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:

Assigning mutational signatures to individual samples and individual somatic mutations with SigProfilerAssignment
Marcos Díaz‐Gay, Raviteja Vangara, Mark Barnes, et al.
Bioinformatics (2023) Vol. 39, Iss. 12
Open Access | Times Cited: 46

Showing 1-25 of 46 citing articles:

Geographic variation of mutagenic exposures in kidney cancer genomes
S. Senkin, Sarah Moody, Marcos Díaz‐Gay, et al.
Nature (2024) Vol. 629, Iss. 8013, pp. 910-918
Open Access | Times Cited: 25

Whole genome and transcriptome integrated analyses guide clinical care of pediatric poor prognosis cancers
Rebecca Deyell, Yaoqing Shen, Emma Titmuss, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 9

TEX264 drives selective autophagy of DNA lesions to promote DNA repair and cell survival
Pauline Lascaux, Gwendoline Hoslett, Sara Tribble, et al.
Cell (2024)
Open Access | Times Cited: 9

Arsenic is a potent co-mutagen of ultraviolet light
Rachel M. Speer, Shuvro P. Nandi, Karen L. Cooper, et al.
Communications Biology (2023) Vol. 6, Iss. 1
Open Access | Times Cited: 18

A review on trends in development and translation of omics signatures in cancer
Wei Ma, Wenshu Tang, Jamie Sui-Lam Kwok, et al.
Computational and Structural Biotechnology Journal (2024) Vol. 23, pp. 954-971
Open Access | Times Cited: 7

A comprehensive comparison of tools for fitting mutational signatures
Matúš Medo, Charlotte K.Y. Ng, Michaela Medová
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 5

Evaluating topography of mutational signatures with SigProfilerTopography
Burçak Otlu, Ludmil B. Alexandrov
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 4

Mutational signatures of colorectal cancers according to distinct computational workflows
Paolo Battuello, Giorgio Corti, Alice Bartolini, et al.
Briefings in Bioinformatics (2024) Vol. 25, Iss. 4
Open Access | Times Cited: 4

DeepSomatic: Accurate somatic small variant discovery for multiple sequencing technologies
J.H. Park, Daniel E. Cook, Pi-Chuan Chang, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 4

Geographic and age-related variations in mutational processes in colorectal cancer
Marcos Díaz‐Gay, Wellington dos Santos, Sarah Moody, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access

A Pulmonary Nodule with an Unexpected Mutation Profile
Lulu Sun, Hannah R. Krigman, Anjali Rohatgi, et al.
Clinical Chemistry (2025) Vol. 71, Iss. 3, pp. 351-355
Closed Access

Deciphering lung adenocarcinoma evolution and the role of LINE-1 retrotransposition
Tongwu Zhang, Wei Zhao, Christopher L. Wirth, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access

Mutational signature-based biomarker to predict the response of immune checkpoint inhibitors therapy in cancers
Yue Huang, Shunheng Zhou, Sina Chen, et al.
International Journal of Biological Macromolecules (2025) Vol. 308, pp. 142585-142585
Closed Access

The complexity of tobacco smoke-induced mutagenesis in head and neck cancer
Laura Torrens, Sarah Moody, Ana Carolina de Carvalho, et al.
Nature Genetics (2025)
Open Access

Germline mutation rates and fine-scale recombination parameters in zebra finch
Djivan Prentout, Daria Bykova, Carla Hoge, et al.
PLoS Genetics (2025) Vol. 21, Iss. 4, pp. e1011661-e1011661
Open Access

Constitutional mismatch repair deficiency mimicking Lynch syndrome is associated with hypomorphic mismatch repair gene variants
Richard Gallon, Carlijn Brekelmans, Marie Martin, et al.
npj Precision Oncology (2024) Vol. 8, Iss. 1
Open Access | Times Cited: 3

DNA polymerase ε and δ variants drive mutagenesis in polypurine tracts in human tumors
Daria Ostroverkhova, Kathrin Tyryshkin, Annette K. Beach, et al.
Cell Reports (2024) Vol. 43, Iss. 1, pp. 113655-113655
Open Access | Times Cited: 2

G-Quadruplex Forming DNA Sequence Context Is Enriched around Points of Somatic Mutations in a Subset of Multiple Myeloma Patients
Anna S. Zhuk, Elena I. Stepchenkova, Irina V. Zotova, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 10, pp. 5269-5269
Open Access | Times Cited: 2

Revealing SARS-CoV-2 Mpro Mutation Cold and Hot Spots: Dynamic Residue Network Analysis Meets Machine Learning
Victor Barozi, Shrestha Chakraborty, S. Govender, et al.
Computational and Structural Biotechnology Journal (2024) Vol. 23, pp. 3800-3816
Open Access | Times Cited: 2

The mutagenic forces shaping the genomic landscape of lung cancer in never smokers
Marcos Díaz‐Gay, Tongwu Zhang, Phuc H. Hoang, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1

Glioma oncogenesis in the constitutional mismatch repair deficiency (CMMRD) syndrome
Léa Guerrini‐Rousseau, Jane Merlevede, Philippe Denizeau, et al.
Neuro-Oncology Advances (2024) Vol. 6, Iss. 1
Open Access | Times Cited: 1

Detecting HRD in whole-genome and whole-exome sequenced breast and ovarian cancers
Ammal Abbasi, Christopher D. Steele, Erik N. Bergstrom, et al.
(2024)
Open Access | Times Cited: 1

Protein and mRNA Expression in Uveal Melanoma Cell Lines Are Related to GNA and BAP1 Mutation Status
Maria C. Gelmi, Arnoud H. de Ru, Peter A. van Veelen, et al.
Investigative Ophthalmology & Visual Science (2024) Vol. 65, Iss. 8, pp. 37-37
Open Access | Times Cited: 1

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