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5. Novel missense SETD1A variants in Japanese patients with schizophrenia: Resequencing and association analysis. Morikawa R; Watanabe Y; Igeta H; Arta RK; Ikeda M; Okazaki S; Hoya S; Saito T; Otsuka I; Egawa J; Tanifuji T; Iwata N; Someya T Psychiatry Res; 2022 Apr; 310():114481. PubMed ID: 35235885 [TBL] [Abstract][Full Text] [Related]
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7. Setd1a Insufficiency in Mice Attenuates Excitatory Synaptic Function and Recapitulates Schizophrenia-Related Behavioral Abnormalities. Nagahama K; Sakoori K; Watanabe T; Kishi Y; Kawaji K; Koebis M; Nakao K; Gotoh Y; Aiba A; Uesaka N; Kano M Cell Rep; 2020 Sep; 32(11):108126. PubMed ID: 32937141 [TBL] [Abstract][Full Text] [Related]
8. Loss-of-function variants in the schizophrenia risk gene SETD1A alter neuronal network activity in human neurons through the cAMP/PKA pathway. Wang S; Rhijn JV; Akkouh I; Kogo N; Maas N; Bleeck A; Ortiz IS; Lewerissa E; Wu KM; Schoenmaker C; Djurovic S; van Bokhoven H; Kleefstra T; Nadif Kasri N; Schubert D Cell Rep; 2022 May; 39(5):110790. PubMed ID: 35508131 [TBL] [Abstract][Full Text] [Related]
9. SETD1A variant-associated psychosis: A systematic review of the clinical literature and description of two new cases. Colijn MA; Carrion P; Poirier-Morency G; Rogic S; Torres I; Menon M; Lisonek M; Cook C; DeGraaf A; Thammaiah SP; Neelakant H; Willaeys V; Leonova O; White RF; Yip S; Mungall AJ; MacLeod PM; Gibson WT; Sullivan PF; Honer WG; Pavlidis P; Stowe RM Prog Neuropsychopharmacol Biol Psychiatry; 2024 Feb; 129():110888. PubMed ID: 37918557 [TBL] [Abstract][Full Text] [Related]
10. Developmental disruption to the cortical transcriptome and synaptosome in a model of SETD1A loss-of-function. Clifton NE; Bosworth ML; Haan N; Rees E; Holmans PA; Wilkinson LS; Isles AR; Collins MO; Hall J Hum Mol Genet; 2022 Sep; 31(18):3095-3106. PubMed ID: 35531971 [TBL] [Abstract][Full Text] [Related]
11. Recapitulation and Reversal of Schizophrenia-Related Phenotypes in Setd1a-Deficient Mice. Mukai J; Cannavò E; Crabtree GW; Sun Z; Diamantopoulou A; Thakur P; Chang CY; Cai Y; Lomvardas S; Takata A; Xu B; Gogos JA Neuron; 2019 Nov; 104(3):471-487.e12. PubMed ID: 31606247 [TBL] [Abstract][Full Text] [Related]
12. 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]
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14. De Novo and Inherited SETD1A Variants in Early-onset Epilepsy. Yu X; Yang L; Li J; Li W; Li D; Wang R; Wu K; Chen W; Zhang Y; Qiu Z; Zhou W Neurosci Bull; 2019 Dec; 35(6):1045-1057. PubMed ID: 31197650 [TBL] [Abstract][Full Text] [Related]
15. Common genetic variants contribute to risk of rare severe neurodevelopmental disorders. Niemi MEK; Martin HC; Rice DL; Gallone G; Gordon S; Kelemen M; McAloney K; McRae J; Radford EJ; Yu S; Gecz J; Martin NG; Wright CF; Fitzpatrick DR; Firth HV; Hurles ME; Barrett JC Nature; 2018 Oct; 562(7726):268-271. PubMed ID: 30258228 [TBL] [Abstract][Full Text] [Related]
16. The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability. Singh T; Walters JTR; Johnstone M; Curtis D; Suvisaari J; Torniainen M; Rees E; Iyegbe C; Blackwood D; McIntosh AM; Kirov G; Geschwind D; Murray RM; Di Forti M; Bramon E; Gandal M; Hultman CM; Sklar P; ; ; Palotie A; Sullivan PF; O'Donovan MC; Owen MJ; Barrett JC Nat Genet; 2017 Aug; 49(8):1167-1173. PubMed ID: 28650482 [TBL] [Abstract][Full Text] [Related]
17. Clinical features of UK Biobank subjects carrying protein-truncating variants in genes implicated in schizophrenia pathogenesis. Curtis D Psychiatr Genet; 2022 Aug; 32(4):156-161. PubMed ID: 35749744 [TBL] [Abstract][Full Text] [Related]
18. Epigenotype-genotype-phenotype correlations in SETD1A and SETD2 chromatin disorders. Lee S; Menzies L; Hay E; Ochoa E; Docquier F; Rodger F; Deshpande C; Foulds NC; Jacquemont S; Jizi K; Kiep H; Kraus A; Löhner K; Morrison PJ; Popp B; Richardson R; van Haeringen A; Martin E; Toribio A; Li F; Jones WD; Sansbury FH; Maher ER Hum Mol Genet; 2023 Nov; 32(22):3123-3134. PubMed ID: 37166351 [TBL] [Abstract][Full Text] [Related]
19. SETD1A Mediated H3K4 Methylation and Its Role in Neurodevelopmental and Neuropsychiatric Disorders. Wang S; Bleeck A; Nadif Kasri N; Kleefstra T; van Rhijn JR; Schubert D Front Mol Neurosci; 2021; 14():772000. PubMed ID: 34803610 [TBL] [Abstract][Full Text] [Related]
20. Assessment of Potential Clinical Role for Exome Sequencing in Schizophrenia. Balakrishna T; Curtis D Schizophr Bull; 2020 Feb; 46(2):328-335. PubMed ID: 31112269 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]