DNA Methylation of ADME Genes von Fisel, P, Schaeffeler, E, Schwab, M

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Implementing Pharmacogenomics in Europe: Design and Implementation Strategy of the Ubiquitous Pharmacogenomics Consortium von van der Wouden, CH, Cambon‐Thomsen, A, Cecchin, E, Cheung, KC, Dávila‐Fajardo, CL, Deneer, VH, Dolžan, V, Ingelman‐Sundberg, M, Jönsson, S, Karlsson, MO, Kriek, M, Mitropoulou, C, Patrinos, GP, Pirmohamed, M, Samwald, M, Schaeffeler, E, Schwab, M, Steinberger, D, Stingl, J, Sunder‐Plassmann, G, Toffoli, G, Turner, RM, van Rhenen, MH, Swen, JJ, Guchelaar, H‐J

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Polymorphic Variation in TPMT Is the Principal Determinant of TPMT Phenotype: A Meta‐Analysis of Three Genome‐Wide Association Studies von Tamm, R, Mägi, R, Tremmel, R, Winter, S, Mihailov, E, Smid, A, Möricke, A, Klein, K, Schrappe, M, Stanulla, M, Houlston, R, Weinshilboum, R, Mlinarič Raščan, Irena, Metspalu, A, Milani, L, Schwab, M, Schaeffeler, E

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Tamoxifen metabolism predicts drug concentrations and outcome in premenopausal patients with early breast cancer von Saladores, P, Mürdter, T, Eccles, D, Chowbay, B, Zgheib, N K, Winter, S, Ganchev, B, Eccles, B, Gerty, S, Tfayli, A, Lim, J S L, Yap, Y S, Ng, R C H, Wong, N S, Dent, R, Habbal, M Z, Schaeffeler, E, Eichelbaum, M, Schroth, W, Schwab, M, Brauch, H

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Genetic variation of platelet function and pharmacology: An update of current knowledge von Geisler, Tobias, Schaeffeler, Elke, Gawaz, Meinrad, Schwab, Matthias

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Stratified medicine for the use of antidiabetic medication in treatment of type II diabetes and cancer: where do we go from here? von Emami‐Riedmaier, A., Schaeffeler, E., Nies, A. T., Mörike, K., Schwab, M.

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ABCB1 genotype of the donor but not of the recipient is a major risk factor for cyclosporine-related nephrotoxicity after renal transplantation von HAUSER, Ingeborg A, SCHAEFFELER, Elke, GEIGER, Helmut, EICHELBAUM, Michel, SCHWAB, Matthias, GAUER, Stefan, SCHEUERMANN, Ernst H, WEGNER, Binytha, GOSSMANN, Jan, ACKERMANN, Hanns, SEIDL, Christian, HOCHER, Berthold, ZANGER, Ulrich M

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Immunological markers and somatic mutations as predictors for therapy selection in metastatic renal cell carcinoma von Bedke, J., Herrmann, L., Stühler, V., Winter, S., Reustle, A., Stenzl, A., Schaeffeler, E., Schwab, M.

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Adherence to thiopurine treatment in out‐patients with Crohn’s disease von BOKEMEYER, B., TEML, A., ROGGEL, C., HARTMANN, P., FISCHER, C., SCHAEFFELER, E., SCHWAB, M.

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Variability in human hepatic MRP4 expression: influence of cholestasis and genotype von Gradhand, U, Lang, T, Schaeffeler, E, Glaeser, H, Tegude, H, Klein, K, Fritz, P, Jedlitschky, G, Kroemer, H K, Bachmakov, I, Anwald, B, Kerb, R, Zanger, U M, Eichelbaum, M, Schwab, M, Fromm, M F

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ABCB1 Single‐Nucleotide Polymorphisms Determine Tacrolimus Response in Patients With Ulcerative Colitis von Herrlinger, KR, Koc, H, Winter, S, Teml, A, Stange, EF, Fellermann, K, Fritz, P, Schwab, M, Schaeffeler, E

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Clinical and Functional Relevance of the Monocarboxylate Transporter Family in Disease Pathophysiology and Drug Therapy von Fisel, Pascale, Schaeffeler, Elke, Schwab, Matthias

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Adme-wide analysis of Copy Number Variation using Targeted exome resequencing and their functional relevance in Human Liver von Tremmel, R, Fehr, S, Battke, F, Klein, K, Schaeffeler, E, Schwab, M, Biskup, S, Zanger, U.M

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Targeted Exome Resequencing: Adme Pharmacogenetics In Human Liver von Klein, K, Fehr, S, Tremmel, R, Schaeffeler, E, Winter, S, Schwab, M, Biskup, S, Zanger, U.M

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Challenges and opportunities associated with rare-variant pharmacogenomics br von Zhou, Y, Tremmel, R, Schaeffeler, E, Schwab, M, Lauschke, VM

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Safe treatment of thiopurine S-methyltransferase deficient Crohn’s disease patients with azathioprine von Kaskas, B A, Louis, E, Hindorf, U, Schaeffeler, E, Deflandre, J, Graepler, F, Schmiegelow, K, Gregor, M, Zanger, U M, Eichelbaum, M, Schwab, M

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CD147, The Ancillary protein of MCT4, as marker for prognosis and clinical outcome in primary clear cell renal cell Carcinoma and Metastasis von Fisel, P, Stühler, V, Winter, S, Rausch, S, Hennenlotter, J, Nies, A.T, Stenzl, A, Scharpf, M, Fend, F, Kruck, S, Bedke, J, Schwab, M, Schaeffeler, E

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Challenges and opportunities associated with rare-variant pharmacogenomics von Zhou, Yitian, Tremmel, Roman, Schaeffeler, Elke, Schwab, Matthias, Lauschke, Volker M.

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Human Pregnane X Receptor Genotype of the Donor but Not of the Recipient Is a Risk Factor for Delayed Graft Function After Renal Transplantation von Hauser, I A, Kruck, S, Gauer, S, Nies, A T, Winter, S, Bedke, J, Geiger, H, Hoefeld, H, Kleemann, J, Asbe-Vollkopf, A, Engel, J, Burk, O, Schwab, M, Schaeffeler, E

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Pretreatment determination of TPMT - state of the art in clinical practice von Teml, A, Schaeffeler, E, Schwab, M

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