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Journal of Neurochemistry|July 8, 2024
DDX3X syndrome: From clinical phenotypes to biological insightsAlexa von Mueffling, Marta Garcia-Forn, Silvia De Rubeis
Cells|November 21, 2020
Linking Autism Risk Genes to Disruption of Cortical DevelopmentMarta Garcia-Forn, Andrea Boitnott, Zeynep Akpinar, et al.
Methods in Cell Biology|June 16, 2024
Assessing motor development and function in mouse models of neurodevelopmental disordersLauren Dierdorff, Marta Garcia-Forn, Alexa von Mueffling, et al.
Biorxiv : the Preprint Server for Biology|November 28, 2024
Sex-specific perturbations of neuronal development caused by mutations in the autism risk gene <i>DDX3X</i>Adele Mossa, Lauren Dierdorff, Jeronimo Lukin, et al.
Biology Open|January 29, 2025
A subpopulation of cortical neurons altered by mutations in the autism risk gene DDX3XMichael A Flores, Marta Garcia-Forn, Alexa von Mueffling, et al.
Nature Communications|May 15, 2025
Sex-specific perturbations of neuronal development caused by mutations in the autism risk gene DDX3XAdele Mossa, Lauren Dierdorff, Jeronimo Lukin, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|August 7, 2025
Sertraline treatment prevents motor dysfunction in a Huntington's disease mouse model and functional decline in patientsMarta Garcia-Forn, Carla Castany-Pladevall, Jordi Creus-Muncunill, et al.
Brain : a Journal of Neurology|August 1, 2019
Increased translation as a novel pathogenic mechanism in Huntington's diseaseJordi Creus-Muncunill, Raquel Badillos-Rodríguez, Marta Garcia-Forn, et al.
Biomolecules|January 21, 2022
RTP801/REDD1 Is Involved in Neuroinflammation and Modulates Cognitive Dysfunction in Huntington's DiseaseLeticia Pérez-Sisqués, Júlia Solana-Balaguer, Genís Campoy-Campos, et al.
The American Journal of Pathology|December 21, 2020
Lack of Annexin A6 Exacerbates Liver Dysfunction and Reduces Lifespan of Niemann-Pick Type C Protein-Deficient MiceElsa Meneses-Salas, Marta Garcia-Forn, Carla Castany-Pladevall, et al.
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