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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:

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: 765

Showing 1-25 of 765 citing articles:

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: 3045
Comprehensive Characterization of Cancer Driver Genes and Mutations
Matthew H. Bailey, Collin Tokheim, Eduard Porta‐Pardo, et al.
Cell (2018) Vol. 173, Iss. 2, pp. 371-385.e18
Open Access | Times Cited: 2033
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
Disease variant prediction with deep generative models of evolutionary data
Jonathan Frazer, Pascal Notin, Mafalda Dias, et al.
Nature (2021) Vol. 599, Iss. 7883, pp. 91-95
Open Access | Times Cited: 558
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: 475
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: 398
Regional missense constraint improves variant deleteriousness prediction
Kaitlin E. Samocha, Jack A. Kosmicki, Konrad J. Karczewski, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2017)
Open Access | Times Cited: 357
Managing computational complexity using surrogate models: a critical review
Reza Alizadeh, Janet K. Allen, Farrokh Mistree
Research in Engineering Design (2020) Vol. 31, Iss. 3, pp. 275-298
Closed Access | Times Cited: 300
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Jason Flannick, Josep M. Mercader, Christian Fuchsberger, et al.
Nature (2019) Vol. 570, Iss. 7759, pp. 71-76
Open Access | Times Cited: 293
PMut: a web-based tool for the annotation of pathological variants on proteins, 2017 update
Víctor López-Ferrando, Andrea Gazzo, Xavier de la Cruz, et al.
Nucleic Acids Research (2017) Vol. 45, Iss. W1, pp. W222-W228
Open Access | Times Cited: 237
The Genetic Landscape of Diamond-Blackfan Anemia
Jacob C. Ulirsch, Jeffrey M. Verboon, Shideh Kazerounian, et al.
The American Journal of Human Genetics (2018) Vol. 103, Iss. 6, pp. 930-947
Open Access | Times Cited: 228
Evaluation of in silico algorithms for use with ACMG/AMP clinical variant interpretation guidelines
Rajarshi Ghosh, Ninad Oak, Sharon E. Plon
Genome biology (2017) Vol. 18, Iss. 1
Open Access | Times Cited: 214
The landscape of epilepsy-related GATOR1 variants
Sara Baldassari, Fabienne Picard, Nienke E. Verbeek, et al.
Genetics in Medicine (2018) Vol. 21, Iss. 2, pp. 398-408
Open Access | Times Cited: 201
ClinPred: Prediction Tool to Identify Disease-Relevant Nonsynonymous Single-Nucleotide Variants
Najmeh Alirezaie, Kristin D. Kernohan, Taila Hartley, et al.
The American Journal of Human Genetics (2018) Vol. 103, Iss. 4, pp. 474-483
Open Access | Times Cited: 199
Performance evaluation of pathogenicity-computation methods for missense variants
Jinchen Li, Tingting Zhao, Yi Zhang, et al.
Nucleic Acids Research (2018) Vol. 46, Iss. 15, pp. 7793-7804
Open Access | Times Cited: 198
Pharmacogenomics of CYP2C9: Functional and Clinical Considerations
Ann K. Daly, Allan E. Rettie, Douglas M. Fowler, et al.
Journal of Personalized Medicine (2017) Vol. 8, Iss. 1, pp. 1-1
Open Access | Times Cited: 190
A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function
Michael T. Lam, Simona Coppola, Oliver H.F. Krumbach, et al.
The Journal of Experimental Medicine (2019) Vol. 216, Iss. 12, pp. 2778-2799
Open Access | Times Cited: 170
MVP predicts the pathogenicity of missense variants by deep learning
Hongjian Qi, Haicang Zhang, Yige Zhao, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 150
Loss-of-function mutations in QRICH2 cause male infertility with multiple morphological abnormalities of the sperm flagella
Ying Shen, Feng Zhang, Fuping Li, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 147
Language models enable zero-shot prediction of the effects of mutations on protein function
Joshua Meier, Roshan Rao, Robert Verkuil, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 131
Improved pathogenicity prediction for rare human missense variants
Yingzhou Wu, Hanqing Liu, Roujia Li, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 10, pp. 1891-1906
Open Access | Times Cited: 111
Frequent SLC35A2 brain mosaicism in mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE)
Thomas Bonduelle, Till Hartlieb, Sara Baldassari, et al.
Acta Neuropathologica Communications (2021) Vol. 9, Iss. 1
Open Access | Times Cited: 110
MetaRNN: differentiating rare pathogenic and rare benign missense SNVs and InDels using deep learning
Chang Li, Degui Zhi, Kai Wang, et al.
Genome Medicine (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 101
The landscape of tolerated genetic variation in humans and primates
Hong Gao, Tobias Hamp, Jeffrey M. Ede, et al.
Science (2023) Vol. 380, Iss. 6648
Open Access | Times Cited: 100
GWAS and ExWAS of blood mitochondrial DNA copy number identifies 71 loci and highlights a potential causal role in dementia
Michael Chong, Pedrum Mohammadi‐Shemirani, Nicolas Perrot, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 84
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