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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:

Single-cell eQTL models reveal dynamic T cell state dependence of disease loci
Aparna Nathan, Samira Asgari, Kazuyoshi Ishigaki, et al.
Nature (2022) Vol. 606, Iss. 7912, pp. 120-128
Open Access | Times Cited: 137

Showing 1-25 of 137 citing articles:

Applications of single-cell RNA sequencing in drug discovery and development
Bram Van de Sande, Joon Sang Lee, Euphemia Mutasa-Gottgens, et al.
Nature Reviews Drug Discovery (2023) Vol. 22, Iss. 6, pp. 496-520
Open Access | Times Cited: 207
Impact of the Human Cell Atlas on medicine
Jennifer Rood, Aidan Maartens, Anna Hupalowska, et al.
Nature Medicine (2022) Vol. 28, Iss. 12, pp. 2486-2496
Open Access | Times Cited: 150
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: 102
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: 92
Single-cell genomics meets human genetics
Anna Cuomo, Aparna Nathan, Soumya Raychaudhuri, et al.
Nature Reviews Genetics (2023) Vol. 24, Iss. 8, pp. 535-549
Closed Access | Times Cited: 73
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: 52
Common genetic factors among autoimmune diseases
Adil Harroud, David A. Hafler
Science (2023) Vol. 380, Iss. 6644, pp. 485-490
Closed Access | Times Cited: 48
Single-cell genomics and regulatory networks for 388 human brains
Prashant S. Emani, Jason Liu, Declan Clarke, et al.
Science (2024) Vol. 384, Iss. 6698
Open Access | Times Cited: 43
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: 31
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: 29
Cell-type-specific and disease-associated expression quantitative trait loci in the human lung
Heini M. Natri, Christina B. Azodi, Lance Peter, et al.
Nature Genetics (2024) Vol. 56, Iss. 4, pp. 595-604
Open Access | Times Cited: 23
Tissue-specific enhancer–gene maps from multimodal single-cell data identify causal disease alleles
Saori Sakaue, Kathryn Weinand, Shakson Isaac, et al.
Nature Genetics (2024) Vol. 56, Iss. 4, pp. 615-626
Open Access | Times Cited: 23
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: 22
Single-cell transcriptome landscape of circulating CD4+ T cell populations in autoimmune diseases
Yoshiaki Yasumizu, Daiki Takeuchi, Reo Morimoto, et al.
Cell Genomics (2024) Vol. 4, Iss. 2, pp. 100473-100473
Open Access | Times Cited: 21
Cell state-dependent allelic effects and contextual Mendelian randomization analysis for human brain phenotypes
Alexander Haglund, Verena Zuber, Maya Abouzeid, et al.
Nature Genetics (2025)
Open Access | Times Cited: 3
Interpreting non-coding disease-associated human variants using single-cell epigenomics
Kyle J. Gaulton, Sebastian Preißl, Bing Ren
Nature Reviews Genetics (2023) Vol. 24, Iss. 8, pp. 516-534
Open Access | Times Cited: 39
Cell-type-specific co-expression inference from single cell RNA-sequencing data
Chang Su, Zichun Xu, Xinning Shan, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 33
eQTL studies: from bulk tissues to single cells
Jingfei Zhang, Hongyu Zhao
Journal of genetics and genomics/Journal of Genetics and Genomics (2023) Vol. 50, Iss. 12, pp. 925-933
Open Access | Times Cited: 28
Methods and Insights from Single-Cell Expression Quantitative Trait Loci
Joyce B. Kang, Alessandro Raveane, Aparna Nathan, et al.
Annual Review of Genomics and Human Genetics (2023) Vol. 24, Iss. 1, pp. 277-303
Open Access | Times Cited: 26
Mapping the dynamic genetic regulatory architecture of HLA genes at single-cell resolution
Joyce B. Kang, Amber Shen, Saisriram Gurajala, et al.
Nature Genetics (2023) Vol. 55, Iss. 12, pp. 2255-2268
Open Access | Times Cited: 24
From genetic associations to genes: methods, applications, and challenges
Ting Qi, Liyang Song, Yazhou Guo, et al.
Trends in Genetics (2024) Vol. 40, Iss. 8, pp. 642-667
Open Access | Times Cited: 16
Immune mechanisms in fibrotic interstitial lung disease
Mari Kamiya, Hannah M. Carter, Milena S. Espíndola, et al.
Cell (2024) Vol. 187, Iss. 14, pp. 3506-3530
Closed Access | Times Cited: 15
The chromatin landscape of pathogenic transcriptional cell states in rheumatoid arthritis
Kathryn Weinand, Saori Sakaue, Aparna Nathan, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 13
Integration of functional genomics and statistical fine-mapping systematically characterizes adult-onset and childhood-onset asthma genetic associations.
Xiaoyuan Zhong, Robert D. Mitchell, Christine Billstrand, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access | Times Cited: 1
Single-cell eQTL mapping in yeast reveals a tradeoff between growth and reproduction
James Boocock, Noah Alexander, Leslie Alamo Tapia, et al.
eLife (2025) Vol. 13
Open Access | Times Cited: 1
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