Truncating mutations in RBM12 are associated with psychosis-Reference-Cited by-同舟云学术

Truncating mutations in RBM12 are associated with psychosis

Published:2017-06-19 Issue:8 Volume:49 Page:1251-1254
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Steinberg Stacy,Gudmundsdottir Steinunn,Sveinbjornsson Gardar,Suvisaari Jaana^ORCID,Paunio Tiina,Torniainen-Holm Minna,Frigge Michael L^ORCID,Jonsdottir Gudrun A,Huttenlocher Johanna,Arnarsdottir Sunna,Ingimarsson Oddur,Haraldsson Magnus,Tyrfingsson Thorarinn,Thorgeirsson Thorgeir E,Kong Augustine,Norddahl Gudmundur L,Gudbjartsson Daniel F,Sigurdsson Engilbert,Stefansson Hreinn,Stefansson Kari

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.3894.pdf

Reference53 articles.

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2. Genovese, G. et al. Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia. Nat. Neurosci. 19, 1433–1441 (2016).

3. Singh, T. et al. Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders. Nat. Neurosci. 19, 571–577 (2016).

4. Purcell, S.M. et al. A polygenic burden of rare disruptive mutations in schizophrenia. Nature 506, 185–190 (2014).

5. Fromer, M. et al. De novo mutations in schizophrenia implicate synaptic networks. Nature 506, 179–184 (2014).

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