Petra Seemann - Concepedia

Author

Petra Seemann

Charité - Universitätsmedizin Berlin ORCID

Also Known As

Moroz, Y.S, P Seemann, P. Seemann, Petra Seemann

Publications

4.2K

Citations

H-Index

Concepts

All Affiliations

Charité - Universitätsmedizin Berlin Berlin-Brandenburger Centrum für Regenerative Therapien Max Planck Institute for Molecular Genetics Freie Universität Berlin Humboldt-Universität zu Berlin

About

Petra Seemann is an author at Charité - Universitätsmedizin Berlin specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	20	24	1.9K
2	Natural Sciences	4	4	358
3	Biochemistry	3	3	178
4	Engineering	2	2	62
5	Health Sciences	1	1	49

Petra Seemann

Publications

3.9K

Citations

H-Index

Page 1

	Year	Citations
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, Human Mutation	2008	436
Selenium Deficiency Is Associated with Mortality Risk from COVID-19 Arash Moghaddam, Raban Heller, Qian Sun, Nutrients	2020	358
Mutations in PYCR1 cause cutis laxa with progeroid features Bruno Reversade, Nathalie Escande‐Beillard, Aikaterini Dimopoulou, Nature Genetics BiologyPlant BiologyGeneticsPathogenesisPlant Pathology	2009	252
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, PLoS ONE	2010	240
The fibrodysplasia ossificans progressiva R206H ACVR1 mutation activates BMP-independent chondrogenesis and zebrafish embryo ventralization Qi Shen, Shawn C. Little, Meiqi Xu, Journal of Clinical Investigation	2009	219
Activating and deactivating mutations in the receptor interaction site of GDF5 cause symphalangism or brachydactyly type A2 Petra Seemann Journal of Clinical Investigation SclerostinGeneticsMolecular BiologyCellular PhysiologyGdf5 Receptor-binding Specificity	2005	213
Prediction of survival odds in COVID-19 by zinc, age and selenoprotein P as composite biomarker Raban Heller, Qian Sun, Julian Hackler, Redox Biology	2020	174
Mutations in <i>bone morphogenetic protein receptor 1B</i> cause brachydactyly type A2 Katarina Lehmann, Petra Seemann, Sigmar Stricker, Proceedings of the National Academy of Sciences	2003	164
Duplications Involving a Conserved Regulatory Element Downstream of BMP2 Are Associated with Brachydactyly Type A2 Katarina Dathe, Klaus Kjaer, Anja Brehm, The American Journal of Human Genetics Natural SciencesGeneticsBmp2 Are AssociatedMolecular BiologyGenomic Mechanism	2009	158
Mutations in WNT7A Cause a Range of Limb Malformations, Including Fuhrmann Syndrome and Al-Awadi/Raas-Rothschild/Schinzel Phocomelia Syndrome C. Geoffrey Woods, Sigmar Stricker, Petra Seemann, The American Journal of Human Genetics Developmental AnomalyDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics	2006	158

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