Bruce J. Aronow
Orcid: 0000-0001-5109-6514
According to our database1,
Bruce J. Aronow
authored at least 35 papers
between 2005 and 2024.
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Bibliography
2024
Deep learning-based IDH1 gene mutation prediction using histopathological imaging and clinical data.
Comput. Biol. Medicine, 2024
Vision Transformers and CNN-Based Knowledge-Distillation for Histopathological Image Classification.
Proceedings of the Fuzzy Systems and Data Mining X, 2024
2023
Informative missingness: What can we learn from patterns in missing laboratory data in the electronic health record?
J. Biomed. Informatics, March, 2023
2022
International electronic health record-derived post-acute sequelae profiles of COVID-19 patients.
npj Digit. Medicine, 2022
Data Augmentation Using Generative Adversarial Networks for Multi-Class Segmentation of Lung Confocal IF Images.
J. Adv. Comput. Intell. Intell. Informatics, 2022
Briefings Bioinform., 2022
2021
Ontology-guided segmentation and object identification for developmental mouse lung immunofluorescent images.
BMC Bioinform., 2021
2019
Multi-Class Segmentation of Lung Immunofluorescence Confocal Images Using Deep Learning.
Proceedings of the 2019 IEEE International Conference on Bioinformatics and Biomedicine, 2019
2018
Proceedings of the Biocomputing 2018: Proceedings of the Pacific Symposium, 2018
2017
Proceedings of the Biocomputing 2017: Proceedings of the Pacific Symposium, 2017
Improving the generalization of disease stage classification with deep CNN for Glioma histopathological images.
Proceedings of the 2017 IEEE International Conference on Bioinformatics and Biomedicine, 2017
2016
Nat., 2016
Proceedings of the Biocomputing 2016: Proceedings of the Pacific Symposium, 2016
A Study on Nuclei Segmentation, Feature Extraction and Disease Stage Classification for Human Brain Histopathological Images.
Proceedings of the Knowledge-Based and Intelligent Information & Engineering Systems: Proceedings of the 20th International Conference KES-2016, 2016
A study on feature extraction and disease stage classification for Glioma pathology images.
Proceedings of the 2016 IEEE International Conference on Fuzzy Systems, 2016
2015
Feature extraction and disease stage classification for Glioma histopathology images.
Proceedings of the 17th International Conference on E-health Networking, 2015
Cell nuclei segmentation in glioma histopathology images with color decomposition based active contours.
Proceedings of the 2015 IEEE International Conference on Bioinformatics and Biomedicine, 2015
2014
ToppMiR: ranking microRNAs and their mRNA targets based on biological functions and context.
Nucleic Acids Res., 2014
The International Society of Computational Biology presents: the Great Lakes Bioinformatics Conference, May 16-18, 2014, Cincinnati, Ohio.
Bioinform., 2014
Proceedings of the 2014 Joint 7th International Conference on Soft Computing and Intelligent Systems (SCIS) and 15th International Symposium on Advanced Intelligent Systems (ISIS), 2014
2013
BMC Syst. Biol., 2013
Proceedings of the 13th IEEE International Conference on Data Mining Workshops, 2013
2010
ToppCluster: a multiple gene list feature analyzer for comparative enrichment clustering and network-based dissection of biological systems.
Nucleic Acids Res., 2010
Integrating neighbor clustering, coexpression clustering and subsystems analysis to define dynamic changes in regulatory networks associated with group A streptococcal sociomicrobiology and niche adaptation.
BMC Bioinform., 2010
2009
Nucleic Acids Res., 2009
Inferring novel disease indications for known drugs by semantically linking drug action and disease mechanism relationships.
BMC Bioinform., 2009
Correction: Disease candidate gene identification and prioritization using protein interaction networks.
BMC Bioinform., 2009
Disease candidate gene identification and prioritization using protein interaction networks.
BMC Bioinform., 2009
2008
Identifying disease-causal genes using Semantic Web-based representation of integrated genomic and phenomic knowledge.
J. Biomed. Informatics, 2008
2007
PolyDoms: a whole genome database for the identification of non-synonymous coding SNPs with the potential to impact disease.
Nucleic Acids Res., 2007
GenomeTrafac: a whole genome resource for the detection of transcription factor binding site clusters associated with conventional and microRNA encoding genes conserved between mouse and human gene orthologs.
Nucleic Acids Res., 2007
Bayesian hierarchical model for transcriptional module discovery by jointly modeling gene expression and ChIP-chip data.
BMC Bioinform., 2007
BMC Bioinform., 2007
2005
CisMols Analyzer: identification of compositionally similar <i>cis</i>-element clusters in ortholog conserved regions of coordinately expressed genes.
Nucleic Acids Res., 2005