Human Genome Epidemiology Literature Finder
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Records 1 - 15 (of 15 Records) |
| Query Trace: Disease and CHRNA4[original query] |
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| Association of novel and established polymorphisms in neuronal nicotinic acetylcholine receptors with sporadic Alzheimer's disease. Journal of Alzheimer's disease : JAD 2002 Apr 4 (2): 71-6. Kawamata Jun, Shimohama Sh |
| Polymorphisms of the CHRNA4 gene encoding the alpha4 subunit of nicotinic acetylcholine receptor as related to the oxidative DNA damage and the level of apoptotic proteins in lymphocytes of the patients with Alzheimer's disease. DNA and cell biology 2005 Dec 24 (12): 786-94. Dorszewska Jolanta, Florczak Jolanta, Rózycka Agata, Jaroszewska-Kolecka Joanna, Trzeciak Wieslaw H, Kozubski Wojcie |
| [Polymorphisms of neural nicotinic cholinergic receptor alpha 4 gene of Chinese]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2006 Feb 23 (1): 55-8. Zhang Li-mei, Chen Biao, Feng Xiu-li, Dong Xiu-min, Wang Wei-z |
| CHRNA2 mutations are rare in the NFLE population: evaluation of a large cohort of Italian patients. Sleep medicine 2009 Jan 10 (1): 139-42. Combi Romina, Ferini-Strambi Luigi, Tenchini Maria Lui |
| Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis. Human molecular genetics 2009 Oct 18 (20): 3997-4006. Sabatelli Mario, Eusebi Fabrizio, Al-Chalabi Ammar, Conte Amelia, Madia Francesca, Luigetti Marco, Mancuso Irene, Limatola Cristina, Trettel Flavia, Sobrero Fabrizia, Di Angelantonio Silvia, Grassi Francesca, Di Castro Amalia, Moriconi Claudia, Fucile Sergio, Lattante Serena, Marangi Giuseppe, Murdolo Marina, Orteschi Daniela, Del Grande Alessandra, Tonali Pietro, Neri Giovanni, Zollino Marcel |
| Multiple cholinergic nicotinic receptor genes affect nicotine dependence risk in African and European Americans. Genes, brain, and behavior 2010 Oct 9 (7): 741-50. Saccone N L, Schwantes-An T-H, Wang J C, Grucza R A, Breslau N, Hatsukami D, Johnson E O, Rice J P, Goate A M, Bierut L |
| Genetic variation of CHRNA4 does not modulate attention in Parkinson's disease. Neuroscience letters 2010 Jul 479 (2): 123-5. Hudson Gavin, Stutt Andrea, Eccles Martin, Robinson Louise, Allcock Liesl M, Wesnes Keith A, Chinnery Patrick F, Burn David |
| Most reported genetic associations with general intelligence are probably false positives. Psychological science 2012 23 (11): 1314-23. Chabris Christopher F, Hebert Benjamin M, Benjamin Daniel J, Beauchamp Jonathan, Cesarini David, van der Loos Matthijs, Johannesson Magnus, Magnusson Patrik K E, Lichtenstein Paul, Atwood Craig S, Freese Jeremy, Hauser Taissa S, Hauser Robert M, Christakis Nicholas, Laibson Dav |
| Association of CHRNA4 gene rs1044396 and rs1044397 polymorphisms with Parkinson's disease symptoms and smoking. Genetics and molecular research : GMR 2015 14 (2): 5112-22. Zhang L M, Zhang X P, Chen Y Q, Ye |
| A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences. Molecular psychiatry 2016 May 21 (5): 594-600. Thorgeirsson T E, Steinberg S, Reginsson G W, Bjornsdottir G, Rafnar T, Jonsdottir I, Helgadottir A, Gretarsdottir S, Helgadottir H, Jonsson S, Matthiasson S E, Gislason T, Tyrfingsson T, Gudbjartsson T, Isaksson H J, Hardardottir H, Sigvaldason A, Kiemeney L A, Haugen A, Zienolddiny S, Wolf H J, Franklin W A, Panadero A, Mayordomo J I, Hall I P, Rönmark E, Lundbäck B, Dirksen A, Ashraf H, Pedersen J H, Masson G, Sulem P, Thorsteinsdottir U, Gudbjartsson D F, Stefansson |
| Molecular Genetic Characterization of Patients With Focal Epilepsy Using a Customized Targeted Resequencing Gene Panel. Frontiers in neurology 2018 7 9 515. Tsai Meng-Han, Chan Chung-Kin, Chang Ying-Chao, Lin Chih-Hsiang, Liou Chia-Wei, Chang Wen-Neng, Ng Ching-Ching, Lim Kheng-Seang, Hwang Daw-Ya |
| Epidemiological evidence for associations between variants in CHRNA genes and risk of lung cancer and chronic obstructive pulmonary disease. Frontiers in oncology 2022 12 1001864. Yang Lei, Yang Zelin, Zuo Chunjian, Lv Xiaolong, Liu Tianyu, Jia Chenhao, Chen Huanw |
| Use of dual genomic sequencing to screen mitochondrial diseases in pediatrics: a retrospective analysis. Scientific reports 2023 3 13 (1): 4193. Wu Teng-Hui, Peng Jing, Yang Li, Chen Yan-Hui, Lu Xiu-Lan, Huang Jiao-Tian, You Jie-Yu, Ou-Yang Wen-Xian, Sun Yue-Yu, Xue Yi-Nan, Mao Xiao, Yan Hui-Ming, Ren Rong-Na, Xie Jing, Chen Zhi-Heng, Zhang Victor-Wei, Lyu Gui-Zhen, He Fa |
| Clarifying Chronic Obstructive Pulmonary Disease Genetic Associations Observed in Biobanks via Mediation Analysis of Smoking. AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science 2024 6 2024 499-508. Katrina Bazemore, Jaehyun Joo, Wei-Ting Hwang, Blanca E Him |
| Genome-wide association study identifies novel susceptible loci and evaluation of polygenic risk score for chronic obstructive pulmonary disease in a Taiwanese population. BMC genomics 2024 6 25 (1): 607. Wei-De Lin, Wen-Ling Liao, Wei-Cheng Chen, Ting-Yuan Liu, Yu-Chia Chen, Fuu-Jen Ts |
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