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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:

Quantifying genetic effects on disease mediated by assayed gene expression levels
Douglas Yao, Luke J. O’Connor, Alkes L. Price, et al.
Nature Genetics (2020) Vol. 52, Iss. 6, pp. 626-633
Open Access | Times Cited: 269

Showing 1-25 of 269 citing articles:

Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression
Urmo Võsa, Annique Claringbould, Harm-Jan Westra, et al.
Nature Genetics (2021) Vol. 53, Iss. 9, pp. 1300-1310
Open Access | Times Cited: 1141
A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease
Douglas P. Wightman, Iris E. Jansen, Jeanne E. Savage, et al.
Nature Genetics (2021) Vol. 53, Iss. 9, pp. 1276-1282
Open Access | Times Cited: 704
A compendium of uniformly processed human gene expression and splicing quantitative trait loci
Nurlan Kerimov, James Hayhurst, Kateryna Peikova, et al.
Nature Genetics (2021) Vol. 53, Iss. 9, pp. 1290-1299
Open Access | Times Cited: 306
Where Are the Disease-Associated eQTLs?
Benjamin D. Umans, Alexis Battle, Yoav Gilad
Trends in Genetics (2020) Vol. 37, Iss. 2, pp. 109-124
Open Access | Times Cited: 254
Exploiting the GTEx resources to decipher the mechanisms at GWAS loci
Alvaro Barbeira, Rodrigo Bonazzola, Eric R. Gamazon, et al.
Genome biology (2021) Vol. 22, Iss. 1
Open Access | Times Cited: 242
Systematic differences in discovery of genetic effects on gene expression and complex traits
Hakhamanesh Mostafavi, Jeffrey P. Spence, Sahin Naqvi, et al.
Nature Genetics (2023) Vol. 55, Iss. 11, pp. 1866-1875
Closed Access | Times Cited: 152
Genetic analyses support the contribution of mRNA N6-methyladenosine (m6A) modification to human disease heritability
Zijie Zhang, Kaixuan Luo, Zhongyu Zou, et al.
Nature Genetics (2020) Vol. 52, Iss. 9, pp. 939-949
Open Access | Times Cited: 146
Enhancers in disease: molecular basis and emerging treatment strategies
Annique Claringbould, Judith B. Zaugg
Trends in Molecular Medicine (2021) Vol. 27, Iss. 11, pp. 1060-1073
Open Access | Times Cited: 139
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: 136
Germline genetic contribution to the immune landscape of cancer
Rosalyn W. Sayaman, Mohamad Saad, Vésteinn Thórsson, et al.
Immunity (2021) Vol. 54, Iss. 2, pp. 367-386.e8
Open Access | Times Cited: 129
Combining SNP-to-gene linking strategies to identify disease genes and assess disease omnigenicity
Steven Gazal, Omer Weissbrod, Farhad Hormozdiari, et al.
Nature Genetics (2022) Vol. 54, Iss. 6, pp. 827-836
Open Access | Times Cited: 122
Genetic control of RNA splicing and its distinct role in complex trait variation
Ting Qi, Yang Wu, Hailing Fang, et al.
Nature Genetics (2022) Vol. 54, Iss. 9, pp. 1355-1363
Open Access | Times Cited: 117
RNA editing underlies genetic risk of common inflammatory diseases
Qin Li, Michael J. Gloudemans, Jonathan M. Geisinger, et al.
Nature (2022) Vol. 608, Iss. 7923, pp. 569-577
Open Access | Times Cited: 113
Mendelian randomization for studying the effects of perturbing drug targets
Dipender Gill, Marios K. Georgakis, Venexia Walker, et al.
Wellcome Open Research (2021) Vol. 6, pp. 16-16
Open Access | Times Cited: 108
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: 99
Limited overlap of eQTLs and GWAS hits due to systematic differences in discovery
Hakhamanesh Mostafavi, Jeffrey P. Spence, Sahin Naqvi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 91
A compendium of genetic regulatory effects across pig tissues
Jinyan Teng, Yahui Gao, Hongwei Yin, et al.
Nature Genetics (2024) Vol. 56, Iss. 1, pp. 112-123
Open Access | Times Cited: 87
A mechanistic framework for cardiometabolic and coronary artery diseases
Simon Koplev, Marcus M. Seldin, Katyayani Sukhavasi, et al.
Nature Cardiovascular Research (2022) Vol. 1, Iss. 1, pp. 85-100
Open Access | Times Cited: 79
Single-cell RNA-sequencing of peripheral blood mononuclear cells reveals widespread, context-specific gene expression regulation upon pathogenic exposure
Roy Oelen, Dylan H. de Vries, Harm Brugge, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 71
Transcriptome-wide association studies: recent advances in methods, applications and available databases
Jialin Mai, Mingming Lu, Qianwen Gao, et al.
Communications Biology (2023) Vol. 6, Iss. 1
Open Access | Times Cited: 55
Molecular quantitative trait loci
François Aguet, Kaur Alasoo, Yang Li, et al.
Nature Reviews Methods Primers (2023) Vol. 3, Iss. 1
Closed Access | Times Cited: 50
Adjusting for genetic confounders in transcriptome-wide association studies improves discovery of risk genes of complex traits
Siming Zhao, Wesley L. Crouse, Sheng Qian, et al.
Nature Genetics (2024)
Open Access | Times Cited: 36
Pleiotropy, epistasis and the genetic architecture of quantitative traits
Trudy F. C. Mackay, Robert R. H. Anholt
Nature Reviews Genetics (2024) Vol. 25, Iss. 9, pp. 639-657
Closed Access | Times Cited: 28
Genetic and molecular architecture of complex traits
Tuuli Lappalainen, Yang Li, Sohini Ramachandran, et al.
Cell (2024) Vol. 187, Iss. 5, pp. 1059-1075
Open Access | Times Cited: 21
Cross-ancestry atlas of gene, isoform, and splicing regulation in the developing human brain
Cindy Wen, Michael Margolis, Rujia Dai, et al.
Science (2024) Vol. 384, Iss. 6698
Open Access | Times Cited: 18
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