Jörg Schröder

<scp>DFNB16</scp> is a frequent cause of congenital hearing impairment: implementation of <i><scp>STRC</scp></i> mutation analysis in routine diagnostics

Barbara Vona, Michaela A. H. Hofrichter, Cordula Neuner et al. · Clinical Genetics · 2013 · 110 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Targeted next-generation sequencing of deafness genes in hearing-impaired individuals uncovers informative mutations

Barbara Vona, Tobias Müller, Indrajit Nanda et al. · Genetics in Medicine · 2014 · 106 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Analysis of Procedural Effects of Percutaneous Edge-to-Edge Mitral Valve Repair by 2D and 3D Echocardiography

Ertunc Altiok, Sandra Hamada, Kathrin Brehmer et al. · Circulation Cardiovascular Imaging · 2012 · 106 citations

Medicine, Cardiology, Surgery +17

Structure-Based Design and Synthesis of Potent Matrix Metalloproteinase Inhibitors Derived from a 6<i>H</i>-1,3,4-Thiadiazine Scaffold

Jörg Schröder, Andreas Henke, H. Wenzel et al. · Journal of Medicinal Chemistry · 2001 · 87 citations · Full text

Pharmacy, Medicinal Chemistry, Pharmacology +17

Acetylcholine as an age-dependent non-neuronal source in the heart

Obaida R. Rana, Patrick Schauerte, Rahel Kluttig et al. · Autonomic Neuroscience · 2010 · 87 citations

Life Sciences, Cardiology, Physiology +12