Kamini Kalidas
Guy's Hospital(GB)St George's, University of London(GB)King's College London(GB)Guy's and St Thomas' NHS Foundation Trust(GB)Hubrecht Institute for Developmental Biology and Stem Cell Research(NL)
Publications by Year
Research Areas
Protein Tyrosine Phosphatases, RNA modifications and cancer, Galectins and Cancer Biology, Lymphatic System and Diseases, Adipokines, Inflammation, and Metabolic Diseases
Most-Cited Works
- → Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome(2001)1,728 cited
- → PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity(2002)787 cited
- → The natural history of Noonan syndrome: a long-term follow-up study(2006)285 cited
- → Mutation in Vascular Endothelial Growth Factor-C, a Ligand for Vascular Endothelial Growth Factor Receptor-3, Is Associated With Autosomal Dominant Milroy-Like Primary Lymphedema(2013)167 cited
- → Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype(2011)116 cited
- → Paternal Germline Origin and Sex-Ratio Distortion in Transmission of PTPN11 Mutations in Noonan Syndrome(2004)101 cited