Analysis of Rare, Exonic Variation amongst Subjects with Autism Spectrum Disorders and Population Controls

We report on results from whole-exome sequencing (WES) of 1,039 subjects diagnosed with autism spectrum disorders (ASD) and 870 controls selected from the NIMH repository to be of similar ancestry to cases. The WES data came from two centers using different methods to produce sequence and to call va...

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Detalles Bibliográficos
Autores principales: Liu, Li, Sabo, Aniko, Neale, Benjamin M., Nagaswamy, Uma, Stevens, Christine, Lim, Elaine, Bodea, Corneliu A., Muzny, Donna, Reid, Jeffrey G., Banks, Eric, Coon, Hillary, DePristo, Mark, Dinh, Huyen, Fennel, Tim, Flannick, Jason, Gabriel, Stacey, Garimella, Kiran, Gross, Shannon, Hawes, Alicia, Lewis, Lora, Makarov, Vladimir, Maguire, Jared, Newsham, Irene, Poplin, Ryan, Ripke, Stephan, Shakir, Khalid, Samocha, Kaitlin E., Wu, Yuanqing, Boerwinkle, Eric, Buxbaum, Joseph D., Cook, Edwin H., Devlin, Bernie, Schellenberg, Gerard D., Sutcliffe, James S., Daly, Mark J., Gibbs, Richard A., Roeder, Kathryn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3623759/
https://www.ncbi.nlm.nih.gov/pubmed/23593035
http://dx.doi.org/10.1371/journal.pgen.1003443

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3623759/
https://www.ncbi.nlm.nih.gov/pubmed/23593035
http://dx.doi.org/10.1371/journal.pgen.1003443

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