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

A Pharmacogenomics Clinical Decision Support Service Based on FHIR and CDS Hooks

(2019) A. Boxwala et al.   METHODS OF INFORMATION IN MEDICINE

Use of computer algorithms in the electronic health record to identify and triage primary care patients for hereditary evaluation.

(2019) Wendy Kohlmann et al.   JOURNAL OF CLINICAL ONCOLOGY

Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network

(2019) Hana Zouk et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Physicians’ perspectives on receiving unsolicited genomic results

(2018) Douglas B. Pet et al.   GENETICS IN MEDICINE

Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background

(2018) Kelly E. Ormond et al.   GENETICS IN MEDICINE

Genomics and electronic health record systems

(2018) Lucila Ohno-Machado et al.   HUMAN MOLECULAR GENETICS

ClinGen advancing genomic data-sharing standards as a GA4GH driver project

(2018) Lena Dolman et al.   HUMAN MUTATION

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

(2018) Timothy M Herr et al.   JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION

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

(2017) Carolyn R Rohrer Vitek et al.   PHARMACOGENOMICS

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics

(2016) Sarah S. Kalia et al.   GENETICS IN MEDICINE

Standardizing terms for clinical pharmacogenetic test results: consensus terms from the Clinical Pharmacogenetics Implementation Consortium (CPIC)

(2016) Kelly E. Caudle et al.   GENETICS IN MEDICINE

SMART precision cancer medicine: a FHIR-based app to provide genomic information at the point of care

(2016) Jeremy L Warner et al.   JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION

Context-sensitive decision support (infobuttons) in electronic health records: a systematic review

(2016) David A Cook et al.   JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION

An informatics research agenda to support precision medicine: seven key areas

(2016) Jessica D Tenenbaum et al.   JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION

SMART on FHIR: a standards-based, interoperable apps platform for electronic health records

(2016) Joshua C Mandel et al.   JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION

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

(2016) Casey Overby et al.   Applied Clinical Informatics

Practical considerations for implementing genomic information resources

(2016) Casey Overby et al.   Applied Clinical Informatics

Origins of the Arden Syntax

(2015) George Hripcsak et al.   ARTIFICIAL INTELLIGENCE IN MEDICINE

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

(2015) Sue Richards et al.   GENETICS IN MEDICINE

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

(2015) Brian H Shirts et al.   JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION

SMART on FHIR Genomics: Facilitating standardized clinico-genomic apps

(2015) Gil Alterovitz et al.   JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION

ClinGen — The Clinical Genome Resource

(2015) Heidi L. Rehm et al.   NEW ENGLAND JOURNAL OF MEDICINE

Return of Genomic Results to Research Participants: The Floor, the Ceiling, and the Choices In Between

(2014) Gail P. Jarvik et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Primary-care providers’ perceived barriers to integration of genetics services: a systematic review of the literature

(2014) Natalie A. Mikat-Stevens et al.   GENETICS IN MEDICINE

Technical desiderata for the integration of genomic data with clinical decision support

(2014) Brandon M. Welch et al.   JOURNAL OF BIOMEDICAL INFORMATICS

Return of results in the genomic medicine projects of the eMERGE network

(2014) Iftikhar J. Kullo et al.   Frontiers in Genetics

Opportunities for genomic clinical decision support interventions

(2013) Casey Lynnette Overby et al.   GENETICS IN MEDICINE

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

(2013) Robert C. Green et al.   GENETICS IN MEDICINE

Ethical, legal and social implications of incorporating genomic information into electronic health records

(2013) Ribhi Hazin et al.   GENETICS IN MEDICINE

Crossing the Omic Chasm

(2013) Justin Starren et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Making data on essential pharmacogenes available for every patient everywhere: the Medicine Safety Code initiative

(2013) Matthias Samwald et al.   PHARMACOGENOMICS

Communicating new knowledge on previously reported genetic variants

(2012) Samuel J. Aronson et al.   GENETICS IN MEDICINE

Implementations of the HL7 Context-Aware Knowledge Retrieval (“Infobutton”) Standard: Challenges, strengths, limitations, and uptake

(2012) Guilherme Del Fiol et al.   JOURNAL OF BIOMEDICAL INFORMATICS

Terminology challenges implementing the HL7 context-aware knowledge retrieval (‘Infobutton’) standard

(2012) Howard R Strasberg et al.   JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION

Electronic medical records and personalized medicine

(2011) Mark A. Hoffman et al.   HUMAN GENETICS

Technical desiderata for the integration of genomic data into Electronic Health Records

(2011) Daniel R. Masys et al.   JOURNAL OF BIOMEDICAL INFORMATICS