| Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1 EM Valente, PM Abou-Sleiman, V Caputo, MMK Muqit, K Harvey, ... Science 304 (5674), 1158-1160, 2004 | 4269 | 2004 |
| Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis Nature 476 (7359), 214-219, 2011 | 3050 | 2011 |
| Autism genome-wide copy number variation reveals ubiquitin and neuronal genes JT Glessner, K Wang, G Cai, O Korvatska, CE Kim, S Wood, H Zhang, ... Nature 459 (7246), 569-573, 2009 | 1626 | 2009 |
| Common genetic variants on 5p14. 1 associate with autism spectrum disorders K Wang, H Zhang, D Ma, M Bucan, JT Glessner, BS Abrahams, ... Nature 459 (7246), 528-533, 2009 | 1147 | 2009 |
| Expanding insights of mitochondrial dysfunction in Parkinson's disease PM Abou-Sleiman, MMK Muqit, NW Wood Nature Reviews Neuroscience 7 (3), 207-219, 2006 | 1126 | 2006 |
| A common LRRK2 mutation in idiopathic Parkinson's disease WP Gilks, PM Abou-Sleiman, S Gandhi, S Jain, A Singleton, AJ Lees, ... The Lancet 365 (9457), 415-416, 2005 | 979 | 2005 |
| A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations K Bønnelykke, P Sleiman, K Nielsen, E Kreiner-Møller, JM Mercader, ... Nature genetics 46 (1), 51-55, 2014 | 677 | 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 | 652 | 2011 |
| Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis JS Ried, J Li, XB Zuo, XD Zheng, XY Yin, LD Sun, MA McAleer, ... Nature genetics 47 (12), 1449-1456, 2015 | 630 | 2015 |
| Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions VM Van Deerlin, PMA Sleiman, M Martinez-Lage, A Chen-Plotkin, ... Nature genetics 42 (3), 234-239, 2010 | 625 | 2010 |
| Age group and sex differences in performance on a computerized neurocognitive battery in children age 8− 21. RC Gur, J Richard, ME Calkins, R Chiavacci, JA Hansen, WB Bilker, ... Neuropsychology 26 (2), 251, 2012 | 613 | 2012 |
| Common variants at five new loci associated with early-onset inflammatory bowel disease M Imielinski, RN Baldassano, A Griffiths, RK Russell, V Annese, ... Nature genetics 41 (12), 1335-1340, 2009 | 586 | 2009 |
| The expression of DJ‐1 (PARK7) in normal human CNS and idiopathic Parkinson’s disease R Bandopadhyay, AE Kingsbury, MR Cookson, AR Reid, IM Evans, ... Brain 127 (2), 420-430, 2004 | 584 | 2004 |
| Neuroimaging of the Philadelphia neurodevelopmental cohort TD Satterthwaite, MA Elliott, K Ruparel, J Loughead, K Prabhakaran, ... Neuroimage 86, 544-553, 2014 | 550 | 2014 |
| The role of pathogenic DJ‐1 mutations in Parkinson's disease PM Abou‐Sleiman, DG Healy, N Quinn, AJ Lees, NW Wood Annals of neurology 54 (3), 283-286, 2003 | 540 | 2003 |
| A genome-wide association meta-analysis identifies new childhood obesity loci Nature genetics 44 (5), 526-531, 2012 | 522 | 2012 |
| Common variants at 5q22 associate with pediatric eosinophilic esophagitis ME Rothenberg, JM Spergel, JD Sherrill, K Annaiah, LJ Martin, ... Nature genetics 42 (4), 289-291, 2010 | 481 | 2010 |
| Mitochondrial function and morphology are impaired in parkin‐mutant fibroblasts H Mortiboys, KJ Thomas, WJH Koopman, S Klaffke, P Abou‐Sleiman, ... Annals of Neurology: Official Journal of the American Neurological …, 2008 | 432 | 2008 |
| Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder J Elia, JT Glessner, K Wang, N Takahashi, CJ Shtir, D Hadley, ... Nature genetics 44 (1), 78-84, 2012 | 431 | 2012 |
| PINK1 protein in normal human brain and Parkinson's disease S Gandhi, MMK Muqit, L Stanyer, DG Healy, PM Abou-Sleiman, ... Brain 129 (7), 1720-1731, 2006 | 425 | 2006 |
