Author details

Full Name

Luke V Rasmussen

Affiliation

Northwestern University Feinberg School of Medicine

ORCID

Career Start Year

2007

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36823157	Developing a standardized but extendable framework to increase the findability of infectious disease datasets.	Sci Data	2023
37581309	Pragmatic reproducible research: improving the research process from raw data to results, bit by bit.	J Clin Invest	2023
37188469	Implementation of a culturally competent <i>APOL1</i> genetic testing programme into living donor evaluation: A two-site, non-randomised, pre-post trial design.	BMJ Open	2023
37186083	Challenges of Integrating APOL1 Genetic Test Results into the Electronic Health Record.	Appl Clin Inform	2023
37208478	Comparing the effects of four common drug classes on the progression of mild cognitive impairment to dementia using electronic health records.	Sci Rep	2023
37104035	Machine learning links unresolving secondary pneumonia to mortality in patients with severe pneumonia, including COVID-19.	J Clin Invest	2023
37429512	AD-BERT: Using pre-trained language model to predict the progression from mild cognitive impairment to Alzheimer's disease.	J Biomed Inform	2023
37196047	Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm.	PLoS One	2023
36621880	Returning integrated genomic risk and clinical recommendations: The eMERGE study.	Genet Med	2023
36474423	Characterizing variability of electronic health record-driven phenotype definitions.	J Am Med Inform Assoc	2023
36609415	Prediction of left ventricular ejection fraction changes in heart failure patients using machine learning and electronic health records: a multi-site study.	Sci Rep	2023
36737471	Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network.	Sci Rep	2023
36823198	Addressing barriers in FAIR data practices for biomedical data.	Sci Data	2023
35090449	Under-specification as the source of ambiguity and vagueness in narrative phenotype algorithm definitions.	BMC Med Inform Decis Mak	2022
35508198	Generating and Reporting Electronic Clinical Quality Measures from Electronic Health Records: Strategies from EvidenceNOW Cooperatives.	Appl Clin Inform	2022
35799370	Design and validation of a FHIR-based EHR-driven phenotyping toolbox.	J Am Med Inform Assoc	2022
35936991	ReviewR: a light-weight and extensible tool for manual review of clinical records.	JAMIA Open	2022
33979874	Infobuttons for Genomic Medicine: Requirements and Barriers.	Appl Clin Inform	2021
37920232	Facilitating Genetics Aware Clinical Decision Support: Putting the eMERGE Infrastructure into Practice.	ACI open	2021
33930535	Genomic considerations for FHIRÂ®; eMERGE implementation lessons.	J Biomed Inform	2021
34926996	Development of a repository of computable phenotype definitions using the clinical quality language.	JAMIA Open	2021
34457178	CQL4NLP: Development and Integration of FHIR NLP Extensions in Clinical Quality Language for EHR-driven Phenotyping.	AMIA Jt Summits Transl Sci Proc	2021
34457128	Phenoflow: A Microservice Architecture for Portable Workflow-based Phenotype Definitions.	AMIA Jt Summits Transl Sci Proc	2021
34508578	Desiderata for the development of next-generation electronic health record phenotype libraries.	Gigascience	2021
32308812	Evaluating the Portability of an NLP System for Processing Echocardiograms: A Retrospective, Multi-site Observational Study.	AMIA Annu Symp Proc	2020
31876643	Effects of 2 Forms of Practice Facilitation on Cardiovascular Prevention in Primary Care: A Practice-randomized, Comparative Effectiveness Trial.	Med Care	2020
31911172	Identifying sub-phenotypes of acute kidney injury using structured and unstructured electronic health record data with memory networks.	J Biomed Inform	2020
33083543	Data-driven discovery of probable Alzheimer's disease and related dementia subphenotypes using electronic health records.	Learn Health Syst	2020
33083540	Subphenotyping depression using machine learning and electronic health records.	Learn Health Syst	2020
33083538	Toward cross-platform electronic health record-driven phenotyping using Clinical Quality Language.	Learn Health Syst	2020
33215069	Facilitating reproducible research through direct connection of data analysis with manuscript preparation: StatTag for connecting statistical software to Microsoft Word.	JAMIA Open	2020
32669677	Participant choices for return of genomic results in the eMERGE Network.	Genet Med	2020
32308871	Considerations for Improving the Portability of Electronic Health Record-Based Phenotype Algorithms.	AMIA Annu Symp Proc	2020
32308829	Development of a Genomic Data Flow Framework: Results of a Survey Administered to NIH-NHGRI IGNITE and eMERGE Consortia Participants.	AMIA Annu Symp Proc	2020
30590574	Pharmacogenomic clinical decision support design and multi-site process outcomes analysis in the eMERGE Network.	J Am Med Inform Assoc	2019
32025638	Challenges to electronic clinical quality measurement using third-party platforms in primary care practices: the healthy hearts in the heartland experience.	JAMIA Open	2019
31737042	Genomic Information for Clinicians in the Electronic Health Record: Lessons Learned From the Clinical Genome Resource Project and the Electronic Medical Records and Genomics Network.	Front Genet	2019
31437966	Stratified Mortality Prediction of Patients with Acute Kidney Injury in Critical Care.	Stud Health Technol Inform	2019
31259038	Predictive Modeling of the Risk of Acute Kidney Injury in Critical Care: A Systematic Investigation of The Class Imbalance Problem.	AMIA Jt Summits Transl Sci Proc	2019
31622801	Developing a FHIR-based EHR phenotyping framework: A case study for identification of patients with obesity and multiple comorbidities from discharge summaries.	J Biomed Inform	2019
30778576	An ancillary genomics system to support the return of pharmacogenomic results.	J Am Med Inform Assoc	2019
30976756	Provider perspectives on the integration of patient-reported outcomes in an electronic health record.	JAMIA Open	2019
30943974	Developing a portable natural language processing based phenotyping system.	BMC Med Inform Decis Mak	2019
29608365	Primary Care Practices' Abilities And Challenges In Using Electronic Health Record Data For Quality Improvement.	Health Aff (Millwood)	2018
29860405	Empowering genomic medicine by establishing critical sequencing result data flows: the eMERGE example.	J Am Med Inform Assoc	2018
30124903	A case study evaluating the portability of an executable computable phenotype algorithm across multiple institutions and electronic health record environments.	J Am Med Inform Assoc	2018
29854246	Classifying Clinical Trial Eligibility Criteria to Facilitate Phased Cohort Identification Using Clinical Data Repositories.	AMIA Annu Symp Proc	2018
28639489	Healthcare provider education to support integration of pharmacogenomics in practice: the eMERGE Network experience.	Pharmacogenomics	2017
28222112	Genome-wide study of resistant hypertension identified from electronic health records.	PLoS One	2017
28903894	Prototype Development: Context-Driven Dynamic XML Ophthalmologic Data Capture Application.	JMIR Med Inform	2017

1 - 50 of 91

Simon Lin

The Abigail Wexner Research Institute, Nationwide Children's Hospital

Career Start Year 2015

Number of shared co-authors 0

Emily R Pfaff

University of North Carolina

Career Start Year 2014

Number of shared co-authors 15

Fernanda Polubriaginof

Memorial Sloan Kettering Cancer Center

Career Start Year 2012

Number of shared co-authors 18

Anita Walden

The National Center for Data to Health

Career Start Year 2011

Number of shared co-authors 6

Allison B McCoy

Vanderbilt University Medical Center

Career Start Year 2010

Number of shared co-authors 18

Ioana Danciu

Oak Ridge National Laboratory

Career Start Year 2010

Number of shared co-authors 20

Kavishwar B Wagholikar

Massachusetts General Hospital

Career Start Year 2009

Number of shared co-authors 10

Davera Gabriel

Johns Hopkins University

Career Start Year 2009

Number of shared co-authors 9

David Kreda

Harvard Medical School

Career Start Year 2009

Number of shared co-authors 6

Jeffrey G Klann

Massachusetts General Hospital

Career Start Year 2008

Number of shared co-authors 15

Meredith Zozus

University of Texas Health

Career Start Year 2007

Number of shared co-authors 8

Andrew R Post

Huntsman Cancer Institute, University of Utah

Career Start Year 2006

Number of shared co-authors 0

Jessica D Tenenbaum

Duke University

Career Start Year 2006

Number of shared co-authors 11

Scott L DuVall

University of Utah

Career Start Year 2006

Number of shared co-authors 31

Nicholas R Anderson

University of California davis

Career Start Year 2006

Number of shared co-authors 15

Matvey B Palchuk

Harvard Medical School

Career Start Year 2005

Number of shared co-authors 7

Harry Hochheiser

University of Pittsburgh

Career Start Year 2005

Number of shared co-authors 5

Jomol Mathew

University of Wisconsin-Madison

Career Start Year 2004

Number of shared co-authors 2

Curtis L Cole

Clinical and Translational Science Center

Career Start Year 2004

Number of shared co-authors 3

Philip R O Payne

Institute for Informatics, Washington University School of Medicine in St. Louis

Career Start Year 2003

Number of shared co-authors 15

Nigam H Shah

Stanford University

Career Start Year 2002

Number of shared co-authors 19

Michael Hogarth

university of california san diego

Career Start Year 2000

Number of shared co-authors 0

Peter J Embi

Vanderbilt University Medical Center

Career Start Year 1998

Number of shared co-authors 37

William T Lester

Massachusetts General Hospital

Career Start Year 1998

Number of shared co-authors 1

Adam B Wilcox

Washington University School of Medicine

Career Start Year 1997

Number of shared co-authors 16

John F Hurdle

University of Utah

Career Start Year 1996

Number of shared co-authors 5

Samuel Trent Rosenbloom

Vanderbilt University Medical Center

Career Start Year 1995

Number of shared co-authors 24

Scott P Narus

University of Utah

Career Start Year 1995

Number of shared co-authors 8

Lucila Ohno-Machado

Escola de Administracao de Empresas - FGV, Stanford University, University of California San Diego, University of Sao Paulo, Yale School of Medicine

Career Start Year 1993

Number of shared co-authors 31

Stanley M Huff

University of Utah School of Medicine

Career Start Year 1984

Number of shared co-authors 16

row(s) 1 - 30 of 30

Jennifer A Pacheco

University of Pennsylvania

Co-authored papers 42

Jyotishman Pathak

Cornell University

Co-authored papers 42

Joshua C Denny

Vanderbilt University

Co-authored papers 31

Peggy L Peissig

Center for Precision Medicine Research, Marshfield Clinic Research Institute

Co-authored papers 27

Guoqian Jiang

Mayo Clinic Rochester Minnesota USA.

Co-authored papers 22

Iftikhar J Kullo

Mayo Clinic

Co-authored papers 21

Abel N Kho

Northwestern University Feinberg School of Medicine

Co-authored papers 21

Christopher G Chute

Brown University, Brown University Warren Alpert Medical School, Dartmouth-Hitchcock Medical Center, Harvard School of Public Health, Johns Hopkins Medicine, Mayo Clinic Minnesota

Co-authored papers 20

Justin Starren

Northwestern University Feinberg School of Medicine

Co-authored papers 19

Yuan Luo

Northwestern University Feinberg School of Medicine

Co-authored papers 17

Marc S Williams

University of Washington Medical Center

Co-authored papers 17

Richard C Kiefer

Mayo Clinic Rochester Minnesota USA.