David Carrell
Orcid: 0000-0002-8471-0928
According to our database1,
David Carrell
authored at least 42 papers
between 2005 and 2024.
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Bibliography
2024
Data-driven automated classification algorithms for acute health conditions: applying PheNorm to COVID-19 disease.
J. Am. Medical Informatics Assoc., February, 2024
J. Am. Medical Informatics Assoc., 2024
2023
J. Am. Medical Informatics Assoc., February, 2023
2022
Under-specification as the source of ambiguity and vagueness in narrative phenotype algorithm definitions.
BMC Medical Informatics Decis. Mak., 2022
Development of a machine learning model to predict mild cognitive impairment using natural language processing in the absence of screening.
BMC Medical Informatics Decis. Mak., 2022
Data-driven automated classification algorithms for acute health conditions: Applying PheNorm to COVID-19 disease.
Proceedings of the AMIA 2022, 2022
2021
Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies.
npj Digit. Medicine, 2021
Evaluation of the Portability of Natural Language Processing-based Computable Phenotypes in the eMERGE Network.
Proceedings of the AMIA 2021, American Medical Informatics Association Annual Symposium, San Diego, CA, USA, October 30, 2021, 2021
2020
Resilience of clinical text de-identified with "hiding in plain sight" to hostile reidentification attacks by human readers.
J. Am. Medical Informatics Assoc., 2020
2019
Making work visible for electronic phenotype implementation: Lessons learned from the eMERGE network.
J. Biomed. Informatics, 2019
J. Biomed. Informatics, 2019
Enrichment sampling for a multi-site patient survey using electronic health records and census data.
J. Am. Medical Informatics Assoc., 2019
The machine giveth and the machine taketh away: a parrot attack on clinical text deidentified with hiding in plain sight.
J. Am. Medical Informatics Assoc., 2019
Facilitating Self-reflection about Values and Self-care Among Individuals with Chronic Conditions.
Proceedings of the 2019 CHI Conference on Human Factors in Computing Systems, 2019
2018
Using Natural Language Processing of Free-Text Radiology Reports to Identify Type 1 Modic Endplate Changes.
J. Digit. Imaging, 2018
Proceedings of the AMIA 2018, 2018
Proceedings of the AMIA 2018, 2018
2017
Challenges in adapting existing clinical natural language processing systems to multiple, diverse health care settings.
J. Am. Medical Informatics Assoc., 2017
Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals.
BioData Min., 2017
Is an Algorithm Just an Algorithm? How to Define Clinical Concepts for Use in Comparative Safety and Effectiveness Distributed Research Networks.
Proceedings of the Summit on Clinical Research Informatics, 2017
2016
Optimizing annotation resources for natural language de-identification via a game theoretic framework.
J. Biomed. Informatics, 2016
PheKB: a catalog and workflow for creating electronic phenotype algorithms for transportability.
J. Am. Medical Informatics Assoc., 2016
2015
J. Biomed. Informatics, 2015
Desiderata for computable representations of electronic health records-driven phenotype algorithms.
J. Am. Medical Informatics Assoc., 2015
Int. J. Medical Informatics, 2015
Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR).
BioData Min., 2015
2014
Design patterns for the development of electronic health record-driven phenotype extraction algorithms.
J. Biomed. Informatics, 2014
J. Am. Medical Informatics Assoc., 2014
Int. J. Medical Informatics, 2014
Proceedings of the AMIA 2014, 2014
2013
Hiding in plain sight: use of realistic surrogates to reduce exposure of protected health information in clinical text.
J. Am. Medical Informatics Assoc., 2013
Proceedings of the AMIA 2013, 2013
Proceedings of the AMIA 2013, 2013
2012
Importance of multi-modal approaches to effectively identify cataract cases from electronic health records.
J. Am. Medical Informatics Assoc., 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
Using Electronic Health Records to Identify Heart Failure Cohorts with Differentiation for Preserved and Reduced Ejection Fraction.
Proceedings of the AMIA 2012, 2012
2011
A Strategy for Deploying Secure Cloud-Based Natural Language Processing Systems for Applied Research Involving Clinical Text.
Proceedings of the 44th Hawaii International International Conference on Systems Science (HICSS-44 2011), 2011
2010
An analytical approach to characterize morbidity profile dissimilarity between distinct cohorts using electronic medical records.
J. Biomed. Informatics, 2010
2007
Research Paper: Patient Web Services Integrated with a Shared Medical Record: Patient Use and Satisfaction.
J. Am. Medical Informatics Assoc., 2007
2006
Use and Satisfaction of a Patient Web Portal with a Shared Medical Record between Patients and Providers.
Proceedings of the AMIA 2006, 2006
Variation in Adoption Rates of a Patient Web Portal with a Shared Medical Record by Age, Gender, and Morbidity Level.
Proceedings of the AMIA 2006, 2006
2005
Messages, Strands and Threads: Measuring Use of Electronic Patient-Provider Messaging.
Proceedings of the AMIA 2005, 2005