Katarina Lehmann - Concepedia

Author

Katarina Lehmann

Charité - Universitätsmedizin Berlin

Also Known As

K A Lehmann, K Lehmann, K. Lehmann, Katarina Lehmann, Lehmann, K.

Publications

1.4K

Citations

H-Index

Concepts

All Affiliations

Charité - Universitätsmedizin Berlin Max Planck Institute for Molecular Genetics Heinrich Heine University Düsseldorf Freie Universität Berlin Max Planck Society

About

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

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	627
2	Natural Sciences	4	4	272
3	Biochemistry	1	1	68
4	Biology	1	1	71
5	Biomolecular Engineering	1	1	15

Katarina Lehmann

Publications

1.3K

Citations

H-Index

Page 1

	Year	Citations
Expansion of the genotypic and phenotypic spectrum in patients with <i>KRAS</i> germline mutations Martin Zenker, Katarina Lehmann, D. Hansmann, Journal of Medical Genetics	2006	201
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
Raf plus TGFβ-dependent EMT is initiated by endocytosis and lysosomal degradation of E-cadherin Elżbieta Janda, Maria T. Nevolo, Katarina Lehmann, Oncogene Developmental BiologySignal TransductionSignaling PathwayReceptor Tyrosine KinaseEndocytic Pathway	2006	159
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, The American Journal of Human Genetics SclerostinDevelopmental BiologyNew SubtypePoint MutationsBone Morphogenic Protein	2007	151
A microduplication of the long range SHH limb regulator (ZRS) is associated with triphalangeal thumb-polysyndactyly syndrome Eva Klopocki, Claus‐Eric Ott, N Benatar, Journal of Medical Genetics	2008	120
A new orphan member of the nuclear hormone receptor superfamily closely related to Rev-Erb. Bernard Dumas, Heather P. Harding, Hueng-Sik Choi, Molecular Endocrinology GeneticsMolecular BiologyBd73 Messenger RnaTranscriptional RegulationReceptor Tyrosine Kinase	1994	118
CD73 and CD29 concurrently mediate the mechanically induced decrease of migratory capacity of mesenchymal stromal cells A Ode, J Kopf, Armin Kurtz, European Cells and Materials	2011	106
A novel R486Q mutation in BMPR1B resulting in either a brachydactyly type C/symphalangism-like phenotype or brachydactyly type A2 Katarina Lehmann, Petra Seemann, Jan H. Boergermann, European Journal of Human Genetics BiologyGenetic DisorderNatural SciencesGeneticsMolecular Biology	2006	71
Brachydactyly type A2 associated with a defect in proGDF5 processing Frank Plöger, Petra Seemann, Mareen Schmidt‐von Kegler, Human Molecular Genetics Gdf5 PrecursorProtein ExpressionBiochemistryNatural SciencesGenetics	2008	68
Polyalanine expansion in HOXA13: three new affected families and the molecular consequences in a mouse model Jeffrey W. Innis, Douglas P. Mortlock, Zhi Chen, Human Molecular Genetics Knockout MouseMolecular PharmacologyMutant Limb BudsDevelopmental BiologyGenetic Disorder	2004	45

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