| Clinical sequencing: from raw data to diagnosis with lifetime value SM Caspar, N Dubacher, AM Kopps, J Meienberg, C Henggeler, ... Clinical genetics 93 (3), 508-519, 2018 | 99 | 2018 |
| Celiprolol but not losartan improves the biomechanical integrity of the aorta in a mouse model of vascular Ehlers–Danlos syndrome N Dubacher, J Münger, MC Gorosabel, J Crabb, AA Ksiazek, SM Caspar, ... Cardiovascular research 116 (2), 457-465, 2020 | 26 | 2020 |
| Need for speed in accurate whole-genome data analysis: GENALICE MAP challenges BWA/GATK more than PEMapper/PECaller and Isaac M Plüss, AM Kopps, I Keller, J Meienberg, SM Caspar, N Dubacher, ... Proceedings of the National Academy of Sciences 114 (40), E8320-E8322, 2017 | 23 | 2017 |
| Vascular Ehlers–Danlos syndrome: can the beneficial effect of celiprolol be extrapolated to bisoprolol? MC Gorosabel, N Dubacher, J Meienberg, G Matyas European Heart Journal-Cardiovascular Pharmacotherapy 6 (3), 199-200, 2020 | 6 | 2020 |
| More genes for thoracic aortic aneurysms and dissections SM Caspar, N Dubacher, G Matyas Journal of the American College of Cardiology 73 (4), 528-529, 2019 | 5 | 2019 |
| Novel Insights into the Aortic Mechanical Properties of Mice Modeling Hereditary Aortic Diseases N Dubacher, K Sugiyama, JD Smith, V Nussbaumer, M Csonka, ... bioRxiv, 2023.08. 15.553452, 2023 | | 2023 |
| New uses for old drugs: Added value of celiprolol and pravastatin in vascular EDS N Dubacher, SM Caspar, J Meienberg, G Matyas EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 74-75, 2022 | | 2022 |
| Molecular Aetiology and Therapeutic Approaches of Rare Aortic Diseases in Mouse Models NM Dubacher ETH Zurich, 2022 | | 2022 |
| Medical therapy of vascular Ehlers-Danlos syndrome: Challenging the paradigm of interchangeable antihypertensive drugs N Dubacher, SM Caspar, J Meienberg, G Matyas EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 764-765, 2020 | | 2020 |
| Novel approach reveals celiprolol but not losartan as medical therapy for vascular Ehlers-Danlos syndrome N Dubacher, J Munger, MC Gorosabel, J Crabb, AA Ksiazek, SM Caspar, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1304-1304, 2019 | | 2019 |
| High-throughput sequencing of Mendelian disorders: From raw data to diagnosis with lifetime value J Meienberg, AM Kopps, M Pluss, SM Caspar, N Dubacher, G Matyas EUROPEAN JOURNAL OF HUMAN GENETICS 27, 538-538, 2019 | | 2019 |
