Concepedia

Katarina Lehmann

KL

13

Publications

1.3K

Citations

13

H-Index

1994

Active since

Affiliations

Charité - Universitätsmedizin Berlin(Current)

Max Planck Institute for Molecular Genetics

Heinrich Heine University Düsseldorf

Freie Universität Berlin

Max Planck Society

Katarina Lehmann is an author at Charité - Universitätsmedizin Berlin specializing in medicine, molecular biology, and genetics.

Top concepts

Publications per year

1994–2011

13

Publications

13

Expansion of the genotypic and phenotypic spectrum in patients with <i>KRAS</i> germline mutations

Martin Zenker, Katarina Lehmann, D. Hansmann et al. · Journal of Medical Genetics · 2006 · 201 citations · Full text

Mutations in <i>bone morphogenetic protein receptor 1B</i> cause brachydactyly type A2

Katarina Lehmann, Petra Seemann, Sigmar Stricker et al. · Proceedings of the National Academy of Sciences · 2003 · 164 citations · Full text

Raf plus TGFβ-dependent EMT is initiated by endocytosis and lysosomal degradation of E-cadherin

Elżbieta Janda, Maria T. Nevolo, Katarina Lehmann et al. · Oncogene · 2006 · 159 citations

, , +9

A New Subtype of Brachydactyly Type B Caused by Point Mutations in the Bone Morphogenetic Protein Antagonist NOGGIN

Katarina Lehmann, Petra Seemann, Timm O. Goecke et al. · The American Journal of Human Genetics · 2007 · 151 citations · Full text

, , +9

A microduplication of the long range SHH limb regulator (ZRS) is associated with triphalangeal thumb-polysyndactyly syndrome

Eva Klopocki, Claus‐Eric Ott, N Benatar et al. · Journal of Medical Genetics · 2008 · 120 citations

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