Behavioural and functional evidence revealing the role of RBFOX1 variation in multiple psychiatric disorders and traits

Common variation in the gene encoding the neuron-specific RNA splicing factor RNA Binding Fox-1 Homolog 1 (RBFOX1) has been identified as a risk factor for several psychiatric conditions, and rare genetic variants have been found causal for autism spectrum disorder (ASD). Here, we explored the genet...

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Detalles Bibliográficos
Autores principales: O’Leary, Aet, Fernàndez-Castillo, Noèlia, Gan, Gabriela, Yang, Yunbo, Yotova, Anna Y., Kranz, Thorsten M., Grünewald, Lena, Freudenberg, Florian, Antón-Galindo, Ester, Cabana-Domínguez, Judit, Harneit, Anais, Schweiger, Janina I., Schwarz, Kristina, Ma, Ren, Chen, Junfang, Schwarz, Emanuel, Rietschel, Marcella, Tost, Heike, Meyer-Lindenberg, Andreas, Pané-Farré, Christiane A., Kircher, Tilo, Hamm, Alfons O., Burguera, Demian, Mota, Nina Roth, Franke, Barbara, Schweiger, Susann, Winter, Jennifer, Heinz, Andreas, Erk, Susanne, Romanczuk-Seiferth, Nina, Walter, Henrik, Ströhle, Andreas, Fehm, Lydia, Fydrich, Thomas, Lueken, Ulrike, Weber, Heike, Lang, Thomas, Gerlach, Alexander L., Nöthen, Markus M., Alpers, Georg W., Arolt, Volker, Witt, Stephanie, Richter, Jan, Straube, Benjamin, Cormand, Bru, Slattery, David A., Reif, Andreas
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/PMC9734045/
https://www.ncbi.nlm.nih.gov/pubmed/35948661
http://dx.doi.org/10.1038/s41380-022-01722-4

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