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Eric Vilain

Showing results (151-160 of 177) with videos related to

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Human Molecular Genetics|December 30, 2016
A recurrent p.Arg92Trp variant in steroidogenic factor-1 (NR5A1) can act as a molecular switch in human sex developmentAnu Bashamboo, Patricia A Donohoue, Eric Vilain, et al.
Scandinavian Journal of Medicine & Science in Sports|November 4, 2024
Fair and Safe Eligibility Criteria for Women's Sport: The Proposed Testing Regime Is Not Justified, Ethical, or ViableAlun G Williams, Shane M Heffernan, Adam J Herbert, et al.
The Journal of Clinical Endocrinology and Metabolism|July 10, 2019
Genetic Evidence of the Association of DEAH-Box Helicase 37 Defects With 46,XY Gonadal Dysgenesis SpectrumThatiana Evilen da Silva, Nathalia Lisboa Gomes, Antonio Marcondes Lerário, et al.
The Journal of Pediatrics|June 28, 2021
Multisystem Inflammatory Syndrome of Children: Subphenotypes, Risk Factors, Biomarkers, Cytokine Profiles, and Viral SequencingRoberta L DeBiasi, Ashraf S Harahsheh, Hemalatha Srinivasalu, et al.
Hormone Research in Paediatrics|February 4, 2024
Multi-Stakeholder Opinion Statement on the Care of Individuals Born with Differences of Sex Development: Common Ground and Opportunities for ImprovementMartine Cools, Earl Y Cheng, Joanne Hall, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 20, 2026
Rare heterozygous de novo variants in RAPGEF2 are associated with a neurodevelopmental disorderAli H Bereshneh, Kirkland A Wilson, Xueyang Pan, et al.
The Journal of Infectious Diseases|August 15, 2018
Pan-Filovirus Serum Neutralizing Antibodies in a Subset of Congolese Ebolavirus Infection SurvivorsMatthew S Bramble, Nicole Hoff, Pavlo Gilchuk, et al.
American Journal of Human Genetics|December 30, 2019
Loss-of-Function Variants in PPP1R12A: From Isolated Sex Reversal to Holoprosencephaly Spectrum and Urogenital MalformationsJoel J Hughes, Ebba Alkhunaizi, Paul Kruszka, et al.
European Journal of Human Genetics : EJHG|May 7, 2015
DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct faciesJianling Ji, Hane Lee, Bob Argiropoulos, et al.
British Journal of Sports Medicine|March 4, 2026
Harmful anachronism: World Athletics reinstates gene testing to participate in women's competitionsSilvia Camporesi, Shane M Heffernan, Pascal Borry, et al.
Pageof 18

Showing results (151-160 of 177) with videos related to

Sort By:
Pageof 18
Human Molecular Genetics|December 30, 2016
A recurrent p.Arg92Trp variant in steroidogenic factor-1 (NR5A1) can act as a molecular switch in human sex developmentAnu Bashamboo, Patricia A Donohoue, Eric Vilain, et al.
Scandinavian Journal of Medicine & Science in Sports|November 4, 2024
Fair and Safe Eligibility Criteria for Women's Sport: The Proposed Testing Regime Is Not Justified, Ethical, or ViableAlun G Williams, Shane M Heffernan, Adam J Herbert, et al.
The Journal of Clinical Endocrinology and Metabolism|July 10, 2019
Genetic Evidence of the Association of DEAH-Box Helicase 37 Defects With 46,XY Gonadal Dysgenesis SpectrumThatiana Evilen da Silva, Nathalia Lisboa Gomes, Antonio Marcondes Lerário, et al.
The Journal of Pediatrics|June 28, 2021
Multisystem Inflammatory Syndrome of Children: Subphenotypes, Risk Factors, Biomarkers, Cytokine Profiles, and Viral SequencingRoberta L DeBiasi, Ashraf S Harahsheh, Hemalatha Srinivasalu, et al.
Hormone Research in Paediatrics|February 4, 2024
Multi-Stakeholder Opinion Statement on the Care of Individuals Born with Differences of Sex Development: Common Ground and Opportunities for ImprovementMartine Cools, Earl Y Cheng, Joanne Hall, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 20, 2026
Rare heterozygous de novo variants in RAPGEF2 are associated with a neurodevelopmental disorderAli H Bereshneh, Kirkland A Wilson, Xueyang Pan, et al.
The Journal of Infectious Diseases|August 15, 2018
Pan-Filovirus Serum Neutralizing Antibodies in a Subset of Congolese Ebolavirus Infection SurvivorsMatthew S Bramble, Nicole Hoff, Pavlo Gilchuk, et al.
American Journal of Human Genetics|December 30, 2019
Loss-of-Function Variants in PPP1R12A: From Isolated Sex Reversal to Holoprosencephaly Spectrum and Urogenital MalformationsJoel J Hughes, Ebba Alkhunaizi, Paul Kruszka, et al.
European Journal of Human Genetics : EJHG|May 7, 2015
DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct faciesJianling Ji, Hane Lee, Bob Argiropoulos, et al.
British Journal of Sports Medicine|March 4, 2026
Harmful anachronism: World Athletics reinstates gene testing to participate in women's competitionsSilvia Camporesi, Shane M Heffernan, Pascal Borry, et al.
Pageof 18