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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:

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

Showing 1-25 of 87 citing articles:

The epidemiology of Parkinson's disease
Yoav Ben‐Shlomo, Sirwan K.L. Darweesh, Jorge J. Llibre‐Guerra, et al.
The Lancet (2024) Vol. 403, Iss. 10423, pp. 283-292
Closed Access | Times Cited: 307
A biological classification of Parkinson's disease: the SynNeurGe research diagnostic criteria
Günter U. Höglinger, Charles H. Adler, Daniela Berg, et al.
The Lancet Neurology (2024) Vol. 23, Iss. 2, pp. 191-204
Closed Access | Times Cited: 228
An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA27B/ATX-FGF14
Haloom Rafehi, Justin Read, David J. Szmulewicz, et al.
The American Journal of Human Genetics (2022) Vol. 110, Iss. 1, pp. 105-119
Open Access | Times Cited: 107
Optimized testing strategy for the diagnosis of GAA-FGF14 ataxia/spinocerebellar ataxia 27B
Céline Bonnet, David Pellerin, Virginie Roth, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 50
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
Genetics and Pathogenesis of Dystonia
Mirja Thomsen, Lara M. Lange, Michael Zech, et al.
Annual Review of Pathology Mechanisms of Disease (2023) Vol. 19, Iss. 1, pp. 99-131
Open Access | Times Cited: 39
CAG Repeat Expansion in THAP11 Is Associated with a Novel Spinocerebellar Ataxia
Dandan Tan, Cuijie Wei, Zhao Chen, et al.
Movement Disorders (2023) Vol. 38, Iss. 7, pp. 1282-1293
Open Access | Times Cited: 33
Different pieces of the same puzzle: a multifaceted perspective on the complex biological basis of Parkinson’s disease
Amica Corda Müller-Nedebock, Marieke C. J. Dekker, Matthew J. Farrer, et al.
npj Parkinson s Disease (2023) Vol. 9, Iss. 1
Open Access | Times Cited: 30
Analysis of rare Parkinson’s disease variants in millions of people
Vanessa Pitz, Mary B. Makarious, Sara Bandrés‐Ciga, et al.
npj Parkinson s Disease (2024) Vol. 10, Iss. 1
Open Access | Times Cited: 15
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
Next-generation sequencing and bioinformatics in rare movement disorders
Michael Zech, J C Winkelmann
Nature Reviews Neurology (2024) Vol. 20, Iss. 2, pp. 114-126
Closed Access | Times Cited: 10
Spiking Patterns in the Globus Pallidus Highlight Convergent Neural Dynamics across Diverse Genetic Dystonia Syndromes
Ahmet Kaymak, Fabiana Colucci, Mahboubeh Ahmadipour, et al.
Annals of Neurology (2025)
Open Access | Times Cited: 1
Towards a Biological Definition of Parkinson’s Disease
Günter U. Höglinger, Charles H. Adler, Daniela Berg, et al.
(2023)
Open Access | Times Cited: 18
Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insights
Burcu Atasu, Javier Simón‐Sánchez, Haşmet Hanağası, et al.
Journal of Medical Genetics (2024), pp. jmg-109099
Open Access | Times Cited: 6
The role of the PLA2G6 gene in neurodegenerative diseases
Xinyue Deng, Lamei Yuan, Joseph Jankovic, et al.
Ageing Research Reviews (2023) Vol. 89, pp. 101957-101957
Closed Access | Times Cited: 14
Genetic Testing of Movements Disorders: A Review of Clinical Utility
Dennis Yeow, Laura Ivete Rudaks, Sue‐Faye Siow, et al.
Tremor and Other Hyperkinetic Movements (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 5
The genetic spectrum of a cohort of patients clinically diagnosed as Parkinson’s disease in mainland China
Yi‐Min Sun, Xinyue Zhou, Xiaoniu Liang, et al.
npj Parkinson s Disease (2023) Vol. 9, Iss. 1
Open Access | Times Cited: 12
MDSGene: Extending the List of Isolated Dystonia Genes by VPS16, EIF2AK2, and AOPEP
Mirja Thomsen, Lara M. Lange, Christine Klein, et al.
Movement Disorders (2023) Vol. 38, Iss. 3, pp. 507-508
Open Access | Times Cited: 11
α-synuclein regulates Cyclin D1 to promote abnormal initiation of the cell cycle and induce apoptosis in dopamine neurons
Xiaokang Jia, Qiliang Chen, Ciyu Yao, et al.
Biomedicine & Pharmacotherapy (2024) Vol. 173, pp. 116444-116444
Open Access | Times Cited: 4
Prasinezumab: A Bayesian Perspective on Its Efficacy
Mirella Russo, Tommaso Costa, Dario Calisi, et al.
Movement Disorders (2025)
Open Access
Eye movement disorders in genetic dystonia syndromes: a literature overview
Luca Pollini, Ilaria Pettenuzzo, Marina A.J. Tijssen, et al.
Parkinsonism & Related Disorders (2025), pp. 107325-107325
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
Movement Disorders in Hereditary Cerebellar Ataxia
Joana Damásio, Sara T. Costa, João Moura, et al.
Movement Disorders Clinical Practice (2025)
Closed Access
A De Novo SCN2A Variant in a Patient with Adult‐Onset Dystonia Parkinsonism and Nigrostriatal Denervation
Marco Bisquoli, Francesco Cavallieri, Giulia Di Rauso, et al.
Movement Disorders Clinical Practice (2025)
Closed Access
Genetic Etiology Influences the Low‐Frequency Components of Globus Pallidus Internus Electrophysiology in Dystonia
Ahmet Kaymak, Luigi Romito, Fabiana Colucci, et al.
European Journal of Neurology (2025) Vol. 32, Iss. 3
Open Access
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