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

Neonatal Encephalopathy

13 Jan 2025

Abstract excerpt

Background and Objectives: Neonatal encephalopathy (NE) is characterized by an abnormal level of consciousness with or without seizures in the neonatal period. It affects 1-6/1,000 live term newborns. We applied genome sequencing (GS) in term newborns with NE to investigate the underlying genetic causes. Methods: We enrolled term newborns according to inclusion/exclusion criteria during their Neonatal Intensive...

Read the complete abstract on PubMed

Topics

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

Share to Genomics and Rare Diseases
Share to Machine Learning in Bioinformatics
Share to Neonatal and fetal brain pathology

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Source

Identifiers

PMID: 39810752
DOI: 10.1212/nxg.0000000000200232

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 20 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Neonatal EncephalopathyPMID 39810752Read ↗

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

Genetic Diagnosis in Neonatal Encephalopathy With Hypoxic Brain Damage Using Targeted Gene Panel SequencingSemantic proximity Read ↗

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

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

Gene panel analysis for nonsyndromic cryptogenic neonatal/infantile epileptic encephalopathySemantic proximity Read ↗

Expanded phenotypic spectrum of UDP-glucose-6-dehydrogenase recessive neurodevelopmental disorder: Two novel descriptions with or without epileptic encephalopathy.Semantic proximity Read ↗

Neonatal epilepsy genetics.Semantic proximity Read ↗

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

Early infantile epileptic encephalopathy related to NECAP1: Clinical delineation of the disease and review.Semantic proximity Read ↗

Secondary genomic findings in the 2020 China Neonatal Genomes Project participants.Semantic proximity Read ↗

Identification of a novel GRIN2D variant in a neonate with intractable epileptic encephalopathy-a case report.Semantic proximity Read ↗

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