Bilirubin Uridine Diphosphate-glucuronosyltransferase Polymorphism as a Risk Factor for Prolonged Hyperbilirubinemia in Japanese Preterm Infants

The Genetic Basis of the Reduced Expression of Bilirubin UDP-Glucuronosyltransferase 1 in Gilbert's Syndrome

Piter J. Bosma, Jayanta Roy Chowdhury, Conny Bakker et al. · New England Journal of Medicine · 1995 · 1.5K citations

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

Gemma Monaghan, Máirín Ryan, Robert Hume et al. · The Lancet · 1996 · 588 citations

Allelic Variant, Genetic Disorder, Genetics +9

Sequence of Exons and the Flanking Regions of Human Bilirubin–Udp–Glucuronosyltransferase Gene Complex and Identification of A Genetic Mutation in A Patient With Crigler–Najjar Syndrome, Type I

Piter J. Bosma, Namita Roy Chowdhury, Bart Goldhoorn et al. · Hepatology · 1992 · 201 citations · Full text

Association of Neonatal Hyperbilirubinemia With Bilirubin UDP-Glucuronosyltransferase Polymorphism

Yoshihiro Maruo, Kashiro Nishizawa, Hiroshi Satō et al. · PEDIATRICS · 1999 · 171 citations

Identification of Defect in the Genes for Bilirubin UDP-Glucuronosyltransferase in a Patient with Crigler-Najjar Syndrome Type II

S. Aono, Yasukazu Yamada, Hiroomi Keino et al. · Biochemical and Biophysical Research Communications · 1993 · 159 citations

Mendelian Disorder, Genetic Disorder, Genetics +10