Melissa Sambrotta
King's College London(GB)
Publications by Year
Research Areas
Pediatric Hepatobiliary Diseases and Treatments, Drug Transport and Resistance Mechanisms, Hepatitis B Virus Studies, Liver Disease Diagnosis and Treatment, Barrier Structure and Function Studies
Most-Cited Works
- → Mutations in TJP2 cause progressive cholestatic liver disease(2014)289 cited
- → An expanded role for heterozygous mutations of ABCB4, ABCB11, ATP8B1, ABCC2 and TJP2 in intrahepatic cholestasis of pregnancy(2017)143 cited
- → Mutations in DCDC2 (doublecortin domain containing protein 2) in neonatal sclerosing cholangitis(2016)88 cited
- → Hepatocellular carcinoma associated with tight‐junction protein 2 deficiency(2015)82 cited
- → Mutations inTJP2, encoding zona occludens 2, and liver disease(2015)68 cited
- → Cholestasis Due to USP53 Deficiency(2020)41 cited
- → Study of Acute Liver Failure in Children Using Next Generation Sequencing Technology(2021)25 cited
- → Genetic variation in interleukin-28B locus is associated with spontaneous clearance of HCV in children with non-1 viral genotype infection(2011)19 cited
- → Human iPSC-derived hepatocyte system models cholestasis with tight junction protein 2 deficiency(2022)13 cited
- → LP16 : Mutations in DCDC2, encoding doublecortin domain-containing protein 2, cause neonatal sclerosing cholangitis(2015)1 cited