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English
Enhancing the incidental pipeline in genomic sequencing
scientific article published on 23 January 2014
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
3977220
retrieved
22 August 2017
title
Enhancing the incidental pipeline in genomic sequencing
(English)
1 reference
stated in
Europe PubMed Central
PMCID
3977220
retrieved
22 August 2017
author name string
B D Solomon
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
3977220
retrieved
22 August 2017
publication date
23 January 2014
1 reference
stated in
Europe PubMed Central
PMCID
3977220
retrieved
22 August 2017
published in
Molecular syndromology
1 reference
stated in
Europe PubMed Central
PMCID
3977220
retrieved
22 August 2017
volume
5
1 reference
stated in
Europe PubMed Central
PMCID
3977220
retrieved
22 August 2017
issue
2
1 reference
stated in
Europe PubMed Central
PMCID
3977220
retrieved
22 August 2017
page(s)
47-50
1 reference
stated in
Europe PubMed Central
PMCID
3977220
retrieved
22 August 2017
cites work
Actionable, pathogenic incidental findings in 1,000 participants' exomes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3977220
retrieved
23 August 2017
Databases of genomic variation and phenotypes: existing resources and future needs
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3977220
retrieved
23 August 2017
Recommendations for returning genomic incidental findings? We need to talk!
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3977220
retrieved
23 August 2017
Interpreting secondary cardiac disease variants in an exome cohort
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3977220
retrieved
23 August 2017
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3977220
retrieved
23 August 2017
Clinical genomic database
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3977220
retrieved
23 August 2017
Self-guided management of exome and whole-genome sequencing results: changing the results return model
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3977220
retrieved
23 August 2017
Deleterious- and disease-allele prevalence in healthy individuals: insights from current predictions, mutation databases, and population-scale resequencing
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3977220
retrieved
23 August 2017
Predicting the functional effect of amino acid substitutions and indels
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3977220
retrieved
23 August 2017
An informatics approach to analyzing the incidentalome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3977220
retrieved
23 August 2017
A public resource facilitating clinical use of genomes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3977220
retrieved
23 August 2017
Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3977220
retrieved
23 August 2017
Incidental medical information in whole-exome sequencing
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3977220
retrieved
23 August 2017
Confidence of primary care physicians in their ability to carry out basic medical genetic tasks-a European survey in five countries-Part 1.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3977220
retrieved
23 August 2017
Offering individual genetic research results: context matters
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3977220
retrieved
23 August 2017
Human non-synonymous SNPs: server and survey
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3977220
retrieved
23 August 2017
Genetic service delivery: infrastructure, assessment and information
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3977220
retrieved
6 September 2017
VAR-MD: a tool to analyze whole exome-genome variants in small human pedigrees with mendelian inheritance
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3977220
retrieved
1 September 2018
Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3977220
retrieved
5 November 2018
Identifiers
DOI
10.1159/000357929
1 reference
stated in
Europe PubMed Central
PMCID
3977220
retrieved
22 August 2017
PMCID
3977220
1 reference
stated in
Europe PubMed Central
PMCID
3977220
retrieved
22 August 2017
PubMed ID
24715850
1 reference
stated in
Europe PubMed Central
PMCID
3977220
retrieved
22 August 2017
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