Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: SCN7A[original query] |
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[Association of single nucleotide polymorphism in human SCN7A gene with essential hypertension in Chinese]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2003 Dec 20 (6): 463-7. Zhang Kui-xing, Zhu Ding-liang, He Xin, Zhang Yi, Zhang Hao, Zhao Rong, Lin Jie, Wang Gu-liang, Zhang Kai-yue, Huang W |
Genetic variations associated with echocardiographic left ventricular traits in hypertensive blacks. Hypertension 2007 May 49 (5): 992-9. Meyers Kristin J, Mosley Thomas H, Fox Ervin, Boerwinkle Eric, Arnett Donna K, Devereux Richard B, Kardia Sharon L |
SCN1A variations and response to multiple antiepileptic drugs. The pharmacogenomics journal 2014 Aug 14 (4): 385-9. Yip T S C, O'Doherty C, Tan N C K, Dibbens L M, Suppiah |
Whole-exome sequencing characterizes the landscape of somatic mutations and copy number alterations in adrenocortical carcinoma. The Journal of clinical endocrinology and metabolism 2015 Mar 100 (3): E493-502. Juhlin C Christofer, Goh Gerald, Healy James M, Fonseca Annabelle L, Scholl Ute I, Stenman Adam, Kunstman John W, Brown Taylor C, Overton John D, Mane Shrikant M, Nelson-Williams Carol, Bäckdahl Martin, Suttorp Anna-Carinna, Haase Matthias, Choi Murim, Schlessinger Joseph, Rimm David L, Höög Anders, Prasad Manju L, Korah Reju, Larsson Catharina, Lifton Richard P, Carling Tobi |
The association between the polymorphisms in a sodium channel gene SCN7A and essential hypertension: a case-control study in the Northern Han Chinese. Annals of human genetics 2015 Jan 79 (1): 28-36. Zhang Bei, Li Mei, Wang Lijuan, Li Chuang, Lou Yuqing, Liu Jielin, Liu Ya, Wang Zuoguang, Wen Shaoj |
Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1. BMC medical genetics 2014 15 (1): 2. Xu Wei, Cohen-Woods Sarah, Chen Qian, Noor Abdul, Knight Jo, Hosang Georgina, Parikh Sagar V, De Luca Vincenzo, Tozzi Federica, Muglia Pierandrea, Forte Julia, McQuillin Andrew, Hu Pingzhao, Gurling Hugh M D, Kennedy James L, McGuffin Peter, Farmer Anne, Strauss John, Vincent John |
Germline mutations in young non-smoking women with lung adenocarcinoma. Lung cancer (Amsterdam, Netherlands) 2018 7 122 76-82. Donner Iikki, Katainen Riku, Sipilä Lauri J, Aavikko Mervi, Pukkala Eero, Aaltonen Lauri |
Genomic signatures reveal DNA damage response deficiency in colorectal cancer brain metastases. Nature communications 2019 7 10 (1): 3190. Sun Jing, Wang Cheng, Zhang Yi, Xu Lingyan, Fang Weijia, Zhu Yuping, Zheng Yi, Chen Xiaofeng, Xie Xiju, Hu Xinhua, Hu Weidong, Zheng Jingyu, Li Ping, Yu Jian, Mei Zhu, Cai Xiaomin, Wang Biao, Hu Zhibin, Shu Yongqian, Shen Hongbing, Gu Yanho |
Methylome analysis of ALS patients and presymptomatic mutation carriers in blood cells. Neurobiology of aging 2022 5 116 16-24. Ruf Wolfgang P, Hannon Eilis, Freischmidt Axel, Grozdanov Veselin, Brenner David, Müller Kathrin, Knehr Antje, Günther Kornelia, Dorst Johannes, Ammerpohl Ole, Danzer Karin M, Mill Jonathan, Ludolph Albert C, Weishaupt Jochen |
Peripheral Ion Channel Genes Screening in Painful Small Fiber Neuropathy. International journal of molecular sciences 2022 11 23 (22): . ?l?czkowska Milena, Almomani Rowida, Marchi Margherita, Salvi Erika, de Greef Bianca T A, Sopacua Maurice, Hoeijmakers Janneke G J, Lindsey Patrick, Waxman Stephen G, Lauria Giuseppe, Faber Catharina G, Smeets Hubert J M, Gerrits Monique |
Genomic analyses reveal SCN7A is associated with the prognosis of esophageal squamous cell carcinoma. Esophagus : official journal of the Japan Esophageal Society 2022 1 19 (2): 303-315. Yuan Ping, Rao Wenqing, Lin Zheng, Liu Shuang, Lin Xiuquan, Wu Chaofeng, Lin Xu, Hu Zhijian, Ye Weim |
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- Page last updated:Mar 25, 2024
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