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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 26-50 of 601 citing articles:

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: 200
Project MinE: study design and pilot analyses of a large-scale whole-genome sequencing study in amyotrophic lateral sclerosis

European Journal of Human Genetics (2018) Vol. 26, Iss. 10, pp. 1537-1546
Open Access | Times Cited: 170
Using deep mutational scanning to benchmark variant effect predictors and identify disease mutations
Benjamin Livesey, Joseph A. Marsh
Molecular Systems Biology (2020) Vol. 16, Iss. 7
Open Access | Times Cited: 157
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: 153
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: 116
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: 102
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
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
Critical assessment of missense variant effect predictors on disease-relevant variant data
Ruchir Rastogi, Ryan Chung, Sindy Li, et al.
Human Genetics (2025)
Open Access | Times Cited: 2
VarCards: an integrated genetic and clinical database for coding variants in the human genome
Jinchen Li, Leisheng Shi, Kun Zhang, et al.
Nucleic Acids Research (2017) Vol. 46, Iss. D1, pp. D1039-D1048
Open Access | Times Cited: 162
SNPnexus: assessing the functional relevance of genetic variation to facilitate the promise of precision medicine
Abu Z M Dayem Ullah, Jorge Oscanoa, Jun Wang, et al.
Nucleic Acids Research (2018) Vol. 46, Iss. W1, pp. W109-W113
Open Access | Times Cited: 161
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
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
De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus
Charuta G. Furey, Jungmin Choi, Sheng Chih Jin, et al.
Neuron (2018) Vol. 99, Iss. 2, pp. 302-314.e4
Open Access | Times Cited: 137
Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies
Han Chen, Jennifer E. Huffman, Jennifer A. Brody, et al.
The American Journal of Human Genetics (2019) Vol. 104, Iss. 2, pp. 260-274
Open Access | Times Cited: 125
Systematic tissue-specific functional annotation of the human genome highlights immune-related DNA elements for late-onset Alzheimer’s disease
Qiongshi Lu, Ryan L. Powles, Sarah B. Abdallah, et al.
PLoS Genetics (2017) Vol. 13, Iss. 7, pp. e1006933-e1006933
Open Access | Times Cited: 113
Functional genomics reveal gene regulatory mechanisms underlying schizophrenia risk
Yongxia Huo, Shiwu Li, Jiewei Liu, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 110
Realizing the significance of noncoding functionality in clinical genomics
Brian Gloss, Marcel E. Dinger
Experimental & Molecular Medicine (2018) Vol. 50, Iss. 8, pp. 1-8
Open Access | Times Cited: 104
Regulatory variants: from detection to predicting impact
Elena Rojano, Pedro Seoane, Juan A. G. Ranea, et al.
Briefings in Bioinformatics (2018) Vol. 20, Iss. 5, pp. 1639-1654
Open Access | Times Cited: 101
Variant effect prediction tools assessed using independent, functional assay-based datasets: implications for discovery and diagnostics
Khalid Mahmood, Chol‐Hee Jung, Gayle K. Philip, et al.
Human Genomics (2017) Vol. 11, Iss. 1
Open Access | Times Cited: 90
Xrare: a machine learning method jointly modeling phenotypes and genetic evidence for rare disease diagnosis
Qi-Gang Li, Keyan Zhao, Carlos D. Bustamante, et al.
Genetics in Medicine (2019) Vol. 21, Iss. 9, pp. 2126-2134
Open Access | Times Cited: 88
REVEL and BayesDel outperform other in silico meta-predictors for clinical variant classification
Yuan Tian, Tina Pesaran, Adam Chamberlin, et al.
Scientific Reports (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 87
Whole-genome sequencing analysis of the cardiometabolic proteome
Arthur Gilly, Young‐Chan Park, Grace Png, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 85
AI applications in functional genomics
Claudia Caudai, Antonella Galizia, Filippo Geraci, et al.
Computational and Structural Biotechnology Journal (2021) Vol. 19, pp. 5762-5790
Open Access | Times Cited: 82

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