Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Disease and meta-analysis and CCDC62[original query] |
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Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.
BMC medical genetics 2011 12 (1): 104. Liu Xinmin, Cheng Rong, Verbitsky Miguel, Kisselev Sergey, Browne Andrew, Mejia-Sanatana Helen, Louis Elan D, Cote Lucien J, Andrews Howard, Waters Cheryl, Ford Blair, Frucht Steven, Fahn Stanley, Marder Karen, Clark Lorraine N, Lee Joseph |
| Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.
Lancet (London, England) 2011 Feb 377 (9766): 641-9. , Nalls Michael A, Plagnol Vincent, Hernandez Dena G, Sharma Manu, Sheerin Una-Marie, Saad Mohamad, Simón-Sánchez J, Schulte Claudia, Lesage Suzanne, Sveinbjörnsdóttir Sigurlaug, Stefánsson Kári, Martinez Maria, Hardy John, Heutink Peter, Brice Alexis, Gasser Thomas, Singleton Andrew B, Wood Nicholas |
| Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
PLoS genetics 2012 8 (3): e1002548. Lill Christina M, Roehr Johannes T, McQueen Matthew B, Kavvoura Fotini K, Bagade Sachin, Schjeide Brit-Maren M, Schjeide Leif M, Meissner Esther, Zauft Ute, Allen Nicole C, Liu Tian, Schilling Marcel, Anderson Kari J, Beecham Gary, Berg Daniela, Biernacka Joanna M, Brice Alexis, DeStefano Anita L, Do Chuong B, Eriksson Nicholas, Factor Stewart A, Farrer Matthew J, Foroud Tatiana, Gasser Thomas, Hamza Taye, Hardy John A, Heutink Peter, Hill-Burns Erin M, Klein Christine, Latourelle Jeanne C, Maraganore Demetrius M, Martin Eden R, Martinez Maria, Myers Richard H, Nalls Michael A, Pankratz Nathan, Payami Haydeh, Satake Wataru, Scott William K, Sharma Manu, Singleton Andrew B, Stefansson Kari, Toda Tatsushi, Tung Joyce Y, Vance Jeffery, Wood Nick W, Zabetian Cyrus P, , , , , Young Peter, Tanzi Rudolph E, Khoury Muin J, Zipp Frauke, Lehrach Hans, Ioannidis John P A, Bertram La |
| Genetic association study between STK39 and CCDC62/HIP1R and Parkinson's disease. PloS one 2013 8 (11): e79211. Li Nan-Nan, Tan Eng-King, Chang Xue-Li, Mao Xue-Ye, Zhang Jin-Hong, Zhao Dong-Mei, Liao Qiao, Yu Wen-Juan, Peng Ro |
| CCDC62 variant rs12817488 is associated with the risk of Parkinson's disease in a Han Chinese population. European neurology 2014 71 (1-2): 77-83. Liu Rong-Rong, Zhou Li-Li, Cheng Xing, Sun Miao-Xuan, Hu Yan-Bing, Chen Song-Fang, Zhang Xiong, Zhu Jian-Ho |
| Association analysis of STK39, MCCC1/LAMP3 and sporadic PD in the Chinese Han population. Neuroscience letters 2014 Apr 566 206-9. Wang Ya-qin, Tang Bei-sha, Yu Ri-li, Li Kai, Liu Zhen-hua, Xu Qian, Sun Qi-ying, Yan Xin-xiang, Guo Ji-fe |
| The single nucleotide polymorphism Rs12817488 is associated with Parkinson's disease in the Chinese population. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2015 Jun 22 (6): 1002-4. Yu Ri-li, Guo Ji-feng, Wang Ya-qin, Liu Zhen-hua, Sun Zhan-fang, Su Li, Zhang Yuan, Yan Xin-xiang, Tang Bei-s |
| Possible association of CCDC62 rs12817488 polymorphism and Parkinson's disease risk in Chinese population: a meta-analysis. Scientific reports 2016 6 23991. Lu Yanjun, Tan Lu, Shen Na, Peng Jing, Wang Chunyu, Zhu Yaowu, Wang Xio |
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