Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Multiple System Atrophy and MAPT[original query] |
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| Progranulin Leu271LeufsX10 is one of the most common FTLD and CBS associated mutations worldwide. Neurobiology of disease 2009 Mar 33 (3): 379-85. Benussi Luisa, Ghidoni Roberta, Pegoiani Eleonora, Moretti Davide V, Zanetti Orazio, Binetti Giulia |
| MAPT1 gene rs1052553 variant is unrelated with the risk for restless legs syndrome. Journal of neural transmission (Vienna, Austria : 1996) 2013 Mar 120 (3): 463-7. Roco Angela, Jiménez-Jiménez Félix Javier, Alonso-Navarro Hortensia, Martínez Carmen, Zurdo Martín, Turpín-Fenoll Laura, Millán Jorge, Adeva-Bartolomé Teresa, Cubo Esther, Navacerrada Francisco, Rojo-Sebastián Ana, Rubio Lluisa, Calleja Marisol, Plaza-Nieto José Francisco, Pilo-de-la-Fuente Belén, Arroyo-Solera Margarita, García-Martín Elena, Agúndez José A |
| Association analysis of the GRN ?rs5848 and MAPT rs242557 polymorphisms in Parkinson's disease and multiple system atrophy: a large-scale population-based study and meta-analysis. The International journal of neuroscience 2015 Sep 1-8. Chen YongPing, Cao Bei, Ou RuWei, Chen XuePing, Zhao Bi, Wei QianQian, Wu Ying, Shang Hui-Fa |
| MAPT haplotype diversity in multiple system atrophy. Parkinsonism & related disorders 2016 09 30 40-5. Labbé Catherine, Heckman Michael G, Lorenzo-Betancor Oswaldo, Murray Melissa E, Ogaki Kotaro, Soto-Ortolaza Alexandra I, Walton Ronald L, Fujioka Shinsuke, Koga Shunsuke, Uitti Ryan J, van Gerpen Jay A, Petersen Ronald C, Graff-Radford Neill R, Younkin Steven G, Boeve Bradley F, Cheshire William P, Low Phillip A, Sandroni Paola, Coon Elizabeth A, Singer Wolfgang, Wszolek Zbigniew K, Dickson Dennis W, Ross Owen |
A genome-wide association study in multiple system atrophy.
Neurology 2016 Sep . Sailer Anna, Scholz Sonja W, Nalls Michael A, Schulte Claudia, Federoff Monica, Price T Ryan, Lees Andrew, Ross Owen A, Dickson Dennis W, Mok Kin, Mencacci Niccolo E, Schottlaender Lucia, Chelban Viorica, Ling Helen, O'Sullivan Sean S, Wood Nicholas W, Traynor Bryan J, Ferrucci Luigi, Federoff Howard J, Mhyre Timothy R, Morris Huw R, Deuschl Günther, Quinn Niall, Widner Hakan, Albanese Alberto, Infante Jon, Bhatia Kailash P, Poewe Werner, Oertel Wolfgang, Höglinger Günter U, Wüllner Ullrich, Goldwurm Stefano, Pellecchia Maria Teresa, Ferreira Joaquim, Tolosa Eduardo, Bloem Bastiaan R, Rascol Olivier, Meissner Wassilios G, Hardy John A, Revesz Tamas, Holton Janice L, Gasser Thomas, Wenning Gregor K, Singleton Andrew B, Houlden Henry, |
| Analysis of GWAS-linked variants in multiple system atrophy. Neurobiology of aging 2018 Mar . Gu XiaoJing, Chen YongPing, Zhou QingQing, Lu Ying-Che, Cao Bei, Zhang LingYu, Kuo Ming-Che, Wu Yih-Ru, Wu Ruey-Meei, Tan Eng-King, Shang Hui-Fang, |
| Coexisting Lewy body disease and clinical parkinsonism in frontotemporal lobar degeneration. Neurology 2019 4 92 (21): e2472-e2482. Forrest Shelley L, Crockford Daniel R, Sizemova Anastasia, McCann Heather, Shepherd Claire E, McGeachie Andrew B, Affleck Andrew J, Carew-Jones Francine, Bartley Lauren, Kwok John B, Kim Woojin Scott, Jary Eve, Tan Rachel H, McGinley Ciara V, Piguet Olivier, Hodges John R, Kril Jillian J, Halliday Glenda |
| Diagnosis Across the Spectrum of Progressive Supranuclear Palsy and Corticobasal Syndrome. JAMA neurology 2019 12 77 (3): 377-387. Jabbari Edwin, Holland Negin, Chelban Viorica, Jones P Simon, Lamb Ruth, Rawlinson Charlotte, Guo Tong, Costantini Alyssa A, Tan Manuela M X, Heslegrave Amanda J, Roncaroli Federico, Klein Johannes C, Ansorge Olaf, Allinson Kieren S J, Jaunmuktane Zane, Holton Janice L, Revesz Tamas, Warner Thomas T, Lees Andrew J, Zetterberg Henrik, Russell Lucy L, Bocchetta Martina, Rohrer Jonathan D, Williams Nigel M, Grosset Donald G, Burn David J, Pavese Nicola, Gerhard Alexander, Kobylecki Christopher, Leigh P Nigel, Church Alistair, Hu Michele T M, Woodside John, Houlden Henry, Rowe James B, Morris Huw |
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