Literature DB >> 21309042

Emerging landscape of genomics in the Electronic Health Record for personalized medicine.

Mollie H Ullman-Cullere1, Jomol P Mathew.   

Abstract

The Information Technology (IT) roadmap for personalized medicine requires Electronic Health Records (EHRs), extension of Healthcare IT (HIT) standards, and understanding of how genetics/genomics should be integrated into the clinical applications. For reduced overall costs and development times, these three initiatives should run in parallel. EHRs must contain structured data and infrastructure that enables quality analysis, Clinical Decision Support (CDS) and messaging within the healthcare information network. Fortunately, as a result of sustained financial commitment to nongenetic-based healthcare, the industry has HIT data standards and understanding of EHR functionality that improves patient safety and outcomes while reducing overall healthcare costs. However, the HIT standards and EHR functional requirements, needed for personalized medicine, are only beginning to support simple genetic tests and need significant extension. In addition, our understanding of the clinical implications of genomic data is evolving and translation of new discovery into clinical care remains a challenge. Therefore, priority areas include CDS, educational resources, and knowledgebases for the EHR, clinical and research data warehouses, messaging frameworks, and continued review of healthcare policies and regulations supporting personalized medicine. Where core infrastructure remains to be developed and implemented, funding is needed for pilot projects, data standards, policy, and stakeholder collaboration.
© 2011 Wiley-Liss, Inc.

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Year:  2011        PMID: 21309042     DOI: 10.1002/humu.21456

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  18 in total

Review 1.  Clinical implementation of comprehensive strategies to characterize cancer genomes: opportunities and challenges.

Authors:  Laura E MacConaill; Paul Van Hummelen; Matthew Meyerson; William C Hahn
Journal:  Cancer Discov       Date:  2011-09       Impact factor: 39.397

2.  Supporting interoperability of genetic data with LOINC.

Authors:  Jamalynne Deckard; Clement J McDonald; Daniel J Vreeman
Journal:  J Am Med Inform Assoc       Date:  2015-02-05       Impact factor: 4.497

Review 3.  Clinical decision support for genetically guided personalized medicine: a systematic review.

Authors:  Brandon M Welch; Kensaku Kawamoto
Journal:  J Am Med Inform Assoc       Date:  2012-08-25       Impact factor: 4.497

4.  Implementing the VMC Specification to Reduce Ambiguity in Genomic Variant Representation.

Authors:  Michael Watkins; Shawn Rynearson; Alex Henrie; Karen Eilbeck
Journal:  AMIA Annu Symp Proc       Date:  2020-03-04

5.  Genetic testing behavior and reporting patterns in electronic medical records for physicians trained in a primary care specialty or subspecialty.

Authors:  Jeremiah Geronimo Ronquillo; Cheng Li; William T Lester
Journal:  J Am Med Inform Assoc       Date:  2012-04-17       Impact factor: 4.497

6.  How the electronic health record will change the future of health care.

Authors:  Jeremiah Geronimo Ronquillo
Journal:  Yale J Biol Med       Date:  2012-09-25

7.  Using electronic patient records to discover disease correlations and stratify patient cohorts.

Authors:  Francisco S Roque; Peter B Jensen; Henriette Schmock; Marlene Dalgaard; Massimo Andreatta; Thomas Hansen; Karen Søeby; Søren Bredkjær; Anders Juul; Thomas Werge; Lars J Jensen; Søren Brunak
Journal:  PLoS Comput Biol       Date:  2011-08-25       Impact factor: 4.475

8.  Systems medicine and integrated care to combat chronic noncommunicable diseases.

Authors:  Jean Bousquet; Josep M Anto; Peter J Sterk; Ian M Adcock; Kian Fan Chung; Josep Roca; Alvar Agusti; Chris Brightling; Anne Cambon-Thomsen; Alfredo Cesario; Sonia Abdelhak; Stylianos E Antonarakis; Antoine Avignon; Andrea Ballabio; Eugenio Baraldi; Alexander Baranov; Thomas Bieber; Joël Bockaert; Samir Brahmachari; Christian Brambilla; Jacques Bringer; Michel Dauzat; Ingemar Ernberg; Leonardo Fabbri; Philippe Froguel; David Galas; Takashi Gojobori; Peter Hunter; Christian Jorgensen; Francine Kauffmann; Philippe Kourilsky; Marek L Kowalski; Doron Lancet; Claude Le Pen; Jacques Mallet; Bongani Mayosi; Jacques Mercier; Andres Metspalu; Joseph H Nadeau; Grégory Ninot; Denis Noble; Mehmet Oztürk; Susanna Palkonen; Christian Préfaut; Klaus Rabe; Eric Renard; Richard G Roberts; Boleslav Samolinski; Holger J Schünemann; Hans-Uwe Simon; Marcelo Bento Soares; Giulio Superti-Furga; Jesper Tegner; Sergio Verjovski-Almeida; Peter Wellstead; Olaf Wolkenhauer; Emiel Wouters; Rudi Balling; Anthony J Brookes; Dominique Charron; Christophe Pison; Zhu Chen; Leroy Hood; Charles Auffray
Journal:  Genome Med       Date:  2011-07-06       Impact factor: 11.117

9.  How to build personalized multi-omics comorbidity profiles.

Authors:  Mohammad Ali Moni; Pietro Liò
Journal:  Front Cell Dev Biol       Date:  2015-06-24

Review 10.  Genetic data and electronic health records: a discussion of ethical, logistical and technological considerations.

Authors:  Kimberly Shoenbill; Norman Fost; Umberto Tachinardi; Eneida A Mendonca
Journal:  J Am Med Inform Assoc       Date:  2013-06-14       Impact factor: 4.497

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