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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:

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

Showing 1-25 of 72 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
A genomic mutational constraint map using variation in 76,156 human genomes
Siwei Chen, Laurent C. Francioli, Julia K. Goodrich, et al.
Nature (2023) Vol. 625, Iss. 7993, pp. 92-100
Closed Access | Times Cited: 525
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
A genome-wide mutational constraint map quantified from variation in 76,156 human genomes
Siwei Chen, Laurent C. Francioli, Julia K. Goodrich, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 278
Leveraging polygenic enrichments of gene features to predict genes underlying complex traits and diseases
E. Weeks, Jacob C. Ulirsch, Nathan Cheng, et al.
Nature Genetics (2023) Vol. 55, Iss. 8, pp. 1267-1276
Open Access | Times Cited: 174
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
The genetic and biochemical determinants of mRNA degradation rates in mammals
Vikram Agarwal, David R. Kelley
Genome biology (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 78
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
Predicting RNA-seq coverage from DNA sequence as a unifying model of gene regulation
Johannes Linder, Divyanshi Srivastava, Han Yuan, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 50
Benchmarking of deep neural networks for predicting personal gene expression from DNA sequence highlights shortcomings
Alexander Sasse, Bernard Ng, Anna Spiro, et al.
Nature Genetics (2023) Vol. 55, Iss. 12, pp. 2060-2064
Open Access | Times Cited: 47
Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries
Zhili Zheng, Shouye Liu, Julia Sidorenko, et al.
Nature Genetics (2024) Vol. 56, Iss. 5, pp. 767-777
Open Access | Times Cited: 34
Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseases
Kai Yuan, Ryan J. Longchamps, Antonio F. Pardiñas, et al.
Nature Genetics (2024) Vol. 56, Iss. 9, pp. 1841-1850
Closed Access | Times Cited: 30
MESuSiE enables scalable and powerful multi-ancestry fine-mapping of causal variants in genome-wide association studies
Boran Gao, Xiang Zhou
Nature Genetics (2024) Vol. 56, Iss. 1, pp. 170-179
Closed Access | Times Cited: 25
Tissue-specific enhancer–gene maps from multimodal single-cell data identify causal disease alleles
Saori Sakaue, Kathryn Weinand, Shakson Isaac, et al.
Nature Genetics (2024) Vol. 56, Iss. 4, pp. 615-626
Open Access | Times Cited: 23
Deciphering the impact of genomic variation on function
J Engreitz, Heather A. Lawson, Harinder Singh, et al.
Nature (2024) Vol. 633, Iss. 8028, pp. 47-57
Closed Access | Times Cited: 22
Predicting RNA-seq coverage from DNA sequence as a unifying model of gene regulation
Johannes Linder, Divyanshi Srivastava, Han Yuan, et al.
Nature Genetics (2025)
Open Access | Times Cited: 11
Insights from complex trait fine-mapping across diverse populations
Masahiro Kanai, Jacob C. Ulirsch, Juha Karjalainen, et al.
medRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 81
Effective gene expression prediction from sequence by integrating long-range interactions
Žiga Avsec, Vikram Agarwal, Daniel Visentin, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 63
Personal transcriptome variation is poorly explained by current genomic deep learning models
Connie Huang, Richard W. Shuai, Parth Baokar, et al.
Nature Genetics (2023) Vol. 55, Iss. 12, pp. 2056-2059
Open Access | Times Cited: 39
Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseases
Kai Yuan, Ryan J. Longchamps, Antonio F. Pardiñas, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 24
Massively parallel screen uncovers many rare 3′ UTR variants regulating mRNA abundance of cancer driver genes
Ting Fu, Kofi Amoah, Tracey W. Chan, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 11
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
ChromBPNet: bias factorized, base-resolution deep learning models of chromatin accessibility reveal cis-regulatory sequence syntax, transcription factor footprints and regulatory variants
Anusri Pampari, Anna Shcherbina, Evgeny Z. Kvon, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 11
Regulatory features aid interpretation of 3′UTR variants
Lindsay Romo, Scott D. Findlay, Christopher B. Burge
The American Journal of Human Genetics (2024) Vol. 111, Iss. 2, pp. 350-363
Open Access | Times Cited: 10
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