Bruce J. Aronow

Orcid: 0000-0001-5109-6514

According to our database1, Bruce J. Aronow authored at least 33 papers between 2005 and 2023.

Collaborative distances:
  • Dijkstra number2 of four.
  • Erdős number3 of four.

Timeline

Legend:

Book 
In proceedings 
Article 
PhD thesis 
Dataset
Other 

Links

Online presence:

On csauthors.net:

Bibliography

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

CellDrift: inferring perturbation responses in temporally sampled single-cell data.
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
Session Introduction.
Proceedings of the Biocomputing 2018: Proceedings of the Pacific Symposium, 2018

2017
Session Introduction.
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
Single-cell analysis of mixed-lineage states leading to a binary cell fate choice.
Nat., 2016

Session Introduction.
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

Comparative study on feature descriptors for brain image analysis.
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
Computational drug repositioning through heterogeneous network clustering.
BMC Syst. Biol., 2013

A Biclustering Algorithm to Discover Functional Modules from ENCODE ChIP-Seq Data.
Proceedings of the 13th IEEE International Conference on Data Mining Workshops, 2013

2010
PhenoHM: human-mouse comparative phenome-genome server.
Nucleic Acids Res., 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
ToppGene Suite for gene list enrichment analysis and candidate gene prioritization.
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

Improved human disease candidate gene prioritization using mouse phenotype.
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


  Loading...