Luke V. Rasmussen

Orcid: 0000-0002-4497-8049

According to our database1, Luke V. Rasmussen authored at least 76 papers between 2012 and 2024.

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

Timeline

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Bibliography

2024
Seamless Integration of Computer-Adaptive Patient Reported Outcomes into an Electronic Health Record.
Appl. Clin. Inform., January, 2024

2023
AD-BERT: Using pre-trained language model to predict the progression from mild cognitive impairment to Alzheimer's disease.
J. Biomed. Informatics, August, 2023

Characterizing variability of electronic health record-driven phenotype definitions.
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

Design and validation of a FHIR-based EHR-driven phenotyping toolbox.
J. Am. Medical Informatics Assoc., 2022

AD-BERT: Using Pre-trained contextualized embeddings to Predict the Progression from Mild Cognitive Impairment to Alzheimer's Disease.
CoRR, 2022

2021
Genomic considerations for FHIR®; eMERGE implementation lessons.
J. Biomed. Informatics, 2021

Infobuttons for Genomic Medicine: Requirements and Barriers.
Appl. Clin. Inform., 2021

On Constraints and Considerations for Extending Support for Natural Language Processing-Based FHIR Resource Generation.
Proceedings of the AMIA 2021, American Medical Informatics Association Annual Symposium, San Diego, CA, USA, October 30, 2021, 2021

FHIRTime: Standardizing Temporal Patterns Identified from Clinical Narratives Using HL7 FHIR.
Proceedings of the AMIA 2021, American Medical Informatics Association Annual Symposium, San Diego, CA, USA, October 30, 2021, 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

A Deep Learning Framework Using a Pre-trained BERT Model to Predict the Risk of Progression from Mild Cognitive Impairment to Alzheimer's Disease.
Proceedings of the AMIA 2021, American Medical Informatics Association Annual Symposium, San Diego, CA, USA, October 30, 2021, 2021

Impact of Sex and Gender Disparities on Computational Phenotyping: A Potential Barrier to an Equitable Learning Health System.
Proceedings of the AMIA 2021, American Medical Informatics Association Annual Symposium, San Diego, CA, USA, October 30, 2021, 2021

Supporting EHR-based Cohort Discovery Through User-centered Design: Results of an Early Formative Usability Study.
Proceedings of the AMIA 2021, American Medical Informatics Association Annual Symposium, San Diego, CA, USA, October 30, 2021, 2021

Multi-site Evaluation of Longitudinal Changes in Ejection Fraction in Heart Failure Patients Through Data-driven Phenotyping.
Proceedings of the AMIA 2021, American Medical Informatics Association Annual Symposium, San Diego, CA, USA, October 30, 2021, 2021

2020
Identifying sub-phenotypes of acute kidney injury using structured and unstructured electronic health record data with memory networks.
J. Biomed. Informatics, 2020

Design Principles Developed through User-Centered and Socio-Technical Methods Improve Clinician Satisfaction, Speed, and Confidence in Pharmacogenomic Clinical Decision Support.
CoRR, 2020

Identification of Alzheimer's Disease Subtypes from Electronic Health Records Using a Data-Driven Approach.
Proceedings of the AMIA 2020, 2020

Feasibility of Cross-Platform EHR-Driven Phenotyping Using Clinical Quality Language.
Proceedings of the AMIA 2020, 2020

2019
Developing a portable natural language processing based phenotyping system.
BMC Medical Informatics Decis. Mak., 2019

Making work visible for electronic phenotype implementation: Lessons learned from the eMERGE network.
J. Biomed. Informatics, 2019

Facilitating phenotype transfer using a common data model.
J. Biomed. Informatics, 2019

Developing a FHIR-based EHR phenotyping framework: A case study for identification of patients with obesity and multiple comorbidities from discharge summaries.
J. Biomed. Informatics, 2019

An ancillary genomics system to support the return of pharmacogenomic results.
J. Am. Medical Informatics Assoc., 2019

Pharmacogenomic clinical decision support design and multi-site process outcomes analysis in the eMERGE Network.
J. Am. Medical Informatics Assoc., 2019

Identification of Predictive Sub-Phenotypes of Acute Kidney Injury using Structured and Unstructured Electronic Health Record Data with Memory Networks.
CoRR, 2019

Stratified Mortality Prediction of Patients with Acute Kidney Injury in Critical Care.
Proceedings of the MEDINFO 2019: Health and Wellbeing e-Networks for All, 2019

Considerations for Improving the Portability of Electronic Health Record-Based Phenotype Algorithms.
Proceedings of the AMIA 2019, 2019

Development of a Genomic Data Flow Framework: Results of a Survey Administered to NIH-NHGRI IGNITE and eMERGE Consortia Participants.
Proceedings of the AMIA 2019, 2019

Evaluating the Portability of an NLP System for Processing Echocardiograms: A Retrospective, Multi-site Observational Study.
Proceedings of the AMIA 2019, 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

Empowering genomic medicine by establishing critical sequencing result data flows: the eMERGE example.
J. Am. Medical Informatics Assoc., 2018

Portable Phenotyping System: A Portable Machine-Learning Approach to i2b2 Obesity Challenge.
Proceedings of the IEEE International Conference on Healthcare Informatics Workshops, 2018

Characterizing Design Patterns of EHR-Driven Phenotype Extraction Algorithms.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2018

2017
Classifying Clinical Trial Eligibility Criteria to Facilitate Phased Cohort Identification Using Clinical Data Repositories.
Proceedings of the AMIA 2017, 2017

The Phenotype Execution and Modeling Architecture: A Roadmap Towards Next-generation Phenotyping Using EHRs.
Proceedings of the AMIA 2017, 2017

Use of the popHealth Open-Source Quality Measure Engine to Support Cardiovascular Care at Small- and Medium-Sized Practices.
Proceedings of the AMIA 2017, 2017

DocUBuild: A Collaborative System to Enhance Dissemination and Discovery of Genomic Clinical Content.
Proceedings of the AMIA 2017, 2017

Design and Implementation of a Structured Sequencing Report Format: A Multi-Stakeholder Perspective from eMERGE.
Proceedings of the AMIA 2017, 2017

Leveraging Value Sets from the Value Set Authority Center (VSAC) in a Standards-Based Clinical Data Repository.
Proceedings of the AMIA 2017, 2017

Challenges impacting data collection from Electronic Health Record (EHR) Systems in Small and Medium sized practices in the Midwest.
Proceedings of the AMIA 2017, 2017

2016
Developing a data element repository to support EHR-driven phenotype algorithm authoring and execution.
J. Biomed. Informatics, 2016

The genomic CDS sandbox: An assessment among domain experts.
J. Biomed. Informatics, 2016

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

A multi-institution evaluation of clinical profile anonymization.
J. Am. Medical Informatics Assoc., 2016

A multi-site cognitive task analysis for biomedical query mediation.
Int. J. Medical Informatics, 2016

Practical considerations for implementing genomic information resources.
Appl. Clin. Inform., 2016

Seamless Integration of Patient Reported Outcomes Assessments into the EHR Workflow.
Proceedings of the Summit on Clinical Research Informatics, 2016

Data Collection Methods to Support a Multi-State Practice Care Transformation Network.
Proceedings of the Summit on Clinical Research Informatics, 2016

A Decompositional Approach to Executing Quality Data Model Algorithms on the i2b2 Platform.
Proceedings of the Summit on Clinical Research Informatics, 2016

Using Collaboration Networks to Visualize Patterns in Clinical Trial Recruitment.
Proceedings of the Summit on Clinical Research Informatics, 2016

Automatic identification and extraction of design patterns of EHR-driven phenotyping algorithms.
Proceedings of the AMIA 2016, 2016

Design and Implementation of an Ancillary Genomics System for the Return of Pharmacogenetic Results.
Proceedings of the AMIA 2016, 2016

An NLP Extension to the Quality Data Model for EHR-Driven Phenotype Algorithm Authoring and Execution.
Proceedings of the AMIA 2016, 2016

Implementing Pharmacogenomic Clinical Decision Support: Design and Prescriber Response in the eMERGE Network.
Proceedings of the AMIA 2016, 2016

2015
Review and evaluation of electronic health records-driven phenotype algorithm authoring tools for clinical and translational research.
J. Am. Medical Informatics Assoc., 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

A Standards-based Semantic Metadata Repository to Support EHR-driven Phenotype Authoring and Execution.
Proceedings of the MEDINFO 2015: eHealth-enabled Health, 2015

PhEMA: Phenotype Modeling, Sharing and Execution Architecture.
Proceedings of the AMIA 2015, 2015

Usability of a phenotype builder prototype and lessons learned for the design of phenotyping tools.
Proceedings of the AMIA 2015, 2015

Translating Electronic Clinical Quality Measures to Executable, Portable, and Customizable Workflows in KNIME.
Proceedings of the AMIA 2015, 2015

Harmonization of Quality Data Model with HL7 FHIR to Support EHR-driven Phenotype Authoring and Execution: A Pilot Study.
Proceedings of the AMIA 2015, 2015

2014
Design patterns for the development of electronic health record-driven phenotype extraction algorithms.
J. Biomed. Informatics, 2014

Qualitative evaluation of three phenotype information models to find methotrexate liver injury.
Proceedings of the AMIA 2014, 2014

Reproducibility of Health Care Datasets.
Proceedings of the AMIA 2014, 2014

Evaluation of Existing Phenotype Authoring Tools for Clinical Research.
Proceedings of the AMIA 2014, 2014


What Is Asked in Clinical Data Request Forms? A Multi-site Thematic Analysis of Forms Towards Better Data Access Support.
Proceedings of the AMIA 2014, 2014

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

Open Source Workflow Tools for Electronic Health Record Based Phenotyping Algorithms.
Proceedings of the AMIA 2012, 2012

An Evaluation of the NQF Quality Data Model for Representing Electronic Health Record Driven Phenotyping Algorithms.
Proceedings of the AMIA 2012, 2012

Grouping and Translating Value Sets.
Proceedings of the AMIA 2012, 2012

Integrating Research Recruitment into a Clinical Patient Portal.
Proceedings of the AMIA 2012, 2012

Rethinking the "Honest Broker" in the Changing Face of Security and Privacy.
Proceedings of the AMIA 2012, 2012


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