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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:

Genetic and chemotherapeutic influences on germline hypermutation
Joanna Kaplanis, Benjamin Ide, Rashesh Sanghvi, et al.
Nature (2022) Vol. 605, Iss. 7910, pp. 503-508
Open Access | Times Cited: 74

Showing 1-25 of 74 citing articles:

Evolution of the SARS-CoV-2 Mutational Spectrum
Jesse D. Bloom, Annabel C. Beichman, Richard A. Neher, et al.
Molecular Biology and Evolution (2023) Vol. 40, Iss. 4
Open Access | Times Cited: 51
Genetic variation across and within individuals
Zhi Yu, Tim H. H. Coorens, Md Mesbah Uddin, et al.
Nature Reviews Genetics (2024) Vol. 25, Iss. 8, pp. 548-562
Closed Access | Times Cited: 22
Generation of a Commercial-Scale Founder Population of Porcine Reproductive and Respiratory Syndrome Virus Resistant Pigs Using CRISPR-Cas
Brian T. Burger, Benjamin P. Beaton, Matthew A. Campbell, et al.
The CRISPR Journal (2024) Vol. 7, Iss. 1, pp. 12-28
Closed Access | Times Cited: 19
The impact of paternal age on new mutations and disease in the next generation
K Wood, Anne Goriely
Fertility and Sterility (2022) Vol. 118, Iss. 6, pp. 1001-1012
Open Access | Times Cited: 43
Inheritance of paternal DNA damage by histone-mediated repair restriction
Siyao Wang, David H. Meyer, Björn Schumacher
Nature (2022) Vol. 613, Iss. 7943, pp. 365-374
Open Access | Times Cited: 38
Experimental estimates of germline mutation rate in eukaryotes: a phylogenetic meta-analysis
Yiguan Wang, Darren J. Obbard
Evolution Letters (2023) Vol. 7, Iss. 4, pp. 216-226
Open Access | Times Cited: 36
Tracking the Evolution of Therapy-Related Myeloid Neoplasms Using Chemotherapy Signatures
Benjamin Diamond, Bachisio Ziccheddu, Kylee Maclachlan, et al.
Blood (2023)
Closed Access | Times Cited: 26
Variation in mutation, recombination, and transposition rates inDrosophila melanogasterandDrosophila simulans
Yiguan Wang, Paul McNeil, R. Abdulazeez, et al.
Genome Research (2023) Vol. 33, Iss. 4, pp. 587-598
Open Access | Times Cited: 26
Genetic links between ovarian ageing, cancer risk and de novo mutation rates
Stasa Stankovic, Saleh Shekari, Qin Qin Huang, et al.
Nature (2024) Vol. 633, Iss. 8030, pp. 608-614
Open Access | Times Cited: 13
The clock-like accumulation of germline and somatic mutations can arise from the interplay of DNA damage and repair
Natanael Spisak, Marc de Manuel, William Milligan, et al.
PLoS Biology (2024) Vol. 22, Iss. 6, pp. e3002678-e3002678
Open Access | Times Cited: 8
DNA damage in testicular germ cells and spermatozoa. When and how is it induced? How should we measure it? What does it mean?
R. John Aitken, Sheena E.M. Lewis
Andrology (2023) Vol. 11, Iss. 8, pp. 1545-1557
Open Access | Times Cited: 22
Genome Instability and DNA Repair in Somatic and Reproductive Aging
Stephanie Panier, Siyao Wang, Björn Schumacher
Annual Review of Pathology Mechanisms of Disease (2023) Vol. 19, Iss. 1, pp. 261-290
Open Access | Times Cited: 20
Limited role of generation time changes in driving the evolution of the mutation spectrum in humans
Ziyue Gao, Yulin Zhang, Nathan Cramer, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 19
Sequence variants affecting the genome-wide rate of germline microsatellite mutations
Snædís Kristmundsdóttir, Hákon Jónsson, Marteinn T. Hardarson, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 18
Building CRISPR Gene Therapies for the Central Nervous System
Sally Salomonsson, Claire D. Clelland
JAMA Neurology (2024) Vol. 81, Iss. 3, pp. 283-283
Closed Access | Times Cited: 6
Origins of Second Malignancies in Children and Mutational Footprint of Chemotherapy in Normal Tissues
Mònica Sánchez-Guixé, Ferran Muiños, Morena Pinheiro-Santin, et al.
Cancer Discovery (2024) Vol. 14, Iss. 6, pp. 953-964
Open Access | Times Cited: 6
Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair
Kitty Sherwood, Joseph C. Ward, Ignacio Soriano, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 13
Variant in the synaptonemal complex protein SYCE2 associates with pregnancy loss through effect on recombination
Valgerður Steinthórsdóttir, Bjarni V. Halldórsson, Hákon Jónsson, et al.
Nature Structural & Molecular Biology (2024) Vol. 31, Iss. 4, pp. 710-716
Open Access | Times Cited: 5
The Evolutionary Interplay of Somatic and Germline Mutation Rates
Annabel C. Beichman, Luke Zhu, Kelley Harris
Annual Review of Biomedical Data Science (2024) Vol. 7, Iss. 1, pp. 83-105
Closed Access | Times Cited: 5
A naturally occurring variant ofMBD4causes maternal germline hypermutation in primates
Alexandra M. Stendahl, Rashesh Sanghvi, Samuel M. Peterson, et al.
Genome Research (2023) Vol. 33, Iss. 12, pp. 2053-2059
Open Access | Times Cited: 11
Transgenerational effects of paternal exposures: the role of germline de novo mutations
Hojat Dehghanbanadaki, Masaya Jimbo, Kiarad Fendereski, et al.
Andrology (2024)
Open Access | Times Cited: 4
The long-term effects of chemotherapy on normal blood cells
Emily Mitchell, My H. Pham, Anna Clay, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 4
The importance of family-based sampling for biobanks
Neil M Davies, Gibran Hemani, Jenae M. Neiderhiser, et al.
Nature (2024) Vol. 634, Iss. 8035, pp. 795-803
Closed Access | Times Cited: 4
Direct measurement of the male germline mutation rate in individuals using sequential sperm samples
Jonathan E. Shoag, Amoolya Srinivasa, Caitlin A. Loh, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Parental germline mosaicism in genome-wide phased de novo variants: Recurrence risk assessment and implications for precision genetic counselling
François Lecoquierre, Nathalie Drouot, Sophie Coutant, et al.
PLoS Genetics (2025) Vol. 21, Iss. 3, pp. e1011651-e1011651
Open Access
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