Sean D. Mooney

Orcid: 0000-0003-2654-0833

According to our database1, Sean D. Mooney authored at least 51 papers between 2002 and 2023.

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Bibliography

2023
Predicting decompression surgery by applying multimodal deep learning to patients' structured and unstructured health data.
BMC Medical Informatics Decis. Mak., December, 2023

Evaluation of crowdsourced mortality prediction models as a framework for assessing artificial intelligence in medicine.
J. Am. Medical Informatics Assoc., December, 2023

2022
A Multifaceted Benchmarking of Synthetic Electronic Health Record Generation Models.
CoRR, 2022

The NLP Sandbox: an efficient model-to-data system to enable federated and unbiased evaluation of clinical NLP models.
CoRR, 2022

Geospatial divide in real-world EHR data: Analytical workflow to assess regional biases and potential impact on health equity.
Proceedings of the AMIA 2022, 2022

Assessing Machine Learning Based Generators for Synthetic Electronic Health Records: A Benchmarking.
Proceedings of the AMIA 2022, 2022

2021
Considering the possibilities and pitfalls of Generative Pre-trained Transformer 3 (GPT-3) in healthcare delivery.
npj Digit. Medicine, 2021

Information needs and priority use cases of population health researchers to improve preparedness for future hurricanes and floods.
J. Am. Medical Informatics Assoc., 2021

Establishing the reliability of algorithms.
Proceedings of the Biocomputing 2021: Proceedings of the Pacific Symposium, 2021

A Continuous Crowd-sourced Challenge for Benchmarking COVID-19 Health Outcome Prediction.
Proceedings of the AMIA 2021, American Medical Informatics Association Annual Symposium, San Diego, CA, USA, October 30, 2021, 2021

2020
Indicators of retention in remote digital health studies: a cross-study evaluation of 100, 000 participants.
npj Digit. Medicine, 2020

Leaf: an open-source, model-agnostic, data-driven web application for cohort discovery and translational biomedical research.
J. Am. Medical Informatics Assoc., 2020

Piloting a model-to-data approach to enable predictive analytics in health care through patient mortality prediction.
J. Am. Medical Informatics Assoc., 2020

2019
Pathogenicity and functional impact of non-frameshifting insertion/deletion variation in the human genome.
PLoS Comput. Biol., 2019

Continuing challenges swirl around bioinformatics service delivery.
J. Biomed. Informatics, 2019

Automated retrieval, preprocessing, and visualization of gridded hydrometeorology data products for spatial-temporal exploratory analysis and intercomparison.
Environ. Model. Softw., 2019

Indicators of retention in remote digital health studies: A cross-study evaluation of 100, 000 participants.
CoRR, 2019

OPMI: the Ontology of Precision Medicine and Investigation and its Support for Clinical Data and Metadata Representation and Analysis.
Proceedings of the 10th International Conference on Biomedical Ontology (ICBO 2019), Buffalo, New York, USA, July 30, 2019

Detecting Seasonal, Holiday, and Rare Events from Trauma Data in the Electronic Health Record.
Proceedings of the AMIA 2019, 2019

2018
Uncovering exposures responsible for birth season - disease effects: a global study.
J. Am. Medical Informatics Assoc., 2018

KTAO: A Kidney Tissue Atlas Ontology to Support Community-Based Kidney Knowledge Base Development and Data Integration.
Proceedings of the 9th International Conference on Biological Ontology (ICBO 2018), 2018

2017
When loss-of-function is loss of function: assessing mutational signatures and impact of loss-of-function genetic variants.
Bioinform., 2017

Session Introduction.
Proceedings of the Biocomputing 2017: Proceedings of the Pacific Symposium, 2017

The feasibility of using smartphones to assess and remediate depression in Hispanic/Latino individuals nationally.
Proceedings of the Adjunct Proceedings of the 2017 ACM International Joint Conference on Pervasive and Ubiquitous Computing and Proceedings of the 2017 ACM International Symposium on Wearable Computers, 2017

2016
The Loss and Gain of Functional Amino Acid Residues Is a Common Mechanism Causing Human Inherited Disease.
PLoS Comput. Biol., 2016

Session Introduction.
Proceedings of the Biocomputing 2016: Proceedings of the Pacific Symposium, 2016

Use of Genome Data in Newborns as a Starting Point for Life-Long Precision Medicine.
Proceedings of the Biocomputing 2016: Proceedings of the Pacific Symposium, 2016

A New Way of Representing Clinical Reports for Rapid Phenotyping.
Proceedings of the Summit on Clinical Research Informatics, 2016

2015
Ten Simple Rules for a Community Computational Challenge.
PLoS Comput. Biol., 2015

2014
A Probabilistic Model to Predict Clinical Phenotypic Traits from Genome Sequencing.
PLoS Comput. Biol., 2014

The automated function prediction SIG looks back at 2013 and prepares for 2014.
Bioinform., 2014

2013
STOP using just GO: a multi-ontology hypothesis generation tool for high throughput experimentation.
BMC Bioinform., 2013

Toward More Transparent and Reproducible Omics Studies Through a Common Metadata Checklist and Data Publications.
Big Data, 2013

2011
Introduction: Advances in Computational Systems Bioinformatics.
J. Bioinform. Comput. Biol., 2011

Identifying viral integration sites using SeqMap 2.0.
Bioinform., 2011

2010
Structure-based kernels for the prediction of catalytic residues and their involvement in human inherited disease.
BMC Bioinform., 2010

Loss of Post-Translational Modification Sites in Disease.
Proceedings of the Biocomputing 2010: Proceedings of the Pacific Symposium, 2010

2009
Automated inference of molecular mechanisms of disease from amino acid substitutions.
Bioinform., 2009

2008
MutDB: update on development of tools for the biochemical analysis of genetic variation.
Nucleic Acids Res., 2008

Extensible open source content management systems and frameworks: a solution for many needs of a bioinformatics group.
Briefings Bioinform., 2008

Gain and loss of phosphorylation sites in human cancer.
Proceedings of the ECCB'08 Proceedings, 2008

2007
Refining Detection of RNA-Protein Binding Regions by Pyrosequencing of RNA Fragments.
Proceedings of the International Conference on Bioinformatics & Computational Biology, 2007

2005
MutDB services: interactive structural analysis of mutation data.
Nucleic Acids Res., 2005

Bioinformatics approaches and resources for single nucleotide polymorphism functional analysis.
Briefings Bioinform., 2005

Introduction to Informatics Approaches in Structural Genomics: Modeling and Representation of Function from Macromolecular STructure.
Proceedings of the Biocomputing 2005, 2005

2004
Session Introduction.
Proceedings of the Biocomputing 2004, 2004

2003
Analysis of Mutations in the COLIA1 Gene with Second-Order Rule Induction.
Int. J. Pattern Recognit. Artif. Intell., 2003

MutDB: annotating human variation with functionally relevant data.
Bioinform., 2003

Informatics Approaches in Structural Genomics - Session Introduction.
Proceedings of the 8th Pacific Symposium on Biocomputing, 2003

2002
The functional importance of disease-associated mutation.
BMC Bioinform., 2002

Compression-Based Induction and Genome Data.
Proceedings of the Fifteenth International Florida Artificial Intelligence Research Society Conference, 2002


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