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

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

BMC genomics - 31 Jan 2023

Wei Si-Jie, Du Jin-Liang, Wang Yue-Bing, Qu Peng-Fei, Ma Lin, Sun Zhong-Chun, Tang Xue, Liu Kai, Xi Yan-Mei, Nie Sheng-Jie, Jia Peng-Lin, Long Wu, Qu Yong-Qiang, Li Yu-Hua, Lei Pu-Ping

Abstract excerpt

OBJECTIVES: To explore the causes of sudden unexpected death (SUD) and to search for high-risk people, whole exome sequencing (WES) was performed in families with SUDs. METHODS: Whole exome sequencing of 25 people from 14 SUD families were screened based on cardiac disease-associated gene variants, and their echocardiograms and electrocardiograms (ECG) were also examined. The protein function of mutated genes...

Read the complete abstract on PubMed

Topics

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

Share to China
Share to Death, Sudden

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Exome Sequencing

Share to Heart Diseases

Share to Mutation

Source

Open in PubMed Open full text

Identifiers

PMID: 36721086
DOI: 10.1186/s12864-022-09097-0
PMCID: PMC9890689

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Whole exome sequencing with a focus on cardiac disease-associated genes in families of sudden unexplained deaths in Yunnan, southwest of China.PMID 36721086Read ↗

Study on Gene Mutations of Hereditary Heart Diseases in Cases of Yunnan Sudden Unexplained DeathSemantic proximity Read ↗

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 ↗

Genetic variants in incident SUDEP cases from a community-based prospective cohort with epilepsy.Semantic proximity Read ↗

Genetic investigations of sudden unexpected deaths in infancy using next-generation sequencing of 100 genes associated with cardiac diseases.Semantic proximity Read ↗

Exome-based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsy.Semantic proximity Read ↗

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

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

Cardiac Disease Associated Genetic Variants in Yi Nationality in Regions with High Incidence of Yunnan Sudden Unexplained Death.Semantic proximity Read ↗

Genetic investigation of 100 heart genes in sudden unexplained death victims in a forensic setting.Semantic proximity Read ↗

Postmortem Identification of Genetic Variations Associated with Sudden Unexpected Death in Young People.Semantic proximity Read ↗

Young and early‐onset dilated cardiomyopathy with malignant ventricular arrhythmia and sudden cardiac death induced by the heterozygous LDB3, MYH6, and SYNE1 missense mutationsSemantic proximity Read ↗

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