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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 12, 2025. (Total: 235195Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: Schizophrenia and SETD1A[original query]
Loss-of-function variants in schizophrenia risk and SETD1A as a candidate susceptibility gene.
Neuron 2014 May 82 (4): 773-80.
Takata Atsushi, Xu Bin, Ionita-Laza Iuliana, Roos J Louw, Gogos Joseph A, Karayiorgou Mar
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.
Nature neuroscience 2016 Mar .
Singh Tarjinder, Kurki Mitja I, Curtis David, Purcell Shaun M, Crooks Lucy, McRae Jeremy, Suvisaari Jaana, Chheda Himanshu, Blackwood Douglas, Breen Gerome, Pietiläinen Olli, Gerety Sebastian S, Ayub Muhammad, Blyth Moira, Cole Trevor, Collier David, Coomber Eve L, Craddock Nick, Daly Mark J, Danesh John, DiForti Marta, Foster Alison, Freimer Nelson B, Geschwind Daniel, Johnstone Mandy, Joss Shelagh, Kirov Georg, Körkkö Jarmo, Kuismin Outi, Holmans Peter, Hultman Christina M, Iyegbe Conrad, Lönnqvist Jouko, Männikkö Minna, McCarroll Steve A, McGuffin Peter, McIntosh Andrew M, McQuillin Andrew, Moilanen Jukka S, Moore Carmel, Murray Robin M, Newbury-Ecob Ruth, Ouwehand Willem, Paunio Tiina, Prigmore Elena, Rees Elliott, Roberts David, Sambrook Jennifer, Sklar Pamela, St Clair David, Veijola Juha, Walters James T R, Williams Hywel, , , , , Sullivan Patrick F, Hurles Matthew E, O'Donovan Michael C, Palotie Aarno, Owen Michael J, Barrett Jeffrey
De Novo and Inherited SETD1A Variants in Early-onset Epilepsy.
Neuroscience bulletin 2019 6 35 (6): 1045-1057.
Yu Xiuya, Yang Lin, Li Jin, Li Wanxing, Li Dongzhi, Wang Ran, Wu Kai, Chen Wenhao, Zhang Yi, Qiu Zilong, Zhou Wenh
Transcriptional Changes following Cellular Knockdown of the Schizophrenia Risk Gene SETD1A Are Enriched for Common Variant Association with the Disorder.
Molecular neuropsychiatry 2019 6 5 (2): 109-114.
Cameron Darren, Blake Derek J, Bray Nicholas J, Hill Matthew
Assessment of Potential Clinical Role for Exome Sequencing in Schizophrenia.
Schizophrenia bulletin 2019 5 46 (2): 328-335.
Balakrishna Thivia, Curtis Dav
Clinical features of UK Biobank subjects carrying protein-truncating variants in genes implicated in schizophrenia pathogenesis.
Psychiatric genetics 2022 Jun .
Curtis Dav
Novel missense SETD1A variants in Japanese patients with schizophrenia: Resequencing and association analysis.
Psychiatry research 2022 Feb 310 114481.
Morikawa Ryo, Watanabe Yuichiro, Igeta Hirofumi, Arta Reza K, Ikeda Masashi, Okazaki Satoshi, Hoya Satoshi, Saito Takeo, Otsuka Ikuo, Egawa Jun, Tanifuji Takaki, Iwata Nakao, Someya Toshiyu
A case of bipolar I disorder with a loss-of-function variant of schizophrenia risk gene SETD1A: possible expansion of the relevant clinical spectrum supported by a meta-analysis.
Psychiatry and clinical neurosciences 2024 4 .
Tomonori Hara, An-A Kazuno, Tomoko Toyota, Junko Ueda, Takehiko Shuno, Jun Mukai, Taka-Aki Sato, Naomichi Matsumoto, Takeo Yoshikawa, Atsushi Taka
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