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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:

Implementation of Whole-Genome and Transcriptome Sequencing Into Clinical Cancer Care
Edwin Cuppen, Olivier Elemento, Richard Rosenquist, et al.
JCO Precision Oncology (2022), Iss. 6
Open Access | Times Cited: 54

Showing 1-25 of 54 citing articles:

Tumour response to hypoxia: understanding the hypoxic tumour microenvironment to improve treatment outcome in solid tumours
Kamilla J. A. Bigos, Conrado Guerrero Quiles, Sapna Lunj, et al.
Frontiers in Oncology (2024) Vol. 14
Open Access | Times Cited: 27
Precision cancer medicine: Concepts, current practice, and future developments
Anders Edsjö, Louise Holmquist, Birgit Geoerger, et al.
Journal of Internal Medicine (2023) Vol. 294, Iss. 4, pp. 455-481
Open Access | Times Cited: 24
Analysis of 10,478 cancer genomes identifies candidate driver genes and opportunities for precision oncology
Ben Kinnersley, Amit Sud, Andrew Everall, et al.
Nature Genetics (2024) Vol. 56, Iss. 9, pp. 1868-1877
Open Access | Times Cited: 13
Benefits for children with suspected cancer from routine whole-genome sequencing
Angus Hodder, Sarah M. Leiter, Jonathan Kennedy, et al.
Nature Medicine (2024) Vol. 30, Iss. 7, pp. 1905-1912
Open Access | Times Cited: 10
Current challenges and practical aspects of molecular pathology for non-small cell lung cancers
Paul Hofman, Sabina Berezowska, Daniel Kazdal, et al.
Virchows Archiv (2023) Vol. 484, Iss. 2, pp. 233-246
Open Access | Times Cited: 20
Novel precision medicine approaches and treatment strategies in hematological malignancies
Richard Rosenquist, Elsa Bernard, Tom Erkers, et al.
Journal of Internal Medicine (2023) Vol. 294, Iss. 4, pp. 413-436
Open Access | Times Cited: 19
Deep-Learning Model for Tumor-Type Prediction Using Targeted Clinical Genomic Sequencing Data
Madison Darmofal, Shalabh Suman, Gurnit Atwal, et al.
Cancer Discovery (2024) Vol. 14, Iss. 6, pp. 1064-1081
Open Access | Times Cited: 7
Epigenetic biomarkers for disease susceptibility and preventative medicine
Michael K. Skinner
Cell Metabolism (2024) Vol. 36, Iss. 2, pp. 263-277
Closed Access | Times Cited: 6
Long-read sequencing of an advanced cancer cohort resolves rearrangements, unravels haplotypes, and reveals methylation landscapes
Kieran O’Neill, Erin Pleasance, Jeremy Fan, et al.
Cell Genomics (2024) Vol. 4, Iss. 11, pp. 100674-100674
Open Access | Times Cited: 6
Anaesthesia, analgesia, and cancer outcomes: time to think like oncologists?
Joshua S. Mincer, Donal J. Buggy
British Journal of Anaesthesia (2023) Vol. 131, Iss. 2, pp. 193-196
Open Access | Times Cited: 15
Implementing patient derived organoids in functional precision medicine for patients with advanced colorectal cancer
Jérôme Cartry, Sabrina Bedja, Alice Boilève, et al.
Journal of Experimental & Clinical Cancer Research (2023) Vol. 42, Iss. 1
Open Access | Times Cited: 14
High‐throughput molecular assays for inclusion in personalised oncology trials – State‐of‐the‐art and beyond
Anders Edsjö, Hege G. Russnes, Janne Lehtiö, et al.
Journal of Internal Medicine (2024) Vol. 295, Iss. 6, pp. 785-803
Open Access | Times Cited: 5
Exploration of the regulatory mechanism of Norcantharidin on sine oculis homeobox homolog 4 in colon cancer using transcriptome sequencing and bioinformatic
Fanqin Zhang, Chao Wu, Jingyuan Zhang, et al.
Journal of Traditional Chinese Medical Sciences (2025)
Open Access
Simultaneous Ultra-Sensitive Detection of Structural and Single Nucleotide Variants Using Multiplex Droplet Digital PCR in Liquid Biopsies from Children with Medulloblastoma
Cecilia Arthur, Cecilia Jylhä, Teresita Díaz de Ståhl, et al.
Cancers (2023) Vol. 15, Iss. 7, pp. 1972-1972
Open Access | Times Cited: 12
Feasibility to use whole-genome sequencing as a sole diagnostic method to detect genomic aberrations in pediatric B-cell acute lymphoblastic leukemia
Fatemah Rezayee, Jesper Eisfeldt, Aron Skaftason, et al.
Frontiers in Oncology (2023) Vol. 13
Open Access | Times Cited: 11
Sarcoma care in the era of precision medicine
Karin Wallander, Ingegerd Öfverholm, Kjetil Boye, et al.
Journal of Internal Medicine (2023) Vol. 294, Iss. 6, pp. 690-707
Open Access | Times Cited: 11
Current and future trends in whole genome sequencing in cancer
Yuki Katsuya
Cancer Biology and Medicine (2024) Vol. 21, Iss. 1, pp. 16-20
Open Access | Times Cited: 4
A multi-omics strategy to understand PASC through the RECOVER cohorts: a paradigm for a systems biology approach to the study of chronic conditions
Jun Sun, Masanori Aikawa, Hassan Ashktorab, et al.
Frontiers in Systems Biology (2025) Vol. 4
Open Access
Cancer Genomics, Biomarkers and Precision Medicine
Leslie E. Oldfield, Trevor J. Pugh
(2025), pp. 243-252
Closed Access
Genomics in Cancer of Unknown Primary – Utility in Modern Clinical Practice
Andrew J. Dooley, Anne Ramsay Bowden, H. Whatling, et al.
Clinical Oncology (2025) Vol. 41, pp. 103793-103793
Closed Access
Novel Molecular Methods in Soft Tissue Sarcomas: From Diagnostics to Theragnostics
Nicholas Frazzette, George Jour
Cancers (2025) Vol. 17, Iss. 7, pp. 1215-1215
Open Access
The Terry Fox Research Institute Marathon of Hope Cancer Centres Network: A pan-Canadian precision oncology initiative
Tess Aalto, Maria Abacan, Shirin Abadi, et al.
Cancer Cell (2025)
Closed Access
The Use of Artificial Intelligence for Cancer Therapeutic Decision-Making
Olivier Elemento, Sean Khozin, Cora N. Sternberg
NEJM AI (2025)
Closed Access
Current and emerging sequencing-based tools for precision cancer medicine
Anders Edsjö, David Gisselsson, Johan Staaf, et al.
Molecular Aspects of Medicine (2024) Vol. 96, pp. 101250-101250
Closed Access | Times Cited: 3
Comprehensive Genomic Profiling Alters Clinical Diagnoses in a Significant Fraction of Tumors Suspicious of Sarcoma
Ingegerd Öfverholm, Karin Wallander, Cecilia Haglund, et al.
Clinical Cancer Research (2024) Vol. 30, Iss. 12, pp. 2647-2658
Open Access | Times Cited: 3
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