Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: SETD1A[original query] |
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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 |
Genetic mutational status of genes regulating epigenetics: Role of the histone methyltransferase KMT2D in triple negative breast tumors. PloS one 2019 4 14 (4): e0209134. Morcillo-Garcia Sara, Noblejas-Lopez Maria Del Mar, Nieto-Jimenez Cristina, Perez-Peña Javier, Nuncia-Cantarero Miriam, Gy?rffy Balázs, Amir Eitan, Pandiella Atanasio, Galan-Moya Eva M, Ocana Alber |
Genetic Associations With Stable Warfarin Dose Requirements in Han Chinese Patients. Journal of cardiovascular pharmacology 2021 5 78 (1): e105-e111. Xu Qingqing, Zhang Suli, Wu Chaoneng, Xiong Yuyu, Niu Jiamin, Li Fengzhen, Zhu Jinhang, Shen Lu, Zhu Bin, Xing Qinghe, He Lin, Chen Luan, Li Mo, Li Hua, Ge Junbo, Qin Shengyi |
Clinical features of UK Biobank subjects carrying protein-truncating variants in genes implicated in schizophrenia pathogenesis. Psychiatric genetics 2022 Jun . Curtis Dav |
Genetic investigation of syndromic forms of obesity. International journal of obesity (2005) 2022 May . Carvalho Laura Machado Lara, D'Angelo Carla Sustek, Villela Darine, da Costa Silvia Souza, de Lima Jorge Alexander Augusto, da Silva Israel Tojal, de Oliveira Scliar Marília, Chaves Luiza Dias, Krepischi Ana Cristina Victorino, Koiffmann Celia Priszkulnik, Rosenberg Car |
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 |
Epigenotype-genotype-phenotype correlations in SETD1A and SETD2 chromatin disorders. Human molecular genetics 2023 5 . Sunwoo Lee, Lara Menzies, Eleanor Hay, Eguzkine Ochoa, France Docquier, Fay Rodger, Charu Deshpande, Nicola C Foulds, Sébastien Jacquemont, Khadije Jizi, Henriette Kiep, Alison Kraus, Katharina Löhner, Patrick J Morrison, Bernt Popp, Ruth Richardson, Arie Haeringen, Ezequiel Martin, Ana Toribio, Fudong Li, Wendy D Jones, Francis H Sansbury, Eamonn R Mah |
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- Page last updated:Apr 22, 2024
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