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| Cloning of the Gene Containing Mutations that Cause< i> PARK8</i>-Linked Parkinson's Disease C Paisán-Ruı́z, S Jain, EW Evans, WP Gilks, J Simón, M Van Der Brug, ... Neuron 44 (4), 595-600, 2004 | 2947 | 2004 |
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| Genome-wide association study reveals genetic risk underlying Parkinson's disease J Simón-Sánchez, C Schulte, JM Bras, M Sharma, JR Gibbs, D Berg, ... Nature genetics 41 (12), 1308-1312, 2009 | 2371 | 2009 |
| Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study E Majounie, AE Renton, K Mok, EGP Dopper, A Waite, S Rollinson, ... The Lancet Neurology 11 (4), 323-330, 2012 | 1523 | 2012 |
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| Loss of VPS13C function in autosomal-recessive parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ... The American Journal of Human Genetics 98 (3), 500-513, 2016 | 501 | 2016 |
| Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease LA Robak, IE Jansen, J Van Rooij, AG Uitterlinden, R Kraaij, J Jankovic, ... Brain 140 (12), 3191-3203, 2017 | 480 | 2017 |
| 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 | 474 | 2006 |
| Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease A Beilina, IN Rudenko, A Kaganovich, L Civiero, H Chau, SK Kalia, ... Proceedings of the National Academy of Sciences 111 (7), 2626-2631, 2014 | 406 | 2014 |
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| SNCA variants are associated with increased risk for multiple system atrophy SW Scholz, H Houlden, C Schulte, M Sharma, A Li, D Berg, A Melchers, ... Annals of Neurology: Official Journal of the American Neurological …, 2009 | 343 | 2009 |
| 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 genetics 3 (6), e108, 2007 | 339 | 2007 |
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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 | 282 | 2008 |
| Using genome-wide complex trait analysis to quantify ‘missing heritability’in Parkinson's disease MF Keller, M Saad, J Bras, F Bettella, N Nicolaou, J Simón-Sánchez, ... Human molecular genetics 21 (22), 4996-5009, 2012 | 263 | 2012 |
| A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release M Matarín, WM Brown, S Scholz, J Simón-Sánchez, HC Fung, ... The Lancet Neurology 6 (5), 414-420, 2007 | 253 | 2007 |
Andrew SingletonNational Institute on AgingVerified email at mail.nih.gov
