Lista de obras - Casey Lynnette Overby - Dominio Público Uruguay

A Template for Authoring and Adapting Genomic Medicine Content in the eMERGE Infobutton Project

artículo científico publicado en 2014

A collaborative approach to developing an electronic health record phenotyping algorithm for drug-induced liver injury

artículo científico publicado en 2013

An Evaluation of Functional and User Interface Requirements for Pharmacogenomic Clinical Decision Support

Analysis of simulation environments utilized in biomedical research.

artículo científico publicado en 2008

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

artículo científico publicado en 2015

Cancer genetic counselor information needs for risk communication: a qualitative evaluation of interview transcripts

artículo científico publicado en 2013

Clinical Data: Sources and Types, Regulatory Constraints, Applications

artículo científico publicado en 2019

Comorbidity Characterization Among eMERGE Institutions: A Pilot Evaluation with the Johns Hopkins Adjusted Clinical Groups® System.

artículo científico publicado en 2019

Deriving rules and assertions from pharmacogenomics knowledge resources in support of patient drug metabolism efficacy predictions

artículo científico publicado en 2012

Detecting Patterns of Prescription Drug Use During Pregnancy and Lactation with Visualization Techniques.

artículo científico publicado en 2019

Developing a prototype system for integrating pharmacogenomics findings into clinical practice

artículo científico publicado en 2012

Disseminating context-specific access to online knowledge resources within electronic health record systems ⬇️

artículo científico publicado el 1 de enero de 2013

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

artículo científico publicado en 2018

Estimating heritability of drug-induced liver injury from common variants and implications for future study designs

artículo científico publicado en 2014

Evaluation considerations for EHR-based phenotyping algorithms: A case study for drug-induced liver injury ⬇️

artículo científico publicado el 18 de marzo de 2013

Extracting Biomedical Terms from Postpartum Depression Online Health Communities.

artículo científico publicado en 2019

Fast Healthcare Interoperability Resources (FHIR) as a Meta Model to Integrate Common Data Models: Development of a Tool and Quantitative Validation Study

scientific article published on 16 October 2019

Feasibility of incorporating genomic knowledge into electronic medical records for pharmacogenomic clinical decision support

artículo científico publicado en 2010

Harnessing next-generation informatics for personalizing medicine: a report from AMIA's 2014 Health Policy Invitational Meeting.

artículo científico publicado en 2016

Implementation of pharmacogenetics: the University of Maryland Personalized Anti-platelet Pharmacogenetics Program

artículo científico publicado en 2014

Integrating Genomic Resources with Electronic Health Records using the HL7 Infobutton Standard

scientific article published on 31 August 2016

Making pharmacogenomic-based prescribing alerts more effective: A scenario-based pilot study with physicians

artículo científico publicado en 2015

Opportunities for genomic clinical decision support interventions

artículo científico publicado en 2013

Personalized Medicine Implementation with Non-traditional Data Sources: A Conceptual Framework and Survey of the Literature

artículo científico publicado en 2019

Personalized Medicine: Challenges and Opportunities for Translational Bioinformatics ⬇️

artículo científico publicado el 1 de julio de 2013

Physician Attitudes toward Adopting Genome-Guided Prescribing through Clinical Decision Support

artículo científico publicado en 2014

Practical choices for infobutton customization: experience from four sites

artículo científico publicado en 2013

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

artículo científico publicado en 2016

Practical considerations in genomic decision support: The eMERGE experience

artículo científico publicado en 2015

Prioritizing Approaches to Engage Community Members and Build Trust in Biobanks: A Survey of Attitudes and Opinions of Adults within Outpatient Practices at the University of Maryland

artículo científico publicado en 2015

Providing Access to Genomic Variant Knowledge in a Healthcare Setting: A Vision for the ClinGen Electronic Health Records Workgroup

artículo científico publicado en 2015

The CLIPMERGE PGx Program: clinical implementation of personalized medicine through electronic health records and genomics-pharmacogenomics

artículo científico publicado en 2013

The Cancer Biomedical Informatics Grid (caBIG<sup>TM</sup>).

artículo científico publicado en 2005

The association between use of a clinical decision support tool and adherence to monitoring for medication-laboratory guidelines in the ambulatory setting

artículo científico publicado en 2013

The genomic CDS sandbox: An assessment among domain experts

artículo científico publicado en 2016

The potential for automated question answering in the context of genomic medicine: An assessment of existing resources and properties of answers ⬇️

artículo científico publicado el 1 de marzo de 2009

The potential for automated question answering in the context of genomic medicine: an assessment of existing resources and properties of answers

artículo científico publicado en 2009

Usability evaluation of pharmacogenomics clinical decision support aids and clinical knowledge resources in a computerized provider order entry system: a mixed methods approach

artículo científico publicado en 2014

User-centered design of multi-gene sequencing panel reports for clinicians

artículo científico publicado en 2016

Using Workflow Modeling to Identify Areas to Improve Genetic Test Processes in the University of Maryland Translational Pharmacogenomics Project

artículo científico publicado en 2015

Value of Genetics-informed Drug Dosing Guidance in Pregnant Women: A Needs Assessment with Obstetric Healthcare Providers at Johns Hopkins

artículo científico publicado en 2017

Willingness to Share Wearable Device Data for Research Among Mechanical Turk Workers: Web-Based Survey Study

artículo científico publicado en 2021

e-PKGene: a knowledge-based research tool for analysing the impact of genetics on drug exposure

artículo científico publicado en 2011

Lista de obras de Casey Lynnette Overby

A Template for Authoring and Adapting Genomic Medicine Content in the eMERGE Infobutton Project

A collaborative approach to developing an electronic health record phenotyping algorithm for drug-induced liver injury

An Evaluation of Functional and User Interface Requirements for Pharmacogenomic Clinical Decision Support

Analysis of simulation environments utilized in biomedical research.

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

Cancer genetic counselor information needs for risk communication: a qualitative evaluation of interview transcripts

Clinical Data: Sources and Types, Regulatory Constraints, Applications

Comorbidity Characterization Among eMERGE Institutions: A Pilot Evaluation with the Johns Hopkins Adjusted Clinical Groups® System.

Deriving rules and assertions from pharmacogenomics knowledge resources in support of patient drug metabolism efficacy predictions

Detecting Patterns of Prescription Drug Use During Pregnancy and Lactation with Visualization Techniques.

Developing a prototype system for integrating pharmacogenomics findings into clinical practice

Disseminating context-specific access to online knowledge resources within electronic health record systems ⬇️

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

Estimating heritability of drug-induced liver injury from common variants and implications for future study designs

Evaluation considerations for EHR-based phenotyping algorithms: A case study for drug-induced liver injury ⬇️

Extracting Biomedical Terms from Postpartum Depression Online Health Communities.

Fast Healthcare Interoperability Resources (FHIR) as a Meta Model to Integrate Common Data Models: Development of a Tool and Quantitative Validation Study

Feasibility of incorporating genomic knowledge into electronic medical records for pharmacogenomic clinical decision support

Harnessing next-generation informatics for personalizing medicine: a report from AMIA's 2014 Health Policy Invitational Meeting.

Implementation of pharmacogenetics: the University of Maryland Personalized Anti-platelet Pharmacogenetics Program

Integrating Genomic Resources with Electronic Health Records using the HL7 Infobutton Standard

Making pharmacogenomic-based prescribing alerts more effective: A scenario-based pilot study with physicians

Opportunities for genomic clinical decision support interventions

Personalized Medicine Implementation with Non-traditional Data Sources: A Conceptual Framework and Survey of the Literature

Personalized Medicine: Challenges and Opportunities for Translational Bioinformatics ⬇️

Physician Attitudes toward Adopting Genome-Guided Prescribing through Clinical Decision Support

Practical choices for infobutton customization: experience from four sites

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

Practical considerations in genomic decision support: The eMERGE experience

Prioritizing Approaches to Engage Community Members and Build Trust in Biobanks: A Survey of Attitudes and Opinions of Adults within Outpatient Practices at the University of Maryland

Providing Access to Genomic Variant Knowledge in a Healthcare Setting: A Vision for the ClinGen Electronic Health Records Workgroup

The CLIPMERGE PGx Program: clinical implementation of personalized medicine through electronic health records and genomics-pharmacogenomics

The Cancer Biomedical Informatics Grid (caBIG<sup>TM</sup>).

The association between use of a clinical decision support tool and adherence to monitoring for medication-laboratory guidelines in the ambulatory setting

The genomic CDS sandbox: An assessment among domain experts

The potential for automated question answering in the context of genomic medicine: An assessment of existing resources and properties of answers ⬇️

The potential for automated question answering in the context of genomic medicine: an assessment of existing resources and properties of answers

Usability evaluation of pharmacogenomics clinical decision support aids and clinical knowledge resources in a computerized provider order entry system: a mixed methods approach

User-centered design of multi-gene sequencing panel reports for clinicians

Using Workflow Modeling to Identify Areas to Improve Genetic Test Processes in the University of Maryland Translational Pharmacogenomics Project

Value of Genetics-informed Drug Dosing Guidance in Pregnant Women: A Needs Assessment with Obstetric Healthcare Providers at Johns Hopkins

Willingness to Share Wearable Device Data for Research Among Mechanical Turk Workers: Web-Based Survey Study

e-PKGene: a knowledge-based research tool for analysing the impact of genetics on drug exposure