(Q46210261)

20 December 2017

title

Non optical semi-conductor next generation sequencing of the main cardiac QT-interval duration genes in pooled DNA samples (English)

1 reference

20 December 2017

author

César Morís

3

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20 December 2017

Eliecer Coto

5

object named as

Eliecer Coto

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20 December 2017

author name string

Juan Gómez

1

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20 December 2017

Julian R Reguero

2

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20 December 2017

Victoria Alvarez

4

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20 December 2017

language of work or name

English

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publication date

5 November 2013

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20 December 2017

Journal of Cardiovascular Translational Research

published in

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20 December 2017

volume

7

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20 December 2017

issue

1

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20 December 2017

page(s)

133-137

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20 December 2017

https://scigraph.springernature.com/pub.10.1007/s12265-013-9516-6

exact match

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cites work

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https://api.crossref.org/works/10.1007%2FS12265-013-9516-6

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Genetic testing in heritable cardiac arrhythmia syndromes: differentiating pathogenic mutations from background genetic noise

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12265-013-9516-6

Confirmation of associations between ion channel gene SNPs and QTc interval duration in healthy subjects

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12265-013-9516-6

Common candidate gene variants are associated with QT interval duration in the general population

21 January 2018

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Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes

21 January 2018

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An integrated semiconductor device enabling non-optical genome sequencing

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Performance comparison of benchtop high-throughput sequencing platforms

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12265-013-9516-6

A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers

21 January 2018

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Rapid detection of the ACMG/ACOG-recommended 23 CFTR disease-causing mutations using ion torrent semiconductor sequencing

21 January 2018

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Novel strategies for classifying splice-site variants of unknown clinical significance in CFTR.

21 January 2018

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Towards clinical molecular diagnosis of inherited cardiac conditions: a comparison of bench-top genome DNA sequencers

21 January 2018

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Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes

21 January 2018

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Pooled-DNA sequencing identifies novel causative variants in PSEN1, GRN and MAPT in a clinical early-onset and familial Alzheimer's disease Ibero-American cohort

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12265-013-9516-6

Genomic DNA pooling strategy for next-generation sequencing-based rare variant discovery in abdominal aortic aneurysm regions of interest-challenges and limitations

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12265-013-9516-6

Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients

21 January 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/24190697

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Sudden cardiac death and genetic ion channelopathies: long QT, Brugada, short QT, catecholaminergic polymorphic ventricular tachycardia, and idiopathic ventricular fibrillation

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24190697

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12 December 2020

based on heuristic

Nonoptical massive parallel DNA sequencing of BRCA1 and BRCA2 genes in a diagnostic setting.

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24190697

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S12265-013-9516-6

1 reference

20 December 2017

1 reference

20 December 2017