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:

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

Showing 1-25 of 192 citing articles:

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: 831

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

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

The molecular cytoarchitecture of the adult mouse brain
Jonah Langlieb, Nina Sachdev, Karol S. Balderrama, et al.
Nature (2023) Vol. 624, Iss. 7991, pp. 333-342
Open Access | Times Cited: 97

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

SpliceAI-visual: a free online tool to improve SpliceAI splicing variant interpretation
Jean‐Madeleine de Sainte Agathe, Mathilde Filser, Bertrand Isidor, et al.
Human Genomics (2023) Vol. 17, Iss. 1
Open Access | Times Cited: 89

Refining the impact of genetic evidence on clinical success
Eric Vallabh Minikel, Jeffery L. Painter, Coco Chengliang Dong, et al.
Nature (2024) Vol. 629, Iss. 8012, pp. 624-629
Open Access | Times Cited: 88

The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits
Maria C. Costanzo, Marcin von Grotthuss, Jeffrey Massung, et al.
Cell Metabolism (2023) Vol. 35, Iss. 4, pp. 695-710.e6
Open Access | Times Cited: 78

Nuclear genetic control of mtDNA copy number and heteroplasmy in humans
Rahul Gupta, Masahiro Kanai, Timothy Durham, et al.
Nature (2023) Vol. 620, Iss. 7975, pp. 839-848
Open Access | Times Cited: 76

WebCSEA: web-based cell-type-specific enrichment analysis of genes
Yulin Dai, Ruifeng Hu, Andi Liu, et al.
Nucleic Acids Research (2022) Vol. 50, Iss. W1, pp. W782-W790
Open Access | Times Cited: 74

Imputation of low-coverage sequencing data from 150,119 UK Biobank genomes
Simone Rubinacci, Robin J. Hofmeister, Bárbara Sousa da Mota, et al.
Nature Genetics (2023) Vol. 55, Iss. 7, pp. 1088-1090
Open Access | Times Cited: 64

Genome-wide association analysis and Mendelian randomization proteomics identify drug targets for heart failure
Danielle Rasooly, Gina M. Peloso, Alexandre C. Pereira, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 54

High-dimensional phenotyping to define the genetic basis of cellular morphology
Matthew Tegtmeyer, Jatin Arora, Samira Asgari, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 29

Deciphering the impact of genomic variation on function
J Engreitz, Heather A. Lawson, Harinder Singh, et al.
Nature (2024) Vol. 633, Iss. 8028, pp. 47-57
Closed Access | Times Cited: 20

Development of a human genetics-guided priority score for 19,365 genes and 399 drug indications
Áine Duffy, Ben Omega Petrazzini, David Stein, et al.
Nature Genetics (2024) Vol. 56, Iss. 1, pp. 51-59
Closed Access | Times Cited: 17

Disease prediction with multi-omics and biomarkers empowers case–control genetic discoveries in the UK Biobank
Manik Garg, Marcin Karpiński, Dorota Matelska, et al.
Nature Genetics (2024) Vol. 56, Iss. 9, pp. 1821-1831
Open Access | Times Cited: 17

Atlas of the plasma proteome in health and disease in 53,026 adults
Yue‐Ting Deng, Jia You, Yu He, et al.
Cell (2024)
Open Access | Times Cited: 16

A comprehensive spatio-cellular map of the human hypothalamus
John A. Tadross, Lukas Steuernagel, Georgina K.C. Dowsett, et al.
Nature (2025) Vol. 639, Iss. 8055, pp. 708-716
Open Access | Times Cited: 5

MorPhiC Consortium: towards functional characterization of all human genes
Mazhar Adli, Laralynne Przybyla, Tony Burdett, et al.
Nature (2025) Vol. 638, Iss. 8050, pp. 351-359
Closed Access | Times Cited: 3

G6PD deficiency triggers dopamine loss and the initiation of Parkinson’s disease pathogenesis
Morgan G. Stykel, Shehani V. Siripala, Eric Soubeyrand, et al.
Cell Reports (2025) Vol. 44, Iss. 1, pp. 115178-115178
Open Access | Times Cited: 2

Large-scale multi-omics identifies drug targets for heart failure with reduced and preserved ejection fraction
Danielle Rasooly, Claudia Giambartolomei, Gina M. Peloso, et al.
Nature Cardiovascular Research (2025)
Closed Access | Times Cited: 2

Kidney multiome-based genetic scorecard reveals convergent coding and regulatory variants
Hongbo Liu, Amin Abedini, Eunji Ha, et al.
Science (2025) Vol. 387, Iss. 6734
Closed Access | Times Cited: 2

Seven years since the launch of the Matchmaker Exchange: The evolution of genomic matchmaking
Kym M. Boycott, Danielle R. Azzariti, Ada Hamosh, et al.
Human Mutation (2022)
Open Access | Times Cited: 43

The cell type composition of the adult mouse brain revealed by single cell and spatial genomics
Jonah Langlieb, Nina Sachdev, Karol S. Balderrama, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 40

Refining the impact of genetic evidence on clinical success
Eric Vallabh Minikel, Jeffery L. Painter, Coco Chengliang Dong, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 23

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