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Petra Seemann
Petra Seemann
Unknown affiliation
Verified email at nautilos.de
Title
Cited by
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
4912009
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
4312020
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
2842010
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
2782006
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
2752009
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
2672009
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
2542005
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
2022009
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
1992003
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
1882021
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
1472010
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
1312007
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
1232011
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
1222009
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
1212016
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
1082008
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
932005
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
832006
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
812009
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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