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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:

Exome sequencing and analysis of 454,787 UK Biobank participants
Joshua Backman, Alexander Li, Anthony Marcketta, et al.
Nature (2021) Vol. 599, Iss. 7886, pp. 628-634
Open Access | Times Cited: 694

Showing 1-25 of 694 citing articles:

The NHGRI-EBI GWAS Catalog: knowledgebase and deposition resource
Elliot Sollis, Abayomi Mosaku, Ala Abid, et al.
Nucleic Acids Research (2022) Vol. 51, Iss. D1, pp. D977-D985
Open Access | Times Cited: 990
Atherosclerosis: Recent developments
Johan Björkegren, Aldons J. Lusis
Cell (2022) Vol. 185, Iss. 10, pp. 1630-1645
Open Access | Times Cited: 666
A saturated map of common genetic variants associated with human height
Loïc Yengo, Sailaja Vedantam, Eirini Marouli, et al.
Nature (2022) Vol. 610, Iss. 7933, pp. 704-712
Open Access | Times Cited: 490
Stroke genetics informs drug discovery and risk prediction across ancestries
Aniket Mishra, Rainer Malik, Tsuyoshi Hachiya, et al.
Nature (2022) Vol. 611, Iss. 7934, pp. 115-123
Open Access | Times Cited: 338
15 years of GWAS discovery: Realizing the promise
Abdel Abdellaoui, Loïc Yengo, Karin J. H. Verweij, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 2, pp. 179-194
Open Access | Times Cited: 293
The next-generation Open Targets Platform: reimagined, redesigned, rebuilt
David Ochoa, Andrew Hercules, Miguel Carmona, et al.
Nucleic Acids Research (2022) Vol. 51, Iss. D1, pp. D1353-D1359
Open Access | Times Cited: 264
International consensus statement on allergy and rhinology: Allergic rhinitis – 2023
Sarah K. Wise, Cecelia Damask, Lauren T. Roland, et al.
International Forum of Allergy & Rhinology (2023) Vol. 13, Iss. 4, pp. 293-859
Open Access | Times Cited: 231
Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes
Konrad J. Karczewski, Matthew Solomonson, Katherine R. Chao, et al.
Cell Genomics (2022) Vol. 2, Iss. 9, pp. 100168-100168
Open Access | Times Cited: 192
Common and rare variant associations with clonal haematopoiesis phenotypes
Michael D. Kessler, Amy Damask, Sean O’Keeffe, et al.
Nature (2022) Vol. 612, Iss. 7939, pp. 301-309
Open Access | Times Cited: 184
Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease
Julie Horowitz, Jack A. Kosmicki, Amy Damask, et al.
Nature Genetics (2022) Vol. 54, Iss. 4, pp. 382-392
Open Access | Times Cited: 148
Epigenomic and transcriptomic analyses define core cell types, genes and targetable mechanisms for kidney disease
Hongbo Liu, Tomohito Doke, Dong Guo, et al.
Nature Genetics (2022) Vol. 54, Iss. 7, pp. 950-962
Closed Access | Times Cited: 142
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease
Henne Holstege, Marc Hulsman, Camille Charbonnier, et al.
Nature Genetics (2022) Vol. 54, Iss. 12, pp. 1786-1794
Open Access | Times Cited: 137
Evolutionary constraint and innovation across hundreds of placental mammals
Matthew J. Christmas, Irene M. Kaplow, Diane P. Genereux, et al.
Science (2023) Vol. 380, Iss. 6643
Open Access | Times Cited: 137
Polygenic architecture of rare coding variation across 394,783 exomes
Daniel J. Weiner, Ajay Nadig, Karthik A. Jagadeesh, et al.
Nature (2023) Vol. 614, Iss. 7948, pp. 492-499
Open Access | Times Cited: 111
A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases
Stephen F. Kingsmore, Laurie D. Smith, Chris M. Kunard, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 9, pp. 1605-1619
Open Access | Times Cited: 110
The missing link between genetic association and regulatory function
Noah J Connally, Sumaiya Nazeen, Daniel Lee, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 100
Accurate rare variant phasing of whole-genome and whole-exome sequencing data in the UK Biobank
Robin J. Hofmeister, Diogo M. Ribeiro, Simone Rubinacci, et al.
Nature Genetics (2023) Vol. 55, Iss. 7, pp. 1243-1249
Open Access | Times Cited: 93
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
Nick Shrine, Abril G. Izquierdo, Jing Chen, et al.
Nature Genetics (2023) Vol. 55, Iss. 3, pp. 410-422
Open Access | Times Cited: 91
WhichTF is functionally important in your open chromatin data?
Yosuke Tanigawa, Ethan S. Dyer, Gill Bejerano
PLoS Computational Biology (2022) Vol. 18, Iss. 8, pp. e1010378-e1010378
Open Access | Times Cited: 89
Pharmacogenomics: Driving Personalized Medicine
Wolfgang Sadée, Daqing Wang, Katherine E. Hartmann, et al.
Pharmacological Reviews (2023) Vol. 75, Iss. 4, pp. 789-814
Open Access | Times Cited: 87
A practical approach to curate clonal hematopoiesis of indeterminate potential in human genetic datasets
Caitlyn Vlasschaert, Taralynn Mack, J. Brett Heimlich, et al.
Blood (2023)
Open Access | Times Cited: 86
Significant sparse polygenic risk scores across 813 traits in UK Biobank
Yosuke Tanigawa, Junyang Qian, Guhan Venkataraman, et al.
PLoS Genetics (2022) Vol. 18, Iss. 3, pp. e1010105-e1010105
Open Access | Times Cited: 80
Germline Mutations in CIDEB and Protection against Liver Disease
Niek Verweij, Mary E. Haas, Jonas B. Nielsen, et al.
New England Journal of Medicine (2022) Vol. 387, Iss. 4, pp. 332-344
Open Access | Times Cited: 78
Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals
Hang Zhou, Rachel L. Kember, Joseph D. Deak, et al.
Nature Medicine (2023) Vol. 29, Iss. 12, pp. 3184-3192
Open Access | Times Cited: 76
Expanded COVID-19 phenotype definitions reveal distinct patterns of genetic association and protective effects
Genevieve H. L. Roberts, Raghavendran Partha, Brooke Rhead, et al.
Nature Genetics (2022) Vol. 54, Iss. 4, pp. 374-381
Open Access | Times Cited: 75
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