Genotype correlates with the natural history of severe bile salt export pump deficiencyDaan van Wessel, Henkjan J. Verkade, Richard J. Thompson et al.|Journal of Hepatology|2020Cited by 133
Natural history of liver disease in a large international cohort of children with Alagille syndrome: Results from the GALA studyShannon M. Vandriel, Catherine Larson‐Nath, Liting Li et al.|Hepatology|2022Cited by 91
Impact of Genotype, Serum Bile Acids, and Surgical Biliary Diversion on Native Liver Survival in FIC1 DeficiencyDaan van Wessel, Felipe Ordonez, Richard J. Thompson et al.|Hepatology|2021Cited by 56
Event-free survival of maralixibat-treated patients with Alagille syndrome compared to a real-world cohort from GALABettina E. Hansen, Shannon M. Vandriel, Pamela Vig et al.|Hepatology|2023Cited by 33
Genotype-phenotype relationships of truncating mutations, p.E297G and p.D482G in bile salt export pump deficiencyAntonia Felzen, Cristina Targa Ferreira, Daan van Wessel et al.|JHEP Reports|2022Cited by 22