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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:

Identifying disease-critical cell types and cellular processes by integrating single-cell RNA-sequencing and human genetics
Karthik A. Jagadeesh, Kushal K. Dey, Daniel T. Montoro, et al.
Nature Genetics (2022) Vol. 54, Iss. 10, pp. 1479-1492
Open Access | Times Cited: 144

Showing 26-50 of 144 citing articles:

Single-cell omics in inflammatory bowel disease: recent insights and future clinical applications
Victòria Gudiño, Raquel Bartolomé-Casado, Azucena Salas
Gut (2025), pp. gutjnl-334165
Closed Access | Times Cited: 1
HCNetlas: A reference database of human cell type-specific gene networks to aid disease genetic analyses
Jiwon Yu, Junha Cha, Geon Koh, et al.
PLoS Biology (2025) Vol. 23, Iss. 2, pp. e3002702-e3002702
Open Access | Times Cited: 1
Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy
Rafik Tadros, Sean L. Zheng, Christopher Grace, et al.
Nature Genetics (2025)
Open Access | Times Cited: 1
SNP-to-gene linking strategies reveal contributions of enhancer-related and candidate master-regulator genes to autoimmune disease
Kushal K. Dey, Steven Gazal, Bryce van de Geijn, et al.
Cell Genomics (2022) Vol. 2, Iss. 7, pp. 100145-100145
Open Access | Times Cited: 35
Examining the shared etiology of psychopathology with genome-wide association studies
Travis T. Mallard, Andrew D. Grotzinger, Jordan W. Smoller
Physiological Reviews (2023) Vol. 103, Iss. 2, pp. 1645-1665
Open Access | Times Cited: 18
SURGE: uncovering context-specific genetic-regulation of gene expression from single-cell RNA sequencing using latent-factor models
Benjamin J. Strober, Karl Tayeb, Joshua M Popp, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 7
Enhanced In Situ Spatial Proteomics by Effective Combination of MALDI Imaging and LC-MS/MS
Frederike Schäfer, Archana Tomar, Shogo Sato, et al.
Molecular & Cellular Proteomics (2024) Vol. 23, Iss. 8, pp. 100811-100811
Open Access | Times Cited: 6
Mapping cis-regulatory elements in human neurons links psychiatric disease heritability and activity-regulated transcriptional programs
Carlos Sánchez-Priego, Ruiqi Hu, Linda L. Boshans, et al.
Cell Reports (2022) Vol. 39, Iss. 9, pp. 110877-110877
Open Access | Times Cited: 24
Integrating leiomyoma genetics, epigenomics, and single-cell transcriptomics reveals causal genetic variants, genes, and cell types
Kadir Buyukcelebi, Alexander James Duval, Fatih Abdula, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 5
The genetic basis of autoimmunity seen through the lens of T cell functional traits
Kaitlyn A. Lagattuta, Hannah L. Park, Laurie Rumker, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 5
A Novel Macrophage Subpopulation Conveys Increased Genetic Risk of Coronary Artery Disease
Jiahao Jiang, Thomas K. Hiron, Thomas A. Agbaedeng, et al.
Circulation Research (2024) Vol. 135, Iss. 1, pp. 6-25
Open Access | Times Cited: 5
Machine learning integrative approaches to advance computational immunology
Fabiola Curion, Fabian J. Theis
Genome Medicine (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 5
Advances and applications in single-cell and spatial genomics
Jingjing Wang, Fang Ye, Haoxi Chai, et al.
Science China Life Sciences (2024)
Closed Access | Times Cited: 5
Systematically characterizing the roles of E3-ligase family members in inflammatory responses with massively parallel Perturb-seq
Kathryn Geiger‐Schuller, Basak Eraslan, Olena Kuksenko, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 12
Towards interpretable imaging genomics analysis: Methodological developments and applications
Xiaoping Cen, Wei Dong, Wei Lv, et al.
Information Fusion (2023) Vol. 102, pp. 102032-102032
Closed Access | Times Cited: 11
Integration of human organoids single‐cell transcriptomic profiles and human genetics repurposes critical cell type‐specific drug targets for severe COVID‐19
Yunlong Ma, Yijun Zhou, Dingping Jiang, et al.
Cell Proliferation (2023) Vol. 57, Iss. 3
Open Access | Times Cited: 11
Connecting genomic results for psychiatric disorders to human brain cell types and regions reveals convergence with functional connectivity
Shuyang Yao, Arvid Harder, Fahimeh Darki, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 4
RNA Sequencing in Disease Diagnosis
Craig Smail, Stephen B. Montgomery
Annual Review of Genomics and Human Genetics (2024) Vol. 25, Iss. 1, pp. 353-367
Closed Access | Times Cited: 4
Recent developments and new directions in the use of natural products for the treatment of inflammatory bowel disease
Yaqian Feng, Mengting Pan, Ruiqiong Li, et al.
Phytomedicine (2024) Vol. 132, pp. 155812-155812
Closed Access | Times Cited: 4
Oral delivery of sodium alginate/chitosan bilayer microgels loaded with Lactobacillus rhamnosus GG for targeted therapy of ulcerative colitis
Yan Hu, Shengpeng Zhu, Xuexin Ye, et al.
International Journal of Biological Macromolecules (2024) Vol. 278, pp. 134785-134785
Closed Access | Times Cited: 4
Genes with differential expression across ancestries are enriched in ancestry-specific disease effects likely due to gene-by-environment interactions
Juehan Wang, Zixuan Zhang, Zeyun Lu, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 10, pp. 2117-2128
Open Access | Times Cited: 4
Fine-mapping causal tissues and genes at disease-associated loci
Benjamin J. Strober, Martin Jinye Zhang, Tiffany Amariuta, et al.
Nature Genetics (2025)
Closed Access
Connecting genomic results for psychiatric disorders to human brain cell types and regions reveals convergence with functional connectivity
Shuyang Yao, Arvid Harder, Fahimeh Darki, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Efficient count-based models improve power and robustness for large-scale single-cell eQTL mapping
Zixuan Zhang, Artem Kim, Noah Suboc, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Causal modeling of gene effects from regulators to programs to traits: integration of genetic associations and Perturb-seq
Mineto Ota, Jeffrey P. Spence, Tony Zeng, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access

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