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Katarina Lehmann

Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations
2006 · Martin Zenker, Katarina Lehmann, et al. · Journal of Medical Genetics · 202
Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2
2003 · Katarina Lehmann, Petra Seemann, et al. · Proceedings of the National Academy of Sciences · 166
A New Subtype of Brachydactyly Type B Caused by Point Mutations in the Bone Morphogenetic Protein Antagonist NOGGIN
2007 · K. Lehmann, P. Seemann, et al. · The American Journal of Human Genetics · 129
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A microduplication of the long range SHH limb regulator (ZRS) is associated with triphalangeal thumb-polysyndactyly syndrome
2008 · E Klopocki, C-E Ott, et al. · Journal of Medical Genetics · 119
Ring chromosome 6 in three fetuses: Case reports, literature review, and implications for prenatal diagnosis
2002 · Maik Urban, Christiane Bommer, et al. · American Journal of Medical Genetics · 84
A novel R486Q mutation in BMPR1B resulting in either a brachydactyly type C/symphalangism-like phenotype or brachydactyly type A2
2006 · Katarina Lehmann, Petra Seemann, et al. · European Journal of Human Genetics · 73
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Brachydactyly type A2 associated with a defect in proGDF5 processing
2008 · Frank Plöger, Petra Seemann, et al. · Human Molecular Genetics · 68
Antenatal onset of cortical hyperostosis (Caffey disease): Case report and review
2003 · Susann Schweiger, Rabih Chaoui, et al. · American Journal of Medical Genetics Part A · 57
Polyalanine expansion in HOXA13: three new affected families and the molecular consequences in a mouse model
2004 · Jeffrey W. Innis, Douglas Mortlock, et al. · Human Molecular Genetics · 48
Catel–Manzke syndrome: Two new patients and a critical review of the literature
2008 · Hermann Manzke, Katarina Lehmann, et al. · European Journal of Medical Genetics · 32
Compound heterozygosity for GDF5 in Du Pan type chondrodysplasia
2008 · Sofia Douzgou, Katarina Lehmann, et al. · American Journal of Medical Genetics Part A · 25
Prenatal diagnosis of partial agenesis of the corpus callosum in a fetus with thanatophoric dysplasia type 2
2002 · Karim D. Kalache, Katarina Lehmann, et al. · Prenatal Diagnosis · 13
Alterations of BMP signaling pathway(s) in skeletal diseases
2008 · Petra Seemann, Stefan Mundlos, et al. · Birkhäuser Basel eBooks · 7
An unusual combination of EEC syndrome and hypomelanosis Ito due to a p63 mutation
2005 · Katarina Lehmann, Stefan Mundlos, et al. · European Journal of Pediatrics · 4
[Partial monosomy 21 or fetal alcohol embryopathy in a retarded boy?].
1993 · J Müller, G Cobet, et al. · PubMed · 3
Works count: 18
Citation count: 1,030
H-index: 12
I10-index: 12
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