K. Bokelmann

Effects of OCT1 polymorphisms on the cellular uptake, plasma concentrations and efficacy of the 5-HT3 antagonists tropisetron and ondansetron

R. Kaiser, J. Brockmöller, M. Tzvetkov, 2010, The Pharmacogenomics Journal.

Hepatocyte Nuclear Factor 1 Regulates the Expression of the Organic Cation Transporter 1 via Binding to an Evolutionary Conserved Region in Intron 1 of the OCT 1 Gene s

Brien, M. Ratain, J. Brockmöller, 2013 .

Impact of Promoter Polymorphisms on the Transcriptional Regulation of the Organic Cation Transporter OCT1 (SLC22A1)

J. Brockmöller, M. Tzvetkov, K. Bokelmann, 2018, Journal of personalized medicine.

Enhancer-driven transcriptional regulation is a potential key determinant for human visceral and subcutaneous adipocytes.

B. Ghadimi, Robert Liefke, S. Dango, 2018, Biochimica et biophysica acta. Gene regulatory mechanisms.

Functional characterization of a -100_-102delAAG deletion-insertion polymorphism in the promoter region of the HTR3B gene

R. Kaiser, J. Brockmöller, M. Tzvetkov, 2008, Pharmacogenetics and genomics.

A novel missense variant in the SDR domain of the WWOX gene leads to complete loss of WWOX protein with early-onset epileptic encephalopathy and severe developmental delay

F. Kortüm, J. Denecke, G. Rosenberger, 2018, neurogenetics.

Hepatocyte Nuclear Factor 1 Regulates the Expression of the Organic Cation Transporter 1 via Binding to an Evolutionary Conserved Region in Intron 1 of the OCT1 Gene

M. Ratain, J. Brockmöller, M. Tzvetkov, 2013, The Journal of Pharmacology and Experimental Therapeutics.

Does the haplotype Met408-Del420, which was apparently predictive for imatinib efficacy, really exist and how strongly may it affect OCT1 activity?

J. Brockmöller, H. Koepsell, T. Mueller, 2014, Blood.

A novel missense variant in the SDR domain of the WWOX gene leads to complete loss of WWOX protein with early-onset epileptic encephalopathy and severe developmental delay

F. Kortüm, J. Denecke, G. Rosenberger, 2018, neurogenetics.