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Author Details
Full Name
Samuel J Aronson
Affiliation
Georgetown University.
ORCID
Career Start Year
2011
Papers
26
H Index
13
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36350612
Results of a Remotely Delivered Hypertension and Lipid Program in More Than 10⿯000 Patients Across a Diverse Health Care Network.
JAMA Cardiol
2023
36053173
I2b2-etl: Python application for importing electronic health data into the informatics for integrating biology and the bedside platform.
Bioinformatics
2022
35485600
A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources.
J Am Med Inform Assoc
2022
35874460
Use of automatic SQL generation interface to enhance transparency and validity of health-data analysis.
Inform Med Unlocked
2022
34658181
The elusive challenge of leadership development at faith-based institutions.
New Dir Stud Leadersh
2021
37920232
Facilitating Genetics Aware Clinical Decision Support: Putting the eMERGE Infrastructure into Practice.
ACI open
2021
33930535
Genomic considerations for FHIR®; eMERGE implementation lessons.
J Biomed Inform
2021
34758494
Workflow Automation for a Virtual Hypertension Management Program.
Appl Clin Inform
2021
31725920
Rationale and design of a navigator-driven remote optimization of guideline-directed medical therapy in patients with heart failure with reduced ejection fraction.
Clin Cardiol
2020
31143314
Phenotyping to Facilitate Accrual for a Cardiovascular Intervention.
J Clin Med Res
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
31463162
Development of a Calculated Panel Reactive Antibody Web Service with Local Frequencies for Platelet Transfusion Refractoriness Risk Stratification.
J Pathol Inform
2019
31258990
Extending i2b2 into a framework for semantic abstraction of EHR to facilitate rapid development and portability of Health IT applications.
AMIA Jt Summits Transl Sci Proc
2019
29460415
Research Directions in the Clinical Implementation of Pharmacogenomics: An Overview of US Programs and Projects.
Clin Pharmacol Ther
2018
29860405
Empowering genomic medicine by establishing critical sequencing result data flows: the eMERGE example.
J Am Med Inform Assoc
2018
26805890
Information Technology Support for Clinical Genetic Testing within an Academic Medical Center.
J Pers Med
2016
26418054
Providing Access to Genomic Variant Knowledge in a Healthcare Setting: A Vision for the ClinGen Electronic Health Records Workgroup.
Clin Pharmacol Ther
2016
27437054
Evaluation: A Qualitative Pilot Study of Novel Information Technology Infrastructure to Communicate Genetic Variant Updates.
Appl Clin Inform
2016
26142422
CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record.
J Am Med Inform Assoc
2015
26469044
Building the foundation for genomics in precision medicine.
Nature
2015
24013137
A novel clinician interface to improve clinician access to up-to-date genetic results.
J Am Med Inform Assoc
2014
24846037
Using multiplexed assays of oncogenic drivers in lung cancers to select targeted drugs.
JAMA
2014
24071794
A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health record.
Genet Med
2013
22521718
Usability of a novel clinician interface for genetic results.
J Biomed Inform
2012
22481129
Communicating new knowledge on previously reported genetic variants.
Genet Med
2012
21432942
The GeneInsight Suite: a platform to support laboratory and provider use of DNA-based genetic testing.
Hum Mutat
2011
1 - 26 of 26
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