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

Post-mortem whole-exome analysis in a large sudden infant death syndrome cohort with a focus on cardiovascular and metabolic genetic diseases

11 Jan 2017

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Cardiac electrophysiology and arrhythmias
Share to Ion channel regulation and function
Share to Neuroscience of respiration and sleep

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 28074886
DOI: 10.1038/ejhg.2016.199

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Post-mortem whole-exome analysis in a large sudden infant death syndrome cohort with a focus on cardiovascular and metabolic genetic diseasesPMID 28074886Read ↗

Post-mortem Whole Exome Sequencing with Gene-Specific Analysis for Autopsy-Negative Sudden Unexplained Death in the Young: A Case SeriesSemantic proximity Read ↗

Exome analysis–based molecular autopsy in cases of sudden unexplained death in the youngSemantic proximity Read ↗

Postmortem genetic analysis of sudden unexplained death syndrome under 50 years of age: A next-generation sequencing studySemantic proximity Read ↗

Clinical utility of exome sequencing in infantile heart failureSemantic proximity Read ↗

Neuroendocrinology: Exome sequencing aids targeted treatment of inborn errors of metabolism.Semantic proximity Read ↗

Exome analysis focusing on epilepsy-related genes in children and adults with sudden unexplained deathSemantic proximity Read ↗

Known pathogenic gene variants and new candidates detected in Sudden Unexpected Infant Death using Whole Genome SequencingSemantic proximity Read ↗

Known pathogenic gene variants and new candidates detected in sudden unexpected infant death using whole genome sequencing.Semantic proximity Read ↗

High-Resolution and Noninvasive Fetal Exome ScreeningSemantic proximity Read ↗

Genetic analysis of Yunnan sudden unexplained death by whole genome sequencing in Southwest of China.Semantic proximity Read ↗

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

Characterization of clinically relevant copy-number variants from exomes of patients with inherited heart disease and unexplained sudden cardiac deathSemantic proximity Read ↗

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