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Facial Emotion Recognition in Psychosis and Associations With Polygenic Risk for Schizophrenia: Findings From the Multi-Center EU-GEI Case-Control Study.
Tripoli G, Quattrone D, Ferraro L, Gayer-Anderson C, La Cascia C, La Barbera D, Sartorio C, Seminerio F, Rodriguez V, Tarricone I, Berardi D, Jamain S, Arango C, Tortelli A, Llorca PM, de Haan L, Velthorst E, Bobes J, Bernardo M, Sanjuán J, Luis Santos J, Arrojo M, Marta Del-Ben C, Rossi Menezes P, van der Ven E, Jones PB, Jongsma HE, Kirkbride JB, Tosato S, Lasalvia A, Richards A, O'Donovan M, Rutten BPF, van Os J, Morgan C, Sham PC, Di Forti M, Murray RM, Murray GK. Tripoli G, et al. Schizophr Bull. 2022 Sep 1;48(5):1104-1114. doi: 10.1093/schbul/sbac022. Schizophr Bull. 2022. PMID: 35325253 Free PMC article.
Neurexin 1 (NRXN1) deletions in schizophrenia.
Kirov G, Rujescu D, Ingason A, Collier DA, O'Donovan MC, Owen MJ. Kirov G, et al. Schizophr Bull. 2009 Sep;35(5):851-4. doi: 10.1093/schbul/sbp079. Epub 2009 Aug 12. Schizophr Bull. 2009. PMID: 19675094 Free PMC article. Review. No abstract available.
TCF4, schizophrenia, and Pitt-Hopkins Syndrome.
Blake DJ, Forrest M, Chapman RM, Tinsley CL, O'Donovan MC, Owen MJ. Blake DJ, et al. Schizophr Bull. 2010 May;36(3):443-7. doi: 10.1093/schbul/sbq035. Epub 2010 Apr 26. Schizophr Bull. 2010. PMID: 20421335 Free PMC article.
Analysis of neurogranin (NRGN) in schizophrenia.
Smith RL, Knight D, Williams H, Dwyer S, Richards A, Kirov G, O'Donovan MC, Owen MJ. Smith RL, et al. Am J Med Genet B Neuropsychiatr Genet. 2011 Jul;156B(5):532-5. doi: 10.1002/ajmg.b.31191. Epub 2011 May 2. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21538840
Common variants at VRK2 and TCF4 conferring risk of schizophrenia.
Steinberg S, de Jong S; Irish Schizophrenia Genomics Consortium; Andreassen OA, Werge T, Børglum AD, Mors O, Mortensen PB, Gustafsson O, Costas J, Pietiläinen OP, Demontis D, Papiol S, Huttenlocher J, Mattheisen M, Breuer R, Vassos E, Giegling I, Fraser G, Walker N, Tuulio-Henriksson A, Suvisaari J, Lönnqvist J, Paunio T, Agartz I, Melle I, Djurovic S, Strengman E; GROUP; Jürgens G, Glenthøj B, Terenius L, Hougaard DM, Ørntoft T, Wiuf C, Didriksen M, Hollegaard MV, Nordentoft M, van Winkel R, Kenis G, Abramova L, Kaleda V, Arrojo M, Sanjuán J, Arango C, Sperling S, Rossner M, Ribolsi M, Magni V, Siracusano A, Christiansen C, Kiemeney LA, Veldink J, van den Berg L, Ingason A, Muglia P, Murray R, Nöthen MM, Sigurdsson E, Petursson H, Thorsteinsdottir U, Kong A, Rubino IA, De Hert M, Réthelyi JM, Bitter I, Jönsson EG, Golimbet V, Carracedo A, Ehrenreich H, Craddock N, Owen MJ, O'Donovan MC; Wellcome Trust Case Control Consortium 2; Ruggeri M, Tosato S, Peltonen L, Ophoff RA, Collier DA, St Clair D, Rietschel M, Cichon S, Stefansson H, Rujescu D, Stefansson K. Steinberg S, et al. Hum Mol Genet. 2011 Oct 15;20(20):4076-81. doi: 10.1093/hmg/ddr325. Epub 2011 Jul 26. Hum Mol Genet. 2011. PMID: 21791550 Free PMC article.
De novo mutation in schizophrenia.
Rees E, Kirov G, O'Donovan MC, Owen MJ. Rees E, et al. Schizophr Bull. 2012 May;38(3):377-81. doi: 10.1093/schbul/sbs047. Epub 2012 Mar 26. Schizophr Bull. 2012. PMID: 22451492 Free PMC article.
1,300 results