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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:

DeepSVP: integration of genotype and phenotype for structural variant prioritization using deep learning
Azza Althagafi, Lamia Alsubaie, Nagarajan Kathiresan, et al.
Bioinformatics (2021) Vol. 38, Iss. 6, pp. 1677-1684
Open Access | Times Cited: 13

Showing 13 citing articles:

AnnotSV and knotAnnotSV: a web server for human structural variations annotations, ranking and analysis
Véronique Geoffroy, Thomas Guignard, Arnaud Kress, et al.
Nucleic Acids Research (2021) Vol. 49, Iss. W1, pp. W21-W28
Open Access | Times Cited: 59
RExPRT: a machine learning tool to predict pathogenicity of tandem repeat loci
Sarah Fazal, Matt C. Danzi, Isaac Xu, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 11
Assessing the utility of large language models for phenotype-driven gene prioritization in the diagnosis of rare genetic disease
Junyoung Kim, Kai Wang, Chunhua Weng, et al.
The American Journal of Human Genetics (2024)
Open Access | Times Cited: 6
Computational Tools for Studying Genome Structural Variation
Xingyu Chen, Siyu Wei, Chen Sun, et al.
OMICS A Journal of Integrative Biology (2025)
Closed Access
The AnnotSV webserver in 2023: updated visualization and ranking
Véronique Geoffroy, Jean-Baptiste Lamouche, Thomas Guignard, et al.
Nucleic Acids Research (2023) Vol. 51, Iss. W1, pp. W39-W45
Open Access | Times Cited: 10
PhenoSV: interpretable phenotype-aware model for the prioritization of genes affected by structural variants
Zhuoran Xu, Quan Li, Luigi Marchionni, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 6
RExPRT: a machine learning tool to predict pathogenicity of tandem repeat loci
Sarah Fazal, Matt C. Danzi, Isaac Xu, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 4
Toward understanding the role of genomic repeat elements in neurodegenerative diseases
Zhengyu An, Aidi Jiang, Jingqi Chen
Neural Regeneration Research (2024) Vol. 20, Iss. 3, pp. 646-659
Open Access | Times Cited: 1
Systematic assessment of structural variant annotation tools for genomic interpretation
Xuanshi Liu, Lei Gu, Chanjuan Hao, et al.
Life Science Alliance (2024) Vol. 8, Iss. 3, pp. e202402949-e202402949
Open Access | Times Cited: 1
The informatics of developmental phenotypes
Paul N. Schofield, Robert Hoehndorf, Georgios V. Gkoutos, et al.
Elsevier eBooks (2024), pp. 457-470
Closed Access
DBFE: distribution-based feature extraction from structural variants in whole-genome data
Maciej Piernik, Dariusz Brzeziński, Paweł Sztromwasser, et al.
Bioinformatics (2022) Vol. 38, Iss. 19, pp. 4466-4473
Closed Access | Times Cited: 1
Improving the classification of cardinality phenotypes using collections
Sarah M. Alghamdi, Robert Hoehndorf
Journal of Biomedical Semantics (2023) Vol. 14, Iss. 1
Open Access
Advancements in Genomic and Behavioral Neuroscience Analysis for the Study of Normal and Pathological Brain Function
Annalisa M. Baratta, Adam J. Brandner, Sonja L. Plasil, et al.
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access
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