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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:

Saturation mutagenesis of twenty disease-associated regulatory elements at single base-pair resolution
Martin Kircher, Chenling Xiong, Beth Martin, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 210

Showing 1-25 of 210 citing articles:

Effective gene expression prediction from sequence by integrating long-range interactions
Žiga Avsec, Vikram Agarwal, Daniel Visentin, et al.
Nature Methods (2021) Vol. 18, Iss. 10, pp. 1196-1203
Open Access | Times Cited: 721
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
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
Molecular and evolutionary processes generating variation in gene expression
Mark S. Hill, Pétra Vande Zande, Patricia J. Wittkopp
Nature Reviews Genetics (2020) Vol. 22, Iss. 4, pp. 203-215
Open Access | Times Cited: 227
MaveDB: an open-source platform to distribute and interpret data from multiplexed assays of variant effect
Daniel Esposito, Jochen Weile, Jay Shendure, et al.
Genome biology (2019) Vol. 20, Iss. 1
Open Access | Times Cited: 218
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
The evolution, evolvability and engineering of gene regulatory DNA
Eeshit Dhaval Vaishnav, Carl G. de Boer, Jennifer Molinet, et al.
Nature (2022) Vol. 603, Iss. 7901, pp. 455-463
Open Access | Times Cited: 198
A systematic evaluation of the design and context dependencies of massively parallel reporter assays
Jason C. Klein, Vikram Agarwal, Fumitaka Inoue, et al.
Nature Methods (2020) Vol. 17, Iss. 11, pp. 1083-1091
Open Access | Times Cited: 177
Melanoma models for the next generation of therapies
E. Elizabeth Patton, Kristen L. Mueller, David J. Adams, et al.
Cancer Cell (2021) Vol. 39, Iss. 5, pp. 610-631
Open Access | Times Cited: 162
Sequence determinants of human gene regulatory elements
Biswajyoti Sahu, Tuomo Hartonen, Päivi Pihlajamaa, et al.
Nature Genetics (2022) Vol. 54, Iss. 3, pp. 283-294
Open Access | Times Cited: 157
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
Multiple causal variants underlie genetic associations in humans
Nathan S. Abell, Marianne K. DeGorter, Michael J. Gloudemans, et al.
Science (2022) Vol. 375, Iss. 6586, pp. 1247-1254
Open Access | Times Cited: 138
CADD v1.7: using protein language models, regulatory CNNs and other nucleotide-level scores to improve genome-wide variant predictions
Max Schubach, Thorben Maaß, Lusiné Nazaretyan, et al.
Nucleic Acids Research (2024) Vol. 52, Iss. D1, pp. D1143-D1154
Open Access | Times Cited: 135
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
From variant to function in human disease genetics
Tuuli Lappalainen, Daniel G. MacArthur
Science (2021) Vol. 373, Iss. 6562, pp. 1464-1468
Closed Access | Times Cited: 124
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
Current sequence-based models capture gene expression determinants in promoters but mostly ignore distal enhancers
Alexander Karollus, Thomas Mauermeier, Julien Gagneur
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 76
Cell-type-directed design of synthetic enhancers
Ibrahim Ihsan Taskiran, Katina I. Spanier, Hannah Dickmänken, et al.
Nature (2023) Vol. 626, Iss. 7997, pp. 212-220
Open Access | Times Cited: 73
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
Affinity-optimizing enhancer variants disrupt development
Fabian Lim, Joe J. Solvason, Genevieve E. Ryan, et al.
Nature (2024) Vol. 626, Iss. 7997, pp. 151-159
Open Access | Times Cited: 53
Massively parallel characterization of transcriptional regulatory elements in three diverse human cell types
Vikram Agarwal, Fumitaka Inoue, Max Schubach, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 46
Hold out the genome: a roadmap to solving the cis-regulatory code
Carl G. de Boer, Jussi Taipale
Nature (2023) Vol. 625, Iss. 7993, pp. 41-50
Open Access | Times Cited: 46
Identification of constrained sequence elements across 239 primate genomes
Lukas F. K. Kuderna, Jacob C. Ulirsch, Sabrina Mohd Rashid, et al.
Nature (2023) Vol. 625, Iss. 7996, pp. 735-742
Open Access | Times Cited: 44
CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods
Shantanu Jain, Constantina Bakolitsa, Steven E. Brenner, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 38
Single-cell spatial multi-omics and deep learning dissect enhancer-driven gene regulatory networks in liver zonation
Carmen Bravo González‐Blas, Irina Matetovici, Hanne Hillen, et al.
Nature Cell Biology (2024) Vol. 26, Iss. 1, pp. 153-167
Open Access | Times Cited: 24
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