| 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 | 1532 | 2019 |
| Parkinson's disease age at onset genome‐wide association study: defining heritability, genetic loci, and α‐synuclein mechanisms C Blauwendraat, K Heilbron, CL Vallerga, S Bandres‐Ciga, R Von Coelln, ... Movement Disorders 34 (6), 866-875, 2019 | 288 | 2019 |
| 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 | 178 | 2020 |
| Features of GBA-associated Parkinson’s disease at presentation in the UK Tracking Parkinson’s study N Malek, RS Weil, C Bresner, MA Lawton, KA Grosset, M Tan, N Bajaj, ... Journal of Neurology, Neurosurgery & Psychiatry 89 (7), 702-709, 2018 | 131 | 2018 |
| Genome‐wide association studies of cognitive and motor progression in Parkinson's disease MMX Tan, MA Lawton, E Jabbari, RH Reynolds, H Iwaki, C Blauwendraat, ... Movement Disorders 36 (2), 424-433, 2021 | 130 | 2021 |
| Diagnosis across the spectrum of progressive supranuclear palsy and corticobasal syndrome E Jabbari, N Holland, V Chelban, PS Jones, R Lamb, C Rawlinson, T Guo, ... JAMA neurology 77 (3), 377-387, 2020 | 123 | 2020 |
| 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 |
| Mitochondria function associated genes contribute to Parkinson’s Disease risk and later age at onset KJ Billingsley, IA Barbosa, S Bandrés-Ciga, JP Quinn, VJ Bubb, ... npj Parkinson's Disease 5 (1), 8, 2019 | 99 | 2019 |
| System Genomics of Parkinson’s Disease Consortium; International Parkinson’s Disease Genomics Consortium. Identification of novel risk loci, causal insights, and heritable risk … MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ... Lancet Neurol 18 (12), 1091-1102, 2019 | 94 | 2019 |
| Expanding Parkinson’s disease genetics: novel risk loci, genomic context, causal insights and heritable risk MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ... BioRxiv, 388165, 2019 | 92 | 2019 |
| Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson’s disease heritability RH Reynolds, J Botía, MA Nalls, J Hardy, SA Gagliano Taliun, M Ryten npj Parkinson's Disease 5 (1), 6, 2019 | 91 | 2019 |
| Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study E Jabbari, S Koga, RR Valentino, RH Reynolds, R Ferrari, MMX Tan, ... The Lancet Neurology 20 (2), 107-116, 2021 | 83 | 2021 |
| The endocytic membrane trafficking pathway plays a major role in the risk of Parkinson's disease S Bandres‐Ciga, S Saez‐Atienzar, L Bonet‐Ponce, K Billingsley, D Vitale, ... Movement Disorders 34 (4), 460-468, 2019 | 78 | 2019 |
| Genetic analysis of Mendelian mutations in a large UK population-based Parkinson’s disease study MMX Tan, N Malek, MA Lawton, L Hubbard, AM Pittman, T Joseph, ... Brain 142 (9), 2828-2844, 2019 | 77 | 2019 |
| Sequence of clinical and neurodegeneration events in Parkinson’s disease progression NP Oxtoby, LA Leyland, LM Aksman, GEC Thomas, EL Bunting, ... Brain 144 (3), 975-988, 2021 | 64 | 2021 |
| Penetrance of Parkinson's Disease in LRRK2 p.G2019S Carriers Is Modified by a Polygenic Risk Score H Iwaki, C Blauwendraat, MB Makarious, S Bandrés‐Ciga, HL Leonard, ... Movement Disorders 35 (5), 774-780, 2020 | 61 | 2020 |
| The genetic architecture of Parkinson disease in Spain: characterizing population‐specific risk, differential haplotype structures, and providing etiologic insight S Bandres‐Ciga, S Ahmed, MS Sabir, C Blauwendraat, ... Movement Disorders 34 (12), 1851-1863, 2019 | 54 | 2019 |
| Parkinson’s disease genetics: identifying novel risk loci, providing causal insights and improving estimates of heritable risk MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ... BioRxiv, 388165, 2018 | 54 | 2018 |
| Variation at the TRIM11 locus modifies progressive supranuclear palsy phenotype E Jabbari, J Woodside, MMX Tan, M Shoai, A Pittman, R Ferrari, KY Mok, ... Annals of neurology 84 (4), 485-496, 2018 | 52 | 2018 |
| Investigation of autosomal genetic sex differences in Parkinson's disease C Blauwendraat, H Iwaki, MB Makarious, S Bandres‐Ciga, HL Leonard, ... Annals of neurology 90 (1), 35-42, 2021 | 41 | 2021 |
