Human Genome Epidemiology Literature Finder
Records 1 - 21 (of 21 Records) |
Query Trace: MCCC1[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 |
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 |
MCCC1/LAMP3 reduces risk of sporadic Parkinson's disease in Han Chinese. Acta neurologica Scandinavica 2013 Mar . Li NN, Tan EK, Chang XL, Mao XY, Zhao DM, Zhang JH, Liao Q, Peng R |
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 |
Metabolic heritability at birth: implications for chronic disease research. Human genetics 2014 Aug 133 (8): 1049-57. Ryckman Kelli K, Smith Caitlin J, Jelliffe-Pawlowski Laura L, Momany Allison M, Berberich Stanton L, Murray Jeffrey |
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 |
Analysis of non-synonymous-coding variants of Parkinson's disease-related pathogenic and susceptibility genes in East Asian populations. Human molecular genetics 2014 Jul 23 (14): 3891-7. Foo Jia Nee, Tan Louis C, Liany Herty, Koh Tat Hung, Irwan Ishak D, Ng Yen Yek, Ahmad-Annuar Azlina, Au Wing-Lok, Aung Tin, Chan Anne Y Y, Chong Siow-Ann, Chung Sun Ju, Jung Yusun, Khor Chiea Chuen, Kim Juyeon, Lee Jimmy, Lim Shen-Yang, Mok Vincent, Prakash Kumar-M, Song Kyuyoung, Tai E-Shyong, Vithana Eranga N, Wong Tien-Yin, Tan Eng-King, Liu Jianj |
Variants in GBA, SNCA, and MAPT influence Parkinson disease risk, age at onset, and progression. Neurobiology of aging 2015 Sep . Davis Albert A, Andruska Kristin M, Benitez Bruno A, Racette Brad A, Perlmutter Joel S, Cruchaga Carl |
Mapping adipose and muscle tissue expression quantitative trait loci in African Americans to identify genes for type 2 diabetes and obesity. Human genetics 2016 08 135 (8): 869-80. Sajuthi Satria P, Sharma Neeraj K, Chou Jeff W, Palmer Nicholette D, McWilliams David R, Beal John, Comeau Mary E, Ma Lijun, Calles-Escandon Jorge, Demons Jamehl, Rogers Samantha, Cherry Kristina, Menon Lata, Kouba Ethel, Davis Donna, Burris Marcie, Byerly Sara J, Ng Maggie C Y, Maruthur Nisa M, Patel Sanjay R, Bielak Lawrence F, Lange Leslie A, Guo Xiuqing, Sale Michèle M, Chan Kei Hang K, Monda Keri L, Chen Gary K, Taylor Kira, Palmer Cameron, Edwards Todd L, North Kari E, Haiman Christopher A, Bowden Donald W, Freedman Barry I, Langefeld Carl D, Das Swapan |
Association of three candidate genetic variants in RAB7L1/NUCKS1, MCCC1 and STK39 with sporadic Parkinson's disease in Han Chinese. Journal of neural transmission (Vienna, Austria : 1996) 2016 Apr 123 (4): 425-30. Wang Ling, Cheng Lan, Lu Zhong-Jiao, Sun Xiao-Yi, Li Jun-Ying, Peng Ro |
Genome-wide association study of Parkinson's disease in East Asians.
Human molecular genetics 2016 Dec . Foo Jia Nee, Tan Louis C, Irwan Ishak D, Au Wing-Lok, Low Hui Qi, Prakash Kumar-M, Ahmad-Annuar Azlina, Bei Jinxin, Chan Anne Yy, Chen Chiung Mei, Chen Yi-Chun, Chung Sun Ju, Deng Hao, Lim Shen-Yang, Mok Vincent, Pang Hao, Pei Zhong, Peng Rong, Shang Hui-Fang, Song Kyuyoung, Tan Ai Huey, Wu Yih-Ru, Aung Tin, Cheng Ching-Yu, Chew Fook Tim, Chew Soo-Hong, Chong Siow-Ann, Ebstein Richard P, Lee Jimmy, Saw Seang-Mei, Seow Adeline, Subramaniam Mythily, Tai E-Shyong, Vithana Eranga N, Wong Tien-Yin, Heng Khai Koon, Meah Wee-Yang, Khor Chiea Chuen, Liu Hong, Zhang Furen, Liu Jianjun, Tan Eng-Ki |
Association of Parkinson's Disease GWAS-Linked Loci with Alzheimer's Disease in Han Chinese. Molecular neurobiology 2017 01 54 (1): 308-318. Zhu Xi-Chen, Cao Lei, Tan Meng-Shan, Jiang Teng, Wang Hui-Fu, Lu Huan, Tan Chen-Chen, Zhang Wei, Tan Lan, Yu Jin-T |
Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and ?-synuclein mechanisms.
Movement disorders : official journal of the Movement Disorder Society 2019 Jun 34 (6): 866-875. Blauwendraat Cornelis, Heilbron Karl, Vallerga Costanza L, Bandres-Ciga Sara, von Coelln Rainer, Pihlstrøm Lasse, Simón-Sánchez Javier, Schulte Claudia, Sharma Manu, Krohn Lynne, Siitonen Ari, Iwaki Hirotaka, Leonard Hampton, Noyce Alastair J, Tan Manuela, Gibbs J Raphael, Hernandez Dena G, Scholz Sonja W, Jankovic Joseph, Shulman Lisa M, Lesage Suzanne, Corvol Jean-Christophe, Brice Alexis, van Hilten Jacobus J, Marinus Johan, , Eerola-Rautio Johanna, Tienari Pentti, Majamaa Kari, Toft Mathias, Grosset Donald G, Gasser Thomas, Heutink Peter, Shulman Joshua M, Wood Nicolas, Hardy John, Morris Huw R, Hinds David A, Gratten Jacob, Visscher Peter M, Gan-Or Ziv, Nalls Mike A, Singleton Andrew B, |
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- |
Expanded Newborn Screening for Inborn Errors of Metabolism by Tandem Mass Spectrometry in Suzhou, China: Disease Spectrum, Prevalence, Genetic Characteristics in a Chinese Population. Frontiers in genetics 2019 11 10 1052. Wang Ting, Ma Jun, Zhang Qin, Gao Ang, Wang Qi, Li Hong, Xiang Jingjing, Wang Benji |
3-Methylcrotonyl-CoA carboxylase deficiency newborn screening in a population of 536,008: is routine screening necessary? Journal of pediatric endocrinology & metabolism : JPEM 2019 Nov . Wang Huaiyan, Liu Shuang, Wang Benjing, Yang Yuqi, Yu Bin, Wang Leilei, Wang Ti |
SNPs in SNCA, MCCC1, DLG2, GBF1 and MBNL2 are associated with Parkinson's disease in southern Chinese population. Journal of cellular and molecular medicine 2020 Jul . Zhao Aonan, Li Yuanyuan, Niu Mengyue, Li Guanglu, Luo Ningdi, Zhou Liche, Kang Wenyan, Liu J |
Association study of MCCC1/LAMP3 and DGKQ variants with Parkinson's disease in patients of Malay ancestry. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2021 Feb . Lim Jia Lun, Ng Ebonne Yulin, Lim Shen-Yang, Tan Ai Huey, Abdul-Aziz Zariah, Ibrahim Khairul Azmi, Gopalai Aroma Agape, Tay Yi Wen, Vijayanathan Yuganthini, Toh Tzi Shin, Lim Soo Kun, Bee Ping-Chong, Puvanarajah Santhi Datuk, Viswanathan Shanthi, Looi Irene, Lim Thien Thien, Eow Gaik Bee, Cheah Wee Kooi, Tan Eng-King, Ahmad-Annuar Azli |
Allele-specific expression of Parkinson's disease susceptibility genes in human brain. Scientific reports 2021 Jan 11 (1): 504. Langmyhr Margrete, Henriksen Sandra Pilar, Cappelletti Chiara, van de Berg Wilma D J, Pihlstrøm Lasse, Toft Mathi |
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