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Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Elizabeth S Barrie

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European Journal of Medical Genetics|March 25, 2018

Pericentromeric regions of homozygosity on the X chromosome: Another likely benign population variantElizabeth S Barrie, Yu Li, Devon Lamb-Thrush, et al.

Journal of Developmental and Physical Disabilities|September 11, 2018

Testing genetic modifiers of behavior and response to atomoxetine in autism spectrum disorder with ADHDElizabeth S Barrie, Julia K Pinsonneault, Wolfgang Sadee, et al.

Human Mutation|August 10, 2019

Mutations in PLS1, encoding fimbrin, cause autosomal dominant nonsyndromic hearing lossAnna Morgan, Daniel C Koboldt, Elizabeth S Barrie, et al.

American Journal of Medical Genetics. Part A|February 27, 2020

Expanding the spectrum of CEP55-associated disease to viable phenotypesElizabeth S Barrie, Eline Overwater, Mieke M van Haelst, et al.

Plos One|May 6, 2016

Human Bacterial Artificial Chromosome (BAC) Transgenesis Fully Rescues Noradrenergic Function in Dopamine β-Hydroxylase Knockout MiceJoseph F Cubells, Jason P Schroeder, Elizabeth S Barrie, et al.

Circulation Research|October 19, 2014

Regulatory polymorphisms in human DBH affect peripheral gene expression and sympathetic activityElizabeth S Barrie, David Weinshenker, Anurag Verma, et al.

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Search research articles

Showing results (11-20 of 16) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 16 results.

European Journal of Medical Genetics|March 25, 2018

Pericentromeric regions of homozygosity on the X chromosome: Another likely benign population variantElizabeth S Barrie, Yu Li, Devon Lamb-Thrush, et al.

Journal of Developmental and Physical Disabilities|September 11, 2018

Testing genetic modifiers of behavior and response to atomoxetine in autism spectrum disorder with ADHDElizabeth S Barrie, Julia K Pinsonneault, Wolfgang Sadee, et al.

Human Mutation|August 10, 2019

Mutations in PLS1, encoding fimbrin, cause autosomal dominant nonsyndromic hearing lossAnna Morgan, Daniel C Koboldt, Elizabeth S Barrie, et al.

American Journal of Medical Genetics. Part A|February 27, 2020

Expanding the spectrum of CEP55-associated disease to viable phenotypesElizabeth S Barrie, Eline Overwater, Mieke M van Haelst, et al.

Plos One|May 6, 2016

Human Bacterial Artificial Chromosome (BAC) Transgenesis Fully Rescues Noradrenergic Function in Dopamine β-Hydroxylase Knockout MiceJoseph F Cubells, Jason P Schroeder, Elizabeth S Barrie, et al.

Circulation Research|October 19, 2014

Regulatory polymorphisms in human DBH affect peripheral gene expression and sympathetic activityElizabeth S Barrie, David Weinshenker, Anurag Verma, et al.

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