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Petra Seemann
Petra Seemann
Unknown affiliation
Verified email at nautilos.de
Title
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Cited by
Year
Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1
FS Kaplan, M Xu, P Seemann, JM Connor, DL Glaser, L Carroll, P Delai, ...
Human mutation 30 (3), 379-390, 2009
4762009
Selenium deficiency is associated with mortality risk from COVID-19
A Moghaddam, RA Heller, Q Sun, J Seelig, A Cherkezov, L Seibert, ...
Nutrients 12 (7), 2098, 2020
4042020
Somatic mutation profiles of MSI and MSS colorectal cancer identified by whole exome next generation sequencing and bioinformatics analysis
B Timmermann, M Kerick, C Roehr, A Fischer, M Isau, ST Boerno, ...
PloS one 5 (12), e15661, 2010
2782010
Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome
CG Woods, S Stricker, P Seemann, R Stern, J Cox, E Sherridan, ...
The American Journal of Human Genetics 79 (2), 402-408, 2006
2762006
Mutations in PYCR1 cause cutis laxa with progeroid features
B Reversade, N Escande-Beillard, A Dimopoulou, B Fischer, SC Chng, ...
Nature genetics 41 (9), 1016-1021, 2009
2632009
The fibrodysplasia ossificans progressiva R206H ACVR1 mutation activates BMP-independent chondrogenesis and zebrafish embryo ventralization
Q Shen, SC Little, M Xu, J Haupt, C Ast, T Katagiri, S Mundlos, ...
The Journal of clinical investigation 119 (11), 3462-3472, 2009
2612009
Activating and deactivating mutations in the receptor interaction site of GDF5 cause symphalangism or brachydactyly type A2
P Seemann, R Schwappacher, KW Kjaer, D Krakow, K Lehmann, ...
The Journal of clinical investigation 115 (9), 2373-2381, 2005
2512005
Duplications involving a conserved regulatory element downstream of BMP2 are associated with brachydactyly type A2
K Dathe, KW Kjaer, A Brehm, P Meinecke, P Nürnberg, JC Neto, ...
The American Journal of Human Genetics 84 (4), 483-492, 2009
1972009
Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2
K Lehmann, P Seemann, S Stricker, M Sammar, B Meyer, K Süring, ...
Proceedings of the National Academy of Sciences 100 (21), 12277-12282, 2003
1952003
Prediction of survival odds in COVID-19 by zinc, age and selenoprotein P as composite biomarker
RA Heller, Q Sun, J Hackler, J Seelig, L Seibert, A Cherkezov, WB Minich, ...
Redox biology 38, 101764, 2021
1822021
Deletion and point mutations of PTHLH cause brachydactyly type E
E Klopocki, BP Hennig, K Dathe, R Koll, T de Ravel, E Baten, E Blom, ...
The American Journal of Human Genetics 86 (3), 434-439, 2010
1432010
A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGIN
K Lehmann, P Seemann, F Silan, TO Goecke, S Irgang, KW Kjaer, ...
The American Journal of Human Genetics 81 (2), 388-396, 2007
1292007
Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis
E Klopocki, S Lohan, F Brancati, R Koll, A Brehm, P Seemann, K Dathe, ...
The American Journal of Human Genetics 88 (1), 70-75, 2011
1222011
Mutations in GDF5 reveal a key residue mediating BMP inhibition by NOGGIN
P Seemann, A Brehm, J König, C Reissner, S Stricker, P Kuss, J Haupt, ...
PLoS genetics 5 (11), e1000747, 2009
1202009
BMPs in bone regeneration: Less is more effective, a paradigm-shift
K Schmidt-Bleek, BM Willie, P Schwabe, P Seemann, GN Duda
Cytokine & growth factor reviews 27, 141-148, 2016
1182016
Skeletal metamorphosis in fibrodysplasia ossificans progressiva (FOP)
FS Kaplan, Q Shen, V Lounev, P Seemann, J Groppe, T Katagiri, ...
Journal of bone and mineral metabolism 26, 521-530, 2008
1032008
An inversion involving the mouse Shh locus results in brachydactyly through dysregulation of Shh expression
M Niedermaier, GC Schwabe, S Fees, A Helmrich, N Brieske, P Seemann, ...
The Journal of clinical investigation 115 (4), 900-909, 2005
912005
A novel R486Q mutation in BMPR1B resulting in either a brachydactyly type C/symphalangism-like phenotype or brachydactyly type A2
K Lehmann, P Seemann, J Boergermann, G Morin, S Reif, P Knaus, ...
European Journal of Human Genetics 14 (12), 1248-1254, 2006
812006
Mutant Hoxd13 induces extra digits in a mouse model of synpolydactyly directly and by decreasing retinoic acid synthesis
P Kuss, P Villavicencio-Lorini, F Witte, J Klose, AN Albrecht, P Seemann, ...
The Journal of clinical investigation 119 (1), 146-156, 2009
802009
Brachydactyly type A2 associated with a defect in proGDF5 processing
F Plöger, P Seemann, M Schmidt-von Kegler, K Lehmann, J Seidel, ...
Human molecular genetics 17 (9), 1222-1233, 2008
772008
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