|
Hyperbilirubinemia, Neonatal
|
|
0.100 |
GeneticVariation
|
BEFREE |
This meta-analysis confirms that UGT1A1 Gly71Arg polymorphism significantly increases the risk of neonatal hyperbilirubinemia in Asian population, but results from the Caucasians were conflicting and further well-designed epidemiological studies are, therefore, required to more adequately assess this correlation.
|
29179591 |
2019 |
|
Hyperbilirubinemia, Neonatal
|
|
0.100 |
GeneticVariation
|
BEFREE |
Additionally, multivariate logistic regression analysis identified that the mutant genotype of rs4148323 in the UGT1A1 gene, ABO incompatibility, G6PD deficiency, and SS genotype at rs1805173 locus of the HO-1 gene were genetic risk factors of neonatal hyperbilirubinemia.
|
30298137 |
2018 |
|
Hyperbilirubinemia, Neonatal
|
|
0.100 |
GeneticVariation
|
BEFREE |
We found that UGT1A1 G71R mutation is a risk factor for neonatal hyperbilirubinemia in Guangxi Heiyi Zhuang and Han populations.
|
26200705 |
2015 |
|
Hyperbilirubinemia, Neonatal
|
|
0.100 |
GeneticVariation
|
BEFREE |
This meta-analysis demonstrated that UGT1A1 polymorphisms (Gly71Arg and TATA promoter) significantly increase the risk of neonatal hyperbilirubinemia.
|
26467199 |
2015 |
|
Hyperbilirubinemia, Neonatal
|
|
0.100 |
GeneticVariation
|
BEFREE |
UGT1A1 gene variants, namely, c.211G>A, g.-3279T>G, TATA box polymorphism and CAT insertion were identified as independent molecular risk factors for neonatal hyperbilirubinemia, whereas c.686C>A, c.1091C>T and c.1456T>G were not detected in study cohort.
|
24232666 |
2014 |
|
Hyperbilirubinemia, Neonatal
|
|
0.100 |
GeneticVariation
|
BEFREE |
The effect of G71R mutation on neonatal hyperbilirubinemia is significant in neonates with 5% or greater maximal body weight loss and its influence increases in parallel with the degree of maximal body weight loss.
|
23014115 |
2013 |
|
Hyperbilirubinemia, Neonatal
|
|
0.100 |
GeneticVariation
|
BEFREE |
Short (GT)n repeats of HO-1 gene, c.211G>A variant of UGT1A1 gene, and excessive weight loss were independent risk factors for neonatal hyperbilirubinemia.
|
23877636 |
2013 |
|
Hyperbilirubinemia, Neonatal
|
|
0.100 |
GeneticVariation
|
BEFREE |
Neonatal hyperbilirubinemia and G71R mutation of the UGT1A1 gene in Turkish patients.
|
20528217 |
2011 |
|
Hyperbilirubinemia, Neonatal
|
|
0.100 |
GeneticVariation
|
BEFREE |
The UGT1A1 211G>A mutation is associated with neonatal hyperbilirubinemia in Asians, but not in Caucasians.
|
21272068 |
2011 |
|
Hyperbilirubinemia, Neonatal
|
|
0.100 |
GeneticVariation
|
BEFREE |
The UGT1A1 gene codon G71R allele is a risk factor for neonatal hyperbilirubinemia in the Chinese population.
|
17888052 |
2007 |