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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:

Accurate classification of BRCA1 variants with saturation genome editing
Gregory M. Findlay, Riza M. Daza, Beth Martin, et al.
Nature (2018) Vol. 562, Iss. 7726, pp. 217-222
Open Access | Times Cited: 710

Showing 1-25 of 710 citing articles:

The mutational constraint spectrum quantified from variation in 141,456 humans
Konrad J. Karczewski, Laurent C. Francioli, Grace Tiao, et al.
Nature (2020) Vol. 581, Iss. 7809, pp. 434-443
Open Access | Times Cited: 8031
CADD: predicting the deleteriousness of variants throughout the human genome
Philipp Rentzsch, Daniela Witten, Gregory M. Cooper, et al.
Nucleic Acids Research (2018) Vol. 47, Iss. D1, pp. D886-D894
Open Access | Times Cited: 3074
The mutational constraint spectrum quantified from variation in 141,456 humans
Konrad J. Karczewski, Laurent C. Francioli, Grace Tiao, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2019)
Open Access | Times Cited: 1045
Accurate proteome-wide missense variant effect prediction with AlphaMissense
Jun Cheng, Guido Novati, Joshua Pan, et al.
Science (2023) Vol. 381, Iss. 6664
Open Access | Times Cited: 882
CRISPR technology: A decade of genome editing is only the beginning
Joy Y. Wang, Jennifer A. Doudna
Science (2023) Vol. 379, Iss. 6629
Closed Access | Times Cited: 634
A brief history of human disease genetics
Melina Claussnitzer, Judy H. Cho, Rory Collins, et al.
Nature (2020) Vol. 577, Iss. 7789, pp. 179-189
Open Access | Times Cited: 615
Deep generative models of genetic variation capture the effects of mutations
Adam J. Riesselman, John Ingraham, Debora S. Marks
Nature Methods (2018) Vol. 15, Iss. 10, pp. 816-822
Open Access | Times Cited: 577
Disease variant prediction with deep generative models of evolutionary data
Jonathan Frazer, Pascal Notin, Mafalda Dias, et al.
Nature (2021) Vol. 599, Iss. 7883, pp. 91-95
Open Access | Times Cited: 563
Mechanical regulation of glycolysis via cytoskeleton architecture
Jin Suk Park, Christoph J. Burckhardt, Rossana Lazcano, et al.
Nature (2020) Vol. 578, Iss. 7796, pp. 621-626
Open Access | Times Cited: 457
Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework
Sarah E. Brnich, Ahmad Abou Tayoun, Fergus J. Couch, et al.
Genome Medicine (2019) Vol. 12, Iss. 1
Open Access | Times Cited: 439
High-content CRISPR screening
Christoph Bock, Paul Datlinger, Florence M. Chardon, et al.
Nature Reviews Methods Primers (2022) Vol. 2, Iss. 1
Open Access | Times Cited: 381
Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions
Akl C. Fahed, Minxian Wang, Julian R. Homburger, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 364
Learning the protein language: Evolution, structure, and function
Tristan Bepler, Bonnie Berger
Cell Systems (2021) Vol. 12, Iss. 6, pp. 654-669.e3
Open Access | Times Cited: 359
Tumour lineage shapes BRCA-mediated phenotypes
Philip Jonsson, Chaitanya Bandlamudi, Michael L. Cheng, et al.
Nature (2019) Vol. 571, Iss. 7766, pp. 576-579
Open Access | Times Cited: 355
Genetic Testing and Results in a Population-Based Cohort of Breast Cancer Patients and Ovarian Cancer Patients
Allison W. Kurian, Kevin C. Ward, Nadia Howlader, et al.
Journal of Clinical Oncology (2019) Vol. 37, Iss. 15, pp. 1305-1315
Open Access | Times Cited: 317
Massively parallel assessment of human variants with base editor screens
Ruth E. Hanna, Mudra Hegde, Christian Fagre, et al.
Cell (2021) Vol. 184, Iss. 4, pp. 1064-1080.e20
Open Access | Times Cited: 259
The impact of nonsense-mediated mRNA decay on genetic disease, gene editing and cancer immunotherapy
Rik G.H. Lindeboom, Michiel Vermeulen, Ben Lehner, et al.
Nature Genetics (2019) Vol. 51, Iss. 11, pp. 1645-1651
Open Access | Times Cited: 233
Translating cancer genomics into precision medicine with artificial intelligence: applications, challenges and future perspectives
Jia Xu, Pengwei Yang, Shang Xue, et al.
Human Genetics (2019) Vol. 138, Iss. 2, pp. 109-124
Open Access | Times Cited: 227
Genomic Medicine–Progress, Pitfalls, and Promise
Jay Shendure, Gregory M. Findlay, Matthew W. Snyder
Cell (2019) Vol. 177, Iss. 1, pp. 45-57
Open Access | Times Cited: 225
MaveDB: an open-source platform to distribute and interpret data from multiplexed assays of variant effect
Daniel Esposito, Jochen Weile, Jay Shendure, et al.
Genome biology (2019) Vol. 20, Iss. 1
Open Access | Times Cited: 218
Genetics of Common, Complex Coronary Artery Disease
Kiran Musunuru, Sekar Kathiresan
Cell (2019) Vol. 177, Iss. 1, pp. 132-145
Open Access | Times Cited: 211
High-content CRISPR screening
Christoph Bock, Paul Datlinger, Florence M. Chardon, et al.
Nature Reviews Methods Primers (2022) Vol. 2, Iss. 1
Open Access | Times Cited: 209
Functional interrogation of DNA damage response variants with base editing screens
Raquel Cuella-Martin, Samuel B. Hayward, Xiao Fan, et al.
Cell (2021) Vol. 184, Iss. 4, pp. 1081-1097.e19
Open Access | Times Cited: 208
ClinPred: Prediction Tool to Identify Disease-Relevant Nonsynonymous Single-Nucleotide Variants
Najmeh Alirezaie, Kristin D. Kernohan, Taila Hartley, et al.
The American Journal of Human Genetics (2018) Vol. 103, Iss. 4, pp. 474-483
Open Access | Times Cited: 201
A new era in functional genomics screens
Laralynne Przybyla, Luke A. Gilbert
Nature Reviews Genetics (2021) Vol. 23, Iss. 2, pp. 89-103
Closed Access | Times Cited: 184
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