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 1-25 of 144 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: 199

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: 143

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

Current insights and future perspectives of ultraviolet radiation (UV) exposure: Friends and foes to the skin and beyond the skin
X. Tang, Tingyi Yang, Daojiang Yu, et al.
Environment International (2024) Vol. 185, pp. 108535-108535
Open Access | Times Cited: 81

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: 72

Polygenic regression uncovers trait-relevant cellular contexts through pathway activation transformation of single-cell RNA sequencing data
Yunlong Ma, Chunyu Deng, Yijun Zhou, et al.
Cell Genomics (2023) Vol. 3, Iss. 9, pp. 100383-100383
Open Access | Times Cited: 48

Convergence of coronary artery disease genes onto endothelial cell programs
Gavin R. Schnitzler, Helen Y. Kang, Shi Fang, et al.
Nature (2024) Vol. 626, Iss. 8000, pp. 799-807
Open Access | Times Cited: 34

Landscape of human organoids: Ideal model in clinics and research
Xinxin Han, Chunhui Cai, Wei Deng, et al.
The Innovation (2024) Vol. 5, Iss. 3, pp. 100620-100620
Open Access | Times Cited: 30

Integrating genetic regulation and single-cell expression with GWAS prioritizes causal genes and cell types for glaucoma
Andrew R. Hamel, Wenjun Yan, John M. Rouhana, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 29

Genetic variation across and within individuals
Zhi Yu, Tim H. H. Coorens, Md Mesbah Uddin, et al.
Nature Reviews Genetics (2024) Vol. 25, Iss. 8, pp. 548-562
Closed Access | Times Cited: 21

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: 19

Leveraging single-cell ATAC-seq and RNA-seq to identify disease-critical fetal and adult brain cell types
Samuel S. Kim, Buu Truong, Karthik A. Jagadeesh, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 18

GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets
Nick Dand, Philip E. Stuart, John Bowes, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access | Times Cited: 2

Repression and 3D-restructuring resolves regulatory conflicts in evolutionarily rearranged genomes
Alessa R. Ringel, Quentin Szabo, Andrea M. Chiariello, et al.
Cell (2022) Vol. 185, Iss. 20, pp. 3689-3704.e21
Open Access | Times Cited: 41

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: 38

Scalable genetic screening for regulatory circuits using compressed Perturb-seq
Douglas Yao, Loïc Binan, Jon Bezney, et al.
Nature Biotechnology (2023) Vol. 42, Iss. 8, pp. 1282-1295
Open Access | Times Cited: 37

Genome-wide association study identifies 30 obsessive-compulsive disorder associated loci
Nora I. Strom, Zachary F. Gerring, Marco Galimberti, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 12

sc2GWAS: a comprehensive platform linking single cell and GWAS traits of human
Mingxue Yin, Chenchen Feng, Zhengmin Yu, et al.
Nucleic Acids Research (2024) Vol. 53, Iss. D1, pp. D1151-D1161
Open Access | Times Cited: 12

Schizophrenia genomics: genetic complexity and functional insights
Patrick F. Sullivan, Shuyang Yao, Jens Hjerling‐Leffler
Nature reviews. Neuroscience (2024) Vol. 25, Iss. 9, pp. 611-624
Closed Access | Times Cited: 11

Single-cell RNA sequencing of human tissue supports successful drug targets
Emma Dann, Erin Teeple, Rasa Elmentaite, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 10

Sequential immunotherapy: towards cures for autoimmunity
Francisco Ramírez‐Valle, Joseph Maranville, Sophie Roy, et al.
Nature Reviews Drug Discovery (2024) Vol. 23, Iss. 7, pp. 501-524
Closed Access | Times Cited: 10

Machine learning-driven identification of critical gene programs and key transcription factors in migraine
Lei Zhang, Yujie Li, Yunhao Xu, et al.
The Journal of Headache and Pain (2025) Vol. 26, Iss. 1
Open Access | Times Cited: 1

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