Human Genome Epidemiology Literature Finder
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Records 1 - 24 (of 24 Records) |
| Query Trace: Disease and STK39[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 |
| Large-scale replication and heterogeneity in Parkinson disease genetic loci. Neurology 2012 Aug 79 (7): 659-67. Sharma Manu, Ioannidis John P A, Aasly Jan O, Annesi Grazia, Brice Alexis, Van Broeckhoven Christine, Bertram Lars, Bozi Maria, Crosiers David, Clarke Carl, Facheris Maurizio, Farrer Matthew, Garraux Gaetan, Gispert Suzana, Auburger Georg, Vilariño-Güell Carles, Hadjigeorgiou Georgios M, Hicks Andrew A, Hattori Nobutaka, Jeon Beom, Lesage Suzanne, Lill Christina M, Lin Juei-Jueng, Lynch Timothy, Lichtner Peter, Lang Anthony E, Mok Vincent, Jasinska-Myga Barbara, Mellick George D, Morrison Karen E, Opala Grzegorz, Pramstaller Peter P, Pichler Irene, Park Sung Sup, Quattrone Aldo, Rogaeva Ekaterina, Ross Owen A, Stefanis Leonidas, Stockton Joanne D, Satake Wataru, Silburn Peter A, Theuns Jessie, Tan Eng-King, Toda Tatsushi, Tomiyama Hiroyuki, Uitti Ryan J, Wirdefeldt Karin, Wszolek Zbigniew, Xiromerisiou Georgia, Yueh Kuo-Chu, Zhao Yi, Gasser Thomas, Maraganore Demetrius, Krüger Rejko, |
| 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 |
| Influence of obesity on association between genetic variants identified by genome-wide association studies and hypertension risk in Chinese children. American journal of hypertension 2013 Aug 26 (8): 990-6. Xi Bo, Zhao Xiaoyuan, Chandak Giriraj R, Shen Yue, Cheng Hong, Hou Dongqing, Wang Xingyu, Mi J |
| 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 |
| Comparable autoantibody serum levels against amyloid- and inflammation-associated proteins in Parkinson's disease patients and controls. PloS one 2014 9 (2): e88604. Maetzler Walter, Apel Anja, Langkamp Markus, Deuschle Christian, Dilger Sarah Selina, Stirnkorb Johannes Georg, Schulte Claudia, Schleicher Erwin, Gasser Thomas, Berg Danie |
| 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 |
| Exonic Re-Sequencing of the Chromosome 2q24.3 Parkinson's Disease Locus. PloS one 2015 10 (6): e0128586. Labbé Catherine, Ogaki Kotaro, Lorenzo-Betancor Oswaldo, Carrasquillo Minerva M, Heckman Michael G, McCarthy Allan, Soto-Ortolaza Alexandra I, Walton Ronald L, Lynch Timothy, Siuda Joanna, Opala Grzegorz, Krygowska-Wajs Anna, Barcikowska Maria, Czyzewski Krzysztof, Dickson Dennis W, Uitti Ryan J, Wszolek Zbigniew K, Ross Owen |
| Target gene capture sequencing in Chinese population of sporadic Parkinson disease. Medicine 2015 May 94 (20): e836. Li Zhiming, Lin Qing, Huang Wenqing, Tzeng Chi-Me |
| 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 |
| STK39, But Not BST1, HLA-DQB1, and SPPL2B Polymorphism, Is Associated With Han-Chinese Parkinson's Disease in Taiwan. Medicine 2015 Oct 94 (41): e1690. Chang Kuo-Hsuan, Wu Yih-Ru, Chen Yi-Chun, Fung Hon-Chung, Lee-Chen Guey-Jen, Chen Chiung-M |
| Genome-wide assessment of Parkinson's disease in a Southern Spanish population. Neurobiology of aging 2016 Jun . Bandrés-Ciga Sara, Price Timothy Ryan, Barrero Francisco Javier, Escamilla-Sevilla Francisco, Pelegrina Javier, Arepalli Sampath, Hernández Dena, Gutiérrez Blanca, Cervilla Jorge, Rivera Margarita, Rivera Alberto, Ding Jing-Hui, Vives Francisco, Nalls Michael, Singleton Andrew, Durán Raqu |
| Endothelin-1 genetic polymorphism as predictive marker for bevacizumab in metastatic breast cancer. The pharmacogenomics journal 2016 May . Gampenrieder S P, Hufnagl C, Brechelmacher S, Huemer F, Hackl H, Rinnerthaler G, Romeder F, Monzo Fuentes C, Morre P, Hauser-Kronberger C, Mlineritsch B, Greil |
| 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 |
| Determining the Effect of the HNMT, STK39, and NMD3 Polymorphisms on the Incidence of Parkinson's Disease, Amyotrophic Lateral Sclerosis, and Multiple System Atrophy in Chinese Populations. Journal of molecular neuroscience : MN 2018 Mar . Chen Yongping, Cao Bei, Ou Ruwei, Wei Qianqian, Chen Xueping, Zhao Bi, Wu Ying, Song Wei, Shang Hui-Fa |
| A replication study of GWAS-genetic risk variants associated with Parkinson's disease in a Spanish population. Neuroscience letters 2019 Aug 134425. Tejera-Parrado Cristina, Jesús Silvia, Periñán María Teresa, Buiza-Rueda Dolores, Oliva-Ariza Guillermo, Adarmes-Gómez Astrid D, Macías-García Daniel, Gómez-Garre Pilar, Mir Pab |
| Rare Genetic Variants of Large Effect Influence Risk of Type 1 Diabetes.
Diabetes 2020 Jan . Forgetta Vincenzo, Manousaki Despoina, Istomine Roman, Ross Stephanie, Tessier Marie-Catherine, Marchand Luc, Li Min, Qu Hui-Qi, Bradfield Jonathan P, Grant Struan F A, Hakonarson Hakon, , Paterson Andrew D, Piccirillo Ciriaco, Polychronakos Constantin, Richards J Bre |
| Variant rs6749447 (T?>?G) in the serine threonine kinase gene is associated with cardiovascular complications, the Tampere adult population cardiovascular risk study. Medicine 2021 Oct 100 (42): e27566. Kunnas Tarja, Määttä Kirsi, Nikkari Seppo |
| 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 |
| GWAS identifies candidate susceptibility loci and microRNA biomarkers for acute encephalopathy with biphasic seizures and late reduced diffusion.
Scientific reports 2022 01 12 (1): 1332. Kasai Mariko, Omae Yosuke, Kawai Yosuke, Shibata Akiko, Hoshino Ai, Mizuguchi Masashi, Tokunaga Katsus |
| Identification of novel susceptibility methylation loci for pancreatic cancer in a two-phase epigenome-wide association study. Epigenetics 2022 1 17 (11): 1357-1372. Wang Ziqiao, Lu Yue, Fornage Myriam, Jiao Li, Shen Jianjun, Li Donghui, Wei Pe |
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