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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:

Variants of uncertain significance in the era of high-throughput genome sequencing: a lesson from breast and ovary cancers
G. Federici, Silvia Soddu
Journal of Experimental & Clinical Cancer Research (2020) Vol. 39, Iss. 1
Open Access | Times Cited: 162

Showing 1-25 of 162 citing articles:

CHEK2 Germline Variants in Cancer Predisposition: Stalemate Rather than Checkmate
Lenka Stolařová, Petra Kleiblová, Markéta Janatová, et al.
Cells (2020) Vol. 9, Iss. 12, pp. 2675-2675
Open Access | Times Cited: 158
Patient-derived tumor organoids: a new avenue for preclinical research and precision medicine in oncology
Lucie Thorel, Marion Perréard, Romane Florent, et al.
Experimental & Molecular Medicine (2024) Vol. 56, Iss. 7, pp. 1531-1551
Open Access | Times Cited: 17
The emerging roles of NGS in clinical oncology and personalized medicine
Bashdar Mahmud Hussen, Sara Tharwat Abdullah, Abbas Salihi, et al.
Pathology - Research and Practice (2022) Vol. 230, pp. 153760-153760
Closed Access | Times Cited: 50
RosettaDDGPrediction for high‐throughput mutational scans: From stability to binding
Valentina Sora, Adrian Otamendi Laspiur, Kristine Degn, et al.
Protein Science (2022) Vol. 32, Iss. 1
Open Access | Times Cited: 41
Considerations for hereditary breast and ovarian cancer syndrome molecular diagnosis: experience from the clinical practice
Míriam Potrony, Blai Morales‐Romero, Lorena Moreno, et al.
Breast Cancer Research and Treatment (2025)
Closed Access | Times Cited: 1
Combining Ramachandran plot and molecular dynamics simulation for structural-based variant classification: Using TP53 variants as model
Benjamin Tam, Siddharth Sinha, San Ming Wang
Computational and Structural Biotechnology Journal (2020) Vol. 18, pp. 4033-4039
Open Access | Times Cited: 50
Primary ciliary dyskinesia
Johanna Raidt, Niki T. Loges, Heike Olbrich, et al.
La Presse Médicale (2023) Vol. 52, Iss. 3, pp. 104171-104171
Closed Access | Times Cited: 20
NCSTN In-Frame Deletion in Maltese Patients With Hidradenitis Suppurativa
Dillon Mintoff, Nikolai Paul Pace, Isabella Borg
JAMA Dermatology (2023) Vol. 159, Iss. 9, pp. 939-939
Open Access | Times Cited: 14
Machine learning-based reclassification of germline variants of unknown significance: The RENOVO algorithm
Valentina Favalli, Giulia Tini, Emanuele Bonetti, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 4, pp. 682-695
Open Access | Times Cited: 31
Is there a duty to routinely reinterpret genomic variant classifications?
Gabriel Watts, Ainsley J. Newson
Journal of Medical Ethics (2023) Vol. 49, Iss. 12, pp. 808-814
Open Access | Times Cited: 11
Fusion Challenges in Solid Tumors: Shaping the Landscape of Cancer Care in Precision Medicine
Jibran Ahmed, Carlos Torrado, Anca Chelariu, et al.
JCO Precision Oncology (2024), Iss. 8
Open Access | Times Cited: 4
Clinical and Molecular Characterization of SMAD4 Splicing Variants in Patients with Juvenile Polyposis Syndrome
Giovanna Forte, Antonia Lucia Buonadonna, Candida Fasano, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 14, pp. 7939-7939
Open Access | Times Cited: 4
Exploring the NANOG-TET2 interaction interface. Effects of a selected mutation and hypothesis on the clinical correlation with anemias
Claudia Testi, Roberta Piacentini, Alessandro Perrone, et al.
Frontiers in Chemical Biology (2025) Vol. 3
Open Access
Enhancer regulatory networks globally connect non-coding breast cancer loci to cancer genes
Yihan Wang, Daniel Armendariz, Lei Wang, et al.
Genome biology (2025) Vol. 26, Iss. 1
Open Access
Sudden Cardiac Death: The Role of Molecular Autopsy with Next-Generation Sequencing
Jennifer Fadoni, Agostinho Santos, António Amorim, et al.
Diagnostics (2025) Vol. 15, Iss. 4, pp. 460-460
Open Access
Sudden cardiac death: the role of molecular autopsy with next-generation sequencing
Jennifer Fadoni, Agostinho Santos, Laura Cainé, et al.
Journal of Forensic and Legal Medicine (2025), pp. 102837-102837
Closed Access
Genetic Profiling of Acute and Chronic Leukemia via Next-Generation Sequencing: Current Insights and Future Perspectives
Laras Pratiwi, Fawzia Hanum Mashudi, Mukti Citra Ningtyas, et al.
Hematology Reports (2025) Vol. 17, Iss. 2, pp. 18-18
Open Access
Epigenomic insights and computational advances in hematologic malignancies
Carolyn Lauzon-Young, Ananilia Silva, Bekim Sadiković
Molecular Cytogenetics (2025) Vol. 18, Iss. 1
Open Access
High-Throughput Affinity Measurements of Transcription Factor and DNA Mutations Reveal Affinity and Specificity Determinants
Arjun K. Aditham, Craig J. Markin, Daniel A. Mokhtari, et al.
Cell Systems (2020) Vol. 12, Iss. 2, pp. 112-127.e11
Open Access | Times Cited: 31
Experiences of individuals with a variant of uncertain significance on genetic testing for hereditary cancer risks: a mixed method systematic review
Danielle Gould, Rae Walker, Grace Makari‐Judson, et al.
Journal of Community Genetics (2022) Vol. 13, Iss. 4, pp. 371-379
Open Access | Times Cited: 18
Multiparametric and accurate functional analysis of genetic sequence variants using CRISPR-Select
Yiyuan Niu, Catarina A. Ferreira Azevedo, Xin Li, et al.
Nature Genetics (2022) Vol. 54, Iss. 12, pp. 1983-1993
Open Access | Times Cited: 16
Domain-specific p53 mutants activate EGFR by distinct mechanisms exposing tissue-independent therapeutic vulnerabilities
Teresa L. Ho, May Yin Lee, Hui Chin Goh, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 10
POSTRE: a tool to predict the pathological effects of human structural variants
Víctor Sánchez-Gaya, Álvaro Rada-Iglesias
Nucleic Acids Research (2023) Vol. 51, Iss. 9, pp. e54-e54
Open Access | Times Cited: 10
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
Chromosome 3p gene alterations as biomarkers for immunocombinations in metastatic renal cell carcinoma: A hypothesis-generating analysis
Matteo Rosellini, Veronica Mollica, Andrea Marchetti, et al.
Pathology - Research and Practice (2024) Vol. 254, pp. 155142-155142
Closed Access | Times Cited: 3
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