(Q37633177)

21 August 2017

A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health record (English)

1 reference

electronic health records

21 August 2017

1 reference

based on heuristic

inferred from title

informatics

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whole genome sequencing

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1

1 reference

21 August 2017

Eliezer Van Allen

12

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Karen E Weck

object named as

Karen E Weck

13

0 references

Matthew S Lebo

object named as

Matthew Lebo

10

0 references

Levi A Garraway

4

object named as

Levi Garraway

1 reference

21 August 2017

7

Lucia A Hindorff

1 reference

21 August 2017

Laura Amendola

2

1 reference

21 August 2017

Samuel J Aronson

3

1 reference

21 August 2017

Stacy Gray

5

1 reference

21 August 2017

Robert W Grundmeier

6

1 reference

21 August 2017

Gail Jarvik

8

1 reference

21 August 2017

Dean Karavite

9

1 reference

21 August 2017

Sharon E Plon

11

1 reference

21 August 2017

Peter S White

14

1 reference

21 August 2017

Yaping Yang

15

1 reference

21 August 2017

language of work or name

English

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publication date

26 September 2013

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21 August 2017

1 reference

21 August 2017

15

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21 August 2017

10

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21 August 2017

824-832

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Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium

21 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3951437

Opportunities for genomic clinical decision support interventions

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3951437

Developing a prototype system for integrating pharmacogenomics findings into clinical practice

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3951437

Crossing the omic chasm: a time for omic ancillary systems

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3951437

Communicating new knowledge on previously reported genetic variants

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3951437

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3951437

Disclosing pathogenic genetic variants to research participants: quantifying an emerging ethical responsibility

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3951437

Translational bioinformatics: linking knowledge across biological and clinical realms

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3951437

The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3951437

Feasibility of incorporating genomic knowledge into electronic medical records for pharmacogenomic clinical decision support

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3951437

The genome-enabled electronic medical record

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3951437

GeneTests-GeneClinics: genetic testing information for a growing audience

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3951437

GeneClinics: a hybrid text/data electronic publishing model using XML applied to clinical genetic testing

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3951437

Creation and maintenance of Helix, a Web based database of medical genetics laboratories, to serve the needs of the genetics community

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3951437

Enabling health care decisionmaking through clinical decision support and knowledge management.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3951437

The clinical bioinformatics ontology: a curated semantic network utilizing RefSeq information

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3951437

Charting a course for genomic medicine from base pairs to bedside

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3951437

Efficiency of CYP2C9 genetic test representation for automated pharmacogenetic decision support

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3951437

A clinician-driven automated system for integration of pharmacogenetic interpretations into an electronic medical record

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3951437

Electronic medical records and personalized medicine

25 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3951437

1 September 2018

Identifiers

DOI

10.1038/GIM.2013.120

1 reference

21 August 2017

1 reference

21 August 2017

PubMed publication ID

24071794

1 reference