Contribution of schizophrenia polygenic burden to longitudinal phenotypic variance in 22q11.2 deletion syndrome

While the recurrent 22q11.2 deletion is one of the strongest genetic risk factors for schizophrenia (SCZ), variability of its associated neuropsychiatric endophenotypes reflects its incomplete penetrance for psychosis development. To assess whether this phenotypic variability is linked to common var...

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Detalles Bibliográficos
Autores principales: Alver, Maris, Mancini, Valentina, Läll, Kristi, Schneider, Maude, Romano, Luciana, Mägi, Reedik, Dermitzakis, Emmanouil T., Eliez, Stephan, Reymond, Alexandre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9718680/
https://www.ncbi.nlm.nih.gov/pubmed/35768638
http://dx.doi.org/10.1038/s41380-022-01674-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9718680/
https://www.ncbi.nlm.nih.gov/pubmed/35768638
http://dx.doi.org/10.1038/s41380-022-01674-9

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