Kimberley J Billingsley
Kimberley J Billingsley
Other namesKimberley Bilingsley
Postdoctoral Research Fellow, NIA, NIH
Verified email at
Cited by
Cited by
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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