Kathrin Klein

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The liver proteome of individuals with a natural UGT2B17 complete deficiency.
In silico and biological analyses of missense variants of the human biliary efflux transporter ABCC2: effects of novel rare missense variants.
Consequences of Amyloid-β Deficiency for the Liver.
Cross-ancestry GWAS defines the extended CYP2D6 locus as the principal genetic determinant of endoxifen plasma concentrations
Hepatic Expression of the Na+-Taurocholate Cotransporting Polypeptide Is Independent from Genetic Variation
Copy number variation profiling in pharmacogenes using panel-based exome resequencing and correlation to human liver expression.
A New Panel-Based Next-Generation Sequencing Method for ADME Genes Reveals Novel Associations of Common and Rare Variants With Expression in a Human Liver Cohort
Methyleugenol DNA adducts in human liver are associated with SULT1A1 copy number variations and expression levels.