UGT1A1 sequence variants and bilirubin levels in early postnatal life: a quantitative approach-Reference-Cited by-同舟云学术

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UGT1A1 sequence variants and bilirubin levels in early postnatal life: a quantitative approach

Published:2011-04-22 Issue:1 Volume:12 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Hanchard Neil A,Skierka Jennifer,Weaver Amy,Karon Brad S,Matern Dietrich,Cook Walter,O'Kane Dennis J

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/1471-2350-12-57.pdf

Reference33 articles.

1. Burgos AE, Schmitt SK, Stevenson DK, Phibbs CS: Readmission for Neonatal Jaundice in California, 1991-2000: Trends and Implications. Pediatrics. 2008, 121 (4): e864-869. 10.1542/peds.2007-1214.

2. Grupp-Phelan J, Taylor JA, Liu LL, Davis RL: Early Newborn Hospital Discharge and Readmission for Mild and Severe Jaundice. Arch Pediatr Adolesc Med. 1999, 153 (12): 1283-1288.

3. Management of hyperbilirubinemia in the newborn infant 35 or more weeks of gestation. Pediatrics. 2004, 114 (1): 297-316.

4. Bhutani VK, Johnson L, Sivieri EM: Predictive ability of a predischarge hour-specific serum bilirubin for subsequent significant hyperbilirubinemia in healthy term and near-term newborns. Pediatrics. 1999, 103 (1): 6-14. 10.1542/peds.103.1.6.

5. Keren R, Bhutani VK, Luan X, Nihtianova S, Cnaan A, Schwartz JS: Identifying newborns at risk of significant hyperbilirubinaemia: a comparison of two recommended approaches. Archives of disease in childhood. 2005, 90 (4): 415-421. 10.1136/adc.2004.060079.

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1. Association of UGT1A1 gene variants, expression levels, and enzyme concentrations with 2,3,7,8-TCDD exposure in individuals exposed to Agent Orange/Dioxin;Scientific Reports;2024-02-09

2. The Genetics of Glucose-6-Phosphate-Dehydrogenase (G6PD) and Uridine Diphosphate Glucuronosyl Transferase 1A1 (UGT1A1) Promoter Gene Polymorphism in Relation to Quantitative Biochemical G6PD Activity Measurement and Neonatal Hyperbilirubinemia;Children;2023-07-06

3. UGT1A1 Genetic Variations and a Haplotype Associated with Neonatal Hyperbilirubinemia in Indonesian Population;BioMed Research International;2018

4. Genetic Variations in Bilirubin Metabolism Genes and Their Association with Unconjugated Hyperbilirubinemia in Adults;Annals of Human Genetics;2016-12-12

5. Risk assessment of gene variants for neonatal hyperbilirubinemia in Taiwan;BMC Pediatrics;2016-08-24

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