Follow
Kimberley J Billingsley
Kimberley J Billingsley
Other namesKimberley Bilingsley
Postdoctoral Research Fellow, NIA, NIH
Verified email at nih.gov
Title
Cited by
Cited by
Year
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
16032019
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
2322018
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
1202021
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
1022019
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
912019
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
822020
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
792019
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
612020
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
542019
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
462021
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
332023
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
332022
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
322019
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
312018
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
232023
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
232022
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
222020
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
202022
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
192023
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
182019
The system can't perform the operation now. Try again later.
Articles 1–20