(Q34065138)

30 July 2017

title

Practical considerations to guide development of access controls and decision support for genetic information in electronic medical records (English)

1 reference

30 July 2017

main subject

decision support system

1 reference

Diana C Darcy

1

1 reference

30 July 2017

Eleanor T Lewis

2

1 reference

30 July 2017

Kelly E Ormond

3

1 reference

30 July 2017

David J Clark

4

1 reference

30 July 2017

Jodie A Trafton

5

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30 July 2017

publication date

2 November 2011

1 reference

BMC Health Services Research

30 July 2017

published in

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30 July 2017

volume

11

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30 July 2017

page(s)

294

1 reference

Identification and Management of Women With BRCA Mutations or Hereditary Predisposition for Breast and Ovarian Cancer

30 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

Pharmacogenomics: will the promise be fulfilled?

5 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

Exclusion of genetic information from the medical record: ethical and medical dilemmas

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

Genomic electronic health records: opportunities and challenges

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

The futility of genomic counseling: essential role of electronic health records

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

Delivery of genomic medicine for common chronic adult diseases: a systematic review

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

Associations between anticipated reactions to genetic test results and interest in genetic testing: will self-selection reduce the potential for harm?

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

Patients' and healthcare professionals' views on pharmacogenetic testing and its future delivery in the NHS.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

Status of clinical gene sequencing data reporting and associated risks for information loss

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

The genome-enabled electronic medical record

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

Family history: a comprehensive genetic risk assessment method for the chronic conditions of adulthood

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3229457

Are electronic health records ready for genomic medicine?

5 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F1472-6963-11-294

Confidentiality, privacy, and security of genetic and genomic test information in electronic health records: points to consider

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1472-6963-11-294

Pharmacogenetics of coumarinic oral anticoagulants

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1472-6963-11-294

Variability in interpreting and reporting copy number changes detected by array-based technology in clinical laboratories.

21 January 2018

1 reference

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An agenda for personalized medicine

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1472-6963-11-294

Concordance study of 3 direct-to-consumer genetic-testing services

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1472-6963-11-294

Evaluation of risk prediction updates from commercial genome-wide scans

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1472-6963-11-294

Key Internet genetics resources for the clinician

21 January 2018

1 reference

12 December 2020

Genetic information: Special or not? Responses from focus groups with members of a health maintenance organization

1 reference

12 December 2020

Ensuring security of high-risk information in EHRs

1 reference

12 December 2020

Keeping Pace with the Times — The Genetic Information Nondiscrimination Act of 2008

1 reference

12 December 2020

Family physicians' awareness and knowledge of the Genetic Information Non-Discrimination Act (GINA)

1 reference

12 December 2020

Genetic exceptionalism. Too much of a good thing?

1 reference

12 December 2020

Genetic exceptionalism & legislative pragmatism

1 reference

12 December 2020

Identifiers

DOI

10.1186/1472-6963-11-294

1 reference

Dimensions Publication ID

30 July 2017

0 references

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30 July 2017

1 reference