These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
212 related articles for article (PubMed ID: 27211562)
1. Phenotypically distinct subtypes of psychosis accompany novel or rare variants in four different signaling genes. Kranz TM; Berns A; Shields J; Rothman K; Walsh-Messinger J; Goetz RR; Chao MV; Malaspina D EBioMedicine; 2016 Apr; 6():206-214. PubMed ID: 27211562 [TBL] [Abstract][Full Text] [Related]
2. De novo mutations from sporadic schizophrenia cases highlight important signaling genes in an independent sample. Kranz TM; Harroch S; Manor O; Lichtenberg P; Friedlander Y; Seandel M; Harkavy-Friedman J; Walsh-Messinger J; Dolgalev I; Heguy A; Chao MV; Malaspina D Schizophr Res; 2015 Aug; 166(1-3):119-24. PubMed ID: 26091878 [TBL] [Abstract][Full Text] [Related]
3. Prefrontal neuronal integrity predicts symptoms and cognition in schizophrenia and is sensitive to genetic heterogeneity. Malaspina D; Kranz TM; Heguy A; Harroch S; Mazgaj R; Rothman K; Berns A; Hasan S; Antonius D; Goetz R; Lazar M; Chao MV; Gonen O Schizophr Res; 2016 Apr; 172(1-3):94-100. PubMed ID: 26925801 [TBL] [Abstract][Full Text] [Related]
4. Rare variants in the neurotrophin signaling pathway implicated in schizophrenia risk. Kranz TM; Goetz RR; Walsh-Messinger J; Goetz D; Antonius D; Dolgalev I; Heguy A; Seandel M; Malaspina D; Chao MV Schizophr Res; 2015 Oct; 168(1-2):421-8. PubMed ID: 26215504 [TBL] [Abstract][Full Text] [Related]
5. Rare missense coding variants in oxytocin receptor (OXTR) in schizophrenia cases are associated with early trauma exposure, cognition and emotional processing. Veras AB; Getz M; Froemke RC; Nardi AE; Alves GS; Walsh-Messinger J; Chao MV; Kranz TM; Malaspina D J Psychiatr Res; 2018 Feb; 97():58-64. PubMed ID: 29190530 [TBL] [Abstract][Full Text] [Related]
6. Support for the N-methyl-D-aspartate receptor hypofunction hypothesis of schizophrenia from exome sequencing in multiplex families. Timms AE; Dorschner MO; Wechsler J; Choi KY; Kirkwood R; Girirajan S; Baker C; Eichler EE; Korvatska O; Roche KW; Horwitz MS; Tsuang DW JAMA Psychiatry; 2013 Jun; 70(6):582-90. PubMed ID: 23553203 [TBL] [Abstract][Full Text] [Related]
7. Whole-genome sequencing in multiplex families with psychoses reveals mutations in the SHANK2 and SMARCA1 genes segregating with illness. Homann OR; Misura K; Lamas E; Sandrock RW; Nelson P; McDonough SI; DeLisi LE Mol Psychiatry; 2016 Dec; 21(12):1690-1695. PubMed ID: 27001614 [TBL] [Abstract][Full Text] [Related]
8. GRIN3B missense mutation as an inherited risk factor for schizophrenia: whole-exome sequencing in a family with a familiar history of psychotic disorders. Hornig T; Grüning B; Kundu K; Houwaart T; Backofen R; Biber K; Normann C Genet Res (Camb); 2017 Jan; 99():e1. PubMed ID: 28132660 [TBL] [Abstract][Full Text] [Related]
9. Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population. Moens LN; De Rijk P; Reumers J; Van den Bossche MJ; Glassee W; De Zutter S; Lenaerts AS; Nordin A; Nilsson LG; Medina Castello I; Norrback KF; Goossens D; Van Steen K; Adolfsson R; Del-Favero J PLoS One; 2011; 6(8):e23450. PubMed ID: 21853134 [TBL] [Abstract][Full Text] [Related]
10. Mixture model clustering of phenotype features reveals evidence for association of DTNBP1 to a specific subtype of schizophrenia. Wessman J; Paunio T; Tuulio-Henriksson A; Koivisto M; Partonen T; Suvisaari J; Turunen JA; Wedenoja J; Hennah W; Pietiläinen OP; Lönnqvist J; Mannila H; Peltonen L Biol Psychiatry; 2009 Dec; 66(11):990-6. PubMed ID: 19782967 [TBL] [Abstract][Full Text] [Related]
11. [Interest of a new instrument to assess cognition in schizophrenia: The Brief Assessment of Cognition in Schizophrenia (BACS)]. Bralet MC; Navarre M; Eskenazi AM; Lucas-Ross M; Falissard B Encephale; 2008 Dec; 34(6):557-62. PubMed ID: 19081451 [TBL] [Abstract][Full Text] [Related]
12. Polygenic risk for schizophrenia and measured domains of cognition in individuals with psychosis and controls. Shafee R; Nanda P; Padmanabhan JL; Tandon N; Alliey-Rodriguez N; Kalapurakkel S; Weiner DJ; Gur RE; Keefe RSE; Hill SK; Bishop JR; Clementz BA; Tamminga CA; Gershon ES; Pearlson GD; Keshavan MS; Sweeney JA; McCarroll SA; Robinson EB Transl Psychiatry; 2018 Apr; 8(1):78. PubMed ID: 29643358 [TBL] [Abstract][Full Text] [Related]
14. Effect of DISC1 polymorphisms on the long-term course of neurocognitive deficits in non-affective psychosis. Vázquez-Bourgon J; Ayesa-Arriola R; Fatjó-Vilas M; Roiz-Santiañez R; Fañanás L; Crespo-Facorro B Eur Psychiatry; 2015 Oct; 30(7):861-7. PubMed ID: 26443054 [TBL] [Abstract][Full Text] [Related]
15. Rare UNC13B variations and risk of schizophrenia: Whole-exome sequencing in a multiplex family and follow-up resequencing and a case-control study. Egawa J; Hoya S; Watanabe Y; Nunokawa A; Shibuya M; Ikeda M; Inoue E; Okuda S; Kondo K; Saito T; Kaneko N; Muratake T; Igeta H; Iwata N; Someya T Am J Med Genet B Neuropsychiatr Genet; 2016 Sep; 171(6):797-805. PubMed ID: 26990377 [TBL] [Abstract][Full Text] [Related]
16. A Missense Variant in CASKIN1's Proline-Rich Region Segregates with Psychosis in a Three-Generation Family. Wahbeh MH; Peng X; Bacharaki S; Hatzimanolis A; Dimitrakopoulos S; Wohler E; Yang X; Yovo C; Maher BJ; Sobreira N; Stefanis NC; Avramopoulos D Genes (Basel); 2023 Jan; 14(1):. PubMed ID: 36672919 [TBL] [Abstract][Full Text] [Related]
17. Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism. Chen R; Davis LK; Guter S; Wei Q; Jacob S; Potter MH; Cox NJ; Cook EH; Sutcliffe JS; Li B Mol Autism; 2017; 8():14. PubMed ID: 28344757 [TBL] [Abstract][Full Text] [Related]
18. Resequencing and association analysis of PTPRA, a possible susceptibility gene for schizophrenia and autism spectrum disorders. Xing J; Wang C; Kimura H; Takasaki Y; Kunimoto S; Yoshimi A; Nakamura Y; Koide T; Banno M; Kushima I; Uno Y; Okada T; Aleksic B; Ikeda M; Iwata N; Ozaki N PLoS One; 2014; 9(11):e112531. PubMed ID: 25393624 [TBL] [Abstract][Full Text] [Related]
19. Resequencing and association analysis of coding regions at twenty candidate genes suggest a role for rare risk variation at AKAP9 and protective variation at NRXN1 in schizophrenia susceptibility. Suárez-Rama JJ; Arrojo M; Sobrino B; Amigo J; Brenlla J; Agra S; Paz E; Brión M; Carracedo Á; Páramo M; Costas J J Psychiatr Res; 2015; 66-67():38-44. PubMed ID: 25943950 [TBL] [Abstract][Full Text] [Related]
20. De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia. Rees E; Han J; Morgan J; Carrera N; Escott-Price V; Pocklington AJ; Duffield M; Hall LS; Legge SE; Pardiñas AF; Richards AL; Roth J; Lezheiko T; Kondratyev N; Kaleda V; Golimbet V; Parellada M; González-Peñas J; Arango C; ; Gawlik M; Kirov G; Walters JTR; Holmans P; O'Donovan MC; Owen MJ Nat Neurosci; 2020 Feb; 23(2):179-184. PubMed ID: 31932766 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]