Ruud Berger

A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis

Laura N. Bull, Michiel J. T. van Eijk, Ludmila Pawlikowska et al. · Nature Genetics · 1998 · 738 citations

Life Sciences, Genetics, Molecular Genetics +12

Benign recurrent intrahepatic cholestasis type 2 is caused by mutations in ABCB11

Saskia W. C. van Mil, Wendy L. van der Woerd, Gerda van der Brugge et al. · Gastroenterology · 2004 · 343 citations

Medicine, Genetics, Molecular Genetics +10

Characterization of mutations in ATP8B1 associated with hereditary cholestasis

Leo W. J. Klomp, Julie C. Vargas, Saskia W. C. van Mil et al. · Hepatology · 2004 · 293 citations · Full text

Medicine, Genetics, Molecular Genetics +17

The Signal Transducer and Activator of Transcription STAT5b Gene Is a New Partner of Retinoic Acid Receptor   in Acute Promyelocytic-Like Leukaemia

Cécile Arnould, Christophe Philippe, Violaine Bourdon et al. · Human Molecular Genetics · 1999 · 262 citations · Full text

Life Sciences, Genetics, Molecular Biology +15

Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of β-oxidation in insulin secretion

Peter T. Clayton, Simon Eaton, A Aynsley‐Green et al. · Journal of Clinical Investigation · 2001 · 253 citations

Life Sciences, Biochemistry, Endocrinology +15