(Q30524344)

12 August 2017

Usability of a novel clinician interface for genetic results (English)

1 reference

12 August 2017

1 reference

Heidi L Rehm

8

0 references

Lynn A Volk

3

object named as

Lynn A Volk

1 reference

12 August 2017

9

David W Bates

1 reference

12 August 2017

Pamela M Neri

1

1 reference

12 August 2017

Stephanie E Pollard

2

1 reference

12 August 2017

Lisa P Newmark

4

1 reference

12 August 2017

Matthew Varugheese

5

1 reference

12 August 2017

Samantha Baxter

6

1 reference

12 August 2017

Samuel J Aronson

7

1 reference

12 August 2017

language of work or name

1 reference

12 April 2012

1 reference

Journal of Biomedical Informatics

12 August 2017

1 reference

12 August 2017

45

1 reference

12 August 2017

5

1 reference

12 August 2017

950-957

1 reference

Communicating new knowledge on previously reported genetic variants

12 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3426649

The GeneInsight Suite: a platform to support laboratory and provider use of DNA-based genetic testing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3426649

Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathy

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3426649

Health information technology: fallacies and sober realities

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3426649

Use and interpretation of genetic tests in cardiovascular genetics

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3426649

The Path to Personalized Medicine

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3426649

The extent and importance of unintended consequences related to computerized provider order entry

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3426649

Conclusion: You need human factors engineering expertise to see design hazards that are hiding in "plain sight!".

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3426649

Cognitive and usability engineering methods for the evaluation of clinical information systems

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3426649

Ten commandments for effective clinical decision support: making the practice of evidence-based medicine a reality

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3426649

Current challenges and opportunities for better integration of human factors research with development of clinical information systems.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3426649

Are electronic health records ready for genomic medicine?

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3426649

The think aloud method: a guide to user interface design.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3426649

Deficiency of knowledge of genetics and genetic tests among general practitioners, gynecologists, and pediatricians: a global problem

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22521718

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22521718

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Structural genomic variation and personalized medicine

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22521718

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.JBI.2012.03.007

1 reference

journals/jbi/NeriPVNVBARB12

12 August 2017

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

12 August 2017

PubMed publication ID

22521718

1 reference