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Genetic variants in GCKR and PNPLA3 confer susceptibility to nonalcoholic fatty liver disease in obese individuals

The American journal of clinical nutrition, 2014-04, Vol.99 (4), p.869-874

2014

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Genetic determinants of hepatic steatosis and serum cytokeratin‐18 fragment levels in Taiwanese children

Liver international, 2018-07, Vol.38 (7), p.1300-1307

2018

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Molecular biology of glucose-6-phosphate dehydrogenase and UDP-glucuronosyltransferase 1A1 in the development of neonatal unconjugated hyperbilirubinemia

Pediatrics and neonatology, 2024-09, Vol.65 (5), p.419-426

2024

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Updated upper limits of normal serum alanine aminotrasferase levels for screening metabolic dysfunction-associated fatty liver disease in obese children

Journal of the Formosan Medical Association, 2022-12, Vol.121 (12), p.2548-2555

2022

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A Common Variant in the PNPLA3 Gene is a Risk Factor for Non-Alcoholic Fatty Liver Disease in Obese Taiwanese Children

The Journal of pediatrics, 2011-05, Vol.158 (5), p.740-744

2011

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Predictors for incidence and remission of nonalcoholic fatty liver disease in obese children and adolescents

Journal of the Formosan Medical Association, 2022-01, Vol.121 (1), p.36-42

2022

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Integrated Counts of Carbohydrate-Active Protein Domains as Metabolic Readouts to Distinguish Probiotic Biology and Human Fecal Metagenomes

Scientific reports, 2019-11, Vol.9 (1), p.16836-12, Article 16836

2019

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Effects of variation status and enzyme activity for UDP-glucuronosyltransferase 1A1 gene on neonatal hyperbilirubinemia

Pediatrics and neonatology, 2020-10, Vol.61 (5), p.506-512

2020

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A Male Adolescent With Vomiting for 2 Weeks

Annals of emergency medicine, 2023-04, Vol.81 (4), p.e51-e52

2023

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Usefulness of the Triglyceride Glucose Index to Predict Nonalcoholic Fatty Liver Disease in Children With Obesity

The Journal of pediatrics, 2023-04, Vol.255, p.260-261

2023

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Variants in the autophagy-related gene IRGM confer susceptibility to non-alcoholic fatty liver disease by modulating lipophagy

Journal of hepatology, 2016-12, Vol.65 (6), p.1209-1216

2016

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Identifying term breast-fed infants at risk of significant hyperbilirubinemia

Pediatric research, 2013-07, Vol.74 (4), p.408-412

2013

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Risk of Hyperbilirubinemia in Breast-Fed Infants

The Journal of pediatrics, 2011-10, Vol.159 (4), p.561-565

2011

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Reply to: “Normal serum alanine aminotransferase levels for screening metabolic dysfunction associated fatty liver disease”

Journal of the Formosan Medical Association, 2023-10, Vol.122 (10), p.1094-1095

2023

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Differences of microbiota in small bowel and faeces between irritable bowel syndrome patients and healthy subjects

Scandinavian journal of gastroenterology, 2016-04, Vol.51 (4), p.410-419

2016

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A common variant in the peroxisome proliferator―activated receptor-γ coactivator-1α gene is associated with nonalcoholic fatty liver disease in obese children

The American journal of clinical nutrition, 2013-02, Vol.97 (2), p.326-331

2013

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Prolonged Unconjugated Hyperbiliriubinemia in Breast-fed Male Infants with a Mutation of Uridine Diphosphate-Glucuronosyl Transferase

The Journal of pediatrics, 2009-12, Vol.155 (6), p.860-863

2009

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Risk Factors for Liver Steatosis in Obese Children and Adolescents

Pediatrics and neonatology, 2010-06, Vol.51 (3), p.149-154

2010

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Variants in the UGT1A1 gene and the risk of pediatric nonalcoholic fatty liver disease

Pediatrics (Evanston), 2009-12, Vol.124 (6), p.e1221-e1227

2009

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Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyl transferase 1A1 gene, and neonatal hyperbilirubinemia

Gastroenterology (New York, N.Y. 1943), 2002-07, Vol.123 (1), p.127-133

2002

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Relationship between bilirubin UDP-glucuronosyl transferase 1A1 gene and neonatal hyperbilirubinemia

Pediatric research, 2002-10, Vol.52 (4), p.601-605

2002

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Effects of the infant stool color card screening program on 5‐year outcome of biliary atresia in taiwan

Hepatology (Baltimore, Md.), 2011-01, Vol.53 (1), p.202-208

2011

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Universal screening for biliary atresia using an infant stool color card in Taiwan

Hepatology (Baltimore, Md.), 2008-04, Vol.47 (4), p.1233-1240

2008

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Percutaneous endoscopic gastrostomy to set up a long-term enteral feeding route in children: an encouraging result

Pediatric surgery international, 2003-06, Vol.19 (4), p.283-285

2003

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Biliary Atresia in Preterm Infants in Taiwan: A Nationwide Survey

The Journal of pediatrics, 2013-07, Vol.163 (1), p.100-103.e1

2013

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Genetic variants in GCKR and PNPLA3 confer susceptibility to nonalcoholic fatty liver disease in obese individuals

Genetic determinants of hepatic steatosis and serum cytokeratin‐18 fragment levels in Taiwanese children

Molecular biology of glucose-6-phosphate dehydrogenase and UDP-glucuronosyltransferase 1A1 in the development of neonatal unconjugated hyperbilirubinemia

Updated upper limits of normal serum alanine aminotrasferase levels for screening metabolic dysfunction-associated fatty liver disease in obese children

A Common Variant in the PNPLA3 Gene is a Risk Factor for Non-Alcoholic Fatty Liver Disease in Obese Taiwanese Children

Predictors for incidence and remission of nonalcoholic fatty liver disease in obese children and adolescents

Integrated Counts of Carbohydrate-Active Protein Domains as Metabolic Readouts to Distinguish Probiotic Biology and Human Fecal Metagenomes

Effects of variation status and enzyme activity for UDP-glucuronosyltransferase 1A1 gene on neonatal hyperbilirubinemia

A Male Adolescent With Vomiting for 2 Weeks

Usefulness of the Triglyceride Glucose Index to Predict Nonalcoholic Fatty Liver Disease in Children With Obesity

Variants in the autophagy-related gene IRGM confer susceptibility to non-alcoholic fatty liver disease by modulating lipophagy

Identifying term breast-fed infants at risk of significant hyperbilirubinemia

Risk of Hyperbilirubinemia in Breast-Fed Infants

Reply to: “Normal serum alanine aminotransferase levels for screening metabolic dysfunction associated fatty liver disease”

Differences of microbiota in small bowel and faeces between irritable bowel syndrome patients and healthy subjects

A common variant in the peroxisome proliferator―activated receptor-γ coactivator-1α gene is associated with nonalcoholic fatty liver disease in obese children

Prolonged Unconjugated Hyperbiliriubinemia in Breast-fed Male Infants with a Mutation of Uridine Diphosphate-Glucuronosyl Transferase

Risk Factors for Liver Steatosis in Obese Children and Adolescents

Variants in the UGT1A1 gene and the risk of pediatric nonalcoholic fatty liver disease

Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyl transferase 1A1 gene, and neonatal hyperbilirubinemia

Relationship between bilirubin UDP-glucuronosyl transferase 1A1 gene and neonatal hyperbilirubinemia

Effects of the infant stool color card screening program on 5‐year outcome of biliary atresia in taiwan

Universal screening for biliary atresia using an infant stool color card in Taiwan

Percutaneous endoscopic gastrostomy to set up a long-term enteral feeding route in children: an encouraging result

Biliary Atresia in Preterm Infants in Taiwan: A Nationwide Survey

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