Literature DB >> 16616698

The genome-enabled electronic medical record.

M A Hoffman1.   

Abstract

The integration of patient-specific genomic information into the electronic medical record (EMR) will create many opportunities to improve patient care. Key to the successful incorporation of genomic information into the EMR will be the development of laboratory information systems capable of appropriately formatting molecular diagnostic and cytogenetic findings in the EMR. Due to the lack of granular genomics-related content in existing medical vocabularies, the adoption of new standards for describing clinically significant genomic information will be an important step toward recognizing the genome-enabled EMR. Appropriate capture of patient-specific genomic results in the EMR will generate new opportunities to utilize this information in clinical decision support, including automated response to pharmacogenomic-based risks.

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Year:  2006        PMID: 16616698     DOI: 10.1016/j.jbi.2006.02.010

Source DB:  PubMed          Journal:  J Biomed Inform        ISSN: 1532-0464            Impact factor:   6.317


  34 in total

1.  Electronic medical records and personalized medicine.

Authors:  Mark A Hoffman; Marc S Williams
Journal:  Hum Genet       Date:  2011-04-26       Impact factor: 4.132

2.  Practical considerations to guide development of access controls and decision support for genetic information in electronic medical records.

Authors:  Diana C Darcy; Eleanor T Lewis; Kelly E Ormond; David J Clark; Jodie A Trafton
Journal:  BMC Health Serv Res       Date:  2011-11-02       Impact factor: 2.655

3.  Robust replication of genotype-phenotype associations across multiple diseases in an electronic medical record.

Authors:  Marylyn D Ritchie; Joshua C Denny; Dana C Crawford; Andrea H Ramirez; Justin B Weiner; Jill M Pulley; Melissa A Basford; Kristin Brown-Gentry; Jeffrey R Balser; Daniel R Masys; Jonathan L Haines; Dan M Roden
Journal:  Am J Hum Genet       Date:  2010-04-01       Impact factor: 11.025

4.  Adding a genomic healthcare component to a health information management curriculum.

Authors:  Bailee Ludwig; Leming Zhou; Valerie Watzlaf; Mervat Abdelhak
Journal:  Perspect Health Inf Manag       Date:  2010-10-01

5.  Consensus: a framework for evaluation of uncertain gene variants in laboratory test reporting.

Authors:  David K Crockett; Perry G Ridge; Andrew R Wilson; Elaine Lyon; Marc S Williams; Scott P Narus; Julio C Facelli; Joyce A Mitchell
Journal:  Genome Med       Date:  2012-05-28       Impact factor: 11.117

6.  An Extended SNOMED CT Concept Model for Observations in Molecular Genetics.

Authors:  James R Campbell; Geoffrey Talmon; Allison Cushman-Vokoun; Daniel Karlsson; W Scott Campbell
Journal:  AMIA Annu Symp Proc       Date:  2017-02-10

7.  Bio*Medical Informatics and Genomic Medicine: Research and Training.

Authors: 
Journal:  J Biomed Inform       Date:  2007-02       Impact factor: 6.317

8.  Development of a large-scale de-identified DNA biobank to enable personalized medicine.

Authors:  D M Roden; J M Pulley; M A Basford; G R Bernard; E W Clayton; J R Balser; D R Masys
Journal:  Clin Pharmacol Ther       Date:  2008-05-21       Impact factor: 6.875

9.  Advancing personalized health care through health information technology: an update from the American Health Information Community's Personalized Health Care Workgroup.

Authors:  John Glaser; Douglas E Henley; Gregory Downing; Kristin M Brinner
Journal:  J Am Med Inform Assoc       Date:  2008-04-24       Impact factor: 4.497

10.  Genetic counselors' current use of personal health records-based family histories in genetic clinics and considerations for their future adoption.

Authors:  Chaney Widmer; Jonathan P Deshazo; Joann Bodurtha; John Quillin; Heather Creswick
Journal:  J Genet Couns       Date:  2012-12-16       Impact factor: 2.537

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