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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.

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Showing 1-25 of 1302 citing articles:

Analysis of protein-coding genetic variation in 60,706 humans
Monkol Lek, Konrad J. Karczewski, Eric Vallabh Minikel, et al.
Nature (2016) Vol. 536, Iss. 7616, pp. 285-291
Open Access | Times Cited: 9752
MutationTaster2: mutation prediction for the deep-sequencing age
Jana Marie Schwarz, D.N. Cooper, Markus Schuelke, et al.
Nature Methods (2014) Vol. 11, Iss. 4, pp. 361-362
Closed Access | Times Cited: 3401
Predicting the sequence specificities of DNA- and RNA-binding proteins by deep learning
Babak Alipanahi, Andrew Delong, Matthew T. Weirauch, et al.
Nature Biotechnology (2015) Vol. 33, Iss. 8, pp. 831-838
Open Access | Times Cited: 2774
REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants
Nilah M. Ioannidis, Joseph H. Rothstein, Vikas Pejaver, et al.
The American Journal of Human Genetics (2016) Vol. 99, Iss. 4, pp. 877-885
Open Access | Times Cited: 2158
Predicting effects of noncoding variants with deep learning–based sequence model
Jian Zhou, Olga G. Troyanskaya
Nature Methods (2015) Vol. 12, Iss. 10, pp. 931-934
Open Access | Times Cited: 2144
Architecture of the human interactome defines protein communities and disease networks
Edward L. Huttlin, Raphael J. Bruckner, João A. Paulo, et al.
Nature (2017) Vol. 545, Iss. 7655, pp. 505-509
Open Access | Times Cited: 1397
A Proteome-Scale Map of the Human Interactome Network
Thomas Rolland, Murat Taşan, Benoît Charloteaux, et al.
Cell (2014) Vol. 159, Iss. 5, pp. 1212-1226
Open Access | Times Cited: 1364
The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies
Peter D. Stenson, Matthew Mort, Edward V. Ball, et al.
Human Genetics (2017) Vol. 136, Iss. 6, pp. 665-677
Open Access | Times Cited: 1290
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease
William J. Astle, Heather Elding, Tao Jiang, et al.
Cell (2016) Vol. 167, Iss. 5, pp. 1415-1429.e19
Open Access | Times Cited: 1225
High-throughput discovery of novel developmental phenotypes
Mary E. Dickinson, Ann M. Flenniken, Xiao Ji, et al.
Nature (2016) Vol. 537, Iss. 7621, pp. 508-514
Open Access | Times Cited: 1156
dbNSFP v3.0: A One-Stop Database of Functional Predictions and Annotations for Human Nonsynonymous and Splice-Site SNVs
Xiaoming Liu, Chunlei Wu, Chang Li, et al.
Human Mutation (2015) Vol. 37, Iss. 3, pp. 235-241
Open Access | Times Cited: 954
Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders
Hane Lee, Joshua L. Deignan, Naghmeh Dorrani, et al.
JAMA (2014) Vol. 312, Iss. 18, pp. 1880-1880
Open Access | Times Cited: 923
Clinical application of whole-exome sequencing across clinical indications
Kyle Retterer, Jane Juusola, Megan T. Cho, et al.
Genetics in Medicine (2015) Vol. 18, Iss. 7, pp. 696-704
Open Access | Times Cited: 918
InterVar: Clinical Interpretation of Genetic Variants by the 2015 ACMG-AMP Guidelines
Quan Li, Kai Wang
The American Journal of Human Genetics (2017) Vol. 100, Iss. 2, pp. 267-280
Open Access | Times Cited: 883
M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity
Karthik A. Jagadeesh, Aaron M. Wenger, Mark J. Berger, et al.
Nature Genetics (2016) Vol. 48, Iss. 12, pp. 1581-1586
Closed Access | Times Cited: 767
An integrative approach to predicting the functional effects of non-coding and coding sequence variation
Hashem A. Shihab, Mark F. Rogers, Julian Gough, et al.
Bioinformatics (2015) Vol. 31, Iss. 10, pp. 1536-1543
Open Access | Times Cited: 654
DISEASES: Text mining and data integration of disease–gene associations
Sune Pletscher-Frankild, Albert Pallejá, Kalliopi Tsafou, et al.
Methods (2014) Vol. 74, pp. 83-89
Open Access | Times Cited: 559
Widespread Macromolecular Interaction Perturbations in Human Genetic Disorders
Nidhi Sahni, S. Stephen Yi, Mikko Taipale, et al.
Cell (2015) Vol. 161, Iss. 3, pp. 647-660
Open Access | Times Cited: 555
Tau and tauopathies
Thomas Arendt, Jens Stieler, Max Holzer
Brain Research Bulletin (2016) Vol. 126, pp. 238-292
Closed Access | Times Cited: 520
Building the foundation for genomics in precision medicine
Samuel Aronson, Heidi L. Rehm
Nature (2015) Vol. 526, Iss. 7573, pp. 336-342
Open Access | Times Cited: 471
Quantifying prion disease penetrance using large population control cohorts
Eric Vallabh Minikel, Sonia M. Vallabh, Monkol Lek, et al.
Science Translational Medicine (2016) Vol. 8, Iss. 322
Open Access | Times Cited: 417
Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease
Keren Carss, Gavin Arno, Marie Erwood, et al.
The American Journal of Human Genetics (2016) Vol. 100, Iss. 1, pp. 75-90
Open Access | Times Cited: 417
Erratum: Guidelines for diagnostic next-generation sequencing
Gert Matthijs, Erika Souche, Mariëlle Alders, et al.
European Journal of Human Genetics (2016) Vol. 24, Iss. 10, pp. 1515-1515
Open Access | Times Cited: 412
Predicting the clinical impact of human mutation with deep neural networks
Laksshman Sundaram, Hong Gao, Samskruthi Reddy Padigepati, et al.
Nature Genetics (2018) Vol. 50, Iss. 8, pp. 1161-1170
Open Access | Times Cited: 400
Structure of the F-actin–tropomyosin complex
Julian von der Ecken, Mirco Müller, William Lehman, et al.
Nature (2014) Vol. 519, Iss. 7541, pp. 114-117
Open Access | Times Cited: 359
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