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

Understanding neonatal hyperbilirubinaemia in the era of genomics.

Seminars in neonatology : SN - 1 Apr 2002

Watchko Jon F, Daood Monica J, Biniwale Manoj

Abstract excerpt

The genomics revolution offers novel approaches to scientific investigation. Application of genomics technologies including microarray gene chips will provide a more complete picture of biological phenomena and help define the genetic contribution to disease by monitoring changes in expression across thousands of genes in physiological and clinical contexts. We briefly summarize identified genetic components that...

Read the complete abstract on PubMed

Topics

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

Share to Bilirubin
Share to Crigler-Najjar Syndrome
Share to Gilbert Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Heme Oxygenase (Decyclizing)

Share to Jaundice, Neonatal

Share to Metabolic Clearance Rate

Share to Metabolism, Inborn Errors

Share to Oxidoreductases Acting on CH-CH Group Donors

Source

Identifiers

PMID: 12208099
DOI: 10.1053/siny.2002.0102

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Understanding neonatal hyperbilirubinaemia in the era of genomics.PMID 12208099Read ↗

Exploring the genetic architecture of neonatal hyperbilirubinemia.Semantic proximity Read ↗

Bilirubin and the Genome: The Hereditary Basis of Unconjugated Neonatal Hyperbilirubinemia.Semantic proximity Read ↗

Neonatal hemolysis and risk of bilirubin-induced neurologic dysfunction.Semantic proximity Read ↗

Genome-wide expression in neonatal encephalopathySemantic proximity Read ↗

DNA microarray gene expression analysis technology and its application to neurological disorders.Semantic proximity Read ↗

Acute neonatal bilirubin encephalopathy in the State of Utah 2009-2018.Semantic proximity Read ↗

Genomics and neurological phenotypes: applications for seizure-induced damage.Semantic proximity Read ↗

Genome-wide analyses of neonatal jaundice reveal a marked departure from adult bilirubin metabolism.Semantic proximity Read ↗

DNA microarrays: an overview of technologies and applications to toxicology.Semantic proximity Read ↗

Elucidating the role of genomics in neonatal sepsis.Semantic proximity Read ↗

Neonatal hemolytic jaundice: morphologic features of erythrocytes that will help you diagnose the underlying condition.Semantic proximity Read ↗

Extreme neonatal hyperbilirubinemia, acute bilirubin encephalopathy, and kernicterus spectrum disorder in children with galactosemia.Semantic proximity Read ↗

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