Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Parkinson Disease and VPS35[original query] |
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VPS35 gene variants are not associated with Parkinson's disease in the mainland Chinese population. Parkinsonism & related disorders 2012 Sep 18 (8): 983-5. Guo Ji-feng, Sun Qi-ying, Lv Zhan-yun, Yu Ri-li, Li Kai, Zhang Yu-han, Tian Jin-yong, Xia Kun, Yan Xin-xiang, Tang Bei-s |
Contribution of VPS35 genetic variability to LBD in the Flanders-Belgian population. Neurobiology of aging 2012 Aug 33 (8): 1844.e11-3. Verstraeten Aline, Wauters Eline, Crosiers David, Meeus Bram, Corsmit Ellen, Elinck Ellen, Mattheijssens Maria, Peeters Karin, Cras Patrick, Pickut Barbara, Vandenberghe Rik, Engelborghs Sebastiaan, De Deyn Peter Paul, Van Broeckhoven Christine, Theuns Jess |
VPS35 Asp620Asn and EIF4G1 Arg1205His mutations are rare in Parkinson disease from southwest China. Neurobiology of aging 2012 Dec . Chen Y, Chen K, Song W, Chen X, Cao B, Huang R, Zhao B, Guo X, Burgunder J, Li J, Shang HF |
A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants. Journal of medical genetics 2012 Nov 49 (11): 721-6. Sharma Manu, Ioannidis John P A, Aasly Jan O, Annesi Grazia, Brice Alexis, Bertram Lars, Bozi Maria, Barcikowska Maria, Crosiers David, Clarke Carl E, Facheris Maurizio F, Farrer Matthew, Garraux Gaetan, Gispert Suzana, Auburger Georg, Vilariño-Güell Carles, Hadjigeorgiou Georgios M, Hicks Andrew A, Hattori Nobutaka, Jeon Beom S, Jamrozik Zygmunt, Krygowska-Wajs Anna, Lesage Suzanne, Lill Christina M, Lin Juei-Jueng, Lynch Timothy, Lichtner Peter, Lang Anthony E, Libioulle Cecile, Murata Miho, Mok Vincent, Jasinska-Myga Barbara, Mellick George D, Morrison Karen E, Meitnger Thomas, Zimprich Alexander, 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, Strom Tim M, Theuns Jessie, Tan Eng-King, Toda Tatsushi, Tomiyama Hiroyuki, Uitti Ryan J, Van Broeckhoven Christine, Wirdefeldt Karin, Wszolek Zbigniew, Xiromerisiou Georgia, Yomono Harumi S, Yueh Kuo-Chu, Zhao Yi, Gasser Thomas, Maraganore Demetrius, Krüger Rejko, |
Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease. Neurology 2013 Mar 80 (11): 982-9. Nuytemans Karen, Bademci Guney, Inchausti Vanessa, Dressen Amy, Kinnamon Daniel D, Mehta Arpit, Wang Liyong, Züchner Stephan, Beecham Gary W, Martin Eden R, Scott William K, Vance Jeffery |
DNAJC13 mutations in Parkinson disease. Human molecular genetics 2014 Apr 23 (7): 1794-801. Vilariño-Güell Carles, Rajput Alex, Milnerwood Austen J, Shah Brinda, Szu-Tu Chelsea, Trinh Joanne, Yu Irene, Encarnacion Mary, Munsie Lise N, Tapia Lucia, Gustavsson Emil K, Chou Patrick, Tatarnikov Igor, Evans Daniel M, Pishotta Frederick T, Volta Mattia, Beccano-Kelly Dayne, Thompson Christina, Lin Michelle K, Sherman Holly E, Han Heather J, Guenther Bruce L, Wasserman Wyeth W, Bernard Virginie, Ross Colin J, Appel-Cresswell Silke, Stoessl A Jon, Robinson Christopher A, Dickson Dennis W, Ross Owen A, Wszolek Zbigniew K, Aasly Jan O, Wu Ruey-Meei, Hentati Faycal, Gibson Rachel A, McPherson Peter S, Girard Martine, Rajput Michele, Rajput Ali H, Farrer Matthew |
VPS35 and DNAJC13 disease-causing variants in essential tremor. European journal of human genetics : EJHG 2015 Jun 23 (6): 887-8. Rajput Alex, Ross Jay P, Bernales Cecily Q, Rayaprolu Sruti, Soto-Ortolaza Alexandra I, Ross Owen A, van Gerpen Jay, Uitti Ryan J, Wszolek Zbigniew K, Rajput Ali H, Vilariño-Güell Carl |
Disease penetrance of late-onset parkinsonism: a meta-analysis. JAMA neurology 2014 Dec 71 (12): 1535-9. Trinh Joanne, Guella Ilaria, Farrer Matthew Jam |
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- Page last updated:May 06, 2024
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