Kamini Kalidas

Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

Marco Tartaglia, Ernest L. Mehler, Rosalie Goldberg et al. · Nature Genetics · 2001 · 1.7K citations

Molecular Physiology, Signal Transduction, Genetic Disorder +8

PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity

Marco Tartaglia, Kamini Kalidas, Adam Shaw et al. · The American Journal of Human Genetics · 2002 · 783 citations · Full text

Mendelian Disorder, Genetic Disorder, Medicine +6

The natural history of Noonan syndrome: a long-term follow-up study

Adam Shaw, Kamini Kalidas, Andrew H. Crosby et al. · Archives of Disease in Childhood · 2006 · 285 citations · Full text

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

Kristiana Gordon, Dörte Schulte, Glen Brice et al. · Circulation Research · 2013 · 167 citations · Full text

Rapid identification of mutations in <i>GJC2</i> in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype

Pia Østergaard, Michael A. Simpson, Glen Brice et al. · Journal of Medical Genetics · 2011 · 116 citations · Full text