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 RNA-sequencing of differentiating iPS cells reveals dynamic genetic effects on gene expression
Anna Cuomo, Daniel D. Seaton, Davis J. McCarthy, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 307

Showing 1-25 of 307 citing articles:

Methods and applications for single-cell and spatial multi-omics
Katy Vandereyken, Alejandro Sifrim, Bernard Thienpont, et al.
Nature Reviews Genetics (2023) Vol. 24, Iss. 8, pp. 494-515
Open Access | Times Cited: 626

From GWAS to Function: Using Functional Genomics to Identify the Mechanisms Underlying Complex Diseases
Eddie Cano-Gamez, Gosia Trynka
Frontiers in Genetics (2020) Vol. 11
Open Access | Times Cited: 483

Computational principles and challenges in single-cell data integration
Ricard Argelaguet, Anna Cuomo, Oliver Stegle, et al.
Nature Biotechnology (2021) Vol. 39, Iss. 10, pp. 1202-1215
Closed Access | Times Cited: 338

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: 314

Single-nucleus cross-tissue molecular reference maps toward understanding disease gene function
Gökçen Eraslan, Eugene Drokhlyansky, Shankara Anand, et al.
Science (2022) Vol. 376, Iss. 6594
Open Access | Times Cited: 279

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: 257

Vireo: Bayesian demultiplexing of pooled single-cell RNA-seq data without genotype reference
Yuanhua Huang, Davis J. McCarthy, Oliver Stegle
Genome biology (2019) Vol. 20, Iss. 1
Open Access | Times Cited: 233

Population-scale single-cell RNA-seq profiling across dopaminergic neuron differentiation
Julie Jerber, Daniel D. Seaton, Anna Cuomo, et al.
Nature Genetics (2021) Vol. 53, Iss. 3, pp. 304-312
Open Access | Times Cited: 220

Targeted Perturb-seq enables genome-scale genetic screens in single cells
Daniel Schraivogel, Andreas R. Gschwind, Jennifer H. Milbank, et al.
Nature Methods (2020) Vol. 17, Iss. 6, pp. 629-635
Open Access | Times Cited: 192

The single-cell eQTLGen consortium
Monique G.P. van der Wijst, DH de Vries, Hilde E. Groot, et al.
eLife (2020) Vol. 9
Open Access | Times Cited: 191

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

Modeling gene regulatory networks using neural network architectures
Hantao Shu, Jingtian Zhou, Qiuyu Lian, et al.
Nature Computational Science (2021) Vol. 1, Iss. 7, pp. 491-501
Closed Access | Times Cited: 119

Immune disease risk variants regulate gene expression dynamics during CD4+ T cell activation
Blagoje Soskic, Eddie Cano-Gamez, Deborah J. Smyth, et al.
Nature Genetics (2022) Vol. 54, Iss. 6, pp. 817-826
Open Access | Times Cited: 111

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

Human-specific genetics: new tools to explore the molecular and cellular basis of human evolution
Alex A. Pollen, Umut Kilik, Craig B. Lowe, et al.
Nature Reviews Genetics (2023) Vol. 24, Iss. 10, pp. 687-711
Open Access | Times Cited: 99

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: 75

Brain Chimeroids reveal individual susceptibility to neurotoxic triggers
Noelia Antón-Bolaños, Irene Faravelli, Tyler Faits, et al.
Nature (2024) Vol. 631, Iss. 8019, pp. 142-149
Closed Access | Times Cited: 39

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

AI‐organoid integrated systems for biomedical studies and applications
Sudhiksha Maramraju, Andrew Kowalczewski, Anirudh Kaza, et al.
Bioengineering & Translational Medicine (2024) Vol. 9, Iss. 2
Open Access | Times Cited: 18

Single-cell network biology for resolving cellular heterogeneity in human diseases
Junha Cha, Insuk Lee
Experimental & Molecular Medicine (2020) Vol. 52, Iss. 11, pp. 1798-1808
Open Access | Times Cited: 118

Engineering islets from stem cells for advanced therapies of diabetes
Johanna Siehler, Anna Karolina Blöchinger, Matthias Meier, et al.
Nature Reviews Drug Discovery (2021) Vol. 20, Iss. 12, pp. 920-940
Closed Access | Times Cited: 99

Guidelines for bioinformatics of single-cell sequencing data analysis in Alzheimer’s disease: review, recommendation, implementation and application
Minghui Wang, Won‐Min Song, Ming Chen, et al.
Molecular Neurodegeneration (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 70

Functional dynamic genetic effects on gene regulation are specific to particular cell types and environmental conditions
Anthony S Findley, Alan Monziani, Allison L. Richards, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 59

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