HuGE Literature Finder
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Records 1-16
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Genetic Mutation Analysis of Parkinson's Disease Patients Using Multigene Next-Generation Sequencing Panels.
Molecular diagnosis & therapy 2016 Jun . Gorostidi Ana, Martí-Massó José Félix, Bergareche Alberto, Rodríguez-Oroz Mari Cruz, de Munain Adolfo López, Ruiz-Martínez Javi |
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Exonic rearrangements in the known Parkinson's disease-causing genes are a rare cause of the disease in South African patients.
Neuroscience letters 2016 Mar 619 168-171. van der Merwe Celia, Carr Jonathan, Glanzmann Brigitte, Bardien Sora |
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An assessment of the frequency of mutations in the GBA and VPS35 genes in Hungarian patients with sporadic Parkinson's disease.
Neuroscience letters 2015 Nov . Török Rita, Zádori Dénes, Török Nóra, Csility Éva, Vécsei László, Klivényi Pét |
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D620N mutation in the VPS35 gene and R1205H mutation in the EIF4G1 gene are uncommon in the Greek population.
Neuroscience letters 2015 Aug 606 113-116. Kalinderi Kallirhoe, Bostantjopoulou Sevasti, Katsarou Zoe, Dimikiotou Maria, Fidani Lia |
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Polygenic determinants of Parkinson's disease in a Chinese population.
Neurobiology of aging 2015 Apr 36 (4): 1765.e1-6. Guo Ji-Feng, Li Kai, Yu Ri-Li, Sun Qi-Yin, Wang Lei, Yao Ling-Yan, Hu Ya-Cen, Lv Zhan-Yun, Luo Lin-Zi, Shen Lu, Jiang Hong, Yan Xin-Xiang, Pan Qian, Xia Kun, Tang Bei-S |
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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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Frequency of the ASP620ASN mutation in VPS35 and Arg1205His mutation in EIF4G1 in familial Parkinson's disease from South Italy.
Neurobiology of aging 2014 Oct 35 (10): 2422.e1-2. Gagliardi Monica, Annesi Grazia, Tarantino Patrizia, Nicoletti Giuseppe, Quattrone Al |
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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 |
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EIF4G1 R1205H and VPS35 D620N mutations are rare in Parkinson's disease from South Africa.
Neurobiology of aging 2014 Feb 35 (2): 445.e1-3. Blanckenberg Janine, Ntsapi Claudia, Carr Jonathan A, Bardien Sora |
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VPS35 and EIF4G1 mutations are rare in Parkinson's disease among Indians.
Neurobiology of aging 2013 Oct 34 (10): 2442.e1-3. Sudhaman Sumedha, Behari Madhuri, Govindappa Shyla T, Muthane Uday B, Juyal Ramesh C, Thelma B |
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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 |
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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 |
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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, |
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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 |
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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 |
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Vacuolar protein sorting 35 Asp620Asn mutation is rare in the ethnic Chinese population with Parkinson's disease.
Parkinsonism & related disorders 2012 Jun 18 (5): 638-40. Zhang Yu, Chen Shuai, Xiao Qin, Cao Li, Liu Jun, Rong Tian-Yi, Ma Jian-Fang, Wang Gang, Wang Ying, Chen Sheng- |
- Page last reviewed:Mar 1, 2018
- Page last updated:Jul 18, 2019
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