| 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 | 1652 | 2019 |
| Genetic risk factors in Parkinson’s disease KJ Billingsley, S Bandres-Ciga, S Saez-Atienzar, AB Singleton Cell and tissue research 373, 9-20, 2018 | 233 | 2018 |
| 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 | 128 | 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 | 105 | 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 | 90 | 2019 |
| The Parkinson's disease genome‐wide association study locus browser FP Grenn, JJ Kim, MB Makarious, H Iwaki, A Illarionova, K Brolin, ... Movement Disorders 35 (11), 2056-2067, 2020 | 84 | 2020 |
| 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 | 80 | 2019 |
| 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 | 64 | 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 | 55 | 2019 |
| 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 | 48 | 2021 |
| Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation M Kolmogorov, KJ Billingsley, M Mastoras, M Meredith, J Monlong, ... Nature Methods 20 (10), 1483-1492, 2023 | 38 | 2023 |
| The role of SINE-VNTR-Alu (SVA) retrotransposons in shaping the human genome O Gianfrancesco, B Geary, AL Savage, KJ Billingsley, VJ Bubb, JP Quinn International journal of molecular sciences 20 (23), 5977, 2019 | 36 | 2019 |
| Heterozygous PRKN mutations are common but do not increase the risk of Parkinson’s disease W Zhu, X Huang, E Yoon, S Bandres-Ciga, C Blauwendraat, ... Brain 145 (6), 2077-2091, 2022 | 34 | 2022 |
| Regulatory characterisation of the schizophrenia-associated CACNA1C proximal promoter and the potential role for the transcription factor EZH2 in schizophrenia aetiology KJ Billingsley, M Manca, O Gianfrancesco, DA Collier, H Sharp, VJ Bubb, ... Schizophrenia research 199, 168-175, 2018 | 30 | 2018 |
| Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study M Rizig, S Bandres-Ciga, MB Makarious, OO Ojo, PW Crea, OV Abiodun, ... The Lancet Neurology 22 (11), 1015-1025, 2023 | 27 | 2023 |
| Genetic risk profiling in Parkinson’s disease and utilizing genetics to gain insight into disease-related biological pathways A Hall, S Bandres-Ciga, M Diez-Fairen, JP Quinn, KJ Billingsley International Journal of Molecular Sciences 21 (19), 7332, 2020 | 25 | 2020 |
| Identification and prediction of Parkinson’s disease subtypes and progression using machine learning in two cohorts A Dadu, V Satone, R Kaur, SH Hashemi, H Leonard, H Iwaki, ... npj Parkinson's Disease 8 (1), 172, 2022 | 24 | 2022 |
| Genome-wide contribution of common short-tandem repeats to Parkinson’s disease genetic risk BI Bustos, K Billingsley, C Blauwendraat, JR Gibbs, Z Gan-Or, D Krainc, ... Brain 146 (1), 65-74, 2023 | 22 | 2023 |
| REViewer: haplotype-resolved visualization of read alignments in and around tandem repeats E Dolzhenko, B Weisburd, K Ibañez, IS Rajan-Babu, C Anyansi, ... Genome medicine 14 (1), 84, 2022 | 22 | 2022 |
| Analysis of repetitive element expression in the blood and skin of patients with Parkinson’s disease identifies differential expression of satellite elements KJ Billingsley, F Lättekivi, A Planken, E Reimann, L Kurvits, ... Scientific Reports 9 (1), 4369, 2019 | 19 | 2019 |
