| Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis MA Van Es, JH Veldink, CGJ Saris, HM Blauw, PWJ van Vught, A Birve, ... Nature genetics 41 (10), 1083-1087, 2009 | 439 | 2009 |
| EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humans A Van Hoecke, L Schoonaert, R Lemmens, M Timmers, KA Staats, ... Nature medicine 18 (9), 1418-1422, 2012 | 348 | 2012 |
| Variants of the elongator protein 3 ( ELP3 ) gene are associated with motor neuron degeneration CL Simpson, R Lemmens, K Miskiewicz, WJ Broom, VK Hansen, ... Human molecular genetics 18 (3), 472-481, 2009 | 339 | 2009 |
| ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study MA Van Es, PW Van Vught, HM Blauw, L Franke, CG Saris, PM Andersen, ... The Lancet Neurology 6 (10), 869-877, 2007 | 280 | 2007 |
| Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis MA Van Es, PWJ Van Vught, HM Blauw, L Franke, CGJ Saris, ... Nature genetics 40 (1), 29-31, 2008 | 273 | 2008 |
| Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis JE Landers, J Melki, V Meininger, JD Glass, LH van den Berg, MA van Es, ... Proceedings of the National Academy of Sciences 106 (22), 9004-9009, 2009 | 225 | 2009 |
| Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis MA Van Es, HJ Schelhaas, PWJ Van Vught, N Ticozzi, PM Andersen, ... Annals of neurology 70 (6), 964-973, 2011 | 212 | 2011 |
| Expanded ATXN2 CAG repeat size in ALS identifies genetic overlap between ALS and SCA2 P Van Damme, JH Veldink, M van Blitterswijk, A Corveleyn, ... Neurology 76 (24), 2066-2072, 2011 | 187 | 2011 |
| Weighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patients CGJ Saris, S Horvath, PWJ van Vught, MA van Es, HM Blauw, TF Fuller, ... BMC genomics 10, 1-16, 2009 | 184 | 2009 |
| Progranulin genetic variability contributes to amyotrophic lateral sclerosis K Sleegers, N Brouwers, S Maurer-Stroh, MA Van Es, PV Damme, ... Neurology 71 (4), 253-259, 2008 | 168 | 2008 |
| VCP mutations in familial and sporadic amyotrophic lateral sclerosis M Koppers, MM van Blitterswijk, L Vlam, PA Rowicka, PWJ van Vught, ... Neurobiology of aging 33 (4), 837. e7-837. e13, 2012 | 149 | 2012 |
| A genome-wide association meta-analysis identifies a novel locus at 17q11. 2 associated with sporadic amyotrophic lateral sclerosis I Fogh, A Ratti, C Gellera, K Lin, C Tiloca, V Moskvina, L Corrado, ... Human molecular genetics 23 (8), 2220-2231, 2014 | 138 | 2014 |
| UNC13A is a modifier of survival in amyotrophic lateral sclerosis FP Diekstra, PWJ van Vught, W van Rheenen, M Koppers, RJ Pasterkamp, ... Neurobiology of aging 33 (3), 630. e3-630. e8, 2012 | 137 | 2012 |
| Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen HM Blauw, JH Veldink, MA van Es, PW van Vught, CGJ Saris, ... The Lancet Neurology 7 (4), 319-326, 2008 | 104 | 2008 |
| The association between H63D mutations in HFE and amyotrophic lateral sclerosis in a Dutch population NA Sutedja, RJ Sinke, PWJ Van Vught, MW Van der Linden, JHJ Wokke, ... Archives of neurology 64 (1), 63-67, 2007 | 96 | 2007 |
| FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands EJN Groen, MA van Es, PWJ van Vught, WGM Spliet, J van Engelen-Lee, ... Archives of neurology 67 (2), 224-230, 2010 | 92 | 2010 |
| Novel optineurin mutations in sporadic amyotrophic lateral sclerosis patients M Van Blitterswijk, PWJ Van Vught, MA Van Es, HJ Schelhaas, ... Neurobiology of aging 33 (5), 1016. e1-1016. e7, 2012 | 88 | 2012 |
| Meta-analysis of vascular endothelial growth factor variations in amyotrophic lateral sclerosis: increased susceptibility in male carriers of the− 2578AA genotype D Lambrechts, K Poesen, R Fernandez-Santiago, A Al-Chalabi, R Del Bo, ... Journal of medical genetics 46 (12), 840-846, 2009 | 88 | 2009 |
| A large genome scan for rare CNVs in amyotrophic lateral sclerosis HM Blauw, A Al-Chalabi, PM Andersen, PWJ van Vught, FP Diekstra, ... Human molecular genetics 19 (20), 4091-4099, 2010 | 75 | 2010 |
| SMN1 gene duplications are associated with sporadic ALS HM Blauw, CP Barnes, PWJ van Vught, W van Rheenen, M Verheul, ... Neurology 78 (11), 776-780, 2012 | 69 | 2012 |
