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Author Details
Full Name
Stephen B Ellis
Affiliation
Icahn School of Medicine at Mount Sinai
ORCID
Career Start Year
2013
Papers
21
H Index
12
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36372942
Prescriber Adoption of SLCO1B1 Genotype-Guided Simvastatin Clinical Decision Support in a Clinical Pharmacogenetics Program.
Clin Pharmacol Ther
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
35244702
Effects of Testing and Disclosing Ancestry-Specific Genetic Risk for Kidney Failure on Patients and Health Care Professionals: A Randomized Clinical Trial.
JAMA Netw Open
2022
33168928
Rapid response to the alpha-1 adrenergic agent phenylephrine in the perioperative period is impacted by genomics and ancestry.
Pharmacogenomics J
2021
33531665
GUÃA: a digital platform to facilitate result disclosure in genetic counseling.
Genet Med
2021
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
31445275
Augmented intelligence with natural language processing applied to electronic health records for identifying patients with non-alcoholic fatty liver disease at risk for disease progression.
Int J Med Inform
2019
28903894
Prototype Development: Context-Driven Dynamic XML Ophthalmologic Data Capture Application.
JMIR Med Inform
2017
28335839
Apolipoprotein L1 Variants and Blood Pressure Traits in African Americans.
J Am Coll Cardiol
2017
28193464
iGAS: A framework for using electronic intraoperative medical records for genomic discovery.
J Biomed Inform
2017
28982267
Institutional profile: translational pharmacogenomics at the Icahn School of Medicine at Mount Sinai.
Pharmacogenomics
2017
27026615
PheKB: a catalog and workflow for creating electronic phenotype algorithms for transportability.
J Am Med Inform Assoc
2016
27393744
Implementing Algorithm-Guided Warfarin Dosing in an Ethnically Diverse Patient Population Using Electronic Health Records and Preemptive CYP2C9 and VKORC1 Genetic Testing.
Clin Pharmacol Ther
2016
26747051
Determining the effects and challenges of incorporating genetic testing into primary care management of hypertensive patients with African ancestry.
Contemp Clin Trials
2016
25460205
Incorporating temporal EHR data in predictive models for risk stratification of renal function deterioration.
J Biomed Inform
2015
26131930
Directional dominance on stature and cognition in diverse human populations.
Nature
2015
25562141
Physician Attitudes toward Adopting Genome-Guided Prescribing through Clinical Decision Support.
J Pers Med
2014
25954398
Development and validation of an electronic phenotyping algorithm for chronic kidney disease.
AMIA Annu Symp Proc
2014
25954377
Disease progression subtype discovery from longitudinal EMR data with a majority of missing values and unknown initial time points.
AMIA Annu Symp Proc
2014
23588317
The CLIPMERGE PGx Program: clinical implementation of personalized medicine through electronic health records and genomics-pharmacogenomics.
Clin Pharmacol Ther
2013
23837993
A collaborative approach to developing an electronic health record phenotyping algorithm for drug-induced liver injury.
J Am Med Inform Assoc
2013
1 - 21 of 21
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row(s) 1 - 30 of 30
Collaborators
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Hasso Plattner Institute for Digital Health at Mount Sinai
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Icahn School of Medicine at Mount Sinai
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Stanford University
Co-authored papers
8
Girish N Nadkarni
Icahn School of Medicine at Mount Sinai
Co-authored papers
6
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Icahn School of Medicine at Mount Sinai
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6
Eimear E Kenny
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5
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University of Pennsylvania
Co-authored papers
4
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Cornell University
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Peggy L Peissig
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Aida Vega
Icahn School of Medicine at Mount Sinai
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George Hripcsak
Columbia University
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Gerard Tromp
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Judy H Cho
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Carol R Horowitz
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