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Benjamin Meder
Benjamin Meder
W3 Professor for Precision Digital Health, University of Heidelberg
Geverifieerd e-mailadres voor benegfx.de - Homepage
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Jaar
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
9392016
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
5742012
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
5402015
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 (7), 1-16, 2013
5102013
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
3882011
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
3582018
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
3342011
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
2672015
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
2322013
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
2162006
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
2022011
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
1992017
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
1992009
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
1892017
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
1602014
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
1592017
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
1442021
Comprehensive analysis of microRNA profiles in multiple sclerosis including next-generation sequencing
A Keller, P Leidinger, F Steinmeyer, C Stähler, A Franke, ...
Multiple Sclerosis Journal 20 (3), 295-303, 2014
1442014
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
1422014
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
1412017
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Artikelen 1–20