Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: Atrophy and MAF[original query] |
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An association analysis of the rs1572931 polymorphism of the RAB7L1 gene in Parkinson's disease, amyotrophic lateral sclerosis and multiple system atrophy in China. European journal of neurology : the official journal of the European Federation of Neurological Societies 2014 Oct 21 (10): 1337-43. Guo X-Y, Chen Y-P, Song W, Zhao B, Cao B, Wei Q-Q, Ou R-W, Yang Y, Yuan L-X, Shang H |
Association analysis of the GRN ?rs5848 and MAPT rs242557 polymorphisms in Parkinson's disease and multiple system atrophy: a large-scale population-based study and meta-analysis. The International journal of neuroscience 2015 Sep 1-8. Chen YongPing, Cao Bei, Ou RuWei, Chen XuePing, Zhao Bi, Wei QianQian, Wu Ying, Shang Hui-Fa |
Genetic Variants of SNCA Are Associated with Susceptibility to Parkinson's Disease but Not Amyotrophic Lateral Sclerosis or Multiple System Atrophy in a Chinese Population. PloS one 2015 10 (7): e0133776. Chen YongPing, Wei Qian-Qian, Ou RuWei, Cao Bei, Chen XuePing, Zhao Bi, Guo XiaoYan, Yang Yuan, Chen Ke, Wu Ying, Song Wei, Shang Hui-Fa |
Integration of bioinformatics and imaging informatics for identifying rare PSEN1 variants in Alzheimer's disease. BMC medical genomics 2016 9 Suppl 1 30. Nho Kwangsik, Horgusluoglu Emrin, Kim Sungeun, Risacher Shannon L, Kim Dokyoon, Foroud Tatiana, Aisen Paul S, Petersen Ronald C, Jack Clifford R, Shaw Leslie M, Trojanowski John Q, Weiner Michael W, Green Robert C, Toga Arthur W, Saykin Andrew J, |
DCTN1 p.K56R in progressive supranuclear palsy. Parkinsonism & related disorders 2016 Apr . Gustavsson Emil K, Trinh Joanne, Guella Ilaria, Szu-Tu Chelsea, Khinda Jaskaran, Lin Chin-Hsien, Wu Ruey-Meei, Stoessl Jon, Appel-Cresswell Silke, McKeown Martin, Rajput Alex, Rajput Ali H, Petersen Maria Skaalum, Jeon Beom S, Aasly Jan O, Farrer Matthew |
Association of TNF-? rs1799964 and IL-1? rs16944 polymorphisms with multiple system atrophy in Chinese Han population. The International journal of neuroscience 2017 Dec 1-16. Zhou Xin, Wang Chunrong, Chen Zhao, Peng Yun, Peng Huirong, Hou Xuan, Ye Wei, Qiu Rong, Xia Kun, Tang Beisha, Jiang Ho |
Association analysis of SNP rs11868035 in SREBF1 with sporadic Parkinson's disease, sporadic amyotrophic lateral sclerosis and multiple system atrophy in a Chinese population. Neuroscience letters 2017 Nov . Yuan XiaoQin, Cao Bei, Wu Ying, Chen YongPing, Wei QianQian, Ou RuWei, Yang Jing, Chen XuePing, Zhao Bi, Song Wei, Shang HuiFa |
Single Nucleotide Polymorphisms of Ubiquitin-Related Genes were Associated with Allograft Fibrosis of Renal Transplant Fibrosis. Annals of transplantation 2019 Oct 24 553-568. Gui Zeping, Li Wencheng, Fei Shuang, Guo Miao, Chen Hao, Sun Li, Han Zhijian, Tao Jun, Ju Xiaobin, Yang Haiwei, Wei Ji-Fu, Tan Ruoyun, Gu M |
CMIP SNPs and their haplotypes are associated with dyslipidaemia and clinicopathologic features of IgA nephropathy. Bioscience reports 2020 10 40 (10): . Pan Ling, Liao Yun-Hua, Mo Man-Qiu, Zhang Qing-Hui, Yin Rui-Xi |
The association of the CMIP rs16955379 polymorphism with dyslipidemia and the clinicopathological features of IgA nephropathy. International journal of clinical and experimental pathology 2020 1 11 (10): 5008-5023. Mo Man-Qiu, Pan Ling, Lu Qing-Mei, Li Qiu-Lin, Liao Yun-H |
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- Page last updated:Apr 16, 2024
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