| 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 | 580 | 2012 |
| 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 | 565 | 2015 |
| 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 | 524 | 2013 |
| 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 | 392 | 2011 |
| 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 | 384 | 2018 |
| 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 | 338 | 2011 |
| 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 | 236 | 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 | 220 | 2017 |
| 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 | 208 | 2011 |
| 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 | 206 | 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 | 167 | 2014 |
| 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 | 166 | 2017 |
| 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 | 155 | 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 | 146 | 2017 |
| Clinical outcomes associated with sarcomere mutations in hypertrophic cardiomyopathy: a meta-analysis on 7675 individuals F Sedaghat-Hamedani, E Kayvanpour, OF Tugrul, A Lai, A Amr, J Haas, ... Clinical Research in Cardiology 107, 30-41, 2018 | 126 | 2018 |
| Physicians' guideline adherence is associated with long‐term heart failure mortality in outpatients with heart failure with reduced ejection fraction: the QUALIFY international … M Komajda, J Schöpe, S Wagenpfeil, L Tavazzi, M Böhm, P Ponikowski, ... European Journal of Heart Failure 21 (7), 921-929, 2019 | 112 | 2019 |
| Immune system-mediated atherosclerosis caused by deficiency of long non-coding RNA MALAT1 in ApoE−/−mice M Gast, BH Rauch, S Nakagawa, A Haghikia, A Jasina, J Haas, N Nath, ... Cardiovascular research 115 (2), 302-314, 2019 | 103 | 2019 |
| Long noncoding RNA NEAT1 modulates immune cell functions and is suppressed in early onset myocardial infarction patients M Gast, BH Rauch, A Haghikia, S Nakagawa, J Haas, A Stroux, D Schmidt, ... Cardiovascular research 115 (13), 1886-1906, 2019 | 98 | 2019 |
| Severe DCM phenotype of patient harboring RBM20 mutation S635A can be modeled by patient-specific induced pluripotent stem cell-derived cardiomyocytes K Streckfuss-Bömeke, M Tiburcy, A Fomin, X Luo, W Li, C Fischer, ... Journal of molecular and cellular cardiology 113, 9-21, 2017 | 97 | 2017 |
| Influence of the confounding factors age and sex on microRNA profiles from peripheral blood B Meder, C Backes, J Haas, P Leidinger, C Stähler, T Großmann, B Vogel, ... Clinical chemistry 60 (9), 1200-1208, 2014 | 97 | 2014 |
