Human Genome Epidemiology Literature Finder
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Records 1 - 14 (of 14 Records) |
| Query Trace: Schizophrenia and ZDHHC8[original query] |
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| Case-control study and transmission disequilibrium test provide consistent evidence for association between schizophrenia and genetic variation in the 22q11 gene ZDHHC8. Human molecular genetics 2004 Dec 13 (23): 2991-5. Chen Wu-Yan, Shi Yong-Yong, Zheng Yong-Lan, Zhao Xin-Zhi, Zhang Guang-Ji, Chen Sheng-Qi, Yang Pei-Di, He L |
| The ZDHHC8 gene did not associate with bipolar disorder or schizophrenia. Neuroscience letters 2005 Dec 390 (3): 166-70. Otani Kyohei, Ujike Hiroshi, Tanaka Yuji, Morita Yukitaka, Kishimoto Makiko, Morio Akiko, Uchida Naohiko, Nomura Akira, Kuroda Shigetos |
| No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples. Biological psychiatry 2005 Jul 58 (1): 78-80. Glaser Beate, Schumacher Johannes, Williams Hywel J, Jamra Rami Abou, Ianakiev Nikolai, Milev Radoi, Ohlraun Stephanie, Schulze Thomas G, Czerski Piotr M, Hauser Joanna, Jönsson Erick G, Sedvall Göran C, Klopp Norman, Illig Thomas, Becker Tim, Propping Peter, Williams Nigel M, Cichon Sven, Kirov George, Rietschel Marcella, Murphy Kieran C, O'Donovan Michael C, Nöthen Markus M, Owen Michael |
| ZDHHC8 as a candidate gene for schizophrenia: analysis of a putative functional intronic marker in case-control and family-based association studies. BMC psychiatry 2005 5 (): 35. Faul Thomas, Gawlik Micha, Bauer Martin, Jung Sven, Pfuhlmann Bruno, Jabs Burkhard, Knapp Michael, Stöber Gera |
| No association was found between a functional SNP in ZDHHC8 and schizophrenia in a Japanese case-control population. Neuroscience letters 2005 Feb 374 (1): 21-4. Saito Shinichi, Ikeda Masashi, Iwata Nakao, Suzuki Tatsuyo, Kitajima Tsuyoshi, Yamanouchi Yoshio, Kinoshita Yoko, Takahashi Nagahide, Inada Toshiya, Ozaki Nor |
| Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility. Schizophrenia research 2006 Oct 87 (1-3): 21-7. Glaser Beate, Moskvina Valentina, Kirov George, Murphy Kieran C, Williams Hywel, Williams Nigel, Owen Michael J, O'Donovan Michael |
| HTF9C gene of 22q11.21 region associates with schizophrenia having deficit-sustained attention. Psychiatric genetics 2007 Dec 17 (6): 333-8. Liu Yu-Li, Fann Cathy Shen-Jang, Liu Chih-Min, Chang Chien Ching, Yang Wei-Chih, Wu Jer-Yuarn, Hung Shuen-Iu, Chan Hung-Yu, Chen Jiahn-Jyh, Hsieh Ming H, Hwang Tzung-Jeng, Faraone Stephen V, Tsuang Ming T, Chen Wei J, Hwu Hai-G |
| Testing for genetic association between the ZDHHC8 gene locus and susceptibility to schizophrenia: An integrated analysis of multiple datasets. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010 Oct 153B (7): 1266-75. Xu Mingqing, St Clair David, He L |
| Association of ZDHHC8 polymorphisms with smooth pursuit eye movement abnormality. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010 Sep 153B (6): 1167-72. Shin Hyoung Doo, Park Byung Lae, Bae Joon Seol, Park Tae Joon, Chun Ji Yong, Park Chul Soo, Sohn Jin-Wook, Kim Bong-Jo, Kang Yeo-Hwa, Kim Jae Won, Kim Ki-Hoon, Shin Tae-Min, Woo Sung- |
| ZDHHC8 gene may play a role in cortical volumes of patients with schizophrenia. Schizophrenia research 2013 Apr 145 (1-3): 33-5. Ota Vanessa K, Gadelha Ary, Assunção Idaiane B, Santoro Marcos L, Christofolini Denise M, Bellucco Fernanda T, Santos-Filho Airton F, Ottoni Gustavo L, Lara Diogo R, Mari Jair J, Melaragno Maria I, Smith Marília A C, Bressan Rodrigo A, Belangero Sintia I, Jackowski Andrea |
| Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome. The Journal of biological chemistry 2015 Sep 290 (38): 23240-53. Napoli Eleonora, Tassone Flora, Wong Sarah, Angkustsiri Kathleen, Simon Tony J, Song Gyu, Giulivi Cecil |
| Linkage and Association Analyses of Schizophrenia with Genetic Variations on Chromosome 22q11 in Koreans. Psychiatry investigation 2016 Nov 13 (6): 630-636. Yoon Se Chang, Jang Yong Lee, Kim Jong-Won, Cho Eun-Young, Park Dong Yeon, Hong Kyung Sue, Lee Yu Sa |
| Lack of association between COMT Val158Met and ZDHHC8 rs175174 polymorphisms and susceptibility to schizophrenia in a Brazilian population. Psychiatric genetics 2017 May . Moraes Leopoldo S, Santos Augusto C C, Ferreira-Fernandes Hygor, Yoshioka France K N, Teixeira Silmar S, Guimarães Adriana C, da Rocha Carlos A M, Rey Juan A, Pinto Giovanny R, Burbano Rommel |
| Associations between neurodevelopmental genes, neuroanatomy, and ultra high risk symptoms of psychosis in 22q11.2 deletion syndrome. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2017 Jan . Thompson Carlie A, Karelis Jason, Middleton Frank A, Gentile Karen, Coman Ioana L, Radoeva Petya D, Mehta Rashi, Fremont Wanda P, Antshel Kevin M, Faraone Stephen V, Kates Wendy |
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