Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders

BACKGROUND: Integrating rare variation from trio family and case–control studies has successfully implicated specific genes contributing to risk of neurodevelopmental disorders (NDDs) including autism spectrum disorders (ASD), intellectual disability (ID), developmental disorders (DDs), and epilepsy...

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Detalles Bibliográficos
Autores principales: Nguyen, Hoang T., Bryois, Julien, Kim, April, Dobbyn, Amanda, Huckins, Laura M., Munoz-Manchado, Ana B., Ruderfer, Douglas M., Genovese, Giulio, Fromer, Menachem, Xu, Xinyi, Pinto, Dalila, Linnarsson, Sten, Verhage, Matthijs, Smit, August B., Hjerling-Leffler, Jens, Buxbaum, Joseph D., Hultman, Christina, Sklar, Pamela, Purcell, Shaun M., Lage, Kasper, He, Xin, Sullivan, Patrick F., Stahl, Eli A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5738153/
https://www.ncbi.nlm.nih.gov/pubmed/29262854
http://dx.doi.org/10.1186/s13073-017-0497-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5738153/
https://www.ncbi.nlm.nih.gov/pubmed/29262854
http://dx.doi.org/10.1186/s13073-017-0497-y

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