Publications

Full Paper

M Eidens, A Weise, S Prause, N Dahmen, A Wunsch, M M Weber, T Forst and A Pfuetzner. Development and validation of a high-throughput screening method for two polymorphisms in the serotonin transporter gene. Mol Diagn Ther 13(1):25–29, 2009.

M Klemm, M Eidens, M Lorenz, S Prause, A Weise, N Dahmen, T Forst and A Pfuetzner. Development of a high throughput single nucleotide polymorphism screening method for the cytochrome P450 1A2 polymorphisms CYP1A2*1C and CYP1A2*1F: are they useful as predictive markers in mental disorders. Clin Lab 56(9-10):473–480, 2010.

Marion Lorenz, Alexander Weise, Stefan Prause, Marco Klemm, Moritz Eidens, Massimiliano Luchi, Thomas Forst, Andreas Pfuetzner and Matthias M Weber. Development and validation of a rapid and reliable method for TPMT genotyping using real-time PCR.. Clin Lab 58(9-10):959–971, 2012.

S Prause, M Eidens, A Weise, M M Weber, N Dahmen, A Wunsch, T Forst and A Pfuetzner. Development of a high-throughput method for screening the dopamine D2 (DRD2) receptor gene polymorphisms based on the LightCycler system. Clin Lab 55(9-10):353–8, 2009.

S Rower, U Bienzle, A Weise, U Lambertz, T Forst, R N Otchwemah, A Pfuetzner and F P Mockenhaupt. Short communication: high prevalence of the cytochrome P450 2C8*2 mutation in Northern Ghana. Trop Med Int Health 10(12):1271–3, 2005.

A Weise, S Grundler, D Zaumsegel, M Klotzek, B Grondahl, T Forst and A Pfuetzner. Development and evaluation of a rapid and reliable method for cytochrome P450 2C8 genotyping. Clin Lab 50(3-4):141–8, 2004.

A Weise, S Prause, M Eidens, M M Weber, P H Kann, T Forst and A Pfuetzner. Prevalence of CYP450 gene variations in patients with type 2 diabetes. Clin Lab 56(7-8):311–318, 2010.

 

Reviews

M Eidens, S Prause, A Weise, M Klemm, M M Weber and A Pfützner. Dihydropyrimidine Dehydrogenase Genotyping and Phenotyping for 5-Fluorouracil Dysmetabolism: Moving Towards Personalized Chemotherapy in Patients with Cancer. CPPM 7(4):275–283, 2009.

M Lorenz, S Prause, M Eidens, A Weise, M Klemm, A Pfützner, T Schöndorf and M M Weber. Translation of CYP2D6 Human Genetic Variation into Medical Practice: Lessons Learned and the Way Forward. CPPM 8(4):306–319, 2010.

 

Poster

M Klemm, M Eidens, S Prause, A Weise, R Maurer, A Brauchler, T Forst and A Pfützner. Development of a Novel Method for theranostic Screening of a Dehydropyrimidine Dehydrogenase Deficiency. Poster at 12th Status Seminar Chip Technologies, Sequencing and Functional Genomics, Frankfurt a. M., 2010.

M Klemm, J Zenner, M Lorenz, M Luchi, M Eidens, S Prause, A Weise and A Pfützner. Development of a Novel Screening Method for the Cystic Fibrosis Transmembrane Conductance Regulator Gene based on a Macroarray DNA-Chip Platform. Poster at 22. Jahrestagung der Deutschen Gesellschaft für Humangenetik, Regensburg, 2011.

M Lorenz, J Zenner, M Klemm, M Luchi, M Eidens, S Prause, A Weise, J Eidens, T Schöndorf and A Pfützner. Development of a Macroarray DNA-Chip Platform for the Detection of a Disease Panel relevant in Nutrigenomics. Poster at 22. Jahrestagung der Deutschen Gesellschaft für Humangenetik, Regensburg, 2011.

S Prause, M Eidens, A Brauchler, J Eidens, E Pfützner, A Weise, M Klemm, A Pfützner, T Forst and M M Weber. Development of a CYP2D6 Macroarray Chip for pre-therapeutic Genetic Testing prior to a Tamoxifen Therapy. Poster at EuroEspes, Barcelona, 2010.

A Weise, N Thome, H Hänel, S Prause, M Eidens, T Forst and A Pfützner. Genotypisierung der Cytochrom P450 Isoenzyme bei Patienten mit Typ 2 Diabetes und Normalpersonen. Poster 1. Deutscher Diabetes Diagnostik Kongress, Köln, 2006.