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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Evaluating the Role of SNCA, LRRK2, and GBA in Chinese Patients With Early‐Onset Parkinson's Disease
Yongping Chen, Xiaojing Gu, Ruwei Ou, et al.
Movement Disorders (2020) Vol. 35, Iss. 11, pp. 2046-2055
Closed Access | Times Cited: 39

Showing 1-25 of 39 citing articles:

Prevalence and clinical aspects of depression in Parkinson’s disease: A systematic review and meta‑analysis of 129 studies
Shengri Cong, Chunchen Xiang, Shun Zhang, et al.
Neuroscience & Biobehavioral Reviews (2022) Vol. 141, pp. 104749-104749
Open Access | Times Cited: 107
Classification of GBA1 Variants in Parkinson's Disease: The GBA1‐PD Browser
Sitki Cem Parlar, Francis P. Grenn, Jonggeol Jeffrey Kim, et al.
Movement Disorders (2023) Vol. 38, Iss. 3, pp. 489-495
Closed Access | Times Cited: 63
A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease
Hui Liu, Christos Koros, Timo Strohäker, et al.
Movement Disorders (2021) Vol. 36, Iss. 7, pp. 1624-1633
Open Access | Times Cited: 83
Prevalence of ten LRRK2 variants in Parkinson's disease: A comprehensive review
Christopher S. Simpson, Lisa Vinikoor-Imler, Feiby L. Nassan, et al.
Parkinsonism & Related Disorders (2022) Vol. 98, pp. 103-113
Closed Access | Times Cited: 45
Targeting the GBA1 pathway to slow Parkinson disease: Insights into clinical aspects, pathogenic mechanisms and new therapeutic avenues
Elisa Menozzi, Marco Toffoli, Anthony H.V. Schapira
Pharmacology & Therapeutics (2023) Vol. 246, pp. 108419-108419
Open Access | Times Cited: 24
Clinical, mechanistic, biomarker, and therapeutic advances in GBA1-associated Parkinson’s disease
Xuxiang Zhang, Heng Wu, Beisha Tang, et al.
Translational Neurodegeneration (2024) Vol. 13, Iss. 1
Open Access | Times Cited: 9
Clinical and functional evidence for the pathogenicity of the LRRK2 p.Arg1067Gln variant
Shen‐Yang Lim, Tzi Shin Toh, Jia Wei Hor, et al.
npj Parkinson s Disease (2025) Vol. 11, Iss. 1
Open Access | Times Cited: 1
Single Nucleotide Polymorphisms of Indoleamine 2,3-Dioxygenase 1 Influenced the Age Onset of Parkinson's Disease
Nóra Török, Rita Maszlag-Török, Kinga Molnár, et al.
Frontiers in Bioscience-Landmark (2022) Vol. 27, Iss. 9
Open Access | Times Cited: 35
Role of genetics in amyotrophic lateral sclerosis: a large cohort study in Chinese mainland population
Yongping Chen, Shihui Yu, Qianqian Wei, et al.
Journal of Medical Genetics (2021) Vol. 59, Iss. 9, pp. 840-849
Open Access | Times Cited: 37
α‐Synuclein V15A Variant in Familial Parkinson's Disease Exhibits a Weaker Lipid‐Binding Property
Kensuke Daida, Shotaro Shimonaka, Kahori Shiba‐Fukushima, et al.
Movement Disorders (2022) Vol. 37, Iss. 10, pp. 2075-2085
Open Access | Times Cited: 25
Genetic study of early-onset Parkinson's disease in the Malaysian population
Yi Wen Tay, Ai Huey Tan, Jia Lun Lim, et al.
Parkinsonism & Related Disorders (2023) Vol. 111, pp. 105399-105399
Closed Access | Times Cited: 16
Genetic heterogeneity on sleep disorders in Parkinson’s disease: a systematic review and meta-analysis
Jingxuan Huang, Yangfan Cheng, Chunyu Li, et al.
Translational Neurodegeneration (2022) Vol. 11, Iss. 1
Open Access | Times Cited: 20
The mutation spectrum of Parkinson‐disease‐related genes in early‐onset Parkinson's disease in ethnic Chinese
Yongping Chen, Shihui Yu, Guohui Zhang, et al.
European Journal of Neurology (2022) Vol. 29, Iss. 11, pp. 3218-3228
Closed Access | Times Cited: 20
Mutational spectrum and clinical features of GBA1 variants in a Chinese cohort with Parkinson’s disease
Yangjie Zhou, Yige Wang, Juan Wan, et al.
npj Parkinson s Disease (2023) Vol. 9, Iss. 1
Open Access | Times Cited: 12
The novel p.A30G SNCA pathogenic variant in Greek patients with familial and sporadic Parkinson's disease
Ioanna Alefanti, Christos Koros, Viktoria Tsami, et al.
European Journal of Neurology (2025) Vol. 32, Iss. 2
Open Access
Gene variants and expression changes of SIRT1 and SIRT6 in peripheral blood are associated with Parkinson’s disease
Rita Maszlag-Török, Fanni Annamária Boros, László Vécsei, et al.
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 23
Clinical and Dopamine Transporter Imaging Trajectories in a Cohort of Parkinson's Disease Patients with GBA Mutations
Silvia Paola Caminiti, Giulia Carli, Micol Avenali, et al.
Movement Disorders (2021) Vol. 37, Iss. 1, pp. 106-118
Closed Access | Times Cited: 22
Prevalence and genotype–phenotype correlations of GBA‐related Parkinson disease in a large Chinese cohort
Jingru Ren, Ronggui Zhang, Chenxi Pan, et al.
European Journal of Neurology (2021) Vol. 29, Iss. 4, pp. 1017-1024
Open Access | Times Cited: 20
Genetic Movement Disorders Commonly Seen in Asians
Priya Jagota, Shen‐Yang Lim, Pramod Kumar Pal, et al.
Movement Disorders Clinical Practice (2023) Vol. 10, Iss. 6, pp. 878-895
Closed Access | Times Cited: 7
Genetic Analysis and Literature Review of SNCA Variants in Parkinson's Disease
Yi Guo, Yan Sun, Zhi Song, et al.
Frontiers in Aging Neuroscience (2021) Vol. 13
Open Access | Times Cited: 17
Profiling Non-motor Symptoms in Monogenic Parkinson’s Disease
Xinyao Liu, Weidong Le
Frontiers in Aging Neuroscience (2020) Vol. 12
Open Access | Times Cited: 17
Structural Insights and Development of LRRK2 Inhibitors for Parkinson’s Disease in the Last Decade
Gunjan Thakur, Vikas Kumar, Keun Woo Lee, et al.
Genes (2022) Vol. 13, Iss. 8, pp. 1426-1426
Open Access | Times Cited: 10
Subtyping of early-onset Parkinson’s disease using cluster analysis: A large cohort study
Zhou Zhou, Xiaoxia Zhou, Yaqin Xiang, et al.
Frontiers in Aging Neuroscience (2022) Vol. 14
Open Access | Times Cited: 10
The Influence of GBA and LRRK2 on Mood Disorders in Parkinson's Disease
Jake DeBroff, Nurit Omer, Batsheva Cohen, et al.
Movement Disorders Clinical Practice (2023) Vol. 10, Iss. 4, pp. 606-616
Open Access | Times Cited: 6
Conformational dynamics of A30G α-synuclein that causes familial Parkinson disease
Dorothy Das, Venkata Satish Kumar Mattaparthi
Journal of Biomolecular Structure and Dynamics (2023) Vol. 41, Iss. 24, pp. 14702-14714
Closed Access | Times Cited: 5
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