May–Jen Huang

Cathay General Hospital — Taiwan

Medicine · Health Sciences

11h-index600citations18works0.02yr avg
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Research Topics

Neonatal Health and Biochemistry(17), Methemoglobinemia and Tumor Lysis Syndrome(8), Heme Oxygenase-1 and Carbon Monoxide(5), Erythrocyte Function and Pathophysiology(5), Metabolism and Genetic Disorders(3)

Publications18 total

Effects of variation status and enzyme activity for UDP-glucuronosyltransferase 1A1 gene on neonatal hyperbilirubinemia
Pediatrics & Neonatology·2020· 6 citedOpen Access
Multiple variants in UGT1A1 gene are factors to develop indirect hyper-bilirubinemia.
PubMed·2014· 10 cited
Bilirubin concentrations in thalassemia heterozygotes in university students
European Journal Of Haematology·2011· 7 cited
Variations in the UDP-Glucuronosyltransferase 1A1 Gene for the Development of Unconjugated Hyperbilirubinemia in Taiwanese
Pharmacogenomics·2008· 16 cited
UDP-glucuronosyltransferase 1A7 polymorphisms are associated with liver cirrhosis
Biochemical and Biophysical Research Communications·2007· 13 cited
Crigler-Najjar Syndrome Type 2
Journal of the Formosan Medical Association·2006· 13 citedOpen Access
Polymorphisms of uridine-diphosphoglucuronosyltransferase 1A7 gene in Taiwan Chinese
World Journal of Gastroenterology·2005· 22 citedOpen Access
Genetic factors related to unconjugated hyperbilirubinemia amongst adults
Pharmacogenetics and Genomics·2005· 58 cited
Risk Factors for Severe Hyperbilirubinemia in Neonates
Pediatric Research·2004· 238 citedOpen Access
Coinheritance of variant UDP-glucuronosyl transferase 1A1 gene and glucose-6-phosphate dehydrogenase deficiency in adults with hyperbilirubinemia
Pharmacogenetics·2002· 15 cited
Relationship Between Bilirubin UDP-Glucuronosyl Transferase 1A1 Gene and Neonatal Hyperbilirubinemia
Pediatric Research·2002· 72 cited
Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyl transferase 1A1 gene, and neonatal hyperbilirubinemia
Gastroenterology·2002· 85 citedOpen Access
A novel compound heterozygous variation of the uridine-diphosphoglucuronosyl transferase 1A 1 gene that causes Crigler‐Najjar syndrome type II
Pharmacogenetics·2001· 15 cited
Genetic variations of randomly amplified polymorphic DNA polymorphisms in Taoyuan and Duroc pigs
2001· 2 cited
G6PD IManKang (517 T→C; 173 Phe→Leu): A New Chinese G6PD Variant Associated with Neonatal Jaundice
Human Heredity·1996· 19 cited
Molecular Diagnosis of Glucose-6-Phosphate Dehydrogenase (G6PD) Mutations
Journal of genetics and molecular biology·1992· 3 cited
Diagnosis of Glucose-6-Phosphate Dehydrogenase (G6PD) Mutations by DNA Amplification and Allele-Specific Oligonucleotide Probes
Acta Haematologica·1992· 3 cited
Molecular diagnosis of G6PD mutations
1992· 3 cited

Frequent Co-authors

Ching‐Shan Huang(15), Hsiu‐Chen Teng(4), En–Sung Chen(4), Sien‐Sing Yang(4), Kung-Sheng Tang(3), Pi‐Feng Chang(3), Min-Shung Lin(2), Tang K. Tang(2), Yangyang Huang(2), Tang K. Tang(2), Chieh-Ju C. Tang(2), Jan‐Gowth Chang(2), Ka-Em Kua(1), Hui-Wen Weng(1), W. Chen(1), Kun‐Long Hung(1), Kuo‐Inn Tsou Yau(1), Hua‐Ling Chen(1), Sieng-Sien Yang(1), Guo-An Luo(1)