Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Schizophrenia and AUTS2[original query] |
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Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes. Molecular psychiatry 2010 Jun 15 (6): 637-46. Elia J, Gai X, Xie H M, Perin J C, Geiger E, Glessner J T, D'arcy M, deBerardinis R, Frackelton E, Kim C, Lantieri F, Muganga B M, Wang L, Takeda T, Rappaport E F, Grant S F A, Berrettini W, Devoto M, Shaikh T H, Hakonarson H, White P |
Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies. PLoS genetics 2010 May 6 (5): e1000962. Mefford Heather C, Muhle Hiltrud, Ostertag Philipp, von Spiczak Sarah, Buysse Karen, Baker Carl, Franke Andre, Malafosse Alain, Genton Pierre, Thomas Pierre, Gurnett Christina A, Schreiber Stefan, Bassuk Alexander G, Guipponi Michel, Stephani Ulrich, Helbig Ingo, Eichler Evan |
Increased de novo copy number variants in the offspring of older males. Translational psychiatry 2012 7 1 (8): e34. Flatscher-Bader T, Foldi C J, Chong S, Whitelaw E, Moser R J, Burne T H J, Eyles D W, McGrath J |
Association study identifying a new susceptibility gene (AUTS2) for schizophrenia. International journal of molecular sciences 2014 15 (11): 19406-16. Zhang Bao, Xu Yue-Hong, Wei Shu-Guang, Zhang Hong-Bo, Fu Dong-Ke, Feng Zu-Fei, Guan Fang-Lin, Zhu Yong-Sheng, Li Sheng-B |
Effect of AUTS2 gene rs6943555 variant in male patients with schizophrenia in a Turkish population. Gene 2020 6 756 144913. Ozsoy Filiz, Karakus Nevin Balci, Yigit Serbulent, Kulu Muber |
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- Page last updated:Apr 22, 2024
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