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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:

Bioinformatics: From NGS Data to Biological Complexity in Variant Detection and Oncological Clinical Practice
Serena Dotolo, Riziero Esposito Abate, Cristin Roma, et al.
Biomedicines (2022) Vol. 10, Iss. 9, pp. 2074-2074
Open Access | Times Cited: 22

Showing 22 citing articles:

Multicentric pilot study to standardize clinical whole exome sequencing (WES) for cancer patients
Michael Menzel, Stephan Ossowski, Sebastian Kral, et al.
npj Precision Oncology (2023) Vol. 7, Iss. 1
Open Access | Times Cited: 19
Computational Biology Helps Understand How Polyploid Giant Cancer Cells Drive Tumor Success
Matheus Correia Casotti, Débora Dummer Meira, Aléxia Stefani Siqueira Zetum, et al.
Genes (2023) Vol. 14, Iss. 4, pp. 801-801
Open Access | Times Cited: 15
Revolutionizing Biological Science: The Synergy of Genomics in Health, Bioinformatics, Agriculture, and Artificial Intelligence
Aakanksha Biswas, Aditi Kumari, D. S. Gaikwad, et al.
OMICS A Journal of Integrative Biology (2023) Vol. 27, Iss. 12, pp. 550-569
Closed Access | Times Cited: 11
Leveraging artificial intelligence in next generation sequencing for head & neck cancer: opportunities and challenges
Carlos M. Chiesa‐Estomba, Antonino Maniaci, Luigi Angelo Vaira, et al.
European Archives of Oto-Rhino-Laryngology (2025)
Closed Access
Advancements in Bone Malignancy Research through Next-Generation Sequencing Focussed on Osteosarcoma, Chondrosarcoma, and Ewing sarcoma
Naveen Jeyaraman, Madhan Jeyaraman, Pearl Subramanian, et al.
Pathology - Research and Practice (2025) Vol. 269, pp. 155908-155908
Closed Access
Advancing chronic myeloid leukemia research with next-generation sequencing: potential benefits, limitations, and future clinical integration
Henry Sutanto, Laras Pratiwi, Pradana Zaky Romadhon, et al.
Human Genetics (2025)
Closed Access
Decoding driver and phenotypic genes in cancer: Unveiling the essence behind the phenomenon
Dequan Liu, Lei Liu, Xiaoman Zhang, et al.
Molecular Aspects of Medicine (2025) Vol. 103, pp. 101358-101358
Open Access
Biological and translational attributes of mitochondrial DNA copy number: Laboratory perspective to clinical relevance
Deepak Parchwani, Ragini Singh, Digisha Patel
World Journal of Methodology (2025) Vol. 15, Iss. 3
Closed Access
HybridGWOSPEA2ABC: a novel feature selection algorithm for gene expression data analysis and cancer classification
Ashimjyoti Nath, Chandan Jyoti Kumar, Sanjib Kr. Kalita, et al.
Computer Methods in Biomechanics & Biomedical Engineering (2025), pp. 1-22
Closed Access
Unveiling the genetic and epigenetic landscape of colorectal cancer: new insights into pathogenic pathways
Humzah Postwala, Yesha Shah, Priyajeet S. Parekh, et al.
Medical Oncology (2023) Vol. 40, Iss. 11
Closed Access | Times Cited: 8
Applications of Deep Learning for Drug Discovery Systems with BigData
Yasunari Matsuzaka, Ryu Yashiro
BioMedInformatics (2022) Vol. 2, Iss. 4, pp. 603-624
Open Access | Times Cited: 11
Harmonizing tumor mutational burden analysis: Insights from a multicenter study using in silico reference data sets in clinical whole-exome sequencing (WES)
Lijia Yu, Yuanfeng Zhang, Duo Wang, et al.
American Journal of Clinical Pathology (2024) Vol. 162, Iss. 4, pp. 408-419
Closed Access | Times Cited: 1
From Genomic Exploration to Personalized Treatment: Next-Generation Sequencing in Oncology
Vishakha Vashisht, Ashutosh Vashisht, Ashis K. Mondal, et al.
Current Issues in Molecular Biology (2024) Vol. 46, Iss. 11, pp. 12527-12549
Open Access | Times Cited: 1
Establishment, characterization, and drug screening of low-passage patient individual non-small cell lung cancer in vitro models including the rare pleomorphic subentity
Ingo Andus, Friedrich Prall, Michael Linnebacher, et al.
Frontiers in Oncology (2023) Vol. 13
Open Access | Times Cited: 3
Evaluation and Comparison of Multi-Omics Data Integration Methods for Subtyping of Cutaneous Melanoma
Adriana Amaro, Max J. Pfeffer, Ulrich Pfeffer, et al.
Biomedicines (2022) Vol. 10, Iss. 12, pp. 3240-3240
Open Access | Times Cited: 4
APGW/AKH Precursor from Rotifer Brachionus plicatilis and the DNA Loss Model Explain Evolutionary Trends of the Neuropeptide LWamide, APGWamide, RPCH, AKH, ACP, CRZ, and GnRH Families
Cristian E. Cadena-Caballero, Nestor Munive-Argüelles, Lina M. Vera-Cala, et al.
Journal of Molecular Evolution (2023) Vol. 91, Iss. 6, pp. 882-896
Open Access | Times Cited: 2
Biomarker Testing Journey Among Patients with Advanced Solid Tumors and Treatment Patterns by Homologous Recombination Repair Status: A Clinico-Genomic Database Study
Changxia Shao, Yixin Ren, Heng Zhou, et al.
Advances in Therapy (2024) Vol. 41, Iss. 2, pp. 759-776
Closed Access
Smart variant filtering - A blueprint solution for massively parallel sequencing-based variant analysis
Orlinda Brahimllari, Sandra Eloranta, Patrik Georgii‐Hemming, et al.
Health Informatics Journal (2024) Vol. 30, Iss. 4
Closed Access
Machine Learning Methods for Gene Selection in Uveal Melanoma
Francesco Reggiani, Zeinab El Rashed, Mariangela Petito, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 3, pp. 1796-1796
Open Access
Tools for short variant calling and the way to deal with big datasets
Adrien Le Meur, Rima Zein-Eddine, Ombeline Lamer, et al.
Elsevier eBooks (2024), pp. 219-250
Closed Access
Transcriptomic Module Discovery of Diarrhea-Predominant Irritable Bowel Syndrome: A Causal Network Inference Approach
Davide Guido, Fatima Maqoud, Michelangelo Aloisio, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 17, pp. 9322-9322
Open Access
Precision medicine in cancer treatment: Revolutionizing care through proteomics, genomics, and personalized therapies
Riddhi Jawdekar, Vaishnavi Mishra, Kajal Hatgoankar, et al.
Journal of Cancer Research and Therapeutics (2024) Vol. 20, Iss. 6, pp. 1687-1693
Open Access
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