(Q33894105)

29 July 2017

title

Teaching genomic counseling: preparing the genetic counseling workforce for the genomic era (English)

1 reference

29 July 2017

1

Gillian W Hooker

1 reference

29 July 2017

4

Barbara B Biesecker

1 reference

29 July 2017

Kelly E Ormond

2

1 reference

29 July 2017

Kevin Sweet

series ordinal

3

1 reference

29 July 2017

publication date

8 February 2014

1 reference

Journal of Genetic Counseling

29 July 2017

published in

1 reference

29 July 2017

volume

23

1 reference

29 July 2017

issue

4

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29 July 2017

page(s)

445-451

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Actionable, pathogenic incidental findings in 1,000 participants' exomes

29 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=4096068

Databases of genomic variation and phenotypes: existing resources and future needs

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

ACMG clinical laboratory standards for next-generation sequencing

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Digenic inheritance in medical genetics

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Personal genotypes are teachable moments

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Personal genome testing in medical education: student experiences with genotyping in the classroom

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

A family genetic risk communication framework: guiding tool development in genetics health services

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Patients' understanding of and responses to multiplex genetic susceptibility test results

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Swabbing students: should universities be allowed to facilitate educational DNA testing?

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Managing incidental findings and research results in genomic research involving biobanks and archived data sets

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Identification of functional genetic variation in exome sequence analysis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Varieties of uncertainty in health care: a conceptual taxonomy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Impact of direct-to-consumer predictive genomic testing on risk perception and worry among patients receiving routine care in a preventive health clinic

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduria.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Motivators for participation in a whole-genome sequencing study: implications for translational genomics research

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Long-term outcomes of BRCA1/BRCA2 testing: risk reduction and surveillance

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Effect of direct-to-consumer genomewide profiling to assess disease risk

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Colonoscopy use following mutation detection in Lynch syndrome: exploring a role for cancer screening in adaptation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Impact of communicating personalized genetic risk information on perceived control over the risk: a systematic review

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Consumers' Views of Direct-to-Consumer Genetic Information

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Future health applications of genomics: priorities for communication, behavioral, and social sciences research

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

The behavioral response to personalized genetic information: will genetic risk profiles motivate individuals and families to choose more healthful behaviors?

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Exome sequencing identifies the cause of a mendelian disorder

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Role of in silico tools in gene discovery

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

The Genetic Counseling Video Project (GCVP): models of practice

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Fatalistic responses to different types of genetic risk information: exploring the role of self-malleability

28 July 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9689-4

Generic Consent for Genetic Screening

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9689-4

Massively parallel sequencing and rare disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9689-4

Evidence that personal genome testing enhances student learning in a course on genomics and personalized medicine.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9689-4

Commentary: to genotype or not to genotype? Addressing the debate through the development of a genomics and personalized medicine curriculum.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9689-4

Lessons learned from the introduction of personalized genotyping into a medical school curriculum.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9689-4

Inherited Cardiomyopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9689-4

Mapping the incidentalome: estimating incidental findings generated through clinical pharmacogenomics testing.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9689-4

Point-counterpoint. Patient autonomy and incidental findings in clinical genomics

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9689-4

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Public preferences regarding informed consent models for participation in population-based genomic research

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Sources of uncertainty and their association with medical decision making: exploring mechanisms in Fanconi anemia

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096068

Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24504939

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Goals, benefits, and outcomes of genetic counseling: client and genetic counselor assessment

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24504939

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S10897-014-9689-4

1 reference

29 July 2017

1 reference

29 July 2017

1 reference