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Metabolic Syndrome and Related Disorders|November 11, 2009
Association of the PPARGC1A gene polymorphism with diabetic nephropathy in an Asian Indian population (CURES-41)Sakthi Baby Gayathri, Venkatesan Radha, Karani S Vimaleswaran, et al.
Gene|September 24, 2013
Genetic association of ADIPOQ gene variants with type 2 diabetes, obesity and serum adiponectin levels in south Indian populationKandaswamy Ramya, Kuppuswamy Ashok Ayyappa, Saurabh Ghosh, et al.
Diabetes Technology & Therapeutics|December 24, 2010
Genetic variations in the FTO gene are associated with type 2 diabetes and obesity in south Indians (CURES-79)Kandaswamy Ramya, Venkatesan Radha, Saurabh Ghosh, et al.
Pediatric Diabetes|October 31, 2013
EIF2AK3 mutations in South Indian children with permanent neonatal diabetes mellitus associated with Wolcott-Rallison syndromeSuresh Jahnavi, Varadarajan Poovazhagi, Sekar Kanthimathi, et al.
Indian Pediatrics|March 19, 2013
Clinical profile and outcome of infantile onset diabetes mellitus in southern IndiaPoovazhagi Varadarajan, Thangavelu Sangaralingam, Senthil Senniappan, et al.
Pediatric Diabetes|March 13, 2019
Functional characterization of activating mutations in the sulfonylurea receptor 1 (ABCC8) causing neonatal diabetes mellitus in Asian Indian childrenKandasamy Balamurugan, Babu Kavitha, Zhongying Yang, et al.
Annals of Human Genetics|June 28, 2016
Hexokinase Domain Containing 1 (HKDC1) Gene Variants and their Association with Gestational Diabetes Mellitus in a South Indian PopulationSekar Kanthimathi, Samuel Liju, Dhandapani Laasya, et al.
Annals of Human Genetics|December 3, 2014
Identification and molecular characterization of HNF1B gene mutations in Indian diabetic patients with renal abnormalitiesSekar Kanthimathi, Kandasamy Balamurugan, Viswanathan Mohan, et al.
Diabetes Care|September 28, 2005
A prevalent amino acid polymorphism at codon 98 (Ala98Val) of the hepatocyte nuclear factor-1alpha is associated with maturity-onset diabetes of the young and younger age at onset of type 2 diabetes in Asian IndiansShekher Anuradha, Venkatesan Radha, Raj Deepa, et al.
Acta Diabetologica|October 11, 2023
A novel stop-loss mutation in NKX2-2 gene as a cause of neonatal diabetes mellitus: molecular characterization and structural analysisBabu Kavitha, Kandi Srikanth, Deepshikha Singh, et al.
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