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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:

Perspectives on ENCODE
Federico Abascal, Reyes Acosta, Nicholas J. Addleman, et al.
Nature (2020) Vol. 583, Iss. 7818, pp. 693-698
Open Access | Times Cited: 179

Showing 1-25 of 179 citing articles:

Expanded encyclopaedias of DNA elements in the human and mouse genomes
Federico Abascal, Reyes Acosta, Nicholas J. Addleman, et al.
Nature (2020) Vol. 583, Iss. 7818, pp. 699-710
Open Access | Times Cited: 1827
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations
Cindy G. Boer, Konstantinos Hatzikotoulas, Lorraine Southam, et al.
Cell (2021) Vol. 184, Iss. 18, pp. 4784-4818.e17
Open Access | Times Cited: 330
FunRich enables enrichment analysis of OMICs datasets
Pamali Fonseka, Mohashin Pathan, Sai V. Chitti, et al.
Journal of Molecular Biology (2020) Vol. 433, Iss. 11, pp. 166747-166747
Closed Access | Times Cited: 235
Functional annotations of three domestic animal genomes provide vital resources for comparative and agricultural research
Colin Kern, Ying Wang, Xiaoqin Xu, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 159
Machine learning meets omics: applications and perspectives
Rufeng Li, Lixin Li, Yungang Xu, et al.
Briefings in Bioinformatics (2021) Vol. 23, Iss. 1
Closed Access | Times Cited: 121
Why sequence all eukaryotes?
Mark Blaxter, John M. Archibald, Anna K. Childers, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 4
Open Access | Times Cited: 83
Leveraging base-pair mammalian constraint to understand genetic variation and human disease
Patrick F. Sullivan, Jennifer R. S. Meadows, Steven Gazal, et al.
Science (2023) Vol. 380, Iss. 6643
Open Access | Times Cited: 72
Cooperation between bHLH transcription factors and histones for DNA access
Alicia K. Michael, Lisa Stoos, Priya Crosby, et al.
Nature (2023) Vol. 619, Iss. 7969, pp. 385-393
Open Access | Times Cited: 56
Epigenetic regulatory layers in the 3D nucleus
Andréa Willemin, Dominik Szabó, Ana Pombo
Molecular Cell (2024) Vol. 84, Iss. 3, pp. 415-428
Open Access | Times Cited: 19
Advancing genetic improvement in the omics era: status and priorities for United States aquaculture
Linnea K. Andersen, Neil F. Thompson, Jason Abernathy, et al.
BMC Genomics (2025) Vol. 26, Iss. 1
Open Access | Times Cited: 2
Omics in Systems Biology: Current Progress and Future Outlook
Timothy D. Veenstra
PROTEOMICS (2020) Vol. 21, Iss. 3-4
Closed Access | Times Cited: 74
Reading the chromatinized genome
Alicia K. Michael, Nicolas H. Thomä
Cell (2021) Vol. 184, Iss. 14, pp. 3599-3611
Open Access | Times Cited: 67
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: 39
Leveraging transcriptomics for precision diagnosis: Lessons learned from cancer and sepsis
Maria Tsakiroglou, A.G. Evans, Munir Pirmohamed
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 25
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: 15
Harnessing Artificial Intelligence in Multimodal Omics Data Integration: Paving the Path for the Next Frontier in Precision Medicine
Yonghyun Nam, Jae‐Sik Kim, Sang‐Hyuk Jung, et al.
Annual Review of Biomedical Data Science (2024) Vol. 7, Iss. 1, pp. 225-250
Closed Access | Times Cited: 12
Big data and deep learning for RNA biology
Hyeonseo Hwang, Hyeonseong Jeon, Nagyeong Yeo, et al.
Experimental & Molecular Medicine (2024) Vol. 56, Iss. 6, pp. 1293-1321
Open Access | Times Cited: 12
Single-cell omics: experimental workflow, data analyses and applications
Fengying Sun, Haoyan Li, Dongqing Sun, et al.
Science China Life Sciences (2024)
Closed Access | Times Cited: 11
Multiomic profiling of transcription factor binding and function in human brain
Jacob M. Loupe, Ashlyn G. Anderson, Lindsay F. Rizzardi, et al.
Nature Neuroscience (2024) Vol. 27, Iss. 7, pp. 1387-1399
Closed Access | Times Cited: 9
SETD2: from chromatin modifier to multipronged regulator of the genome and beyond
Thom M. Molenaar, Fred van Leeuwen
Cellular and Molecular Life Sciences (2022) Vol. 79, Iss. 6
Open Access | Times Cited: 34
Transcriptional network orchestrating regional patterning of cortical progenitors
Athéna R. Ypsilanti, Kartik Pattabiraman, Rinaldo Catta-Preta, et al.
Proceedings of the National Academy of Sciences (2021) Vol. 118, Iss. 51
Open Access | Times Cited: 41
Epigenetic editing: Dissecting chromatin function in context
Cristina Policarpi, Juliette Dabin, Jamie A. Hackett
BioEssays (2021) Vol. 43, Iss. 5
Closed Access | Times Cited: 39
Mechanisms underlying divergent responses of genetically distinct macrophages to IL-4
Marten A. Hoeksema, Zeyang Shen, Inge R. Holtman, et al.
Science Advances (2021) Vol. 7, Iss. 25
Open Access | Times Cited: 39
NASA GeneLab RNA-seq consensus pipeline: Standardized processing of short-read RNA-seq data
Eliah Overbey, Amanda Saravia-Butler, Zhe Zhang, et al.
iScience (2021) Vol. 24, Iss. 4, pp. 102361-102361
Open Access | Times Cited: 38
Regulatory variants in TCF7L2 are associated with thoracic aortic aneurysm
Tanmoy Roychowdhury, Haocheng Lu, Whitney Hornsby, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 9, pp. 1578-1589
Open Access | Times Cited: 35
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