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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:

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

Showing 24 citing articles:

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
Updated MDSGene review on the clinical and genetic spectrum of LRRK2 variants in Parkinson´s disease
Cleusa Adriane Menegassi Bianchi Krüger, Shen‐Yang Lim, Alissa Buhrmann, et al.
npj Parkinson s Disease (2025) Vol. 11, Iss. 1
Open Access | Times Cited: 1
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
Clinical genetic testing in Parkinson’s disease should become part of routine patient care
Ziv Gan‐Or
Brain (2024) Vol. 147, Iss. 8, pp. 2595-2597
Closed Access | Times Cited: 5
Large-scale genetic characterization of Parkinson′s disease in the African and African admixed populations
Fulya Akçimen, Kimberly Paquette, Peter Wild Crea, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Classification and Genotype–Phenotype Relationships of GBA1 Variants: MDSGene Systematic Review
Malco Rossi, Susen Schaake, Tatiana Usnich, et al.
Movement Disorders (2025)
Open Access
A novel alpha-synuclein K58N missense variant in a patient with Parkinson's disease
Mohammed Al-Azzani, Sandrina Weber, Nagendran Ramalingam, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
La maladie de Parkinson : de la génétique aux thérapies ciblées
Guillaume Cogan, Alexis Brice
Comptes Rendus Biologies (2025) Vol. 348, Iss. G1, pp. 21-33
Open Access
18F-FDG PET findings in Parkinson's disease associated to RAB 32 S71R variant
Francesco Cavallieri, Alessandro Fraternali, Annachiara Arnone, et al.
Parkinsonism & Related Disorders (2025) Vol. 134, pp. 107343-107343
Closed Access
Polygenic Risk Score Combined with Transcranial Sonography Refines Parkinson's Disease Risk Prediction
Mart Kals, Anu Reigo, Maris Teder‐Laving, et al.
Movement Disorders Clinical Practice (2025)
Open Access
PTEN: a new dawn in Parkinson’s disease treatment
Xiuna Yang, Tianqi Liu, Hong Cheng
Frontiers in Cellular Neuroscience (2025) Vol. 19
Open Access
The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population
Lara M. Lange, Kristin Levine, Susan H. Fox, et al.
npj Parkinson s Disease (2025) Vol. 11, Iss. 1
Open Access
Convention vs. Innovation II: Genetic profiles should be a standard consideration in the assessment for deep brain stimulation candidacy for people with Parkinson’s disease (PSG Debate 2024)
Thomas F. Tropea, Saar Anis, Ramirez-Zamora Adolfo
Parkinsonism & Related Disorders (2025), pp. 107810-107810
Closed Access
RAB32 mutation in Parkinson's disease
Christian Beetz, Mandy Radefeldt, Kornélia Tripolszki, et al.
The Lancet Neurology (2024) Vol. 23, Iss. 10, pp. 961-961
Closed Access | Times Cited: 3
Genetic and Epidemiological Insights into RAB32‐Linked Parkinson's Disease
Mandy Radefeldt, Sabrina Lemke, Kridsadakorn Chaichoompu, et al.
Movement Disorders (2024)
Open Access | Times Cited: 2
A Global Perspective of GBA1-Related Parkinson’s Disease: A Narrative Review
Christos Koros, Anastasia Bougea, Ioanna Alefanti, et al.
Genes (2024) Vol. 15, Iss. 12, pp. 1605-1605
Open Access | Times Cited: 2
Identification of Genetic Variants in Progressive Supranuclear Palsy in Southeast Asia
Adeline Su Lyn Ng, Ai Huey Tan, Yi Jayne Tan, et al.
Movement Disorders (2024) Vol. 39, Iss. 10, pp. 1829-1842
Closed Access | Times Cited: 1
Global Perspectives on Returning Genetic Research Results in Parkinson Disease
Ai Huey Tan, Paula Saffie Awad, Artur Francisco Schumacher Schuh, et al.
Neurology Genetics (2024) Vol. 10, Iss. 6
Closed Access | Times Cited: 1
Exploring Environmental Modifiers of LRRK2-Associated Parkinson’s Disease Penetrance through Exposomics and Metagenomics of Household Dust
Begoña Talavera Andújar, Sandro L. Pereira, Susheel Bhanu Busi, et al.
(2024)
Open Access
Pesticides and lifestyle factors are associated with disease severity of Parkinson's disease: a longitudinal study
Theresa Lüth, Amke Caliebe, Carolin Gabbert, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Are rare heterozygous SYNJ1 variants associated with Parkinson’s disease?
Konstantin Senkevich, Sitki Cem Parlar, Cloe Chantereault, et al.
npj Parkinson s Disease (2024) Vol. 10, Iss. 1
Open Access
Exploring environmental modifiers of LRRK2-associated Parkinson’s disease penetrance: An exposomics and metagenomics pilot study on household dust
Begoña Talavera Andújar, Sandro L. Pereira, Susheel Bhanu Busi, et al.
Environment International (2024) Vol. 194, pp. 109151-109151
Open Access
Genetic-based diagnostics of Parkinson’s disease and other Parkinsonian syndromes
Emma N. Somerville, Ziv Gan-Or
Expert Review of Molecular Diagnostics (2024), pp. 1-13
Closed Access
Cerebral Amyloid-β Deposition, Axial Features, and Cognitive Alterations in Patients with Parkinson’s Disease Treated with Bilateral STN-DBS: A Long-Term Cohort Study
Francesco Cavallieri, Alessandro Fraternali, Annachiara Arnone, et al.
Journal of Personalized Medicine (2024) Vol. 14, Iss. 12, pp. 1150-1150
Open Access
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