OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13.3 Microdeletion Syndrome-Reference-Cited by-同舟云学术

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OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13.3 Microdeletion Syndrome

Published:2018-02 Issue:2 Volume:102 Page:278-295
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Uddin Mohammed,Unda Brianna K.,Kwan Vickie,Holzapfel Nicholas T.,White Sean H.,Chalil Leon,Woodbury-Smith Marc,Ho Karen S.,Harward Erin,Murtaza Nadeem,Dave Biren,Pellecchia Giovanna,D’Abate Lia,Nalpathamkalam Thomas,Lamoureux Sylvia,Wei John,Speevak Marsha,Stavropoulos James,Hope Kristin J.,Doble Brad W.,Nielsen Jacob,Wassman E. Robert,Scherer Stephen W.,Singh Karun K.

Funder

Canadian Institutes of Health Research [CIHR]

Natural Sciences and Engineering Research Council

Brain Canada Platform Support Grant

Ontario Brain Institute-POND study

OB

CIHR

Autism Speaks

Ontario Institute of Cancer Research

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference85 articles.

1. Indexing effects of copy number variation on genes involved in developmental delay;Uddin;Sci. Rep.,2016

2. Genetic variation in the 22q11 locus and susceptibility to schizophrenia;Liu;Proc. Natl. Acad. Sci. USA,2002

3. Palmitoylation-dependent neurodevelopmental deficits in a mouse model of 22q11 microdeletion;Mukai;Nat. Neurosci.,2008

4. Behavioral abnormalities and circuit defects in the basal ganglia of a mouse model of 16p11.2 deletion syndrome;Portmann;Cell Rep.,2014

5. Reversal of dendritic phenotypes in 16p11.2 microduplication mouse model neurons by pharmacological targeting of a network hub;Blizinsky;Proc. Natl. Acad. Sci. USA,2016

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