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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:

The role of genetics in Parkinson’s disease: a large cohort study in Chinese mainland population
Yuwen Zhao, Lixia Qin, Hongxu Pan, et al.
Brain (2020) Vol. 143, Iss. 7, pp. 2220-2234
Open Access | Times Cited: 139

Showing 1-25 of 139 citing articles:

Global Trends in the Incidence, Prevalence, and Years Lived With Disability of Parkinson's Disease in 204 Countries/Territories From 1990 to 2019
Zejin Ou, Jing Pan, Shihao Tang, et al.
Frontiers in Public Health (2021) Vol. 9
Open Access | Times Cited: 465
GP2: The Global Parkinson's Genetics Program

Movement Disorders (2021) Vol. 36, Iss. 4, pp. 842-851
Open Access | Times Cited: 113
Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force – An Update
Lara M. Lange, Paulina González-Latapí, Rajasumi Rajalingam, et al.
Movement Disorders (2022) Vol. 37, Iss. 5, pp. 905-935
Open Access | Times Cited: 87
Parkinson’s Disease is Predominantly a Genetic Disease
Shen‐Yang Lim, Christine Klein
Journal of Parkinson s Disease (2024) Vol. 14, Iss. 3, pp. 467-482
Open Access | Times Cited: 24
Relevance of genetic testing in the gene-targeted trial era: the Rostock Parkinson’s disease study
Ana Westenberger, Volha Skrahina, Tatiana Usnich, et al.
Brain (2024) Vol. 147, Iss. 8, pp. 2652-2667
Open Access | Times Cited: 24
Curcumin can improve Parkinson's disease via activating BDNF/PI3k/Akt signaling pathways
Tian Jin, Yong Zhang, Benson O. A. Botchway, et al.
Food and Chemical Toxicology (2022) Vol. 164, pp. 113091-113091
Closed Access | Times Cited: 65
Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson’s disease in Chinese population
Hongxu Pan, Zhenhua Liu, Jinghong Ma, et al.
npj Parkinson s Disease (2023) Vol. 9, Iss. 1
Open Access | Times Cited: 32
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
Uncovering the genetic basis of Parkinson's disease globally: from discoveries to the clinic
Shen‐Yang Lim, Ai Huey Tan, Azlina Ahmad, et al.
The Lancet Neurology (2024)
Closed 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
Mitochondrial Function and Parkinson’s Disease: From the Perspective of the Electron Transport Chain
Jeng‐Lin Li, Tai-Yi Lin, Po‐Lin Chen, et al.
Frontiers in Molecular Neuroscience (2021) Vol. 14
Open Access | Times Cited: 43
Deficiency in endocannabinoid synthase DAGLB contributes to early onset Parkinsonism and murine nigral dopaminergic neuron dysfunction
Zhenhua Liu, Nannan Yang, Jie Dong, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 38
Risk factors associated with age at onset of Parkinson’s disease in the UK Biobank
Yuanfeng Huang, Qian Chen, Zheng Wang, et al.
npj Parkinson s Disease (2024) Vol. 10, Iss. 1
Open Access | Times Cited: 7
Early Onset Parkinsonism: Differential diagnosis and what not to miss
Norlinah Mohamed Ibrahim, Chin Hsien Lin
Parkinsonism & Related Disorders (2024) Vol. 129, pp. 107100-107100
Closed Access | Times Cited: 6
Genotype-phenotype correlation of Parkinson's disease with PRKN variants
Hiroyo Yoshino, Yuanzhe Li, Kenya Nishioka, et al.
Neurobiology of Aging (2022) Vol. 114, pp. 117-128
Open Access | Times Cited: 24
The Chinese Parkinson's Disease Registry (CPDR): Study Design and Baseline Patient Characteristics
Xiaoxia Zhou, Zhenhua Liu, Xiaoting Zhou, et al.
Movement Disorders (2022) Vol. 37, Iss. 7, pp. 1335-1345
Closed Access | Times Cited: 23
Characteristics of fatigue in Parkinson’s disease: A longitudinal cohort study
Xiaoxia Zhou, Yaqin Xiang, Tingwei Song, et al.
Frontiers in Aging Neuroscience (2023) Vol. 15
Open Access | Times Cited: 16
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
Long‐Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's Disease
Kensuke Daida, Manabu Funayama, Kimberley Billingsley, et al.
Movement Disorders (2023) Vol. 38, Iss. 12, pp. 2249-2257
Open Access | Times Cited: 15
The Genetic Drivers of Juvenile, Young, and Early‐Onset Parkinson's Disease in India
Shan V. Andrews, Prashanth Lingappa Kukkle, Ramesh Menon, et al.
Movement Disorders (2023) Vol. 39, Iss. 2, pp. 339-349
Open Access | Times Cited: 13
Recent progresses in natural based therapeutic materials for Alzheimer's disease
Tayebeh Zivari‐Ghader, Ferzane Valioğlu, Aziz Eftekhari, et al.
Heliyon (2024) Vol. 10, Iss. 4, pp. e26351-e26351
Open Access | Times Cited: 5
Deficiency of parkin causes neurodegeneration and accumulation of pathological α-synuclein in monkey models
Rui Han, Qi Wang, Xin Xiong, et al.
Journal of Clinical Investigation (2024) Vol. 134, Iss. 20
Closed Access | Times Cited: 5
Glucocerebrosidase (GBA) gene variants in a multi-ethnic Asian cohort with Parkinson’s disease: mutational spectrum and clinical features
Jia Lun Lim, Katja Lohmann, Ai Huey Tan, et al.
Journal of Neural Transmission (2021) Vol. 129, Iss. 1, pp. 37-48
Closed Access | Times Cited: 32
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
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