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Eric Vilain

Showing results (161-170 of 177) with videos related to

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The Journal of Sexual Medicine|May 25, 2021
The Neuroanatomy of Transgender Identity: Mega-Analytic Findings From the ENIGMA Transgender Persons Working GroupSven C Mueller, Antonio Guillamon, Leire Zubiaurre-Elorza, et al.
Transgender Health|December 30, 2020
Consensus Parameter: Research Methodologies to Evaluate Neurodevelopmental Effects of Pubertal Suppression in Transgender YouthDiane Chen, John F Strang, Victoria D Kolbuck, et al.
Arxiv|January 7, 2025
GREGoR: Accelerating Genomics for Rare DiseasesMoez Dawood, Ben Heavner, Marsha M Wheeler, et al.
Nature|November 12, 2025
GREGoR: accelerating genomics for rare diseasesMoez Dawood, Ben Heavner, Marsha M Wheeler, et al.
Medrxiv : the Preprint Server for Health Sciences|January 7, 2025
Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed casesSarah L Stenton, Kristen Laricchia, Nicole J Lake, et al.
HGG Advances|April 17, 2025
Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed casesSarah L Stenton, Kristen Laricchia, Nicole J Lake, et al.
Pediatric Research|January 3, 2025
Building a growing genomic repository for maternal and fetal health through the PING ConsortiumClara M Abdelmalek, Shriya Singh, Blain Fasil, et al.
Medrxiv : the Preprint Server for Health Sciences|June 3, 2024
Building a growing genomic data repository for maternal and fetal health through the PING ConsortiumClara M Abdelmalek, Shriya Singh, Blain Fasil, et al.
Biorxiv : the Preprint Server for Biology|June 4, 2026
Building an Interoperable Rare Disease Multi-omic Resource: The GREGoR Data Model and DatasetBenjamin D Heavner, Marsha M Wheeler, Jesse D Bengtsson, et al.
American Journal of Human Genetics|January 29, 2025
Sequence variants in HECTD1 result in a variable neurodevelopmental disorderGazelle Zerafati-Jahromi, Elias Oxman, Hieu D Hoang, et al.
Pageof 18

Showing results (161-170 of 177) with videos related to

Sort By:
Pageof 18
The Journal of Sexual Medicine|May 25, 2021
The Neuroanatomy of Transgender Identity: Mega-Analytic Findings From the ENIGMA Transgender Persons Working GroupSven C Mueller, Antonio Guillamon, Leire Zubiaurre-Elorza, et al.
Transgender Health|December 30, 2020
Consensus Parameter: Research Methodologies to Evaluate Neurodevelopmental Effects of Pubertal Suppression in Transgender YouthDiane Chen, John F Strang, Victoria D Kolbuck, et al.
Arxiv|January 7, 2025
GREGoR: Accelerating Genomics for Rare DiseasesMoez Dawood, Ben Heavner, Marsha M Wheeler, et al.
Nature|November 12, 2025
GREGoR: accelerating genomics for rare diseasesMoez Dawood, Ben Heavner, Marsha M Wheeler, et al.
Medrxiv : the Preprint Server for Health Sciences|January 7, 2025
Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed casesSarah L Stenton, Kristen Laricchia, Nicole J Lake, et al.
HGG Advances|April 17, 2025
Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed casesSarah L Stenton, Kristen Laricchia, Nicole J Lake, et al.
Pediatric Research|January 3, 2025
Building a growing genomic repository for maternal and fetal health through the PING ConsortiumClara M Abdelmalek, Shriya Singh, Blain Fasil, et al.
Medrxiv : the Preprint Server for Health Sciences|June 3, 2024
Building a growing genomic data repository for maternal and fetal health through the PING ConsortiumClara M Abdelmalek, Shriya Singh, Blain Fasil, et al.
Biorxiv : the Preprint Server for Biology|June 4, 2026
Building an Interoperable Rare Disease Multi-omic Resource: The GREGoR Data Model and DatasetBenjamin D Heavner, Marsha M Wheeler, Jesse D Bengtsson, et al.
American Journal of Human Genetics|January 29, 2025
Sequence variants in HECTD1 result in a variable neurodevelopmental disorderGazelle Zerafati-Jahromi, Elias Oxman, Hieu D Hoang, et al.
Pageof 18