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Page 1
Heritability of Clinically Diagnosed Obsessive-Compulsive Disorder Among Twins.
Mataix-Cols D, Fernández de la Cruz L, Beucke JC, De Schipper E, Kuja-Halkola R, Lichtenstein P, Pol-Fuster J. Mataix-Cols D, et al. Among authors: pol fuster j. JAMA Psychiatry. 2024 Apr 3:e240299. doi: 10.1001/jamapsychiatry.2024.0299. Online ahead of print. JAMA Psychiatry. 2024. PMID: 38568562 Free PMC article.
Role of PATJ in stroke prognosis by modulating endothelial to mesenchymal transition through the Hippo/Notch/PI3K axis.
Medina-Dols A, Cañellas G, Capó T, Solé M, Mola-Caminal M, Cullell N, Jaume M, Nadal-Salas L, Llinàs J, Gómez L, Tur S, Jiménez C, Díaz RM, Carrera C, Muiño E, Gallego-Fabrega C, Soriano-Tárraga C, Ruiz-Guerra L, Pol-Fuster J, Asensio V, Muncunill J, Fleischer A, Iglesias A, Giralt-Steinhauer E, Lazcano U, Fernández-Pérez I, Jiménez-Balado J, Gabriel-Salazar M, Garcia-Gabilondo M, Lei T, Torres-Aguila NP, Cárcel-Márquez J, Lladó J, Olmos G, Rosell A, Montaner J, Planas AM, Rabionet R, Hernández-Guillamon M, Jiménez-Conde J, Fernández-Cadenas I, Vives-Bauzá C. Medina-Dols A, et al. Among authors: pol fuster j. Cell Death Discov. 2024 Feb 17;10(1):85. doi: 10.1038/s41420-024-01857-z. Cell Death Discov. 2024. PMID: 38368420 Free PMC article.
The conserved ASTN2/BRINP1 locus at 9q33.1-33.2 is associated with major psychiatric disorders in a large pedigree from Southern Spain.
Pol-Fuster J, Cañellas F, Ruiz-Guerra L, Medina-Dols A, Bisbal-Carrió B, Ortega-Vila B, Llinàs J, Hernandez-Rodriguez J, Lladó J, Olmos G, Strauch K, Heine-Suñer D, Vives-Bauzà C, Flaquer A. Pol-Fuster J, et al. Sci Rep. 2021 Jul 15;11(1):14529. doi: 10.1038/s41598-021-93555-4. Sci Rep. 2021. PMID: 34267256 Free PMC article.
Familial Psychosis Associated With a Missense Mutation at MACF1 Gene Combined With the Rare Duplications DUP3p26.3 and DUP16q23.3, Affecting the CNTN6 and CDH13 Genes.
Pol-Fuster J, Cañellas F, Ruiz-Guerra L, Medina-Dols A, Bisbal-Carrió B, Asensio V, Ortega-Vila B, Marzese D, Vidal C, Santos C, Lladó J, Olmos G, Heine-Suñer D, Strauch K, Flaquer A, Vives-Bauzà C. Pol-Fuster J, et al. Front Genet. 2021 Apr 7;12:622886. doi: 10.3389/fgene.2021.622886. eCollection 2021. Front Genet. 2021. PMID: 33897758 Free PMC article.
Non-motor symptoms burden, mood, and gait problems are the most significant factors contributing to a poor quality of life in non-demented Parkinson's disease patients: Results from the COPPADIS Study Cohort.
Santos García D, de Deus Fonticoba T, Suárez Castro E, Borrué C, Mata M, Solano Vila B, Cots Foraster A, Álvarez Sauco M, Rodríguez Pérez AB, Vela L, Macías Y, Escalante S, Esteve P, Reverté Villarroya S, Cubo E, Casas E, Arnaiz S, Carrillo Padilla F, Pueyo Morlans M, Mir P, Martinez-Martin P; Coppadis Study Group. Santos García D, et al. Parkinsonism Relat Disord. 2019 Sep;66:151-157. doi: 10.1016/j.parkreldis.2019.07.031. Epub 2019 Jul 29. Parkinsonism Relat Disord. 2019. PMID: 31409572
Disrupted in schizophrenia 1 (DISC1) is a constituent of the mammalian mitochondrial contact site and cristae organizing system (MICOS) complex, and is essential for oxidative phosphorylation.
Piñero-Martos E, Ortega-Vila B, Pol-Fuster J, Cisneros-Barroso E, Ruiz-Guerra L, Medina-Dols A, Heine-Suñer D, Lladó J, Olmos G, Vives-Bauzà C. Piñero-Martos E, et al. Among authors: pol fuster j. Hum Mol Genet. 2016 Oct 1;25(19):4157-4169. doi: 10.1093/hmg/ddw250. Epub 2016 Jul 27. Hum Mol Genet. 2016. PMID: 27466199 Free PMC article.