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ABOUT JoVE

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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Scott Barish

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Human Molecular Genetics|April 11, 2022

The microRNA processor DROSHA is a candidate gene for a severe progressive neurological disorderScott Barish, Mumine Senturk, Kelly Schoch, et al.

American Journal of Human Genetics|October 12, 2023

Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomaliesZelha Nil, Ashish R Deshwar, Yan Huang, et al.

American Journal of Human Genetics|October 29, 2024

Homozygous variants in WDR83OS lead to a neurodevelopmental disorder with hypercholanemiaScott Barish, Sheng-Jia Lin, Reza Maroofian, et al.

American Journal of Human Genetics|November 24, 2020

BICRA, a SWI/SNF Complex Member, Is Associated with BAF-Disorder Related Phenotypes in Humans and Model OrganismsScott Barish, Tahsin Stefan Barakat, Brittany C Michel, et al.

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Search research articles

Showing results (11-20 of 14) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 14 results.

Human Molecular Genetics|April 11, 2022

The microRNA processor DROSHA is a candidate gene for a severe progressive neurological disorderScott Barish, Mumine Senturk, Kelly Schoch, et al.

American Journal of Human Genetics|October 12, 2023

Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomaliesZelha Nil, Ashish R Deshwar, Yan Huang, et al.

American Journal of Human Genetics|October 29, 2024

Homozygous variants in WDR83OS lead to a neurodevelopmental disorder with hypercholanemiaScott Barish, Sheng-Jia Lin, Reza Maroofian, et al.

American Journal of Human Genetics|November 24, 2020

BICRA, a SWI/SNF Complex Member, Is Associated with BAF-Disorder Related Phenotypes in Humans and Model OrganismsScott Barish, Tahsin Stefan Barakat, Brittany C Michel, et al.

Pageof 2