| MDS clinical diagnostic criteria for Parkinson's disease RB Postuma, D Berg, M Stern, W Poewe, CW Olanow, W Oertel, J Obeso, ... Movement disorders 30 (12), 1591-1601, 2015 | 6888 | 2015 |
| Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology A Zimprich, S Biskup, P Leitner, P Lichtner, M Farrer, S Lincoln, ... Neuron 44 (4), 601-607, 2004 | 3551 | 2004 |
| Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease E Sidransky, MA Nalls, JO Aasly, J Aharon-Peretz, G Annesi, ER Barbosa, ... New England Journal of Medicine 361 (17), 1651-1661, 2009 | 2408 | 2009 |
| 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 | 2265 | 2009 |
| The ubiquitin pathway in Parkinson's disease E Leroy, R Boyer, G Auburger, B Leube, G Ulm, E Mezey, G Harta, ... Nature 395 (6701), 451-452, 1998 | 2147 | 1998 |
| 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 | 2082 | 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 | 1980 | 2019 |
| Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study DG Healy, M Falchi, SS O'Sullivan, V Bonifati, A Durr, S Bressman, ... The Lancet Neurology 7 (7), 583-590, 2008 | 1754 | 2008 |
| Analysis of shared heritability in common disorders of the brain Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ... Science 360 (6395), eaap8757, 2018 | 1550 | 2018 |
| MDS research criteria for prodromal Parkinson's disease D Berg, RB Postuma, CH Adler, BR Bloem, P Chan, B Dubois, T Gasser, ... Movement Disorders 30 (12), 1600-1611, 2015 | 1490 | 2015 |
| Association between early-onset Parkinson's disease and mutations in the parkin gene CB Lucking, A Durr, V Bonifati, J Vaughan, G De Michele, T Gasser, ... New England Journal of Medicine 342 (21), 1560-1567, 2000 | 1259 | 2000 |
| Neuropathological assessment of Parkinson's disease: refining the diagnostic criteria DW Dickson, H Braak, JE Duda, C Duyckaerts, T Gasser, GM Halliday, ... The Lancet Neurology 8 (12), 1150-1157, 2009 | 1192 | 2009 |
| Intraoperative MRI guidance and extent of resection in glioma surgery: a randomised, controlled trial C Senft, A Bink, K Franz, H Vatter, T Gasser, V Seifert The lancet oncology 12 (11), 997-1003, 2011 | 964 | 2011 |
| The phenotypic spectrum of CADASIL: clinical findings in 102 cases M Dichgans, M Mayer, I Uttner, R Brüning, J Müller‐Höcker, G Rungger, ... Annals of neurology 44 (5), 731-739, 1998 | 911 | 1998 |
| Association between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene CB Lücking, A Dürr, V Bonifati, J Vaughan, G De Michele, T Gasser, ... New England Journal of Medicine 342 (21), 1560-1567, 2000 | 813* | 2000 |
| Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease KM Strauss, LM Martins, H Plun-Favreau, FP Marx, S Kautzmann, D Berg, ... Human molecular genetics 14 (15), 2099-2111, 2005 | 760 | 2005 |
| Analysis of shared heritability in common disorders of the brain Brainstorm Consortium Science (New York, NY) 360 (6395), eaap8757, 2018 | 717 | 2018 |
| A Wide Variety of Mutations in the Parkin Gene Are Responsible for Autosomal Recessive Parkinsonism in Europe N Abbas, CB Lücking, S Ricard, A Dürr, V Bonifati, G De Michele, ... Human molecular genetics 8 (4), 567-574, 1999 | 715 | 1999 |
| Update of the MDS research criteria for prodromal Parkinson's disease S Heinzel, D Berg, T Gasser, H Chen, C Yao, RB Postuma, ... Movement Disorders 34 (10), 1464-1470, 2019 | 678 | 2019 |
| EFNS/MDS‐ES recommendations for the diagnosis of P arkinson's disease A Berardelli, GK Wenning, A Antonini, D Berg, BR Bloem, V Bonifati, ... European journal of neurology 20 (1), 16-34, 2013 | 666 | 2013 |