Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: Abnormalities and HTT[original query] |
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Attempted suicide and polymorphism of the serotonin transporter gene in Chinese patients with schizophrenia. Psychiatry research 2000 Dec 97 (2-3): 101-6. Chong S A, Lee W L, Tan C H, Tay A H, Chan A O, Tan E |
Serotonin transporter and tryptophan hydroxylase gene polymorphisms in Chinese patients with generalized anxiety disorder. Psychiatric genetics 2005 Mar 15 (1): 7-11. You Jin-Song, Hu Sui-Yu, Chen Binglai, Zhang Hong-G |
Genetic and expression analyses reveal elevated expression of syntaxin 1A ( STX1A) in high functioning autism. The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP) 2008 Dec 11 (8): 1073-84. Nakamura Kazuhiko, Anitha Ayyappan, Yamada Kazuo, Tsujii Masatsugu, Iwayama Yoshimi, Hattori Eiji, Toyota Tomoko, Suda Shiro, Takei Noriyoshi, Iwata Yasuhide, Suzuki Katsuaki, Matsuzaki Hideo, Kawai Masayoshi, Sekine Yoshimoto, Tsuchiya Kenji J, Sugihara Gen-Ichi, Ouchi Yasuomi, Sugiyama Toshiro, Yoshikawa Takeo, Mori Nor |
Reported childhood abuse is associated with low serotonin transporter binding in vivo in major depressive disorder. Synapse (New York, N.Y.) 2009 Jul 63 (7): 565-73. Miller Jeffrey M, Kinnally Erin L, Ogden R Todd, Oquendo Maria A, Mann J John, Parsey Ramin |
The gene coding for PGC-1alpha modifies age at onset in Huntington's Disease. Molecular neurodegeneration 2009 4 (1): 3. Weydt Patrick, Soyal Selma M, Gellera Cinzia, Didonato Stefano, Weidinger Claus, Oberkofler Hannes, Landwehrmeyer G Bernhard, Patsch Wolfga |
Systemic energy homeostasis in Huntington's disease patients. Journal of neurology, neurosurgery, and psychiatry 2010 Nov 81 (11): 1233-7. Aziz N Ahmad, Pijl Hanno, Frölich Marijke, Snel Marieke, Streefland Trea C M, Roelfsema Ferdinand, Roos Raymund A |
Replication study of Japanese cohorts supports the role of STX1A in autism susceptibility. Progress in neuro-psychopharmacology & biological psychiatry 2011 Mar 35 (2): 454-8. Nakamura Kazuhiko, Iwata Yasuhide, Anitha Ayyappan, Miyachi Taishi, Toyota Tomoko, Yamada Satoru, Tsujii Masatsugu, Tsuchiya Kenji J, Iwayama Yoshimi, Yamada Kazuo, Hattori Eiji, Matsuzaki Hideo, Matsumoto Kaori, Suzuki Katsuaki, Suda Shiro, Takebayashi Kiyokazu, Takei Nori, Ichikawa Hironobu, Sugiyama Toshiro, Yoshikawa Takeo, Mori Nor |
Insulin sensitivity and early-phase insulin secretion in normoglycemic Huntington's disease patients. Journal of Huntington's disease 2013 2 (4): 501-7. Russo Cinzia V, Salvatore Elena, Saccà Francesco, Tucci Tecla, Rinaldi Carlo, Sorrentino Pierpaolo, Massarelli Marco, Rossi Fabiana, Savastano Silvia, Di Maio Luigi, Filla Alessandro, Colao Annamaria, De Michele Giusep |
The First 5-Year-Long Survey on Intrauterine Unexplained Sudden Deaths from the Northeast Italy. Fetal and pediatric pathology 2016 Jun 1-12. Roncati Luca, Pusiol Teresa, Piscioli Francesco, Barbolini Giuseppe, Maiorana Antonio, Lavezzi An |
Developmental malformations in Huntington disease: neuropathologic evidence of focal neuronal migration defects in a subset of adult brains. Acta neuropathologica 2021 1 141 (3): 399-413. Hickman R A, Faust P L, Rosenblum M K, Marder K, Mehler M F, Vonsattel J |
DNA methylation age acceleration is associated with age of onset in Chinese spinocerebellar ataxia type 3 patients. Neurobiology of aging 2022 3 113 1-6. Li Jiahao, Shu Anli, Sun Yimin, Yang Wanli, Tang Xuelin, Pu Hongjiang, Peng Yun, Hu Xiaowen, Qing Ying, Wang Jian, Wan Chunling, Zhou Mingcheng, Zhang Mi |
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- Page last updated:Apr 16, 2024
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