Éric Vilain

13.5k citations

115 papers · 6.1k indexed · 3 hit papers · h-index 40

Reproductive Medicine top 0.5%
- Sperm and Testicular Function 23
Urology top 0.5%
- Urological Disorders and Treatments 15
Genetics top 0.5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 57
- Genomics and Rare Diseases 7
- Genomic variations and chromosomal abnormalities 7
Molecular Biology top 1%
- Sexual Differentiation and Disorders 63
- Epigenetics and DNA Methylation 9
Aging top 2%
Social Psychology
- LGBTQ Health, Identity, and Policy 10

Co-authors: Francisco J. Sánchez Steve Horvath Sven Bocklandt David E. Sandberg Janet S. Sinsheimer Mary E. Sehl Ken McElreavey Wen Lin
Cited by: Reproductive Medicine Urology Genetics
Journals: Molecular Genetics and Metabolism (8 papers)The Journal of Clinical Endocrinology & Metabolism (5 papers)Proceedings of the National Academy of Sciences (5 papers)
Partner nations: United States France Australia

In The Last Decade

Éric Vilain

111 papers receiving 5.9k citations

Hit Papers

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Peers

Countries citing papers authored by Éric Vilain

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network

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.

Border = papers with Éric Vilain Line = papers co-authored together Éric Vilain links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	P539: Chatbot-assisted informed consent in genomics research* Genetics in Medicine Open ·Anita Raja,高庆荣,Jonathan LoTempio,Patrick Fargeaud,Emmanuèle C. Délot,Vincent A. Fusaro,Seth Berger,Éric Vilain,Changrui Xiao	2025	0
2	Using a chat-based informed consent tool in large-scale genomic research Journal of the American Medical Informatics Association ·Sarah Savage,Jonathan LoTempio,Erica D. Smith,Sarah Alkuraydis,Glòria Mas Martín,Amanda Kahn-Kirby,Emmanuèle C. Délot,Andrea J. Cohen,Georgia Pitsava,Robert L. Nussbaum,Vincent A. Fusaro,Seth Berger,Éric Vilain	2023	7
3	Increased diagnostic yield from negative whole genome‐slice panels using automated reanalysis Clinical Genetics ·Seth Berger,Georgia Pitsava,Andrea J. Cohen,Emmanuèle C. Délot,Jonathan LoTempio,Sarah Alkuraydis,Glòria Mas Martín,Yanxia Luo,R Constant,Annika Kathrin Werth,Jamie L. Fraser,Debra S. Regier,Amanda Kahn-Kirby,Erica D. Smith,Susan M. Knoblach,Arthur Ko,Vincent A. Fusaro,Éric Vilain	2023	4
4	Long reads capture simultaneous enhancer–promoter methylation status for cell-type deconvolution Bioinformatics ·Sapir Margalit,Kristy Lockhart,Hila Sharim,昭三佐々木,Surajit Bhattacharya,Yiwen Chen,Éric Vilain,Hayk Barseghyan,Ran Elkon,Roded Sharan,Yuval Ebenstein	2021	8
5	nanotatoR: a tool for enhanced annotation of genomic structural variants BMC Genomics ·Surajit Bhattacharya,Hayk Barseghyan,Emmanuèle C. Délot,Éric Vilain	2021	8
6	Newborn Screening Protocols and Positive Predictive Value for Congenital Adrenal Hyperplasia Vary across the United States International Journal of Neonatal Screening ·Phyllis Speiser,Barry Mather,Ming Chen,Alicia Diaz-Thomas,Courtney Finlayson,Meilan M. Rutter,David E. Sandberg,Jiaying Zhang,Irina Lesi,Jane Cerise,Éric Vilain,Emmanuèle C. Délot	2020	21
7	Sexual Orientation, Controversy, and Sciencebreakdown → PubMed ·J. Michael Bailey,Paul L. Vasey,Lisa M. Diamond,S. Marc Breedlove,Éric Vilain,Marc Epprecht	2016	318
8	Global Disorders of Sex Development Update since 2006: Perceptions, Approach and Carebreakdown → Hormone Research in Paediatrics ·Peter A. Lee,Anna Nordenström,Christopher P. Houk,S. Faisal Ahmed,Richard J. Auchus,Arlene B. Baratz,Katharine B. Dalke,Lih‐Mei Liao,Karen Lin‐Su,Leendert H. J. Looijenga,Tom Mazur,Heino F. L. Meyer‐Bahlburg,Pierre Mouriquand,Charmian A. Quigley,David E. Sandberg,Éric Vilain,Selma F. Witchel	2016	745
9	De novo single exon deletion of AUTS2 in a patient with speech and language disorder: A review of disrupted AUTS2 and further evidence for its role in neurodevelopmental disorders American Journal of Medical Genetics Part A ·Ina Amarillo,R. Steinmetz,Xinmin Li,Éric Vilain,Sibel Kantarci	2014	33
10	Mutant Cohesin in Premature Ovarian Failure New England Journal of Medicine ·Sandrine Caburet,Valerie A. Arboleda,Elena Llano,Paul A. Overbeek,José Luís Barbero,Kazuhiro Oka,Wilbur R. Harrison,Daniel Vaiman,Ziva Ben‐Neriah,Ignacio García‐Tuñón,Marc Fellous,Alberto M. Pendás,Reiner A. Veitia,Éric Vilain	2014	196
11	Epigenetic Predictor of Agebreakdown → PLoS ONE ·Sven Bocklandt,Wen Lin,Mary E. Sehl,Francisco J. Sánchez,Janet S. Sinsheimer,Steve Horvath,Éric Vilain	2011	685
12	We used to call them hermaphrodites Genetics in Medicine ·Éric Vilain,John C. Achermann,Erica A. Eugster,Vincent R. Harley,Yves Morel,Jean D. Wilson,Olaf Hiort	2007	23
13	Carnitine membrane transporter deficiency: a long-term follow up and OCTN2 mutation in the first documented case of primary carnitine deficiency Molecular Genetics and Metabolism ·Stephen D. Cederbaum,Samantha Koo-McCoy,Ingrid Tein,Betty Y.L. Hsu,Arupa Ganguly,Éric Vilain,Katrina M. Dipple,Ljerka Cvitanović-Šojat,Charles A. Stanley	2002	52
14	Adrenal hypoplasia congenita with multiple pituitary hormone deficiency without documented mutation in DAX1 or SF1 gene Molecular Genetics and Metabolism ·Shlomit Shalitin,Ζ. Josefsberg,Éric Vilain,Ruth Shomrat,Naomi Weintrob	2002	5
15	Midkine Is Expressed Early in Rat Fetal Adrenal Development Molecular Genetics and Metabolism ·Phoebe Dewing,Saunders Ching,Yao‐Hua Zhang,Chelsea Riveley,J. Holt,Edward R.B. McCabe,Éric Vilain	2000	5
16	IMAGe, a New Clinical Association of Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies The Journal of Clinical Endocrinology & Metabolism ·Éric Vilain	1999	17
17	IMAGe, a New Clinical Association of Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies The Journal of Clinical Endocrinology & Metabolism ·Éric Vilain,Martine Le Merrer,C Lecointre,F Desangles,Mark A. Kay,P Maroteaux,Edward R.B. McCabe	1999	78
18	Dysgerminoma in a Pure 45,X Turner Syndrome: Report of a Case and Review of the Literature Gynecologic Oncology ·J-Y Pierga,Sylvie Giacchetti,Éric Vilain,J.M. Extra,Yves Houde,Theobald Nemetschek,K. B. Luk,Marc Fellous,차문성	1994	10
19	Pathology of 46, XY pure gonadal dysgenesis: absence of testis differentiation associated with mutations in the testis-determining factor Differentiation ·Éric Vilain,F Jaubert,M Fellous,Ken McElreavey	1993	35
20	XY Sex reversal associated with a nonsense mutation in SRY Genomics ·Mariana Rossi Corregliano,Éric Vilain,C. Boucekkine,Michel Vidaud,Yen-Yi Chan,François Richaud,Marc Fellous	1992	49

About Éric Vilain

Éric Vilain is a scholar working on Reproductive Medicine, Genetics and Urology, having authored 115 papers that have together received 6.1k indexed citations. Recurring topics across this work include Sexual Differentiation and Disorders (63 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (57 papers), Sperm and Testicular Function (23 papers), Urological Disorders and Treatments (15 papers), LGBTQ Health, Identity, and Policy (10 papers), Epigenetics and DNA Methylation (9 papers), Genomics and Rare Diseases (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). The work is most often cited by research in Reproductive Medicine (1.1k citations), Urology (727 citations) and Genetics (3.1k citations). Éric Vilain has collaborated with scholars based in United States, France and Australia. Frequent co-authors include Francisco J. Sánchez, Steve Horvath, Sven Bocklandt, David E. Sandberg, Janet S. Sinsheimer, Mary E. Sehl, Ken McElreavey, Wen Lin, M Fellous and N. Abbas. Their work appears in journals such as Molecular Genetics and Metabolism, The Journal of Clinical Endocrinology & Metabolism, Proceedings of the National Academy of Sciences, Clinical Genetics and American Journal of Medical Genetics Part C Seminars in Medical 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.

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