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Methods in Molecular Biology (Clifton, N.J.)|May 3, 2018
Quantitation of JAK2 V617F Allele Burden by Using the QuantStudio™ 3D Digital PCR SystemElena Kinz, Axel Muendlein
Molecular and Cellular Endocrinology|November 27, 2013
Hypoxia induces a HIF-1α dependent signaling cascade to make a complex metabolic switch in SGBS-adipocytesAndreas Leiherer, Kathrin Geiger, Axel Muendlein, et al.
International Journal of Molecular Sciences|September 27, 2025
Persistent Hypercalcemia Despite Parathyroidectomy for Primary Hyperparathyroidism in an Adult with Nephrocalcinosis and Nephrolithiasis Caused by a Novel Combination of Two Pathogenic CYP24A1 MutationsSijun Zhang, Axel Muendlein, Edgar Meusburger, et al.
Frontiers in Genetics|June 14, 2019
Unrecognized High Occurrence of Genetically Confirmed Hereditary Carnitine Palmitoyltransferase II Deficiency in an Austrian Family Points to the Ongoing Underdiagnosis of the DiseaseChristina Zach, Karl Unterkofler, Peter Fraunberger, et al.
Scientific Reports|September 8, 2019
Serotonin is elevated in risk-genotype carriers of TCF7L2 - rs7903146Andreas Leiherer, Axel Muendlein, Christoph H Saely, et al.
Atherosclerosis|April 3, 2010
Serial decline of kidney function as a novel biomarker for the progression of atherothrombotic diseasePhilipp Rein, Christoph H Saely, Axel Muendlein, et al.
HLA|November 22, 2019
Real-time PCR based HLA-B*27 screening directly in whole bloodKathrin Geiger, Christina Zach, Andreas Leiherer, et al.
American Journal of Physiology. Renal Physiology|December 10, 2019
Evaluation of the associations between circulating microRNAs and kidney function in coronary angiography patientsAxel Muendlein, Kathrin Geiger, Andreas Leiherer, et al.
European Heart Journal Open|January 31, 2024
Ceramides improve cardiovascular risk prediction beyond low-density lipoprotein cholesterolAndreas Leiherer, Axel Muendlein, Christoph H Saely, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 16, 2018
Direct blood PCR: TaqMan-probe based detection of the venous thromboembolism associated mutations factor V Leiden and prothrombin c.20210G>A without DNA extractionKathrin Geiger, Andreas Leiherer, Eva-Maria Brandtner, et al.
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