| 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 | 1540 | 2019 |
| Genetic correction of a LRRK2 mutation in human iPSCs links parkinsonian neurodegeneration to ERK-dependent changes in gene expression P Reinhardt, B Schmid, LF Burbulla, DC Schöndorf, L Wagner, M Glatza, ... Cell stem cell 12 (3), 354-367, 2013 | 546 | 2013 |
| A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies MA Nalls, R Duran, G Lopez, M Kurzawa-Akanbi, IG McKeith, ... JAMA neurology 70 (6), 727-735, 2013 | 474 | 2013 |
| 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 | 412 | 2016 |
| 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 | 380 | 2014 |
| 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 | 375 | 2017 |
| GBA-associated PD presents with nonmotor characteristics K Brockmann, K Srulijes, AK Hauser, C Schulte, I Csoti, T Gasser, D Berg Neurology 77 (3), 276-280, 2011 | 298 | 2011 |
| GBA‐associated Parkinson's disease: Reduced survival and more rapid progression in a prospective longitudinal study K Brockmann, K Srulijes, S Pflederer, AK Hauser, C Schulte, W Maetzler, ... Movement Disorders 30 (3), 407-411, 2015 | 265 | 2015 |
| Genetic modifiers of risk and age at onset in GBA associated Parkinson’s disease and Lewy body dementia C Blauwendraat, X Reed, L Krohn, K Heilbron, S Bandres-Ciga, M Tan, ... Brain 143 (1), 234-248, 2020 | 180 | 2020 |
| Gait analysis with wearables predicts conversion to parkinson disease S Del Din, M Elshehabi, B Galna, MA Hobert, E Warmerdam, U Suenkel, ... Annals of neurology 86 (3), 357-367, 2019 | 174 | 2019 |
| Arm swing as a potential new prodromal marker of Parkinson's disease A Mirelman, H Bernad‐Elazari, A Thaler, E Giladi‐Yacobi, T Gurevich, ... Movement Disorders 31 (10), 1527-1534, 2016 | 170 | 2016 |
| Enlarged hyperechogenic substantia nigra as a risk marker for Parkinson's disease D Berg, S Behnke, K Seppi, J Godau, S Lerche, P Mahlknecht, ... Movement Disorders 28 (2), 216-219, 2013 | 163 | 2013 |
| Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non‐Ashkenazi Jewish ancestry AJ Lee, Y Wang, RN Alcalay, H Mejia‐Santana, R Saunders‐Pullman, ... Movement Disorders 32 (10), 1432-1438, 2017 | 155 | 2017 |
| Interrogating Parkinson's disease LRRK2 kinase pathway activity by assessing Rab10 phosphorylation in human neutrophils Y Fan, AJM Howden, AR Sarhan, P Lis, G Ito, TN Martinez, K Brockmann, ... Biochemical Journal 475 (1), 23-44, 2018 | 151 | 2018 |
| Prodromal features for P arkinson's disease–baseline data from the TREND study A Gaenslen, I Wurster, K Brockmann, H Huber, J Godau, B Faust, ... European journal of neurology 21 (5), 766-772, 2014 | 151 | 2014 |
| 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 | 138 | 2013 |
| Poor trail making test performance is directly associated with altered dual task prioritization in the elderly–baseline results from the TREND study MA Hobert, R Niebler, SI Meyer, K Brockmann, C Becker, H Huber, ... PloS one 6 (11), e27831, 2011 | 127 | 2011 |
| Mitochondrial damage-associated inflammation highlights biomarkers in PRKN/PINK1 parkinsonism M Borsche, IR König, S Delcambre, S Petrucci, A Balck, N Brüggemann, ... Brain 143 (10), 3041-3051, 2020 | 122 | 2020 |
| Cognitive changes in prodromal Parkinson's disease: a review S Fengler, I Liepelt‐Scarfone, K Brockmann, E Schäffer, D Berg, E Kalbe Movement Disorders 32 (12), 1655-1666, 2017 | 120 | 2017 |
| Identification of candidate Parkinson disease genes by integrating genome-wide association study, expression, and epigenetic data sets DA Kia, D Zhang, S Guelfi, C Manzoni, L Hubbard, RH Reynolds, J Botía, ... JAMA neurology 78 (4), 464-472, 2021 | 116 | 2021 |
