Literature DB >> 17238523

Integrating genetic information resources with an EHR.

Guilherme Del Fiol1, Marc S Williams, Naveen Maram, Roberto A Rocha, Grant M Wood, Joyce A Mitchell.   

Abstract

As the knowledge about the genetic factors associated with clinical conditions increases, access to information that can help practicing clinicians better understand these factors becomes essential for optimal care and communication with patients. We describe the implementation of 'infobuttons' from the problem list module of an electronic health record (EHR) to on-line genetic resources.

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Mesh:

Year:  2006        PMID: 17238523      PMCID: PMC1839246     

Source DB:  PubMed          Journal:  AMIA Annu Symp Proc        ISSN: 1559-4076


  1 in total

1.  Supporting infobuttons with terminological knowledge.

Authors:  J J Cimino; G Elhanan; Q Zeng
Journal:  Proc AMIA Annu Fall Symp       Date:  1997
  1 in total
  11 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.  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

3.  Evaluation: A Qualitative Pilot Study of Novel Information Technology Infrastructure to Communicate Genetic Variant Updates.

Authors:  Stephanie Klinkenberg-Ramirez; Pamela M Neri; Lynn A Volk; Sara J Samaha; Lisa P Newmark; Stephanie Pollard; Matthew Varugheese; Samantha Baxter; Samuel J Aronson; Heidi L Rehm; David W Bates
Journal:  Appl Clin Inform       Date:  2016-06-01       Impact factor: 2.342

4.  Charting a course for genomic medicine from base pairs to bedside.

Authors:  Eric D Green; Mark S Guyer
Journal:  Nature       Date:  2011-02-10       Impact factor: 49.962

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

Authors:  Bret S E Heale; Casey Lynnette Overby; Guilherme Del Fiol; Wendy S Rubinstein; Donna R Maglott; Tristan H Nelson; Aleksandar Milosavljevic; Christa L Martin; Scott R Goehringer; Robert Freimuth; Marc S Williams
Journal:  Appl Clin Inform       Date:  2016-08-31       Impact factor: 2.342

Review 6.  Building the foundation for genomics in precision medicine.

Authors:  Samuel J Aronson; Heidi L Rehm
Journal:  Nature       Date:  2015-10-15       Impact factor: 49.962

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

Authors:  Elizabeth Cutting; Meghan Banchero; Amber L Beitelshees; James J Cimino; Guilherme Del Fiol; Ayse P Gurses; Mark A Hoffman; Linda Jo Bone Jeng; Kensaku Kawamoto; Mark Kelemen; Harold Alan Pincus; Alan R Shuldiner; Marc S Williams; Toni I Pollin; Casey Lynnette Overby
Journal:  J Biomed Inform       Date:  2016-07-14       Impact factor: 6.317

8.  Opportunities for genomic clinical decision support interventions.

Authors:  Casey Lynnette Overby; Isaac Kohane; Joseph L Kannry; Marc S Williams; Justin Starren; Erwin Bottinger; Omri Gottesman; Joshua C Denny; Chunhua Weng; Peter Tarczy-Hornoch; George Hripcsak
Journal:  Genet Med       Date:  2013-09-19       Impact factor: 8.822

9.  Developing a prototype system for integrating pharmacogenomics findings into clinical practice.

Authors:  Casey Lynnette Overby; Peter Tarczy-Hornoch; Ira J Kalet; Kenneth E Thummel; Joe W Smith; Guilherme Del Fiol; David Fenstermacher; Emily Beth Devine
Journal:  J Pers Med       Date:  2012-11-20

10.  Perspectives on what is needed to implement genomic medicine.

Authors:  Marc S Williams
Journal:  Mol Genet Genomic Med       Date:  2015-05       Impact factor: 2.183

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