Dan M. Roden

According to our database1, Dan M. Roden authored at least 28 papers between 2006 and 2021.

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Bibliography

2021
A retrospective approach to evaluating potential adverse outcomes associated with delay of procedures for cardiovascular and cancer-related diagnoses in the context of COVID-19.
J. Biomed. Informatics, 2021

Phenotyping coronavirus disease 2019 during a global health pandemic: Lessons learned from the characterization of an early cohort.
J. Biomed. Informatics, 2021

DDIWAS: High-throughput electronic health record-based screening of drug-drug interactions.
J. Am. Medical Informatics Assoc., 2021

Real-time clinical note monitoring to detect conditions for rapid follow-up: A case study of clinical trial enrollment in drug-induced torsades de pointes and Stevens-Johnson syndrome.
J. Am. Medical Informatics Assoc., 2021

2020
A structural variation reference for medical and population genetics.
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Nat., 2020

PheMap: a multi-resource knowledge base for high-throughput phenotyping within electronic health records.
J. Am. Medical Informatics Assoc., 2020

The All of Us Research Program Researcher Workbench: Cloud based access and analytics to advance precision medicine.
Proceedings of the AMIA 2020, 2020

The All of Us Research Program Researcher Workbench Phenotype Library: Five Disease Implementations.
Proceedings of the AMIA 2020, 2020

Real-time Clinical Note Monitoring to Detect Conditions for Follow-up: a Case Study of Clinical Trial Enrollment in Drug-induced Torsades de Pointes and Stevens-Johnson Syndrome.
Proceedings of the AMIA 2020, 2020

2019
Improving the phenotype risk score as a scalable approach to identifying patients with Mendelian disease.
J. Am. Medical Informatics Assoc., 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

Evaluating statistical approaches to leverage large clinical datasets for uncovering therapeutic and adverse medication effects.
Bioinform., 2018

Evaluation of a Novel System to Enhance Clinicians' Recognition of Preadmission Adverse Drug Reactions.
Appl. Clin. Inform., 2018

2017
Evaluating electronic health record data sources and algorithmic approaches to identify hypertensive individuals.
J. Am. Medical Informatics Assoc., 2017

Strategies for Equitable Pharmacogenomic-Guided Warfarin Dosing Among European and African American Individuals in a Clinical Population.
Proceedings of the Biocomputing 2017: Proceedings of the Pacific Symposium, 2017

A comparative study of different methods for automatic identification of clopidogrel-induced bleedings in electronic health records.
Proceedings of the Summit on Clinical Research Informatics, 2017

2016
PheKB: a catalog and workflow for creating electronic phenotype algorithms for transportability.
J. Am. Medical Informatics Assoc., 2016

2015
Deciphering Signaling Pathway Networks to Understand the Molecular Mechanisms of Metformin Action.
PLoS Comput. Biol., 2015

Validating drug repurposing signals using electronic health records: a case study of metformin associated with reduced cancer mortality.
J. Am. Medical Informatics Assoc., 2015

Desiderata for computable representations of electronic health records-driven phenotype algorithms.
J. Am. Medical Informatics Assoc., 2015

2014
Size matters: How population size influences genotype-phenotype association studies in anonymized data.
J. Biomed. Informatics, 2014

Utilization of an EMR-Biorepository to Identify the Genetic Predictors of Calcineurin-Inhibitor Toxicity in Heart Transplant Recipients.
Proceedings of the Biocomputing 2014: Proceedings of the Pacific Symposium, 2014

Replication of SCN5A Associations with Electrocardiographic Traits in African Americans from Clinical and Epidemiologic Studies.
Proceedings of the Applications of Evolutionary Computation - 17th European Conference, 2014

2011
Facilitating pharmacogenetic studies using electronic health records and natural-language processing: a case study of warfarin.
J. Am. Medical Informatics Assoc., 2011

Visual Integration of Results from a Large Dna Biobank (Biovu) Using Synthesis-View.
Proceedings of the Biocomputing 2011: Proceedings of the Pacific Symposium, 2011

2010
An analytical approach to characterize morbidity profile dissimilarity between distinct cohorts using electronic medical records.
J. Biomed. Informatics, 2010

PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associations.
Bioinform., 2010

2006
Risk Factor Interactions and Genetic Effects Associated with Post-Operative Atrial Fibrillation.
Proceedings of the Biocomputing 2006, 2006


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