Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Syndrome and DISC1[original query] |
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| Evidence for statistical epistasis between catechol-O-methyltransferase (COMT) and polymorphisms in RGS4, G72 (DAOA), GRM3, and DISC1: influence on risk of schizophrenia. Human genetics 2007 Feb 120 (6): 889-906. Nicodemus Kristin K, Kolachana Bhaskar S, Vakkalanka Radhakrishna, Straub Richard E, Giegling Ina, Egan Michael F, Rujescu Dan, Weinberger Daniel |
| Association of DISC1 with autism and Asperger syndrome. Molecular psychiatry 2008 Feb 13 (2): 187-96. Kilpinen H, Ylisaukko-Oja T, Hennah W, Palo O M, Varilo T, Vanhala R, Nieminen-von Wendt T, von Wendt L, Paunio T, Peltonen |
| DISC1 association, heterogeneity and interplay in schizophrenia and bipolar disorder. Molecular psychiatry 2009 Sep 14 (9): 865-73. Hennah W, Thomson P, McQuillin A, Bass N, Loukola A, Anjorin A, Blackwood D, Curtis D, Deary I J, Harris S E, Isometsä E T, Lawrence J, Lönnqvist J, Muir W, Palotie A, Partonen T, Paunio T, Pylkkö E, Robinson M, Soronen P, Suominen K, Suvisaari J, Thirumalai S, St Clair D, Gurling H, Peltonen L, Porteous |
| A threonine to isoleucine missense mutation in the pericentriolar material 1 gene is strongly associated with schizophrenia. Molecular psychiatry 2010 Jun 15 (6): 615-28. Datta S R, McQuillin A, Rizig M, Blaveri E, Thirumalai S, Kalsi G, Lawrence J, Bass N J, Puri V, Choudhury K, Pimm J, Crombie C, Fraser G, Walker N, Curtis D, Zvelebil M, Pereira A, Kandaswamy R, St Clair D, Gurling H M |
| Association between genes of Disrupted in schizophrenia 1 (DISC1) interactors and schizophrenia supports the role of the DISC1 pathway in the etiology of major mental illnesses. Biological psychiatry 2009 Jun 65 (12): 1055-62. Tomppo Liisa, Hennah William, Lahermo Päivi, Loukola Anu, Tuulio-Henriksson Annamari, Suvisaari Jaana, Partonen Timo, Ekelund Jesper, Lönnqvist Jouko, Peltonen Lee |
| A functional polymorphism in the disrupted-in schizophrenia 1 gene is associated with chronic fatigue syndrome. Life sciences 2010 May 86 (19-20): 722-5. Fukuda Sanae, Hashimoto Ryota, Ohi Kazutaka, Yamaguti Kouzi, Nakatomi Yasuhito, Yasuda Yuka, Kamino Kouzin, Takeda Masatoshi, Tajima Seiki, Kuratsune Hirohiko, Nishizawa Yoshiki, Watanabe Yasuyos |
| Evidence for association between Disrupted-in-Schizophrenia 1 (DISC1) gene polymorphisms and autism in Chinese Han population: a family-based association study. Behavioral and brain functions : BBF 2011 7 (1): 14. Zheng Fanfan, Wang Lifang, Jia Meixiang, Yue Weihua, Ruan Yan, Lu Tianlan, Liu Jing, Li Jun, Zhang D |
| Limited association between Disrupted in Schizophrenia 1 (DISC1) gene and bipolar disorder in the Chinese population. Psychiatric genetics 2011 Feb 21 (1): 42-6. Xiao Yue, Zhang Jing, Wang Yang, Wang Peng, Li Xingwang, Ji Jue, Yang Fengping, Feng Guoyin, He Lin, He Gua |
| Genetic variability testing of neurodevelopmental genes in schizophrenic patients. Journal of molecular neuroscience : MN 2015 May 56 (1): 205-11. Terzi? Tea, Kastelic Matej, Dolžan Vita, Plesni?ar Blanka Kor |
| Family-Based Analysis Combined with Case-Controls Study Implicate Roles of PCNT in Tourette Syndrome. Neuropsychiatric disease and treatment 2020 16 349-354. Liu Wenmiao, Guo Yixia, Liu Xiumei, Zhang Ru, Dong Jicheng, Deng Hao, He Fan, Che Fengyuan, Liu Shiguo, Yi Ming |
| Structural Variants and Implicated Processes Associated with Familial Tourette Syndrome. International journal of molecular sciences 2024 6 25 (11): . Jakub P Fichna, Mateusz Chili?ski, Anup Kumar Halder, Pawe? Ci?szczyk, Dariusz Plewczynski, Cezary ?ekanowski, Piotr Jan |
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