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:

Genome-wide enhancer maps link risk variants to disease genes
Joseph Nasser, Drew T. Bergman, Charles P. Fulco, et al.
Nature (2021) Vol. 593, Iss. 7858, pp. 238-243
Open Access | Times Cited: 528

Showing 1-25 of 528 citing articles:

Long non-coding RNAs: definitions, functions, challenges and recommendations
John S. Mattick, Paulo Amaral, Piero Carninci, et al.
Nature Reviews Molecular Cell Biology (2023) Vol. 24, Iss. 6, pp. 430-447
Open Access | Times Cited: 1143

Genome-wide association studies
Emil Uffelmann, Qin Qin Huang, Nchangwi Syntia Munung, et al.
Nature Reviews Methods Primers (2021) Vol. 1, Iss. 1
Open Access | Times Cited: 1084

A single-cell atlas of chromatin accessibility in the human genome
Kai Zhang, James D. Hocker, Michael Miller, et al.
Cell (2021) Vol. 184, Iss. 24, pp. 5985-6001.e19
Open Access | Times Cited: 327

Advancing the use of genome-wide association studies for drug repurposing
William R. Reay, Murray J. Cairns
Nature Reviews Genetics (2021) Vol. 22, Iss. 10, pp. 658-671
Closed Access | Times Cited: 211

Systematic differences in discovery of genetic effects on gene expression and complex traits
Hakhamanesh Mostafavi, Jeffrey P. Spence, Sahin Naqvi, et al.
Nature Genetics (2023) Vol. 55, Iss. 11, pp. 1866-1875
Closed Access | Times Cited: 155

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: 145

Epigenomic and transcriptomic analyses define core cell types, genes and targetable mechanisms for kidney disease
Hongbo Liu, Tomohito Doke, Dong Guo, et al.
Nature Genetics (2022) Vol. 54, Iss. 7, pp. 950-962
Closed Access | Times Cited: 139

Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention
Zhe Wang, Andrew Emmerich, Nicolas J. Pillon, et al.
Nature Genetics (2022) Vol. 54, Iss. 9, pp. 1332-1344
Open Access | Times Cited: 130

Compatibility rules of human enhancer and promoter sequences
Drew T. Bergman, Thouis R. Jones, Vincent Liu, et al.
Nature (2022) Vol. 607, Iss. 7917, pp. 176-184
Open Access | Times Cited: 124

Combining SNP-to-gene linking strategies to identify disease genes and assess disease omnigenicity
Steven Gazal, Omer Weissbrod, Farhad Hormozdiari, et al.
Nature Genetics (2022) Vol. 54, Iss. 6, pp. 827-836
Open Access | Times Cited: 122

Building regulatory landscapes reveals that an enhancer can recruit cohesin to create contact domains, engage CTCF sites and activate distant genes
Niels J. Rinzema, Konstantinos Sofiadis, Sjoerd J. D. Tjalsma, et al.
Nature Structural & Molecular Biology (2022) Vol. 29, Iss. 6, pp. 563-574
Open Access | Times Cited: 117

DNA methylation QTL mapping across diverse human tissues provides molecular links between genetic variation and complex traits
Meritxell Oliva, Kathryn Demanelis, Yihao Lu, et al.
Nature Genetics (2022) Vol. 55, Iss. 1, pp. 112-122
Open Access | Times Cited: 115

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: 110

Discovery of target genes and pathways at GWAS loci by pooled single-cell CRISPR screens
John Morris, Christina M. Caragine, Zharko Daniloski, et al.
Science (2023) Vol. 380, Iss. 6646
Open Access | Times Cited: 110

Genetics of the human microglia regulome refines Alzheimer’s disease risk loci
Roman Kosoy, John F. Fullard, Biao Zeng, et al.
Nature Genetics (2022) Vol. 54, Iss. 8, pp. 1145-1154
Open Access | Times Cited: 106

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: 100

Single-nucleus chromatin accessibility profiling highlights regulatory mechanisms of coronary artery disease risk
Adam W. Turner, Shengen Hu, José Verdezoto Mosquera, et al.
Nature Genetics (2022) Vol. 54, Iss. 6, pp. 804-816
Open Access | Times Cited: 92

Limited overlap of eQTLs and GWAS hits due to systematic differences in discovery
Hakhamanesh Mostafavi, Jeffrey P. Spence, Sahin Naqvi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 91

WhichTF is functionally important in your open chromatin data?
Yosuke Tanigawa, Ethan S. Dyer, Gill Bejerano
PLoS Computational Biology (2022) Vol. 18, Iss. 8, pp. e1010378-e1010378
Open Access | Times Cited: 87

Complementary Alu sequences mediate enhancer–promoter selectivity
Liang Liang, Changchang Cao, Lei Ji, et al.
Nature (2023) Vol. 619, Iss. 7971, pp. 868-875
Closed Access | Times Cited: 86

Intestinal epithelial cell metabolism at the interface of microbial dysbiosis and tissue injury
Eva Rath, Dirk Haller
Mucosal Immunology (2022) Vol. 15, Iss. 4, pp. 595-604
Open Access | Times Cited: 82

The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits
Maria C. Costanzo, Marcin von Grotthuss, Jeffrey Massung, et al.
Cell Metabolism (2023) Vol. 35, Iss. 4, pp. 695-710.e6
Open Access | Times Cited: 78

Single-cell DNA methylation and 3D genome architecture in the human brain
Wei Tian, Jingtian Zhou, Anna Bartlett, et al.
Science (2023) Vol. 382, Iss. 6667
Open Access | Times Cited: 74

Lactate limits CNS autoimmunity by stabilizing HIF-1α in dendritic cells
Liliana M. Sanmarco, Joseph M. Rone, Carolina Manganeli Polonio, et al.
Nature (2023) Vol. 620, Iss. 7975, pp. 881-889
Closed Access | Times Cited: 73

An atlas of transcribed human cardiac promoters and enhancers reveals an important role of regulatory elements in heart failure
Ruslan Deviatiiarov, Anna Gams, Ivan V. Kulakovskiy, et al.
Nature Cardiovascular Research (2023) Vol. 2, Iss. 1, pp. 58-75
Open Access | Times Cited: 65

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