Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Re-evaluation of single nucleotide variants and identification of structural variants in a cohort of 45 sudden unexplained death cases.

International journal of legal medicine - 1 Jul 2021

Neubauer Jacqueline, Wang Shouyu, Russo Giancarlo, Haas Cordula

Abstract excerpt

Sudden unexplained death (SUD) takes up a considerable part in overall sudden death cases, especially in adolescents and young adults. During the past decade, many channelopathy- and cardiomyopathy-associated single nucleotide variants (SNVs) have been identified in SUD studies by means of postmortem molecular autopsy, yet the number of cases that remain inconclusive is still high. Recent studies had suggested...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Alkyl and Aryl Transferases
Share to Death, Sudden

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Dystrophin-Associated Proteins

Share to Genomic Structural Variation

Share to Heart Diseases

Share to NAV1.5 Voltage-Gated Sodium Channel

Share to Switzerland

Share to TRPM Cation Channels

Source

Open in PubMed Open full text

Identifiers

PMID: 33895855
DOI: 10.1007/s00414-021-02580-5
PMCID: PMC8205883

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Re-evaluation of single nucleotide variants and identification of structural variants in a cohort of 45 sudden unexplained death cases.PMID 33895855Read ↗

Post-mortem whole-exome sequencing (WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death (SUD) cases.Semantic proximity Read ↗

Post-mortem genetic analysis of sudden unexplained death in a young cohort: a whole-exome sequencing study.Semantic proximity Read ↗

Importance of Variant Interpretation in Whole-Exome Molecular Autopsy: Population-Based Case Series.Semantic proximity Read ↗

From Death to Life/Back to the Future: Detailed Premorbid Clinical and Family History Can Save Lives and Address the Final Diagnosis in Sudden Unexplained Deaths With Negative Autopsy.Semantic proximity Read ↗

Exome analysis in 34 sudden unexplained death (SUD) victims mainly identified variants in channelopathy-associated genesSemantic proximity Read ↗

Unveiling a sudden unexplained death case by whole exome sequencing and bioinformatic analysis.Semantic proximity Read ↗

Ion channelopathies associated genetic variants as the culprit for sudden unexplained death.Semantic proximity Read ↗

[Molecular Genetic Analysis of One Sudden Unexplained Death in the Young by Whole Exome Sequencing].Semantic proximity Read ↗

Next-generation sequencing of 34 genes in sudden unexplained death victims in forensics and in patients with channelopathic cardiac diseases.Semantic proximity Read ↗

Whole exome sequencing with a focus on cardiac disease-associated genes in families of sudden unexplained deaths in Yunnan, southwest of China.Semantic proximity Read ↗

Targeted next generation sequencing application in cardiac channelopathies: Analysis of a cohort of autopsy-negative sudden unexplained deaths.Semantic proximity Read ↗

Cardiac channelopathy testing in 274 ethnically diverse sudden unexplained deaths.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.