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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:

A spectral approach integrating functional genomic annotations for coding and noncoding variants
Iuliana Ionita‐Laza, K. J. McCallum, Bin Xu, et al.
Nature Genetics (2016) Vol. 48, Iss. 2, pp. 214-220
Open Access | Times Cited: 601

Showing 1-25 of 601 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: 3056
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
Brian W. Kunkle, Benjamin Grenier‐Boley, Rebecca Sims, et al.
Nature Genetics (2019) Vol. 51, Iss. 3, pp. 414-430
Open Access | Times Cited: 2492
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
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: 2040
Accurate proteome-wide missense variant effect prediction with AlphaMissense
Jun Cheng, Guido Novati, Joshua Pan, et al.
Science (2023) Vol. 381, Iss. 6664
Open Access | Times Cited: 882
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
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: 563
CADD-Splice—improving genome-wide variant effect prediction using deep learning-derived splice scores
Philipp Rentzsch, Max Schubach, Jay Shendure, et al.
Genome Medicine (2021) Vol. 13, Iss. 1
Open Access | Times Cited: 540
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
Discovery of common and rare genetic risk variants for colorectal cancer
Jeroen R. Huyghe, Stephanie A. Bien, Tabitha A. Harrison, et al.
Nature Genetics (2018) Vol. 51, Iss. 1, pp. 76-87
Open Access | Times Cited: 476
An xQTL map integrates the genetic architecture of the human brain's transcriptome and epigenome
Bernard Ng, Charles C. White, Hans‐Ulrich Klein, et al.
Nature Neuroscience (2017) Vol. 20, Iss. 10, pp. 1418-1426
Open Access | Times Cited: 438
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
Whole-genome sequencing identifies common-to-rare variants associated with human blood metabolites
Tao Long, Michael Hicks, Hung‐Chun Yu, et al.
Nature Genetics (2017) Vol. 49, Iss. 4, pp. 568-578
Closed Access | Times Cited: 397
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
The impact of rare and low-frequency genetic variants in common disease
Lorenzo Bomba, Klaudia Walter, Nicole Soranzo
Genome biology (2017) Vol. 18, Iss. 1
Open Access | Times Cited: 334
Systematic Functional Dissection of Common Genetic Variation Affecting Red Blood Cell Traits
Jacob C. Ulirsch, Satish K. Nandakumar, Li Wang, et al.
Cell (2016) Vol. 165, Iss. 6, pp. 1530-1545
Open Access | Times Cited: 333
The sequences of 150,119 genomes in the UK Biobank
Bjarni V. Halldórsson, Hannes P. Eggertsson, Kristjan H. S. Moore, et al.
Nature (2022) Vol. 607, Iss. 7920, pp. 732-740
Open Access | Times Cited: 333
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
Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis
Eleni Zengini, Konstantinos Hatzikotoulas, Ioanna Tachmazidou, et al.
Nature Genetics (2018) Vol. 50, Iss. 4, pp. 549-558
Open Access | Times Cited: 282
Gene discovery in amyotrophic lateral sclerosis: implications for clinical management
Ammar Al‐Chalabi, Leonard H. van den Berg, Jan H. Veldink
Nature Reviews Neurology (2016) Vol. 13, Iss. 2, pp. 96-104
Open Access | Times Cited: 274
A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease
Damian Smedley, Max Schubach, Julius O.B. Jacobsen, et al.
The American Journal of Human Genetics (2016) Vol. 99, Iss. 3, pp. 595-606
Open Access | Times Cited: 265
Human gene essentiality
István Bartha, Julia di Iulio, J. Craig Venter, et al.
Nature Reviews Genetics (2017) Vol. 19, Iss. 1, pp. 51-62
Closed Access | Times Cited: 241
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
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
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: 200
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