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Molecular and Cellular Probes|September 15, 2011
Next-generation sequencing entering the clinical arenaJan Haas, Hugo A Katus, Benjamin MederPersonalized Medicine|May 16, 2018
Targeted next-generation sequencing: the clinician's stethoscope for genetic disordersJan Haas, Ioana Barb, Hugo A Katus, et al.Current Heart Failure Reports|August 3, 2015
Determined to Fail--the Role of Genetic Mechanisms in Heart FailureElham Kayvanpour, Hugo A Katus, Benjamin MederBriefings in Bioinformatics|February 2, 2015
Pathogenicity prediction of non-synonymous single nucleotide variants in dilated cardiomyopathySabine C Mueller, Christina Backes, Jan Haas, et al.Genes & Development|December 6, 2008
Right into the heart of microRNA-133aBenjamin Meder, Hugo A Katus, Wolfgang RottbauerBiology|May 17, 2014
Next-generation sequencing: from understanding biology to personalized medicineKaren S Frese, Hugo A Katus, Benjamin MederPlos One|August 18, 2022
Multi-omics assessment of dilated cardiomyopathy using non-negative matrix factorizationRewati Tappu, Jan Haas, David H Lehmann, et al.Biochemical and Biophysical Research Communications|April 2, 2019
ANK2 functionally interacts with KCNH2 aggravating long QT syndrome in a double mutation carrierGuido Gessner, Sarah Runge, Michael Koenen, et al.Clinical Research in Cardiology : Official Journal of the German Cardiac Society|October 4, 2023
Improving sudden cardiac death risk stratification in hypertrophic cardiomyopathy using established clinical variables and genetic informationAli Amr, Jan Koelemen, Christoph Reich, et al.Clinical Research in Cardiology : Official Journal of the German Cardiac Society|August 26, 2017
Clinical outcomes associated with sarcomere mutations in hypertrophic cardiomyopathy: a meta-analysis on 7675 individualsFarbod Sedaghat-Hamedani, Elham Kayvanpour, Oguz Firat Tugrul, et al.Pageof 125