Peggy L. Peissig
Orcid: 0000-0003-4156-0189Affiliations:
- Marshfield Clinic Research Foundation, Marshfield, WI, USA
According to our database1,
Peggy L. Peissig
authored at least 61 papers
between 2005 and 2022.
Collaborative distances:
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Bibliography
2022
Under-specification as the source of ambiguity and vagueness in narrative phenotype algorithm definitions.
BMC Medical Informatics Decis. Mak., 2022
2021
Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies.
npj Digit. Medicine, 2021
2020
High-Throughput Approach to Modeling Healthcare Costs Using Electronic Healthcare Records.
CoRR, 2020
Adverse drug reaction discovery from electronic health records with deep neural networks.
Proceedings of the ACM CHIL '20: ACM Conference on Health, 2020
2019
J. Biomed. Informatics, 2019
J. Biomed. Informatics, 2019
Pharmacogenomic clinical decision support design and multi-site process outcomes analysis in the eMERGE Network.
J. Am. Medical Informatics Assoc., 2019
Proceedings of the 2019 IEEE EMBS International Conference on Biomedical & Health Informatics, 2019
2018
A case study evaluating the portability of an executable computable phenotype algorithm across multiple institutions and electronic health record environments.
J. Am. Medical Informatics Assoc., 2018
Quantifying predictive capability of electronic health records for the most harmful breast cancer.
Proceedings of the Medical Imaging 2018: Image Perception, 2018
Object Detection to Assist Visually Impaired People: A Deep Neural Network Adventure.
Proceedings of the Advances in Visual Computing - 13th International Symposium, 2018
Proceedings of the 35th International Conference on Machine Learning, 2018
Diagnostic Classification of Lung CT Images Using Deep 3D Multi-Scale Convolutional Neural Network.
Proceedings of the IEEE International Conference on Healthcare Informatics, 2018
Improving breast cancer risk prediction by using demographic risk factors, abnormality features on mammograms and genetic variants.
Proceedings of the AMIA 2018, 2018
2017
Evaluating electronic health record data sources and algorithmic approaches to identify hypertensive individuals.
J. Am. Medical Informatics Assoc., 2017
Hawkes Process Modeling of Adverse Drug Reactions with Longitudinal Observational Data.
Proceedings of the Machine Learning for Health Care Conference, 2017
Proceedings of the Machine Learning and Data Mining in Pattern Recognition, 2017
Pharmacovigilance via Baseline Regularization with Large-Scale Longitudinal Observational Data.
Proceedings of the 23rd ACM SIGKDD International Conference on Knowledge Discovery and Data Mining, Halifax, NS, Canada, August 13, 2017
Proceedings of the 2017 IEEE International Conference on Healthcare Informatics, 2017
Proceedings of the Summit on Clinical Research Informatics, 2017
Proceedings of the Summit on Clinical Research Informatics, 2017
bigNN: An open-source big data toolkit focused on biomedical sentence classification.
Proceedings of the 2017 IEEE International Conference on Big Data (IEEE BigData 2017), 2017
2016
Proceedings of the Computational Sustainability, 2016
J. Mach. Learn. Res., 2016
PheKB: a catalog and workflow for creating electronic phenotype algorithms for transportability.
J. Am. Medical Informatics Assoc., 2016
J. Am. Medical Informatics Assoc., 2016
Identification of genetic interaction networks via an evolutionary algorithm evolved Bayesian network.
BioData Min., 2016
Appl. Clin. Inform., 2016
Biofilter as a Functional Annotation Pipeline for Common and Rare Copy Number Burden.
Proceedings of the Biocomputing 2016: Proceedings of the Pacific Symposium, 2016
Knowledge Driven Binning and PheWAS Analysis in Marshfield Personalized Medicine Research Project Using BioBin.
Proceedings of the Biocomputing 2016: Proceedings of the Pacific Symposium, 2016
Discriminatory power of common genetic variants in personalized breast cancer diagnosis.
Proceedings of the Medical Imaging 2016: Image Perception, Observer Performance, and Technology Assessment, San Diego, California, United States, 27 February, 2016
Proceedings of the 22nd ACM SIGKDD International Conference on Knowledge Discovery and Data Mining, 2016
OCR as a Service: An Experimental Evaluation of Google Docs OCR, Tesseract, ABBYY FineReader, and Transym.
Proceedings of the Advances in Visual Computing - 12th International Symposium, 2016
Baseline Regularization for Computational Drug Repositioning with Longitudinal Observational Data.
Proceedings of the Twenty-Fifth International Joint Conference on Artificial Intelligence, 2016
Proceedings of the AMIA 2016, 2016
2015
CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record.
J. Am. Medical Informatics Assoc., 2015
Desiderata for computable representations of electronic health records-driven phenotype algorithms.
J. Am. Medical Informatics Assoc., 2015
Proceedings of the AMIA 2015, 2015
Proceedings of the Foundations of Biomedical Knowledge Representation, 2015
2014
Design patterns for the development of electronic health record-driven phenotype extraction algorithms.
J. Biomed. Informatics, 2014
J. Biomed. Informatics, 2014
Proceedings of the Applications of Evolutionary Computation - 17th European Conference, 2014
Comparing the Value of Mammographic Features and Genetic Variants in Breast Cancer Risk Prediction.
Proceedings of the AMIA 2014, 2014
Development and validation of an electronic phenotyping algorithm for chronic kidney disease.
Proceedings of the AMIA 2014, 2014
2013
Proceedings of the AMIA 2013, 2013
2012
Proceedings of the Fifteenth International Conference on Artificial Intelligence and Statistics, 2012
Development of an optical character recognition pipeline for handwritten form fields from an electronic health record.
J. Am. Medical Informatics Assoc., 2012
Importance of multi-modal approaches to effectively identify cataract cases from electronic health records.
J. Am. Medical Informatics Assoc., 2012
Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study.
J. Am. Medical Informatics Assoc., 2012
Machine Learning for Personalized Medicine: Predicting Primary Myocardial Infarction from Electronic Health Records.
AI Mag., 2012
Graphical-model Based Multiple Testing under Dependence, with Applications to Genome-wide Association Studies.
Proceedings of the Twenty-Eighth Conference on Uncertainty in Artificial Intelligence, 2012
Proceedings of the 29th International Conference on Machine Learning, 2012
Statistical Relational Learning to Predict Primary Myocardial Infarction from Electronic Health Records.
Proceedings of the Twenty-Fourth Conference on Innovative Applications of Artificial Intelligence, 2012
An Evaluation of the NQF Quality Data Model for Representing Electronic Health Record Driven Phenotyping Algorithms.
Proceedings of the AMIA 2012, 2012
Proceedings of the AMIA 2012, 2012
Using PheWAS to Assess Pleiotropy of Genetic Risk Scores for Rheumatoid Arthritis and Coronary Artery Disease in the eMERGE Network.
Proceedings of the AMIA 2012, 2012
Proceedings of the Twenty-Sixth AAAI Conference on Artificial Intelligence, 2012
2010
An analytical approach to characterize morbidity profile dissimilarity between distinct cohorts using electronic medical records.
J. Biomed. Informatics, 2010
2005
Study of Effect of Drug Lexicons on Medication Extraction from Electronic Medical Records.
Proceedings of the Biocomputing 2005, 2005