KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant-Reference-Cited by-同舟云学术

KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant

Published:2012-05 Issue:7398 Volume:485 Page:363-367
ISSN:0028-0836
Container-title:Nature
language:en
Short-container-title:Nature

Author:

Golzio Christelle,Willer Jason,Talkowski Michael E.,Oh Edwin C.,Taniguchi Yu,Jacquemont Sébastien,Reymond Alexandre,Sun Mei,Sawa Akira,Gusella James F.,Kamiya Atsushi,Beckmann Jacques S.,Katsanis Nicholas

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/nature11091.pdf

Reference31 articles.

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2. Weiss, L. A. et al. Association between microdeletion and microduplication at 16p11.2 and autism. N. Engl. J. Med. 358, 667–675 (2008)

3. McCarthy, S. E. et al. Microduplications of 16p11.2 are associated with schizophrenia. Nature Genet. 41, 1223–1227 (2009)

4. Jacquemont, S. et al. Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus. Nature 478, 97–102 (2011)

5. Walters, R. G. et al. A new highly penetrant form of obesity due to deletions on chromosome 16p11.2. Nature 463, 671–675 (2010)

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