UGT1A1 Gene Polymorphisms in North Indian Neonates Presenting with Unconjugated Hyperbilirubinemia

Management of Hyperbilirubinemia in the Newborn Infant 35 or More Weeks of Gestation

PEDIATRICS · 2004 · 2.8K citations

Medicine, Child Health, Pediatrics +16

Racial variability in the UDP-glucuronosyltransferase 1 ( <i>UGT1A1</i> ) promoter: A balanced polymorphism for regulation of bilirubin metabolism?

Ernest Beutler, Terri Gelbart, Anna Demina · Proceedings of the National Academy of Sciences · 1998 · 852 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndrome

Gemma Monaghan, Máirín Ryan, Robert Hume et al. · The Lancet · 1996 · 589 citations

Life Sciences, Genetics, Molecular Genetics +8

Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: A dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia

Michael Kaplan, Paul Renbaum, Ephrat Levy‐Lahad et al. · Proceedings of the National Academy of Sciences · 1997 · 347 citations

Life Sciences, Genetics, Molecular Genetics +17

Cloning of two human liver bilirubin UDP-glucuronosyltransferase cDNAs with expression in COS-1 cells.

Joseph K. Ritter, John M. Crawford, I S Owens · Journal of Biological Chemistry · 1991 · 265 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +13