
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 identifies celltype-specific cis-eQTLs and co-expression QTLs
Monique G.P. van der Wijst, Harm Brugge, Dylan H. de Vries, et al.
Nature Genetics (2018) Vol. 50, Iss. 4, pp. 493-497
Open Access | Times Cited: 352
Monique G.P. van der Wijst, Harm Brugge, Dylan H. de Vries, et al.
Nature Genetics (2018) Vol. 50, Iss. 4, pp. 493-497
Open Access | Times Cited: 352
Showing 1-25 of 352 citing articles:
Integrative single-cell analysis
Tim Stuart, Rahul Satija
Nature Reviews Genetics (2019) Vol. 20, Iss. 5, pp. 257-272
Closed Access | Times Cited: 1161
Tim Stuart, Rahul Satija
Nature Reviews Genetics (2019) Vol. 20, Iss. 5, pp. 257-272
Closed Access | Times Cited: 1161
Unraveling the polygenic architecture of complex traits using blood eQTL metaanalysis
Urmo Võsa, Annique Claringbould, Harm-Jan Westra, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2018)
Open Access | Times Cited: 516
Urmo Võsa, Annique Claringbould, Harm-Jan Westra, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2018)
Open Access | Times Cited: 516
Cell type–specific genetic regulation of gene expression across human tissues
Sarah Kim-Hellmuth, François Aguet, Meritxell Oliva, et al.
Science (2020) Vol. 369, Iss. 6509
Open Access | Times Cited: 489
Sarah Kim-Hellmuth, François Aguet, Meritxell Oliva, et al.
Science (2020) Vol. 369, Iss. 6509
Open Access | Times Cited: 489
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
Eddie Cano-Gamez, Gosia Trynka
Frontiers in Genetics (2020) Vol. 11
Open Access | Times Cited: 483
Transcriptional and Cellular Diversity of the Human Heart
Nathan R. Tucker, Mark Chaffin, Stephen J. Fleming, et al.
Circulation (2020) Vol. 142, Iss. 5, pp. 466-482
Open Access | Times Cited: 464
Nathan R. Tucker, Mark Chaffin, Stephen J. Fleming, et al.
Circulation (2020) Vol. 142, Iss. 5, pp. 466-482
Open Access | Times Cited: 464
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
Ricard Argelaguet, Anna Cuomo, Oliver Stegle, et al.
Nature Biotechnology (2021) Vol. 39, Iss. 10, pp. 1202-1215
Closed Access | Times Cited: 338
Towards a comprehensive catalogue of validated and target-linked human enhancers
Molly Gasperini, Jacob M. Tome, Jay Shendure
Nature Reviews Genetics (2020) Vol. 21, Iss. 5, pp. 292-310
Open Access | Times Cited: 320
Molly Gasperini, Jacob M. Tome, Jay Shendure
Nature Reviews Genetics (2020) Vol. 21, Iss. 5, pp. 292-310
Open Access | Times Cited: 320
Large eQTL meta-analysis reveals differing patterns between cerebral cortical and cerebellar brain regions
Solveig K. Sieberts, Thanneer M. Perumal, Minerva M. Carrasquillo, et al.
Scientific Data (2020) Vol. 7, Iss. 1
Open Access | Times Cited: 317
Solveig K. Sieberts, Thanneer M. Perumal, Minerva M. Carrasquillo, et al.
Scientific Data (2020) Vol. 7, Iss. 1
Open Access | Times Cited: 317
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
Nurlan Kerimov, James Hayhurst, Kateryna Peikova, et al.
Nature Genetics (2021) Vol. 53, Iss. 9, pp. 1290-1299
Open Access | Times Cited: 314
Single-cell transcriptomics reveals expansion of cytotoxic CD4 T cells in supercentenarians
Kosuke Hashimoto, Tsukasa Kouno, Tomokatsu Ikawa, et al.
Proceedings of the National Academy of Sciences (2019) Vol. 116, Iss. 48, pp. 24242-24251
Open Access | Times Cited: 279
Kosuke Hashimoto, Tsukasa Kouno, Tomokatsu Ikawa, et al.
Proceedings of the National Academy of Sciences (2019) Vol. 116, Iss. 48, pp. 24242-24251
Open Access | Times Cited: 279
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
Gökçen Eraslan, Eugene Drokhlyansky, Shankara Anand, et al.
Science (2022) Vol. 376, Iss. 6594
Open Access | Times Cited: 279
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: 276
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: 276
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles
Heidi Hautakangas, Bendik S. Winsvold, Sanni Ruotsalainen, et al.
Nature Genetics (2022) Vol. 54, Iss. 2, pp. 152-160
Open Access | Times Cited: 258
Heidi Hautakangas, Bendik S. Winsvold, Sanni Ruotsalainen, et al.
Nature Genetics (2022) Vol. 54, Iss. 2, pp. 152-160
Open Access | Times Cited: 258
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
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
Yuanhua Huang, Davis J. McCarthy, Oliver Stegle
Genome biology (2019) Vol. 20, Iss. 1
Open Access | Times Cited: 233
Dream: powerful differential expression analysis for repeated measures designs
Gabriel E. Hoffman, Panos Roussos
Bioinformatics (2020) Vol. 37, Iss. 2, pp. 192-201
Open Access | Times Cited: 229
Gabriel E. Hoffman, Panos Roussos
Bioinformatics (2020) Vol. 37, Iss. 2, pp. 192-201
Open Access | Times Cited: 229
Dynamic landscape of immune cell-specific gene regulation in immune-mediated diseases
Mineto Ota, Yasuo Nagafuchi, Hiroaki Hatano, et al.
Cell (2021) Vol. 184, Iss. 11, pp. 3006-3021.e17
Open Access | Times Cited: 227
Mineto Ota, Yasuo Nagafuchi, Hiroaki Hatano, et al.
Cell (2021) Vol. 184, Iss. 11, pp. 3006-3021.e17
Open Access | Times Cited: 227
The Human Lung Cell Atlas: A High-Resolution Reference Map of the Human Lung in Health and Disease
Herbert B. Schiller, Daniel T. Montoro, Lukas M. Simon, et al.
American Journal of Respiratory Cell and Molecular Biology (2019) Vol. 61, Iss. 1, pp. 31-41
Open Access | Times Cited: 220
Herbert B. Schiller, Daniel T. Montoro, Lukas M. Simon, et al.
American Journal of Respiratory Cell and Molecular Biology (2019) Vol. 61, Iss. 1, pp. 31-41
Open Access | Times Cited: 220
A general approach for detecting expressed mutations in AML cells using single cell RNA-sequencing
Allegra A. Petti, Stephen R. Williams, Christopher A. Miller, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 195
Allegra A. Petti, Stephen R. Williams, Christopher A. Miller, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 195
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
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
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis
Kazuyoshi Ishigaki, Saori Sakaue, Chikashi Terao, et al.
Nature Genetics (2022) Vol. 54, Iss. 11, pp. 1640-1651
Open Access | Times Cited: 192
Kazuyoshi Ishigaki, Saori Sakaue, Chikashi Terao, et al.
Nature Genetics (2022) Vol. 54, Iss. 11, pp. 1640-1651
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
Monique G.P. van der Wijst, DH de Vries, Hilde E. Groot, et al.
eLife (2020) Vol. 9
Open Access | Times Cited: 191
Gene regulatory network inference in the era of single-cell multi-omics
Pau Badia-i-Mompel, Lorna Wessels, Sophia Müller‐Dott, et al.
Nature Reviews Genetics (2023) Vol. 24, Iss. 11, pp. 739-754
Closed Access | Times Cited: 189
Pau Badia-i-Mompel, Lorna Wessels, Sophia Müller‐Dott, et al.
Nature Reviews Genetics (2023) Vol. 24, Iss. 11, pp. 739-754
Closed Access | Times Cited: 189
Large-scale meta-analysis across East Asian and European populations updated genetic architecture and variant-driven biology of rheumatoid arthritis, identifying 11 novel susceptibility loci
Eunji Ha, Sang‐Cheol Bae, Kwang-Woo Kim
Annals of the Rheumatic Diseases (2020) Vol. 80, Iss. 5, pp. 558-565
Open Access | Times Cited: 151
Eunji Ha, Sang‐Cheol Bae, Kwang-Woo Kim
Annals of the Rheumatic Diseases (2020) Vol. 80, Iss. 5, pp. 558-565
Open Access | Times Cited: 151
Brain expression quantitative trait locus and network analyses reveal downstream effects and putative drivers for brain-related diseases
Niek de Klein, Ellen Tsai, Martijn Vochteloo, et al.
Nature Genetics (2023) Vol. 55, Iss. 3, pp. 377-388
Open Access | Times Cited: 148
Niek de Klein, Ellen Tsai, Martijn Vochteloo, et al.
Nature Genetics (2023) Vol. 55, Iss. 3, pp. 377-388
Open Access | Times Cited: 148