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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:

Variant reclassification and clinical implications
Nicola Walsh, Aislinn Cooper, Adrian Dockery, et al.
Journal of Medical Genetics (2024) Vol. 61, Iss. 3, pp. 207-211
Open Access | Times Cited: 22

Showing 22 citing articles:

Long-term experience with gene augmentation therapy in patients with inherited retinal disease associated with biallelic mutations in RPE65
Birgit Lorenz
Medizinische Genetik (2025) Vol. 37, Iss. 1, pp. 47-56
Closed Access | Times Cited: 1
Genetic Counseling and Genetic Testing for Familial Hypercholesterolemia
Hayato Tada, Masa‐aki Kawashiri, Atsushi Nohara, et al.
Genes (2024) Vol. 15, Iss. 3, pp. 297-297
Open Access | Times Cited: 5
A Multidisciplinary Approach to Navigating Variants of Uncertain Significance in Sudden Infant Deaths
Renee Ouellette, Austin Pagani, Lydia D. Hellwig, et al.
American Journal of Forensic Medicine & Pathology (2025)
Closed Access
Functional Characterization and In Silico Prediction Tools Improve the Pathogenicity Prediction of Novel Bile Acid Transporter Variants
Ziyue Peng, Xin Wang, Ying Li, et al.
Clinical Genetics (2025)
Open Access
Hemoglobin Variants as Targets for Stabilizing Drugs
Miroslava Žoldáková, Michal Novotný, Krishna P. Khakurel, et al.
Molecules (2025) Vol. 30, Iss. 2, pp. 385-385
Open Access
Germline variants detected by multigene panel testing in patients with suspected hereditary breast cancer
Yusa Togashi, Masayuki Nagahashi, Mina Kashima, et al.
Surgery Today (2025)
Open Access
Genomic sequencing: the case for equity of care in the era of personalized medicine
Lina Ghaloul‐Gonzalez, Lisa S. Parker, Jonathan M. Davis, et al.
Pediatric Research (2025)
Closed Access
DNA Methylation-Based Classification of the Central Nervous System Tumors, Achievements, and Challenges
Pramath Kakodkar, Kyle Conway, Lucas Santana‐Santos, et al.
IntechOpen eBooks (2025)
Closed Access
Reclassification of variants of uncertain significance by race, ethnicity, and ancestry for patients at risk for breast cancer
Versha Pleasant, James E. Boggan, Blair Richards, et al.
Frontiers in Oncology (2025) Vol. 15
Open Access
Hereditary Angioedema with Normal C1 Inhibitor: an Updated International Consensus Paper on Diagnosis, Pathophysiology, and Treatment
Bruce L. Zuraw, Konrad Bork, Laurence Bouillet, et al.
Clinical Reviews in Allergy & Immunology (2025) Vol. 68, Iss. 1
Open Access
Personalised genomic strategies improve diagnostic yield in inherited retinal dystrophies: a stepwise, patient-centred approach
Cinthia Aguilera, Anna Esteve-Garcia, Ariadna Padró‐Miquel, et al.
Research Square (Research Square) (2025)
Closed Access
Biobanking and gynecologic oncology - Special considerations, challenges and opportunities
Laura Grech, Celine Ann Grech, Jean Calleja‐Agius, et al.
European Journal of Surgical Oncology (2025), pp. 109713-109713
Closed Access
There will always be variants of uncertain significance. Analysis of VUSs
Haoyang Zhang, Muhammad Kabir, Saeed Ahmed, et al.
NAR Genomics and Bioinformatics (2024) Vol. 6, Iss. 4
Open Access | Times Cited: 1
Variability of Clinical Phenotypes Caused by Isolated Defects of Mitochondrial ATP Synthase
Kateřina Tauchmannová, Alena Pecinová, J Houštěk, et al.
Physiological Research (2024), Iss. Suppl 1, pp. S243-S278
Open Access | Times Cited: 1
Unrecognised actionability for breast cancer risk variants identified in a national-level review of Australian familial cancer centres
Cristina Fortuño, Elisa J. Cops, Aimee L. Davidson, et al.
European Journal of Human Genetics (2024)
Open Access | Times Cited: 1
SID/SIEDP expert consensus on optimizing clinical strategies for early detection and management of wolfram syndrome
Giulio Frontino, Maurizio Delvecchio, Sabrina Prudente, et al.
Journal of Endocrinological Investigation (2024)
Open Access | Times Cited: 1
Unrecognised actionability for breast cancer risk variants identified in a national-level review of Australian familial cancer centres
Amanda B. Spurdle, Cristina Fortuño, Elisa J. Cops, et al.
Research Square (Research Square) (2024)
Open Access
Understanding Genetic Testing in Healthy Individuals, and Related Regulations in Korea
Kyung Park, Yoonjung Kim, Saeam Shin, et al.
Laboratory Medicine Online (2024) Vol. 14, Iss. 3, pp. 201-207
Closed Access
Paired comparison of the analytical performance between the Oncomine™ Comprehensive Assay v3 and whole-exome sequencing of ovarian cancer tissue
Joanna Lopacinska‐Jørgensen, Lau K. Vestergaard, Lone Schejbel, et al.
Molecular Biology Reports (2024) Vol. 51, Iss. 1
Open Access
Germline Variants of Uncertain Significance in Gynecologic Oncology Patients
Julia Cooper, Leigha Senter
Clinical Obstetrics & Gynecology (2024)
Closed Access
Automated variant re-evaluation is labor-balanced and gives clinically relevant results: hereditary cardiac disease as a use case.
Anne Grosen, Charlotte Kvist Lautrup, Emil Bahsen, et al.
European Journal of Medical Genetics (2024), pp. 104981-104981
Open Access
The Excess of Carriers in Rare Disorders Suggests a Nonpathogenic Effect for Most Variants of Uncertain Significance
Stefano Medaglia, Jaume Reig‐Palou, Ariadna Bellés, et al.
Clinical Genetics (2024) Vol. 107, Iss. 3, pp. 323-327
Open Access
Successful Transition to Sulfonylurea for Relapsed Monogenic Diabetes Due to Rare 6q23.3 Duplication
Dalia Hassan, David B. Allen, Melinda Chen
JCEM Case Reports (2024) Vol. 2, Iss. 10
Open Access
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