| 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 | 2012 | 2014 |
| Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies International Parkinson Disease Genomics Consortium The Lancet 377 (9766), 641-649, 2011 | 1011 | 2011 |
| 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 | 418 | 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 | 385 | 2017 |
| 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 | 382 | 2014 |
| Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis Y Allanore, M Saad, P Dieudé, J Avouac, JHW Distler, P Amouyel, ... PLoS genetics 7 (7), e1002091, 2011 | 256 | 2011 |
| 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 | 239 | 2012 |
| A two-stage meta-analysis identifies several new loci for Parkinson's disease International Parkinson's Disease Genomics Consortium (IPDGC), ... PLoS genetics 7 (6), e1002142, 2011 | 220 | 2011 |
| Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population M Saad, S Lesage, A Saint-Pierre, JC Corvol, D Zelenika, JC Lambert, ... Human molecular genetics 20 (3), 615-627, 2011 | 196 | 2011 |
| A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease P Holmans, V Moskvina, L Jones, M Sharma, ... Human molecular genetics 22 (5), 1039-1049, 2013 | 139 | 2013 |
| Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing IE Jansen, H Ye, S Heetveld, MC Lechler, H Michels, RI Seinstra, ... Genome biology 18, 1-26, 2017 | 119 | 2017 |
| Germline genetic contribution to the immune landscape of cancer RW Sayaman, M Saad, V Thorsson, D Hu, W Hendrickx, J Roelands, ... Immunity 54 (2), 367-386. e8, 2021 | 118 | 2021 |
| NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases MA Nalls, J Bras, DG Hernandez, MF Keller, E Majounie, AE Renton, ... Neurobiology of aging 36 (3), 1605. e7-1605. e12, 2015 | 113 | 2015 |
| Genetic comorbidities in Parkinson's disease MA Nalls, M Saad, AJ Noyce, MF Keller, A Schrag, JP Bestwick, ... Human molecular genetics 23 (3), 831-841, 2014 | 73 | 2014 |
| Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk V Moskvina, D Harold, GC Russo, A Vedernikov, M Sharma, M Saad, ... JAMA neurology 70 (10), 1268-1276, 2013 | 72 | 2013 |
| Oncogenic states dictate the prognostic and predictive connotations of intratumoral immune response J Roelands, W Hendrickx, G Zoppoli, R Mall, M Saad, K Halliwill, ... Journal for immunotherapy of cancer 8 (1), 2020 | 67 | 2020 |
| Use of support vector machines for disease risk prediction in genome‐wide association studies: Concerns and opportunities F Mittag, F Büchel, M Saad, A Jahn, C Schulte, Z Bochdanovits, ... Human mutation 33 (12), 1708-1718, 2012 | 65 | 2012 |
| Parkinson’s Study Group (PSG) Parkinson’s Research: The Organized GENetics Initiative (PROGENI); 23andMe MA Nalls, N Pankratz, CM Lill, CB Do, DG Hernandez, M Saad, ... GenePD 46 (9), 989-93, 2014 | 58 | 2014 |
| The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism S Klebe, JL Golmard, MA Nalls, M Saad, AB Singleton, JM Bras, J Hardy, ... Journal of Neurology, Neurosurgery & Psychiatry 84 (6), 666-673, 2013 | 56 | 2013 |
| International Parkinson's Disease Genomics Consortium (IPDGC) MA Nalls, N Pankratz, CM Lill, CB Do, DG Hernandez, M Saad, ... Parkinson's Study Group (PSG) Parkinson's Research: The Organized GENetics …, 2014 | 52 | 2014 |
Mike A. NallsFounder/consultant with Data Tecnica International + Data science lead at NIH’s Center for Alzheimer在 mail.nih.gov 的电子邮件经过验证
