The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability

By meta-analyzing rare coding variants in whole-exome sequences of 4,133 schizophrenia cases and 9,274 controls, de novo mutations in 1,077 trios, and copy number variants from 6,882 cases and 11,255 controls, we show that individuals with schizophrenia carry a significant burden of rare damaging va...

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Detalles Bibliográficos
Autores principales: Singh, Tarjinder, Walters, James T. R., Johnstone, Mandy, Curtis, David, Suvisaari, Jaana, Torniainen, Minna, Rees, Elliott, Iyegbe, Conrad, Blackwood, Douglas, McIntosh, Andrew M., Kirov, Georg, Geschwind, Daniel, Murray, Robin M., Di Forti, Marta, Bramon, Elvira, Gandal, Michael, Hultman, Christina M., Sklar, Pamela, Palotie, Aarno, Sullivan, Patrick F., O'Donovan, Michael C., Owen, Michael J., Barrett, Jeffrey C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5533219/
https://www.ncbi.nlm.nih.gov/pubmed/28650482
http://dx.doi.org/10.1038/ng.3903

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5533219/
https://www.ncbi.nlm.nih.gov/pubmed/28650482
http://dx.doi.org/10.1038/ng.3903

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