics and DNA Methylation (7 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genomics and Rare Diseases (5 papers). The work is most often cited by research in Reproductive Medicine (969 citations), Genetics (2.8k citations), Urology (566 citations), Molecular Biology (3.9k citations) and Aging (94 citations). Éric Vilain has collaborated with scholars based in United States, France and Australia. Frequent co-authors include Francisco J. Sánchez, Steve Horvath, David E. Sandberg, Janet S. Sinsheimer, Sven Bocklandt, Mary E. Sehl, Wen Lin, Ken McElreavey, Emmanuèle C. Délot and M Fellous. Their work appears in journals such as Molecular Genetics and Metabolism, Proceedings of the National Academy of Sciences, The Journal of Clinical Endocrinology & Metabolism, American Journal of Medical Genetics Part C Seminars in Medical Genetics and Clinical Genetics.
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.