Area of research
Surgery · Oncology
Research interest
Research interests include Pediatric Hepatobiliary Diseases and Treatments, Drug Transport and Resistance Mechanisms, Liver Disease Diagnosis and Treatment, and Liver Disease and Transplantation.
Phenotypic Divergence of <i>JAG1</i> ‐ and <i>NOTCH2</i> ‐Associated Alagille Syndrome & Disease‐Specific <i>NOTCH2</i> Variant Classification Guidelines
Elevated Serum Bile Acids Predict Poor Liver Outcomes in Children With Alagille Syndrome: Results From the <scp>GALA</scp> Study Group
Condition-Specific Growth Charts for Children With Alagille Syndrome
Efficacy and safety of odevixibat in patients with Alagille syndrome (ASSERT): a phase 3, double-blind, randomised, placebo-controlled trial
Towards a Standardized Classification of the Hepatobiliary Manifestations in Cystic Fibrosis (CFHBI): A Joint ESPGHAN/NASPGHAN Position Paper
EASL-ERN position paper on liver involvement in patients with Fontan-type circulation
Interim results from an ongoing, open-label, single-arm trial of odevixibat in progressive familial intrahepatic cholestasis
Event-free survival of maralixibat-treated patients with Alagille syndrome compared to a real-world cohort from GALA
Odevixibat treatment in progressive familial intrahepatic cholestasis: a randomised, placebo-controlled, phase 3 trial
Natural history of liver disease in a large international cohort of children with Alagille syndrome: Results from the GALA study
Prognosis of Children Undergoing Liver Transplantation: A 30-Year European Study
Genotype-phenotype relationships of truncating mutations, p.E297G and p.D482G in bile salt export pump deficiency
European Liver Transplant Registry: Donor and transplant surgery aspects of 16,641 liver transplantations in children
Hepatocyte‐specific deletion of adipose triglyceride lipase (adipose triglyceride lipase/patatin‐like phospholipase domain containing 2) ameliorates dietary induced steatohepatitis in mice
Impact of Genotype, Serum Bile Acids, and Surgical Biliary Diversion on Native Liver Survival in FIC1 Deficiency
The potential and limitations of intrahepatic cholangiocyte organoids to study inborn errors of metabolism
Abnormal Liver Function Tests in Patients With COVID‐19: Relevance and Potential Pathogenesis
Genotype correlates with the natural history of severe bile salt export pump deficiency
Long‐Term β‐galacto‐oligosaccharides Supplementation Decreases the Development of Obesity and Insulin Resistance in Mice Fed a Western‐Type Diet
Systematic Review and Meta‐analysis
Glucose‐6‐Phosphate Regulates Hepatic Bile Acid Synthesis in Mice
Sex differences in lipid metabolism are affected by presence of the gut microbiota
Intestinal Failure and Aberrant Lipid Metabolism in Patients With DGAT1 Deficiency
The Health Care Transition of Youth With Liver Disease Into the Adult Health System
IVACAFTOR restores FGF19 regulated bile acid homeostasis in cystic fibrosis patients with an S1251N or a G551D gating mutation
Diagnosis and Management of Pediatric Autoimmune Liver Disease
Wilson's Disease in Children
Treatment of Chronic Hepatitis C Virus Infection in Children
Cystic Fibrosis–related Liver Disease
Intestinal PPARδ protects against diet-induced obesity, insulin resistance and dyslipidemia
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