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List of works by Luke V. Rasmussen

A case study evaluating the portability of an executable computable phenotype algorithm across multiple institutions and electronic health record environments

scientific article published on 01 November 2018

A conceptual model for translating omic data into clinical action

scientific article

A multi-institution evaluation of clinical profile anonymization

scientific article

A multi-site cognitive task analysis for biomedical query mediation

scientific article published on 16 June 2016

A rural community's involvement in the design and usability testing of a computer-based informed consent process for the Personalized Medicine Research Project

scientific article published on 22 November 2013

Addressing barriers in FAIR data practices for biomedical data

scientific article published on 23 February 2023

An ancillary genomics system to support the return of pharmacogenomic results

scientific article published on 01 April 2019

Anatomic and advanced adenoma detection rates as quality metrics determined via natural language processing

scientific article published on 17 June 2014

Assessing the spatial implications of interactions among strategic forest management options using a Windows-based harvest simulator

CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record

scientific article published on 03 July 2015

Cataract research using electronic health records

scientific article

Desiderata for computable representations of electronic health records-driven phenotype algorithms

scientific article

Desiderata for the development of next-generation electronic health record phenotype libraries

scientific article published on 01 September 2021

Design and anticipated outcomes of the eMERGE-PGx project: a multicenter pilot for preemptive pharmacogenomics in electronic health record systems

scientific article

Design patterns for the development of electronic health record-driven phenotype extraction algorithms

scientific article

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

scientific article published on 14 October 2019

Developing a data element repository to support EHR-driven phenotype algorithm authoring and execution

scientific article

Developing a portable natural language processing based phenotyping system

scientific article published on 04 April 2019

Development of an optical character recognition pipeline for handwritten form fields from an electronic health record

scientific article

Electronic medical records and genomics (eMERGE) network exploration in cataract: several new potential susceptibility loci.

scientific article

Electronic medical records for genetic research: results of the eMERGE consortium

scientific article published on April 2011

Empowering genomic medicine by establishing critical sequencing result data flows: the eMERGE example

scientific article published on 01 October 2018

Facilitating phenotype transfer using a common data model

scientific article published on 17 July 2019

Facilitating reproducible research through direct connection of data analysis with manuscript preparation: StatTag for connecting statistical software to Microsoft Word

scientific article published on 01 October 2020

Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network

scientific article

Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk

scientific article published on 05 March 2013

Genome-wide study of resistant hypertension identified from electronic health records

scientific article

Healthcare provider education to support integration of pharmacogenomics in practice: the eMERGE Network experience

scientific article published on 22 June 2017

Implementation of workflow engine technology to deliver basic clinical decision support functionality

scientific article

Importance of multi-modal approaches to effectively identify cataract cases from electronic health records

scientific article published on March 2012

Making work visible for electronic phenotype implementation: Lessons learned from the eMERGE network

scientific article published on 19 September 2019

Pharmacogenomic clinical decision support design and multi-site process outcomes analysis in the eMERGE Network

scientific article published on 01 February 2019

PheKB: a catalog and workflow for creating electronic phenotype algorithms for transportability

scientific article

Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality

scientific article

Practical challenges in integrating genomic data into the electronic health record

scientific article

Practical considerations for implementing genomic information resources. Experiences from eMERGE and CSER.

scientific article published on 21 September 2016

Practical considerations in genomic decision support: The eMERGE experience

scientific article

Primary Care Practices' Abilities And Challenges In Using Electronic Health Record Data For Quality Improvement

scientific article published in April 2018

Prototype Development: Context-Driven Dynamic XML Ophthalmologic Data Capture Application.

scientific article published on 13 September 2017

Quality control procedures for genome-wide association studies

scientific article published in 2011

Review and evaluation of electronic health records-driven phenotype algorithm authoring tools for clinical and translational research.

scientific article

Stakeholder engagement: a key component of integrating genomic information into electronic health records

scientific article

Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data

scientific article

The electronic health record for translational research

scientific article

The genomic CDS sandbox: An assessment among domain experts

scientific article

Validation of electronic medical record-based phenotyping algorithms: results and lessons learned from the eMERGE network

scientific article published on 26 March 2013

Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies

scientific article

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