Petra Seemann
Publications by Year
Research Areas
TGF-β signaling in diseases, Heterotopic Ossification and Related Conditions, Connective tissue disorders research, Congenital limb and hand anomalies, Medical Imaging and Pathology Studies
Most-Cited Works
- → Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1(2008)444 cited
- → Selenium Deficiency Is Associated with Mortality Risk from COVID-19(2020)359 cited
- → Mutations in PYCR1 cause cutis laxa with progeroid features(2009)252 cited
- → Somatic Mutation Profiles of MSI and MSS Colorectal Cancer Identified by Whole Exome Next Generation Sequencing and Bioinformatics Analysis(2010)241 cited
- → The fibrodysplasia ossificans progressiva R206H ACVR1 mutation activates BMP-independent chondrogenesis and zebrafish embryo ventralization(2009)219 cited
- → Activating and deactivating mutations in the receptor interaction site of GDF5 cause symphalangism or brachydactyly type A2(2005)213 cited
- → Prediction of survival odds in COVID-19 by zinc, age and selenoprotein P as composite biomarker(2020)176 cited
- → Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2(2003)165 cited
- → Duplications Involving a Conserved Regulatory Element Downstream of BMP2 Are Associated with Brachydactyly Type A2(2009)160 cited
- → Mutations in WNT7A Cause a Range of Limb Malformations, Including Fuhrmann Syndrome and Al-Awadi/Raas-Rothschild/Schinzel Phocomelia Syndrome(2006)158 cited