The Outcome of Patients With Cystic Biliary Atresia With Intact Proximal Hepatic Ducts Following Hepatic-Cyst-Jejunostomy. Journal of Pediatric Gastroenterology and Nutrition. 2022; 75(2):131-137.
Human iPSC-derived hepatocyte system models cholestasis with tight junction protein 2 deficiency. JHEP Reports. 2022; 4(4):100446.
Biliary Atresia and Other Disorders of the Extrahepatic Bile Ducts. In: Liver Disease in Children. Cambridge University Press (CUP); 2021:162-181.
Modeling Human Bile Acid Transport and Synthesis in Stem Cell-Derived Hepatocytes with a Patient-Specific Mutation. Stem Cell Reports. 2021; 16(2):309-323.
Pathogenesis of biliary atresia: defining biology to understand clinical phenotypes. Nature Reviews Gastroenterology and Hepatology. 2015; 12(6):342-352.
Pharmacokinetic Monitoring of JAK Inhibitor and Tacrolimus for Safe and Effective Management of Graft-Versus-Host Disease After Pediatric Liver Transplantation. Pediatric Transplantation. 2025; 29(7):e70187.
Deriving Human Intestinal Organoids with Functional Tissue-Resident Macrophages All From Pluripotent Stem Cells. Cellular and Molecular Gastroenterology and Hepatology (CMGH). 2025; 19(4):101444.
Portal vein hypoplasia is present in patients with biliary atresia at the time of diagnosis. Journal of Pediatric Gastroenterology and Nutrition. 2024; 79(4):818-825.
Induced pluripotent stem cell (iPSC) modeling validates reduced GBE1 enzyme activity due to a novel variant, p.Ile694Asn, found in a patient with suspected glycogen storage disease IV. Molecular Genetics and Metabolism Reports. 2024; 39:101069.
Rapid in vivo evaluation system for cholestasis-related genes in mice with humanized bile acid profiles. Hepatology Communications. 2024; 8(4).
Neonatal cholestasis in children with Alpha-1-AT deficiency is a risk for earlier severe liver disease with male predominance. Hepatology Communications. 2023; 7(12).
Customized Postoperative Therapy Improves Bile Drainage in Biliary Atresia: A Single Center Preliminary Report. Journal of Pediatric Surgery. 2023; 58(8):1483-1488.
Recent Increase in Incidence of Severe Acute Hepatitis of Unknown Etiology in Children is Associated with Infection with Adenovirus and Other Nonhepatotropic Viruses. Journal of Pediatrics. 2023; 259:113439.
Diagnosis and management of glycogen storage disease type IV, including adult polyglucosan body disease: A clinical practice resource. Molecular Genetics and Metabolism. 2023; 138(3):107525.
O18: A path forward for patients with glycogen branching enzyme deficiency: Consensus on diagnosing and managing glycogen storage disease type IV* Genetics in Medicine Open. 2023; 1(1):100114.
Editorial: Infants with cholestasis. Frontiers in Pediatrics. 2023; 11:1175231.
Gas Leak in the Port: Portal Venous Gas Associated With Congenital Cytomegalovirus Colitis. JPGN Rep. 2022; 3(4):e267.
The Outcome of Patients With Cystic Biliary Atresia With Intact Proximal Hepatic Ducts Following Hepatic-Cyst-Jejunostomy. Journal of Pediatric Gastroenterology and Nutrition. 2022; 75(2):131-137.
In vivo partial cellular reprogramming enhances liver plasticity and regeneration. Cell reports. 2022; 39(4):110730.
Human iPSC-derived hepatocyte system models cholestasis with tight junction protein 2 deficiency. JHEP Reports. 2022; 4(4):100446.
Biliary Atresia and Other Disorders of the Extrahepatic Bile Ducts. In: Liver Disease in Children. Cambridge University Press (CUP); 2021:162-181.
Acute liver dysfunction with delayed peak of serum aminotransferase levels as a presentation of ornithine transcarbamylase deficiency in females. American Journal of Medical Genetics, Part A. 2021; 185(3):909-915.
Modeling Human Bile Acid Transport and Synthesis in Stem Cell-Derived Hepatocytes with a Patient-Specific Mutation. Stem Cell Reports. 2021; 16(2):309-323.
High-Fidelity Drug-Induced Liver Injury Screen Using Human Pluripotent Stem Cell-Derived Organoids. Gastroenterology. 2021; 160(3):831-846.e10.