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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:

Challenges of variant reinterpretation: Opinions of stakeholders and need for guidelines
Sara M. Berger, Paul S. Appelbaum, Karolynn Siegel, et al.
Genetics in Medicine (2022) Vol. 24, Iss. 9, pp. 1878-1887
Open Access | Times Cited: 19

Showing 19 citing articles:

Clinical Variant Reclassification in Hereditary Disease Genetic Testing
Yuya Kobayashi, Elaine Chen, Flavia M. Facio, et al.
JAMA Network Open (2024) Vol. 7, Iss. 11, pp. e2444526-e2444526
Open Access | Times Cited: 6
Building a Hand-Curated ceRNET for Endometrial Cancer, Striving for Clinical as Well as Medicolegal Soundness: A Systematic Review
Roberto Piergentili, Stefano Sechi, Lina De Paola, et al.
Non-Coding RNA (2025) Vol. 11, Iss. 3, pp. 34-34
Open Access
Text Mining to Understand Disease-Causing Gene Variants
Leena Nezamuldeen, M. Saleet Jafri
Knowledge (2024) Vol. 4, Iss. 3, pp. 422-443
Open Access | Times Cited: 3
Practical considerations for reinterpretation of individual genetic variants
Paul S. Appelbaum, Sara M. Berger, Elly Brokamp, et al.
Genetics in Medicine (2023) Vol. 25, Iss. 5, pp. 100801-100801
Open Access | Times Cited: 9
Application of next generation sequencing in cardiology: current and future precision medicine implications
Eirini Papadopoulou, Dimitra Bouzarelou, George S. Tsaousis, et al.
Frontiers in Cardiovascular Medicine (2023) Vol. 10
Open Access | Times Cited: 8
The frequency of gene variant reclassification and its impact on clinical management in the inherited arrhythmia clinic
William J. Young, Soe Thiha Maung, Selda Ahmet, et al.
Heart Rhythm (2024) Vol. 21, Iss. 6, pp. 903-910
Open Access | Times Cited: 3
Practices and Views of US Oncologists and Genetic Counselors Regarding Patient Recontact After Variant Reclassification: Results of a Nationwide Survey
Sukh Makhnoon, Elenita Davidson, Brian H. Shirts, et al.
JCO Precision Oncology (2023), Iss. 7
Open Access | Times Cited: 5
Improvement of variant reclassification in genetic neurodevelopmental conditions
Michelle Kowanda, Rebecca Sheedy Smith, Jamie Lundy, et al.
Genetics in Medicine Open (2024) Vol. 2, pp. 101845-101845
Open Access | Times Cited: 1
What do cancer genetic providers want us to know about variant reclassification and recontact that we are not asking? A thematic analysis of open‐ended survey responses
Kerri Brown, Marisel Ponton, Elenita Davidson, et al.
Cancer (2024)
Open Access | Times Cited: 1
Rectifying or Reinforcing? The (In)Equity Implications of Recontacting Practices in Genomic Medicine
Michael P. Mackley, Hanna Faghfoury, Lauren Chad
The Hastings Center Report (2024) Vol. 54, Iss. S2
Open Access | Times Cited: 1
Avoiding Liability and Other Legal Land Mines in the Evolving Genomics Landscape
Ellen Wright Clayton, Alex M. Tritell, Adrian Thorogood
Annual Review of Genomics and Human Genetics (2023) Vol. 24, Iss. 1, pp. 333-346
Open Access | Times Cited: 2
Breast Irradiation Is Well Tolerated in Carriers of a Pathogenic ATM Variant
Andrew H. Zureick, Dana Zakalik, Thomas J. Quinn, et al.
Practical Radiation Oncology (2023) Vol. 14, Iss. 1, pp. e29-e39
Closed Access | Times Cited: 2
Exploring the evolving roles of clinical geneticists and genetic counselors in the era of genomic medicine
Andrew Freiman, Aisha Rekab, Amanda Bergner, et al.
American Journal of Medical Genetics Part A (2023) Vol. 194, Iss. 4
Closed Access | Times Cited: 2
Assessing management practices for variants of uncertain significance among genetic counselors in pediatrics
C. H. Cheung, Sara M. Berger, M. Elizabeth Ross, et al.
Journal of Genetic Counseling (2024)
Closed Access
Variant reclassification and recontact research: A scoping review
Abhinav Thummala, Rhea Sudhakaran, Anoop Gurram, et al.
Genetics in Medicine Open (2024) Vol. 2, pp. 101867-101867
Open Access
Cases in Precision Medicine: Is There an Obligation to Return Reinterpreted Genetic Results to Former Patients?
Paul S. Appelbaum, Wylie Burke, Erik Parens, et al.
Annals of Internal Medicine (2023) Vol. 176, Iss. 4, pp. 563-567
Open Access | Times Cited: 1
Certainty in uncertainty: Determining the rate and reasons for reclassification of variants of uncertain significance in haematological malignancies
Anoop K. Enjeti, Natasha Walker, Oliver Fahey, et al.
eJHaem (2024) Vol. 5, Iss. 5, pp. 957-963
Open Access
Routinely Updating Patients With Cancer About Variant of Uncertain Significance Reclassifications: A Premature Responsibility for Community Oncologists
Linda Battistuzzi, Alberto Puccini, Stefania Sciallero, et al.
Journal of Clinical Oncology (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
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