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

Topics Community

Article

Genetic Diagnosis in Neonatal Encephalopathy With Hypoxic Brain Damage Using Targeted Gene Panel Sequencing

1 Jan 2024

Abstract excerpt

Background and Purpose Neonatal encephalopathy (NE) is a neurological syndrome that presents with severe neurological impairments and complications.Hypoxic-ischemic encephalopathy is a major contributor to poor outcomes, being responsible for 50%-80% of admissions to neonatal intensive care units.However, some cases of NE accompanied by hypoxic brain damage cannot be solely attributed to hypoxia-ischemia.We aimed...

Topics

Join the communities discussing this publication.

Genomics and Rare Diseases
Mitochondrial Function and Pathology
Neonatal and fetal brain pathology

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 39227335
DOI: 10.3988/jcn.2023.0500

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic Diagnosis in Neonatal Encephalopathy With Hypoxic Brain Damage Using Targeted Gene Panel SequencingPMID 39227335Read ↗

Clinical exome sequencing uncovers genetic disorders in neonates with suspected hypoxic-ischemic encephalopathy: A retrospective analysis.Semantic proximity Read ↗

Identifying Genetic Susceptibility in Neonates With Hypoxic-Ischemic Encephalopathy: A Retrospective Case Series.Semantic proximity Read ↗

Genetic and epigenetic contributors and mimickers of phenotypic hypoxic-ischemic encephalopathy (HIE).Semantic proximity Read ↗

Exploring the genetic landscape of neurotransmitter alterations in hypoxic-ischemic encephalopathy: A personalized medicine perspectiveSemantic proximity Read ↗

Prospective cohort study for identification of underlying genetic causes in neonatal encephalopathy using whole-exome sequencing.Semantic proximity Read ↗

Clinical features and underlying genetic causes in neonatal encephalopathy: A large cohort study.Semantic proximity Read ↗

[Genotype and phenotype analysis of neonates with neonatal encephalopathy complicated with perinatal hypoxic event].Semantic proximity Read ↗

The NESHIE and CP Genetics Resource (NCGR): A database of genes and variants reported in neonatal encephalopathy with suspected hypoxic ischemic encephalopathy (NESHIE) and consequential cerebral palsy (CP)Semantic proximity Read ↗

Neonatal EncephalopathySemantic proximity Read ↗

Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era: A ReviewSemantic proximity Read ↗

Genetic diagnosis and clinical characteristics by etiological classification in early-onset epileptic encephalopathy with burst suppression pattern.Semantic proximity Read ↗

Intersociety policy statement on the use of whole-exome sequencing in the critically ill newborn infantSemantic proximity Read ↗

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