Linking spatial gene expression patterns to sex-specific brain structural changes on a mouse model of 16p11.2 hemideletion-Reference-Cited by-同舟云学术

Linking spatial gene expression patterns to sex-specific brain structural changes on a mouse model of 16p11.2 hemideletion

Published:2018-05-29 Issue:1 Volume:8 Page:
ISSN:2158-3188
Container-title:Translational Psychiatry
language:en
Short-container-title:Transl Psychiatry

Author:

Kumar Vinod Jangir,Grissom Nicola M.,McKee Sarah E.,Schoch Hannah,Bowman Nicole,Havekes Robbert^ORCID,Kumar Manoj,Pickup Stephen,Poptani Harish,Reyes Teresa M.,Hawrylycz Mike,Abel Ted^ORCID,Nickl-Jockschat Thomas

Publisher

Springer Science and Business Media LLC

Subject

Biological Psychiatry,Cellular and Molecular Neuroscience,Psychiatry and Mental health

Link

http://www.nature.com/articles/s41398-018-0157-z.pdf

Reference93 articles.

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3. Pinto, D. et al. Functional impact of global rare copy number variation in autism spectrum disorders. Nature 466, 368–372 (2010).

4. Sanders, S. J. et al. Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron 70, 863–885 (2011).

5. Levy, D. et al. Rare de novo and transmitted copy-number variation in autistic spectrum disorders. Neuron 70, 886–897 (2011).

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