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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:

Fast, scalable prediction of deleterious noncoding variants from functional and population genomic data
Yi-Fei Huang, Brad Gulko, Adam Siepel
Nature Genetics (2017) Vol. 49, Iss. 4, pp. 618-624
Open Access | Times Cited: 349

Showing 1-25 of 349 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
CADD: predicting the deleteriousness of variants throughout the human genome
Philipp Rentzsch, Daniela Witten, Gregory M. Cooper, et al.
Nucleic Acids Research (2018) Vol. 47, Iss. D1, pp. D886-D894
Open Access | Times Cited: 3056
Analysis of 100,000 human cancer genomes reveals the landscape of tumor mutational burden
Zachary R. Chalmers, Caitlin Connelly, David Fabrizio, et al.
Genome Medicine (2017) Vol. 9, Iss. 1
Open Access | Times Cited: 3014
Applications of Deep Learning and Reinforcement Learning to Biological Data
Mufti Mahmud, M. Shamim Kaiser, Amir Hussain, et al.
IEEE Transactions on Neural Networks and Learning Systems (2018) Vol. 29, Iss. 6, pp. 2063-2079
Open Access | Times Cited: 782
Deep generative models of genetic variation capture the effects of mutations
Adam J. Riesselman, John Ingraham, Debora S. Marks
Nature Methods (2018) Vol. 15, Iss. 10, pp. 816-822
Open Access | Times Cited: 577
Cell type–specific genetic regulation of gene expression across human tissues
Sarah Kim-Hellmuth, François Aguet, Meritxell Oliva, et al.
Science (2020) Vol. 369, Iss. 6509
Open Access | Times Cited: 489
dbNSFP v4: a comprehensive database of transcript-specific functional predictions and annotations for human nonsynonymous and splice-site SNVs
Xiaoming Liu, Chang Li, Chengcheng Mou, et al.
Genome Medicine (2020) Vol. 12, Iss. 1
Open Access | Times Cited: 478
Deep Learning in Mining Biological Data
Mufti Mahmud, M. Shamim Kaiser, T.M. McGinnity, et al.
Cognitive Computation (2021) Vol. 13, Iss. 1, pp. 1-33
Open Access | Times Cited: 356
Machine learning for integrating data in biology and medicine: Principles, practice, and opportunities
Marinka Žitnik, Francis Nguyen, Bo Wang, et al.
Information Fusion (2018) Vol. 50, pp. 71-91
Open Access | Times Cited: 289
Mapping and characterization of structural variation in 17,795 human genomes
Haley Abel, David E. Larson, Allison Regier, et al.
Nature (2020) Vol. 583, Iss. 7814, pp. 83-89
Open Access | Times Cited: 277
Settling the score: variant prioritization and Mendelian disease
Karen Eilbeck, Aaron R. Quinlan, Mark Yandell
Nature Reviews Genetics (2017) Vol. 18, Iss. 10, pp. 599-612
Open Access | Times Cited: 241
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale
Xihao Li, Zilin Li, Hufeng Zhou, et al.
Nature Genetics (2020) Vol. 52, Iss. 9, pp. 969-983
Open Access | Times Cited: 216
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
A Deep Neural Network for Predicting and Engineering Alternative Polyadenylation
Nicholas Bogard, Johannes Linder, Alexander Rosenberg, et al.
Cell (2019) Vol. 178, Iss. 1, pp. 91-106.e23
Open Access | Times Cited: 200
Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis
Sai Zhang, Johnathan Cooper‐Knock, Annika K. Weimer, et al.
Neuron (2022) Vol. 110, Iss. 6, pp. 992-1008.e11
Open Access | Times Cited: 98
Functional regulatory variants implicate distinct transcriptional networks in dementia
Yonatan A. Cooper, Noam Teyssier, Nina M. Dräger, et al.
Science (2022) Vol. 377, Iss. 6608
Open Access | Times Cited: 88
FAVOR: functional annotation of variants online resource and annotator for variation across the human genome
Hufeng Zhou, Theodore Arapoglou, Xihao Li, et al.
Nucleic Acids Research (2022) Vol. 51, Iss. D1, pp. D1300-D1311
Open Access | Times Cited: 86
Universal annotation of the human genome through integration of over a thousand epigenomic datasets
Ha Vu, Jason Ernst
Genome biology (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 80
Jasmine and Iris: population-scale structural variant comparison and analysis
Melanie Kirsche, Gautam Prabhu, Rachel M. Sherman, et al.
Nature Methods (2023) Vol. 20, Iss. 3, pp. 408-417
Open Access | Times Cited: 75
Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study
Hao Yu Chen, Christian Dina, Aeron Small, et al.
European Heart Journal (2023) Vol. 44, Iss. 21, pp. 1927-1939
Open Access | Times Cited: 61
Bayesian estimation of gene constraint from an evolutionary model with gene features
Tony Zeng, Jeffrey P. Spence, Hakhamanesh Mostafavi, et al.
Nature Genetics (2024) Vol. 56, Iss. 8, pp. 1632-1643
Open Access | Times Cited: 28
Functional dissection of human cardiac enhancers and noncoding de novo variants in congenital heart disease
Feng Xiao, Xiaoran Zhang, Sarah U. Morton, et al.
Nature Genetics (2024) Vol. 56, Iss. 3, pp. 420-430
Open Access | Times Cited: 21
Functional architecture of low-frequency variants highlights strength of negative selection across coding and non-coding annotations
Steven Gazal, Po−Ru Loh, Hilary K. Finucane, et al.
Nature Genetics (2018) Vol. 50, Iss. 11, pp. 1600-1607
Open Access | Times Cited: 161
Incomplete dominance of deleterious alleles contributes substantially to trait variation and heterosis in maize
Jinliang Yang, Sofiane Mezmouk, Andy Baumgarten, et al.
PLoS Genetics (2017) Vol. 13, Iss. 9, pp. e1007019-e1007019
Open Access | Times Cited: 161
The human noncoding genome defined by genetic diversity
Julia di Iulio, István Bartha, Emily H. M. Wong, et al.
Nature Genetics (2018) Vol. 50, Iss. 3, pp. 333-337
Open Access | Times Cited: 159
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