Human Genome Epidemiology Literature Finder
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Records 1 - 12 (of 12 Records) |
| Query Trace: Disease and STX1B[original query] |
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| A two-stage meta-analysis identifies several new loci for Parkinson's disease. PLoS genetics 2011 Jun 7 (6): e1002142. , |
| Supportive evidence for 11 loci from genome-wide association studies in Parkinson's disease. Neurobiology of aging 2012 Nov . Pihlstrøm L, Axelsson G, Bjørnarå KA, Dizdar N, Fardell C, Forsgren L, Holmberg B, Larsen JP, Linder J, Nissbrandt H, Tysnes OB, Ohman E, Dietrichs E, Toft M |
| High-density genotyping of immune loci in Kawasaki disease and IVIG treatment response in European-American case-parent trio study. Genes and immunity 2014 Dec 15 (8): 534-42. Shendre A, Wiener H W, Zhi D, Vazquez A I, Portman M A, Shrestha |
| The RIT2 and STX1B polymorphisms are associated with Parkinson's disease. Parkinsonism & related disorders 2015 Mar 21 (3): 300-2. Wang Jian-Yong, Gong Mei-Ying, Ye Yang-Lie, Ye Jin-Min, Lin Guo-Liang, Zhuang Qing-Qing, Zhang Xiong, Zhu Jian-Ho |
| No association of FAM47E rs6812193, SCARB2 rs6825004 and STX1B rs4889603 polymorphisms with Parkinson's disease in a Chinese Han population. Journal of neural transmission (Vienna, Austria : 1996) 2015 Jul . Chen YongPing, Yuan XiaoQin, Cao Bei, Wei QianQian, Ou RuWei, Yang Jing, Chen XuePing, Zhao Bi, Song Wei, Wu Ying, Shang HuiFa |
| Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies. Molecular syndromology 2016 Sep 7 (4): 210-219. Møller Rikke S, Larsen Line H G, Johannesen Katrine M, Talvik Inga, Talvik Tiina, Vaher Ulvi, Miranda Maria J, Farooq Muhammad, Nielsen Jens E K, Svendsen Lene Lavard, Kjelgaard Ditte B, Linnet Karen M, Hao Qin, Uldall Peter, Frangu Mimoza, Tommerup Niels, Baig Shahid M, Abdullah Uzma, Born Alfred P, Gellert Pia, Nikanorova Marina, Olofsson Kern, Jepsen Birgit, Marjanovic Dragan, Al-Zehhawi Lana I K, Peñalva Sofia J, Krag-Olsen Bente, Brusgaard Klaus, Hjalgrim Helle, Rubboli Guido, Pal Deb K, Dahl Hans |
| Parkinson's disease susceptibility variants and severity of Lewy body pathology. Parkinsonism & related disorders 2017 Sep . Heckman Michael G, Kasanuki Koji, Diehl Nancy N, Koga Shunsuke, Soto Alexandra, Murray Melissa E, Dickson Dennis W, Ross Owen |
| Detergent Insoluble Proteins and Inclusion Body-Like Structures Immunoreactive for PRKDC/DNA-PK/DNA-PKcs, FTL, NNT, and AIFM1 in the Amygdala of Cognitively Impaired Elderly Persons. Journal of neuropathology and experimental neurology 2018 Jan 77 (1): 21-39. Gal Jozsef, Chen Jing, Katsumata Yuriko, Fardo David W, Wang Wang-Xia, Artiushin Sergey, Price Douglas, Anderson Sonya, Patel Ela, Zhu Haining, Nelson Peter |
| An integrative functional genomics framework for effective identification of novel regulatory variants in genome-phenome studies. Genome medicine 2018 1 10 (1): 7. Zhao Junfei, Cheng Feixiong, Jia Peilin, Cox Nancy, Denny Joshua C, Zhao Zhongmi |
| Association of three candidate genetic variants in ACMSD/TMEM163, GPNMB and BCKDK /STX1B with sporadic Parkinson's disease in Han Chinese. Neuroscience letters 2019 Mar 703 45-48. Wang Ling, Li Nan-Nan, Lu Zhong-Jiao, Li Jun-Ying, Peng Jia-Xin, Duan Li-Ren, Peng Ro |
| Polymorphisms of ACMSD-TMEM163, MCCC1, and BCKDK-STX1B Are Not Associated with Parkinson's Disease in Taiwan. Parkinson's disease 2019 2019 3489638. Chang Kuo-Hsuan, Chen Chiung-Mei, Chen Yi-Chun, Fung Hon-Chung, Wu Yih- |
| The Association Between STX1B Polymorphisms and Treatment Response in Patients With Epilepsy. Frontiers in pharmacology 2021 7 12 701575. Wang Shitao, Zhou Liang, He Chenglu, Wang Dan, Cai Xuemei, Yu Yanying, Chen Liling, Lu Di, Bian Ligong, Du Sunbing, Wu Qian, Han Yanbi |
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