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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:

Worldwide barriers to genetic testing for movement disorders
Emilia Gatto, Ruth H. Walker, Claudio González, et al.
European Journal of Neurology (2021) Vol. 28, Iss. 6, pp. 1901-1909
Open Access | Times Cited: 37

Showing 1-25 of 37 citing articles:

Precision medicine for genetic epilepsy on the horizon: Recent advances, present challenges, and suggestions for continued progress
Juliet K. Knowles, Ingo Helbig, Cameron S. Metcalf, et al.
Epilepsia (2022) Vol. 63, Iss. 10, pp. 2461-2475
Open Access | Times Cited: 89
Deep learning-derived 12-lead electrocardiogram-based genotype prediction for hypertrophic cardiomyopathy: a pilot study
Laite Chen, Xia Sheng, Chenyang Jiang
Annals of Medicine (2023) Vol. 55, Iss. 1
Open Access | Times Cited: 17
Genetic Testing in Parkinson's Disease
Gian Pal, Lola Cook, Jeanine Schulze, et al.
Movement Disorders (2023) Vol. 38, Iss. 8, pp. 1384-1396
Open Access | Times Cited: 16
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 Landscape of Complex Childhood‐Onset Hyperkinetic Movement Disorders
Belén Pérez‐Dueñas, Kathleen M. Gorman, Anna Marcé‐Grau, et al.
Movement Disorders (2022) Vol. 37, Iss. 11, pp. 2197-2209
Open Access | Times Cited: 19
Artificial Intelligence‐Based Virtual Assistant for the Diagnostic Approach of Chronic Ataxias
Lucas Alessandro, Nicolas Bianciotti, Luciana Salama, et al.
Movement Disorders (2025)
Closed Access
Hereditary Ataxias in Argentina
Malco Rossi, Marcelo Merello
The Cerebellum (2025) Vol. 24, Iss. 3
Closed Access
International Genetic Testing and Counseling Practices for Parkinson's Disease
Rachel Saunders‐Pullman, Deborah Raymond, Roberto A. Ortega, et al.
Movement Disorders (2023) Vol. 38, Iss. 8, pp. 1527-1535
Closed Access | Times Cited: 10
Parkinson's Disease, Diagnosis
Roongroj Bhidayasiri, Claudia Trenkwalder
Elsevier eBooks (2024)
Closed Access | Times Cited: 2
Genome Sequencing in the Parkinson Disease Clinic
Emily J. Hill, Laurie Robak, Rami Al‐Ouran, et al.
Neurology Genetics (2022) Vol. 8, Iss. 4
Open Access | Times Cited: 12
Global Perspectives on Returning Genetic Research Results in Parkinson's Disease
Ai Huey Tan, Paula Saffie Awad, Artur Francisco Schumacher Schuh, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Genetic Testing for Parkinson's Disease and Movement Disorders in Less Privileged Areas: Barriers and Opportunities
Ai Huey Tan, Mario Cornejo‐Olivas, Njideka Okubadejo, et al.
Movement Disorders Clinical Practice (2023) Vol. 11, Iss. 1, pp. 14-20
Closed Access | Times Cited: 6
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
The importance of genetic testing for dystonia patients and translational research
Jelena Pozojevic, Christian Beetz, Ana Westenberger
Journal of Neural Transmission (2021) Vol. 128, Iss. 4, pp. 473-481
Open Access | Times Cited: 9
Gene-Targeted Therapies in Pediatric Neurology: Challenges and Opportunities in Diagnosis and Delivery
Renée A. Shellhaas, Gabrielle deVeber, Joshua L. Bonkowsky, et al.
Pediatric Neurology (2021) Vol. 125, pp. 53-57
Open Access | Times Cited: 9
The Genetic Testing Experience of Individuals with Parkinson's Disease
Sydney Richards, Weiyi Mu, Rachel Nusbaum, et al.
Movement Disorders Clinical Practice (2022) Vol. 10, Iss. 2, pp. 248-257
Open Access | Times Cited: 4
Short Report: Clinical Features and Epilepsy Monitoring in an Adult With 22q11.2 Deletion Syndrome
Mike W. Zhang, Stephanie Bustros, Tyler E. Gaston, et al.
The Neurohospitalist (2024) Vol. 14, Iss. 3, pp. 273-277
Closed Access
The role of genetics in the treatment of dystonia with deep brain stimulation: Systematic review and Meta-analysis
Harini Sarva, Federico Rodríguez‐Porcel, Francisco Rivera, et al.
Journal of the Neurological Sciences (2024) Vol. 459, pp. 122970-122970
Closed Access
Dystonia
Katja Lohmann, Christine Klein
Elsevier eBooks (2024), pp. 133-170
Closed Access
Factors impacting time to genetic diagnosis for children with epilepsy
Megan Rimmasch, Carey Wilson, Nephi Walton, et al.
Epilepsia Open (2024)
Open Access
Management of rare movement diseases in different world regions
Cèlia Painous, Marı́a José Martı́, Holm Graeßner, et al.
Parkinsonism & Related Disorders (2023) Vol. 108, pp. 105286-105286
Open Access | Times Cited: 1
Assessment of the Needs of Nephrology Divisions to Implement Return of Clinically Significant Research Genetic Results: A Survey of Nephrotic Syndrome Study Network (NEPTUNE) Investigators
Jennifer Fishbein, Loryn W. Dass, Chrysta Lienczewski, et al.
Glomerular Diseases (2023) Vol. 3, Iss. 1, pp. 178-188
Open Access | Times Cited: 1
Systematic mapping review of guidelines forBRCA1/2genetic testing globally: investigating geographic and regional disparities in health equity for women and families at risk for hereditary ovarian cancer
Brittany N. Hughes, Kirsten Jorgensen, Shelly Cummings, et al.
International Journal of Gynecological Cancer (2022) Vol. 33, Iss. 2, pp. 250-256
Closed Access | Times Cited: 1
Revolución genética: apertura a nuevos desafíos y oportunidades
Paula Saffie Awad, Ignácio F. Mata, Pedro Chaná‐Cuevas
Revista médica de Chile (2022) Vol. 150, Iss. 11, pp. 1547-1548
Open Access | Times Cited: 1
Case Reports and Movement Disorder Rounds: Learning through observation, building on collective experiences
Ai Huey Tan, Emilia Gatto
Parkinsonism & Related Disorders (2023) Vol. 110, pp. 105396-105396
Closed Access
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