Kamini Kalidas - Concepedia

Author

Kamini Kalidas

St George's, University of London

Also Known As

E Prappa, K Kalidas, K. Kalidas, Kamini Kalidas

Publications

3.9K

Citations

H-Index

Concepts

All Affiliations

St George's, University of London St George's Hospital Guy's Hospital Istituto Superiore di Sanità Icahn School of Medicine at Mount Sinai

About

Kamini Kalidas is an author at St George's, University of London specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	2.9K
2	Health Sciences	2	2	44
3	Public Health	2	2	112
4	Diabetes	2	2	44
5	Biochemistry	1	1	12

Kamini Kalidas

Publications

3.8K

Citations

H-Index

Page 1

	Year	Citations
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome Marco Tartaglia, Ernest L. Mehler, Rosalie Goldberg, Nature Genetics Molecular PhysiologySignal TransductionGenetic DisorderReceptor Tyrosine KinaseGenetics	2001	1.7K
PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity Marco Tartaglia, Kamini Kalidas, Adam Shaw, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderMedicineGeneticsPathology	2002	783
The natural history of Noonan syndrome: a long-term follow-up study Adam Shaw, Kamini Kalidas, Andrew H. Crosby, Archives of Disease in Childhood	2006	285
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, Circulation Research	2013	167
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, Journal of Medical Genetics	2011	116
Paternal Germline Origin and Sex-Ratio Distortion in Transmission of PTPN11 Mutations in Noonan Syndrome Marco Tartaglia, Viviana Cordeddu, Hong Chang, The American Journal of Human Genetics Genetic DisorderMedicineGeneticsPathologyPaternal Germline Origin	2004	100
Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia Fiona Connell, Kamini Kalidas, Pia Østergaard, Human Genetics Genetic DisorderImmune Cell DevelopmentGeneticsSequence AnalysisPathology	2009	98
Homozygous Mutation of Desmocollin-2 in Arrhythmogenic Right Ventricular Cardiomyopathy with Mild Palmoplantar Keratoderma and Woolly Hair Michael A. Simpson, Sarah Mansour, Dana Ahnood, Cardiology	2008	97
Association of interleukin-6 -174G/C promoter polymorphism with hypertension and left ventricular hypertrophy in dialysis patients Attilio Losito, Kamini Kalidas, Stefania Santoni, Kidney International HypertensionUrologyHemodialysisHeart FailureCardiovascular Disease	2003	84
Emberger syndrome—Primary lymphedema with myelodysplasia: Report of seven new cases Sahar Mansour, Fiona Connell, Colin G. Steward, American Journal of Medical Genetics Part A	2010	82

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