Petra Seemann

Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1

Frederick S. Kaplan, Meiqi Xu, Petra Seemann et al. · Human Mutation · 2008 · 436 citations

Selenium Deficiency Is Associated with Mortality Risk from COVID-19

Arash Moghaddam, Raban Heller, Qian Sun et al. · Nutrients · 2020 · 358 citations · Full text

Mutations in PYCR1 cause cutis laxa with progeroid features

Bruno Reversade, Nathalie Escande‐Beillard, Aikaterini Dimopoulou et al. · Nature Genetics · 2009 · 252 citations

Biology, Plant Biology, Genetics +5

Somatic Mutation Profiles of MSI and MSS Colorectal Cancer Identified by Whole Exome Next Generation Sequencing and Bioinformatics Analysis

Bernd Timmermann, Martin Kerick, Christina Roehr et al. · PLoS ONE · 2010 · 240 citations · Full text

The fibrodysplasia ossificans progressiva R206H ACVR1 mutation activates BMP-independent chondrogenesis and zebrafish embryo ventralization

Qi Shen, Shawn C. Little, Meiqi Xu et al. · Journal of Clinical Investigation · 2009 · 219 citations · Full text