Kerstin Kutsche
Universität Hamburg(DE)University Medical Center Hamburg-Eppendorf(DE)German Centre for Cardiovascular Research(DE)
Publications by Year
Research Areas
Connective tissue disorders research, Genetics and Neurodevelopmental Disorders, Protein Tyrosine Phosphatases, Galectins and Cancer Biology, Aortic Disease and Treatment Approaches
Most-Cited Works
- → Disruption of Neurexin 1 Associated with Autism Spectrum Disorder(2008)580 cited
- → Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes(2010)506 cited
- → Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D(2001)494 cited
- → Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair(2009)413 cited
- → Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardation(2000)372 cited
- → A restricted spectrum of NRAS mutations causes Noonan syndrome(2009)315 cited