| Distribution of miRNA expression across human tissues N Ludwig, P Leidinger, K Becker, C Backes, T Fehlmann, C Pallasch, ... Nucleic acids research 44 (8), 3865-3877, 2016 | 1047 | 2016 |
| Atlas of the clinical genetics of human dilated cardiomyopathy J Haas, KS Frese, B Peil, W Kloos, A Keller, R Nietsch, Z Feng, S Müller, ... European heart journal 36 (18), 1123-1135, 2015 | 606 | 2015 |
| New insights into the Tyrolean Iceman's origin and phenotype as inferred by whole-genome sequencing A Keller, A Graefen, M Ball, M Matzas, V Boisguerin, F Maixner, ... Nature communications 3 (1), 698, 2012 | 586 | 2012 |
| A blood based 12-miRNA signature of Alzheimer disease patients P Leidinger, C Backes, S Deutscher, K Schmitt, SC Mueller, K Frese, ... Genome biology 14, 1-16, 2013 | 552 | 2013 |
| Non-coding RNAs in cardiovascular diseases: diagnostic and therapeutic perspectives W Poller, S Dimmeler, S Heymans, T Zeller, J Haas, M Karakas, ... European heart journal 39 (29), 2704-2716, 2018 | 417 | 2018 |
| Toward the blood-borne miRNome of human diseases A Keller, P Leidinger, A Bauer, A ElSharawy, J Haas, C Backes, ... Nature methods 8 (10), 841-843, 2011 | 397 | 2011 |
| MicroRNA signatures in total peripheral blood as novel biomarkers for acute myocardial infarction B Meder, A Keller, B Vogel, J Haas, F Sedaghat-Hamedani, ... Basic research in cardiology 106, 13-23, 2011 | 346 | 2011 |
| Assessment of myocardial deformation with cardiac magnetic resonance strain imaging improves risk stratification in patients with dilated cardiomyopathy SJ Buss, K Breuninger, S Lehrke, A Voss, C Galuschky, D Lossnitzer, ... European Heart Journal-Cardiovascular Imaging 16 (3), 307-315, 2015 | 305 | 2015 |
| Alterations in cardiac DNA methylation in human dilated cardiomyopathy J Haas, KS Frese, YJ Park, A Keller, B Vogel, AM Lindroth, D Weichenhan, ... EMBO molecular medicine 5 (3), 413-429, 2013 | 254 | 2013 |
| Clinical genetics and outcome of left ventricular non-compaction cardiomyopathy F Sedaghat-Hamedani, J Haas, F Zhu, C Geier, E Kayvanpour, M Liss, ... European heart journal 38 (46), 3449-3460, 2017 | 240 | 2017 |
| Genotype-phenotype associations in dilated cardiomyopathy: meta-analysis on more than 8000 individuals E Kayvanpour, F Sedaghat-Hamedani, A Amr, A Lai, J Haas, DB Holzer, ... Clinical Research in Cardiology 106, 127-139, 2017 | 232 | 2017 |
| Arteriogenesis depends on circulating monocytes and macrophage accumulation and is severely depressed in op/op mice CE Bergmann, IE Hoefer, B Meder, H Roth, N van Royen, SM Breit, ... Journal of leukocyte biology 80 (1), 59-65, 2006 | 222 | 2006 |
| Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect R Tadros, C Francis, X Xu, AMC Vermeer, AR Harper, R Huurman, ... Nature genetics 53 (2), 128-134, 2021 | 220 | 2021 |
| Targeted next-generation sequencing for the molecular genetic diagnostics of cardiomyopathies B Meder, J Haas, A Keller, C Heid, S Just, A Borries, V Boisguerin, ... Circulation: Cardiovascular Genetics 4 (2), 110-122, 2011 | 212 | 2011 |
| Nexilin mutations destabilize cardiac Z-disks and lead to dilated cardiomyopathy D Hassel, T Dahme, J Erdmann, B Meder, A Huge, M Stoll, S Just, A Hess, ... Nature medicine 15 (11), 1281-1288, 2009 | 209 | 2009 |
| Mavacamten favorably impacts cardiac structure in obstructive hypertrophic cardiomyopathy: EXPLORER-HCM cardiac magnetic resonance substudy analysis S Saberi, N Cardim, M Yamani, J Schulz-Menger, W Li, V Florea, ... Circulation 143 (6), 606-608, 2021 | 182 | 2021 |
| Epigenome-wide association study identifies cardiac gene patterning and a novel class of biomarkers for heart failure B Meder, J Haas, F Sedaghat-Hamedani, E Kayvanpour, K Frese, A Lai, ... Circulation 136 (16), 1528-1544, 2017 | 179 | 2017 |
| A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy B Meder, F Rühle, T Weis, G Homuth, A Keller, J Franke, B Peil, ... European heart journal 35 (16), 1069-1077, 2014 | 177 | 2014 |
| The symptom complex of familial sinus node dysfunction and myocardial noncompaction is associated with mutations in the HCN4 channel PA Schweizer, J Schröter, S Greiner, J Haas, P Yampolsky, D Mereles, ... Journal of the American College of Cardiology 64 (8), 757-767, 2014 | 159 | 2014 |
| Catecholamine-dependent β-adrenergic signaling in a pluripotent stem cell model of takotsubo cardiomyopathy T Borchert, D Hübscher, CI Guessoum, TDD Lam, JR Ghadri, ... Journal of the American College of Cardiology 70 (8), 975-991, 2017 | 158 | 2017 |
