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Michael P Epstein

Showing results (111-120 of 140) with videos related to

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Translational Psychiatry|February 18, 2022
Metabolic effects of the schizophrenia-associated 3q29 deletionRebecca M Pollak, Ryan H Purcell, Timothy P Rutkowski, et al.
Genetic Epidemiology|August 19, 2010
Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndromeAdam E Locke, Kenneth J Dooley, Stuart W Tinker, et al.
Nature Medicine|August 31, 2023
Sex differences in brain protein expression and diseaseAliza P Wingo, Yue Liu, Ekaterina S Gerasimov, et al.
American Journal of Human Genetics|August 5, 2022
Loss of function of OTUD7A in the schizophrenia- associated 15q13.3 deletion impairs synapse development and function in human neuronsAlena Kozlova, Siwei Zhang, Alex V Kotlar, et al.
Ebiomedicine|May 31, 2022
Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discoveryKaren L Oliver, Colin A Ellis, Ingrid E Scheffer, et al.
American Journal of Human Genetics|December 31, 2005
Epimerase-deficiency galactosemia is not a binary conditionKimberly K Openo, Jenny M Schulz, Claudia A Vargas, et al.
Nature Genetics|January 29, 2021
Integrating human brain proteomes with genome-wide association data implicates new proteins in Alzheimer's disease pathogenesisAliza P Wingo, Yue Liu, Ekaterina S Gerasimov, et al.
Medrxiv : the Preprint Server for Health Sciences|May 15, 2024
Genome-wide study of gene-by-sex interactions identifies risks for cleft palateKelsey Robinson, Randy Parrish, Wasiu Lanre Adeyemo, et al.
Human Genetics|October 3, 2024
Genome-wide study of gene-by-sex interactions identifies risks for cleft palateKelsey Robinson, Randy Parrish, Wasiu Lanre Adeyemo, et al.
Medrxiv : the Preprint Server for Health Sciences|March 17, 2025
Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 816 triosKelsey R Robinson, Sarah W Curtis, Justin E Paschall, et al.
Pageof 14

Showing results (111-120 of 140) with videos related to

Sort By:
Pageof 14
Translational Psychiatry|February 18, 2022
Metabolic effects of the schizophrenia-associated 3q29 deletionRebecca M Pollak, Ryan H Purcell, Timothy P Rutkowski, et al.
Genetic Epidemiology|August 19, 2010
Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndromeAdam E Locke, Kenneth J Dooley, Stuart W Tinker, et al.
Nature Medicine|August 31, 2023
Sex differences in brain protein expression and diseaseAliza P Wingo, Yue Liu, Ekaterina S Gerasimov, et al.
American Journal of Human Genetics|August 5, 2022
Loss of function of OTUD7A in the schizophrenia- associated 15q13.3 deletion impairs synapse development and function in human neuronsAlena Kozlova, Siwei Zhang, Alex V Kotlar, et al.
Ebiomedicine|May 31, 2022
Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discoveryKaren L Oliver, Colin A Ellis, Ingrid E Scheffer, et al.
American Journal of Human Genetics|December 31, 2005
Epimerase-deficiency galactosemia is not a binary conditionKimberly K Openo, Jenny M Schulz, Claudia A Vargas, et al.
Nature Genetics|January 29, 2021
Integrating human brain proteomes with genome-wide association data implicates new proteins in Alzheimer's disease pathogenesisAliza P Wingo, Yue Liu, Ekaterina S Gerasimov, et al.
Medrxiv : the Preprint Server for Health Sciences|May 15, 2024
Genome-wide study of gene-by-sex interactions identifies risks for cleft palateKelsey Robinson, Randy Parrish, Wasiu Lanre Adeyemo, et al.
Human Genetics|October 3, 2024
Genome-wide study of gene-by-sex interactions identifies risks for cleft palateKelsey Robinson, Randy Parrish, Wasiu Lanre Adeyemo, et al.
Medrxiv : the Preprint Server for Health Sciences|March 17, 2025
Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 816 triosKelsey R Robinson, Sarah W Curtis, Justin E Paschall, et al.
Pageof 14