Literature DB >> 30778576

An ancillary genomics system to support the return of pharmacogenomic results.

Luke V Rasmussen1, Maureen E Smith2,3, Federico Almaraz4, Stephen D Persell3, Laura J Rasmussen-Torvik1, Jennifer A Pacheco2, Rex L Chisholm2, Carl Christensen4,5, Timothy M Herr1, Firas H Wehbe1, Justin B Starren1.   

Abstract

Existing approaches to managing genetic and genomic test results from external laboratories typically include filing of text reports within the electronic health record, making them unavailable in many cases for clinical decision support. Even when structured computable results are available, the lack of adopted standards requires considerations for processing the results into actionable knowledge, in addition to storage and management of the data. Here, we describe the design and implementation of an ancillary genomics system used to receive and process heterogeneous results from external laboratories, which returns a descriptive phenotype to the electronic health record in support of pharmacogenetic clinical decision support.
© The Author(s) 2019. Published by Oxford University Press on behalf of the American Medical Informatics Association. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Keywords:  electronic health record; genetic testing; pharmacogenomics

Year:  2019        PMID: 30778576      PMCID: PMC6402311          DOI: 10.1093/jamia/ocy187

Source DB:  PubMed          Journal:  J Am Med Inform Assoc        ISSN: 1067-5027            Impact factor:   4.497


  6 in total

1.  Managing Increased Accessibility to Pharmacogenomic Data.

Authors:  Susanne B Haga
Journal:  Clin Pharmacol Ther       Date:  2019-09-03       Impact factor: 6.875

Review 2.  Advancing Pharmacogenomics from Single-Gene to Preemptive Testing.

Authors:  Cyrine E Haidar; Kristine R Crews; James M Hoffman; Mary V Relling; Kelly E Caudle
Journal:  Annu Rev Genomics Hum Genet       Date:  2022-05-10       Impact factor: 9.340

Review 3.  Challenges and opportunities for integrating genetic testing into a diagnostic workflow: heritable long QT syndrome as a model.

Authors:  Ira M Lubin; Edward R Lockhart; Julie Frank; Vincent Y See; Sudhir Vashist; Carol Greene
Journal:  Diagnosis (Berl)       Date:  2019-07-09

Review 4.  Pharmacogenomic Clinical Decision Support: A Review, How-to Guide, and Future Vision.

Authors:  Dyson T Wake; D Max Smith; Sadaf Kazi; Henry M Dunnenberger
Journal:  Clin Pharmacol Ther       Date:  2021-08-29       Impact factor: 6.903

5.  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.

Authors:  Marc S Williams; Casey Overby Taylor; Nephi A Walton; Scott R Goehringer; Samuel Aronson; Robert R Freimuth; Luke V Rasmussen; Eric S Hall; Cynthia A Prows; Wendy K Chung; Alexander Fedotov; Jordan Nestor; Chunhua Weng; Robb K Rowley; Georgia L Wiesner; Gail P Jarvik; Guilherme Del Fiol
Journal:  Front Genet       Date:  2019-10-29       Impact factor: 4.599

6.  Advancing precision public health using human genomics: examples from the field and future research opportunities.

Authors:  Megan C Roberts; Alison E Fohner; Latrice Landry; Dana Lee Olstad; Amelia K Smit; Erin Turbitt; Caitlin G Allen
Journal:  Genome Med       Date:  2021-06-01       Impact factor: 11.117

  6 in total

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