OpenAlex Citation Counts

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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:

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

Showing 1-25 of 45 citing articles:

Role of dopamine in the pathophysiology of Parkinson’s disease
Zhidong Zhou, Ling Yi, Qing Wang, et al.
Translational Neurodegeneration (2023) Vol. 12, Iss. 1
Open Access | Times Cited: 75

Perspective on the current state of the LRRK2 field
Jean‐Marc Taymans, Matt Fell, Tim Greenamyre, et al.
npj Parkinson s Disease (2023) Vol. 9, Iss. 1
Open Access | Times Cited: 70

Parkinson’s disease variant detection and disclosure: PD GENEration, a North American study
Lola Cook, Jennifer Verbrugge, Tae‐Hwi Schwantes‐An, et al.
Brain (2024) Vol. 147, Iss. 8, pp. 2668-2679
Open Access | Times Cited: 21

Towards a Global View of Parkinson's Disease Genetics
Marzieh Khani, Catalina Cerquera‐Cleves, Mariam Kekenadze, et al.
Annals of Neurology (2024) Vol. 95, Iss. 5, pp. 831-842
Open Access | Times Cited: 15

Genetic analysis and natural history of Parkinson’s disease due to the LRRK2 G2019S variant
Matthew J. Kmiecik, Steven J. Micheletti, Daniella Coker, et al.
Brain (2024) Vol. 147, Iss. 6, pp. 1996-2008
Open Access | Times Cited: 9

Genetic architecture of Parkinson’s disease subtypes – Review of the literature
Jarosław Dulski, Ryan J. Uitti, Owen A. Ross, et al.
Frontiers in Aging Neuroscience (2022) Vol. 14
Open Access | Times Cited: 34

Novel LRR-ROC Motif That Links the N- and C-terminal Domains in LRRK2 Undergoes an Order–Disorder Transition Upon Activation
Jui-Hung Weng, Chiara R. Trilling, Pallavi Kaila Sharma, et al.
Journal of Molecular Biology (2023) Vol. 435, Iss. 12, pp. 167999-167999
Open Access | Times Cited: 22

LRRK2 kinase inhibition protects against Parkinson's disease-associated environmental toxicants
Neda M. Ilieva, Eric K. Hoffman, Mohammed Ghalib, et al.
Neurobiology of Disease (2024) Vol. 196, pp. 106522-106522
Open Access | Times Cited: 7

The Golgi Apparatus: A Voyage through Time, Structure, Function and Implication in Neurodegenerative Disorders
Aurel George Mohan, Bogdan Calenic, Nicu Adrian Ghiurau, et al.
Cells (2023) Vol. 12, Iss. 15, pp. 1972-1972
Open Access | Times Cited: 13

Human iPSC-derived microglia carrying the LRRK2-G2019S mutation show a Parkinson’s disease related transcriptional profile and function
Sohvi Ohtonen, Luca Giudice, Henna Jäntti, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 11

Editorial on: Confirmation of RAB32 Ser71Arg involvement in Parkinson's disease
Emil K. Gustavsson
Movement Disorders (2025) Vol. 40, Iss. 1, pp. 5-6
Closed Access

Carriers of LRRK2 pathogenic variants show a milder, anatomically distinct brain signature of Parkinson's disease
Jakub Kopál, Andrew Vo, Tao Qin, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access

Investigating the prevalence of the G2019S mutation in Parkinson's disease among a Libyan population
Nuri Awayn, Sara A Hashish, S. A. Salem, et al.
Journal of Parkinson s Disease (2025)
Open Access

Prevalence and Clinical Characteristics of the LRRK2 p.L1795F Variant in Central Europeans with Early‐Onset and Familial Parkinson's Disease
Miriam Ostrožovičová, Gertrúd Tamás, Agsha Atputhavadivel, et al.
Movement Disorders Clinical Practice (2025)
Open Access

Environmental Factors Exacerbate Parkinsonian Phenotypes in an Asian-Specific Knock-In LRRK2 Risk Variant in Mice
Zoë Bichler, Sarivin Vanan, Zhiwei Zhang, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 8, pp. 3556-3556
Open Access

Regulation of Leucine-Rich Repeat Kinase 2 by inflammation and IL-4
Dina Dikovskaya, Rebecca Pemberton, Matthew Taylor, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 3

Leucine-rich repeat kinase 2 at a glance
Christiane Zhu, Susanne Herbst, Patrick A. Lewis
Journal of Cell Science (2023) Vol. 136, Iss. 17
Open Access | Times Cited: 9

The Genetics of Parkinson’s Disease
Zeliha YÜCEL, Levent Şi̇mşek, Emine Berrin YÜKSEL
Genel Tıp Dergisi (2024) Vol. 34, Iss. 1, pp. 136-143
Open Access | Times Cited: 2

The R1441C-Lrrk2 mutation induces myeloid immune cell exhaustion in an age- and sex-dependent manner in mice
Rebecca L. Wallings, Karen N. McFarland, Hannah A. Staley, et al.
Science Translational Medicine (2024) Vol. 16, Iss. 772
Open Access | Times Cited: 2

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

Overview of the Impact of Pathogenic LRRK2 Mutations in Parkinson’s Disease
Genta Ito, Naoko Utsunomiya‐Tate
Biomolecules (2023) Vol. 13, Iss. 5, pp. 845-845
Open Access | Times Cited: 6

The function of Golgi apparatus in LRRK2-associated Parkinson’s disease
Yonghang Wei, Maher Un Nisa Awan, Li‐Ping Bai, et al.
Frontiers in Molecular Neuroscience (2023) Vol. 16
Open Access | Times Cited: 5

Modeling Parkinson’s disease in LRRK2 rodents
Chiara Domenicale, Stefano Magnabosco, Michele Morari
Neuronal Signaling (2023) Vol. 7, Iss. 3
Open Access | Times Cited: 5

Endemic parkinsonism: clusters, biology and clinical features
Kateřina Menšíková, John C. Steele, Raymond L. Rosales, et al.
Nature Reviews Neurology (2023) Vol. 19, Iss. 10, pp. 599-616
Closed Access | Times Cited: 5

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