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| Exome sequencing reveals VCP mutations as a cause of familial ALS JO Johnson, J Mandrioli, M Benatar, Y Abramzon, VM Van Deerlin, ... Neuron 68 (5), 857-864, 2010 | 1502 | 2010 |
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| Genome-wide Analyses Identify KIF5A as a Novel ALS Gene A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ... Neuron 97 (6), 1268-1283. e6, 2018 | 672 | 2018 |
| A genome-wide association study identifies protein quantitative trait loci (pQTLs) D Melzer, JR Perry, D Hernandez, AM Corsi, K Stevens, I Rafferty, ... PLoS Genet 4 (5), e1000072, 2008 | 581 | 2008 |
| Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data HC Fung, S Scholz, M Matarin, J Simón-Sánchez, D Hernandez, A Britton, ... The Lancet Neurology 5 (11), 911-916, 2006 | 472 | 2006 |
| Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms C Blauwendraat, K Heilbron, CL Vallerga, S Bandres‐Ciga, R von Coelln, ... Movement Disorders 34 (6), 866-875, 2019 | 335 | 2019 |
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| Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans J Van de Leemput, J Chandran, MA Knight, LA Holtzclaw, S Scholz, ... PLoS Genet 3 (6), e108, 2007 | 329 | 2007 |
| Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study H Laaksovirta, T Peuralinna, JC Schymick, SW Scholz, SL Lai, ... The Lancet Neurology 9 (10), 978-985, 2010 | 324 | 2010 |
| Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture R Chia, MS Sabir, S Bandres-Ciga, S Saez-Atienzar, RH Reynolds, ... Nature genetics 53 (3), 294-303, 2021 | 308 | 2021 |
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| Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study R Guerreiro, OA Ross, C Kun-Rodrigues, DG Hernandez, T Orme, ... The Lancet Neurology 17 (1), 64-74, 2018 | 272 | 2018 |
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| DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA S Camargos, S Scholz, J Simón-Sánchez, C Paisán-Ruiz, P Lewis, ... The Lancet Neurology 7 (3), 207-215, 2008 | 266 | 2008 |
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Andrew SingletonNational Institute on AgingVerified email at mail.nih.gov
