Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia

Despite considerable progress in schizophrenia genetics, most findings have been for large rare structural variants and common variants in well-imputed regions with few genes implicated from exome sequencing. Whole genome sequencing (WGS) can potentially provide a more complete enumeration of etiolo...

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Detalles Bibliográficos
Autores principales: Halvorsen, Matthew, Huh, Ruth, Oskolkov, Nikolay, Wen, Jia, Netotea, Sergiu, Giusti-Rodriguez, Paola, Karlsson, Robert, Bryois, Julien, Nystedt, Björn, Ameur, Adam, Kähler, Anna K., Ancalade, NaEshia, Farrell, Martilias, Crowley, James J., Li, Yun, Magnusson, Patrik K. E., Gyllensten, Ulf, Hultman, Christina M., Sullivan, Patrick F., Szatkiewicz, Jin P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160146/
https://www.ncbi.nlm.nih.gov/pubmed/32296054
http://dx.doi.org/10.1038/s41467-020-15707-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160146/
https://www.ncbi.nlm.nih.gov/pubmed/32296054
http://dx.doi.org/10.1038/s41467-020-15707-w

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