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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:

High-throughput identification of human SNPs affecting regulatory element activity
J.H.J. Janssen, Ludo Pagie, Vincent FitzPatrick, et al.
Nature Genetics (2019) Vol. 51, Iss. 7, pp. 1160-1169
Open Access | Times Cited: 189

Showing 1-25 of 189 citing articles:

The GTEx Consortium atlas of genetic regulatory effects across human tissues
François Aguet, Shankara Anand, Kristin Ardlie, et al.
Science (2020) Vol. 369, Iss. 6509, pp. 1318-1330
Open Access | Times Cited: 3811
Enhancer RNAs are an important regulatory layer of the epigenome
Vittorio Sartorelli, Shannon Lauberth
Nature Structural & Molecular Biology (2020) Vol. 27, Iss. 6, pp. 521-528
Open Access | Times Cited: 280
Genomic Analysis in the Age of Human Genome Sequencing
Tuuli Lappalainen, Alexandra J. Scott, Margot Brandt, et al.
Cell (2019) Vol. 177, Iss. 1, pp. 70-84
Open Access | Times Cited: 269
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
Enhancer redundancy in development and disease
Evgeny Z. Kvon, Rachel Waymack, Mario Gad, et al.
Nature Reviews Genetics (2021) Vol. 22, Iss. 5, pp. 324-336
Open Access | Times Cited: 202
Comprehensive In Vivo Interrogation Reveals Phenotypic Impact of Human Enhancer Variants
Evgeny Z. Kvon, Yiwen Zhu, Guy Kelman, et al.
Cell (2020) Vol. 180, Iss. 6, pp. 1262-1271.e15
Open Access | Times Cited: 154
Landscape of allele-specific transcription factor binding in the human genome
Sergey Abramov, Alexandr Boytsov, Daria Bykova, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 140
Genome-wide functional screen of 3′UTR variants uncovers causal variants for human disease and evolution
Dustin Griesemer, James R. Xue, Steven K. Reilly, et al.
Cell (2021) Vol. 184, Iss. 20, pp. 5247-5260.e19
Open Access | Times Cited: 128
Systematic analysis of intrinsic enhancer-promoter compatibility in the mouse genome
Miguel Martinez-Ara, Federico Comoglio, J.H.J. Janssen, et al.
Molecular Cell (2022) Vol. 82, Iss. 13, pp. 2519-2531.e6
Open Access | Times Cited: 85
Single nucleus multiomics identifies ZEB1 and MAFB as candidate regulators of Alzheimer’s disease-specific cis-regulatory elements
Ashlyn G. Anderson, Brianne B. Rogers, Jacob M. Loupe, et al.
Cell Genomics (2023) Vol. 3, Iss. 3, pp. 100263-100263
Open Access | Times Cited: 53
Decoding the genetic and epigenetic basis of asthma
Bernard Stikker, Rudi W. Hendriks, Ralph Stadhouders
Allergy (2023) Vol. 78, Iss. 4, pp. 940-956
Open Access | Times Cited: 47
Insights into pancreatic islet cell dysfunction from type 2 diabetes mellitus genetics
Nicole A. J. Krentz, Anna L. Gloyn
Nature Reviews Endocrinology (2020) Vol. 16, Iss. 4, pp. 202-212
Closed Access | Times Cited: 117
A practical view of fine-mapping and gene prioritization in the post-genome-wide association era
Roeland Broekema, Olivier B. Bakker, Iris H. Jonkers
Open Biology (2020) Vol. 10, Iss. 1, pp. 190221-190221
Open Access | Times Cited: 113
Massively parallel discovery of human-specific substitutions that alter enhancer activity
Severin Uebbing, Jake Gockley, Steven K. Reilly, et al.
Proceedings of the National Academy of Sciences (2020) Vol. 118, Iss. 2
Open Access | Times Cited: 98
MPRAnalyze: statistical framework for massively parallel reporter assays
Tal Ashuach, David S. Fischer, Anat Kreimer, et al.
Genome biology (2019) Vol. 20, Iss. 1
Open Access | Times Cited: 86
3D genome architecture coordinates trans and cis regulation of differentially expressed ear and tassel genes in maize
Yonghao Sun, Liang Dong, Ying Zhang, et al.
Genome biology (2020) Vol. 21, Iss. 1
Open Access | Times Cited: 79
Leveraging supervised learning for functionally informed fine-mapping of cis-eQTLs identifies an additional 20,913 putative causal eQTLs
Qingbo Wang, David R. Kelley, Jacob C. Ulirsch, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 72
Identification of non-coding silencer elements and their regulation of gene expression
Baoxu Pang, Jan Hendrik van Weerd, Feija L. Hamoen, et al.
Nature Reviews Molecular Cell Biology (2022) Vol. 24, Iss. 6, pp. 383-395
Open Access | Times Cited: 62
Scalable Functional Assays for the Interpretation of Human Genetic Variation
Daniel Tabet, Victoria N. Parikh, Prashant Mali, et al.
Annual Review of Genetics (2022) Vol. 56, Iss. 1, pp. 441-465
Closed Access | Times Cited: 48
Current challenges in understanding the role of enhancers in disease
Judith B. Zaugg, Pelin Sahlén, Robin Andersson, et al.
Nature Structural & Molecular Biology (2022) Vol. 29, Iss. 12, pp. 1148-1158
Open Access | Times Cited: 48
Regulating specificity in enhancer–promoter communication
Charalampos Chrysovalantis Galouzis, Eileen E. M. Furlong
Current Opinion in Cell Biology (2022) Vol. 75, pp. 102065-102065
Closed Access | Times Cited: 45
Analyses of rare predisposing variants of lung cancer in 6,004 whole genomes in Chinese
Cheng Wang, Juncheng Dai, Na Qin, et al.
Cancer Cell (2022) Vol. 40, Iss. 10, pp. 1223-1239.e6
Open Access | Times Cited: 43
Leveraging massively parallel reporter assays for evolutionary questions
Irene Gallego Romero, Amanda J. Lea
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 33
De novo human brain enhancers created by single-nucleotide mutations
Shan Li, Sridhar Hannenhalli, Ivan Ovcharenko
Science Advances (2023) Vol. 9, Iss. 7
Open Access | Times Cited: 24
Functional dissection of complex and molecular trait variants at single nucleotide resolution
Layla Siraj, Rodrigo Castro, Hannah B. Dewey, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 11
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