Astrid Mühl
Forschungsverbund Berlin(DE)
Publications by Year
Research Areas
Phosphodiesterase function and regulation, Hormonal Regulation and Hypertension, Blood Pressure and Hypertension Studies, Heart Failure Treatment and Management, Genetic Associations and Epidemiology
Most-Cited Works
- → PDE3A mutations cause autosomal dominant hypertension with brachydactyly(2015)170 cited
- → A Cholesterol-Lowering Gene Maps to Chromosome 13q(2000)94 cited
- → Phosphodiesterase 3A and Arterial Hypertension(2020)49 cited
- → Clinical Effects of Phosphodiesterase 3A Mutations in Inherited Hypertension With Brachydactyly(2015)40 cited
- Deletion at 12p in a Japanese child with brachydactyly overlaps the assigned locus of brachydactyly with hypertension in a Turkish family.(1997)
- → Autosomal-Dominant Hypertension With Type E Brachydactyly Is Caused by Rearrangement on the Short Arm of Chromosome 12(2004)35 cited
- → Abstract 054: Mutations In Pde3a Explain Mendelian Hypertension With Brachydactyly(2014)
- → Cell Painting Protocol to Characterize Morphological Profiles of Large Compound Collections Using the EU-OPENSCREEN Library(2026)