| A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD AE Renton, E Majounie, A Waite, J Simón-Sánchez, S Rollinson, ... Neuron 72 (2), 257-268, 2011 | 4765 | 2011 |
| TREM2 Variants in Alzheimer's Disease R Guerreiro, A Wojtas, J Bras, M Carrasquillo, E Rogaeva, E Majounie, ... New England Journal of Medicine 368 (2), 117-127, 2013 | 3125 | 2013 |
| Genome-wide association study reveals genetic risk underlying Parkinson's disease J Simon-Sanchez, C Schulte, JM Bras, M Sharma, JR Gibbs, D Berg, ... Nature genetics 41 (12), 1308-1312, 2009 | 2206 | 2009 |
| Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease MA Nalls, N Pankratz, CM Lill, CB Do, DG Hernandez, M Saad, ... Nature genetics 46 (9), 989-993, 2014 | 2008 | 2014 |
| Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ... The Lancet Neurology 18 (12), 1091-1102, 2019 | 1637 | 2019 |
| 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 | 1447 | 2010 |
| Genotype, haplotype and copy-number variation in worldwide human populations M Jakobsson, SW Scholz, P Scheet, JR Gibbs, JM VanLiere, HC Fung, ... Nature 451 (7181), 998-1003, 2008 | 1022 | 2008 |
| Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain JR Gibbs, MP Van Der Brug, DG Hernandez, BJ Traynor, MA Nalls, SL Lai, ... PLoS genetics 6 (5), e1000952, 2010 | 901 | 2010 |
| Common genetic variants influence human subcortical brain structures DP Hibar, JL Stein, ME Renteria, A Arias-Vasquez, S Desrivières, ... Nature 520 (7546), 224-229, 2015 | 846 | 2015 |
| Genetic variability in the regulation of gene expression in ten regions of the human brain A Ramasamy, D Trabzuni, S Guelfi, V Varghese, C Smith, R Walker, T De, ... Nature neuroscience 17 (10), 1418-1428, 2014 | 686 | 2014 |
| Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy GU Höglinger, NM Melhem, DW Dickson, PMA Sleiman, LS Wang, L Klei, ... Nature genetics 43 (7), 699-705, 2011 | 627 | 2011 |
| The transcriptional landscape of age in human peripheral blood MJ Peters, R Joehanes, LC Pilling, C Schurmann, KN Conneely, J Powell, ... Nature communications 6 (1), 1-14, 2015 | 612 | 2015 |
| 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), 1267-1288, 2018 | 599 | 2018 |
| A survey of genetic human cortical gene expression AJ Myers, JR Gibbs, JA Webster, K Rohrer, A Zhao, L Marlowe, M Kaleem, ... Nature genetics 39 (12), 1494-1499, 2007 | 574 | 2007 |
| A genome-wide association study identifies protein quantitative trait loci (pQTLs) D Melzer, JRB Perry, D Hernandez, AM Corsi, K Stevens, I Rafferty, ... PLoS genetics 4 (5), e1000072, 2008 | 551 | 2008 |
| Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis JO Johnson, EP Pioro, A Boehringer, R Chia, H Feit, AE Renton, ... Nature neuroscience 17 (5), 664-666, 2014 | 528 | 2014 |
| Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease C Cruchaga, CM Karch, SC Jin, BA Benitez, Y Cai, R Guerreiro, O Harari, ... Nature 505 (7484), 550-554, 2014 | 526 | 2014 |
| 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 | 473 | 2006 |
| Genome-wide meta-analysis identifies new susceptibility loci for migraine V Anttila, BS Winsvold, P Gormley, T Kurth, F Bettella, G McMahon, ... Nature genetics 45 (8), 912-917, 2013 | 466 | 2013 |
| Distinct DNA methylation changes highly correlated with chronological age in the human brain DG Hernandez, MA Nalls, JR Gibbs, S Arepalli, M van der Brug, S Chong, ... Human molecular genetics 20 (6), 1164-1172, 2011 | 438 | 2011 |
Andrew SingletonNational Institute on Aging在 mail.nih.gov 的电子邮件经过验证
