(Q33816395)

29 July 2017

title

Whole-genome amplified DNA from stored dried blood spots is reliable in high resolution melting curve and sequencing analysis (English)

1 reference

29 July 2017

main subject

whole genome sequencing

1 reference

7

Jacob Tfelt-Hansen

0 references

Mads Vilhelm Hollegaard

Mads V Hollegaard

2

0 references

Morten Salling Olesen

Morten S Olesen

3

0 references

Jesper Hastrup Svendsen

Jesper H Svendsen

4

0 references

Stig Haunsø

5

Stig Haunsø

1 reference

29 July 2017

1

Bo G Winkel

1 reference

29 July 2017

David M Hougaard

6

1 reference

29 July 2017

publication date

9 February 2011

1 reference

29 July 2017

1 reference

29 July 2017

volume

12

1 reference

29 July 2017

page(s)

22

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2350-12-22

29 July 2017

exact match

0 references

cites work

Inherited cardiac diseases caused by mutations in the Nav1.5 sodium channel

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3045282

Genotyping whole-genome-amplified DNA from 3- to 25-year-old neonatal dried blood spot samples with reference to fresh genomic DNA.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3045282

Genome-wide scans using archived neonatal dried blood spot samples.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3045282

Novel KCNA5 loss-of-function mutations responsible for atrial fibrillation

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3045282

High-resolution melting curve analysis of genomic and whole-genome amplified DNA.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3045282

Assessing quality and functionality of DNA from fresh and archival dried blood spots and recommendations for quality control guidelines

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3045282

Multiple displacement amplification to create a long-lasting source of DNA for genetic studies

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3045282

Storage and use of residual dried blood spots from state newborn screening programs

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3045282

Newborn screening in Japan.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3045282

Validation of dye-binding/high-resolution thermal denaturation for the identification of mutations in the SLC22A5 gene

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3045282

Biological specimen banks in neonatal screening

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3045282

Storage policies and use of the Danish Newborn Screening Biobank.

4 July 2018

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Newborn screening: a national public health programme in Brazil.

21 January 2018

1 reference

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Newborn screening in North America.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-22

Guidelines for the retention, storage, and use of residual dried blood spot samples after newborn screening analysis: statement of the Council of Regional Networks for Genetic Services.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-22

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-22

Four potassium channel mutations account for 73% of the genetic spectrum underlying long-QT syndrome (LQTS) and provide evidence for a strong founder effect in Finland

21 January 2018

1 reference

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Polymorphism screening in the cardiac K+ channel gene KCNA5.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-22

Newborn screening in Australia and New Zealand.

21 January 2018

1 reference

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Genetic aspects and investigation of sudden death in young people

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21306642

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy population

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21306642

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Whole Genome Amplification and Genetic Analysis after Extraction of Proteins from Dried Blood Spots

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21306642

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2350-12-22

1 reference

Dimensions Publication ID

29 July 2017

0 references

1 reference

29 July 2017

1 reference