1. Association of rs11643718 SLC12A3 and rs741301 ELMO1 Variants with Diabetic Nephropathy in South Indian Population. (4th October 2016) Authors: Bodhini, Dhanasekaran; Chidambaram, Manickam; Liju, Samuel; Revathi, Balakannan; Laasya, Dhandapani; Sathish, Natarajan; Kanthimathi, Sekar; Ghosh, Saurabh; Anjana, Ranjit Mohan; Mohan, Viswanathan; Radha, Venkatesan Journal: Annals of human genetics Issue: Volume 80:Number 6(2016:Nov.) Page Start: 336 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. EIF2AK3 mutations in South Indian children with permanent neonatal diabetes mellitus associated with Wolcott–Rallison syndrome. Issue 4 (30th October 2013) Authors: Jahnavi, Suresh; Poovazhagi, Varadarajan; Kanthimathi, Sekar; Gayathri, Vijay; Mohan, Viswanathan; Radha, Venkatesan Journal: Pediatric diabetes Issue: Volume 15:Issue 4(2014:Jun.) Page Start: 313 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Genotype‐phenotype correlation of KATP channel gene defects causing permanent neonatal diabetes in Indian patients. Issue 1 (15th September 2020) Authors: Gopi, Sundaramoorthy; Kavitha, Babu; Kanthimathi, Sekar; Kannan, Alagarsamy; Kumar, Rakesh; Joshi, Rajesh; Kanodia, Swati; Arya, Archana Dayal; Pendsey, Sanket; Pendsey, Sharad; Raghupathy, Palany; Mohan, Viswanathan; Radha, Venkatesan Journal: Pediatric diabetes Issue: Volume 22:Issue 1(2021) Page Start: 82 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Hexokinase Domain Containing 1 (HKDC1) Gene Variants and their Association with Gestational Diabetes Mellitus in a South Indian Population. (July 2016) Authors: Kanthimathi, Sekar; Liju, Samuel; Laasya, Dhandapani; Anjana, Ranjit Mohan; Mohan, Viswanathan; Radha, Venkatesan Journal: Annals of human genetics Issue: Volume 80:Number 4(2016:Jul.) Page Start: 241 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Identification and Molecular Characterization of HNF1B Gene Mutations in Indian Diabetic Patients with Renal Abnormalities. (1st December 2014) Authors: Kanthimathi, Sekar; Balamurugan, Kandasamy; Mohan, Viswanathan; Shanthirani, Coimbatore Subramaniyam; Gayathri, Vijay; Radha, Venkatesan Journal: Annals of human genetics Issue: Volume 79:Number 1(2015:Jan.) Page Start: 10 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Novel ABCC8 (SUR1) Gene Mutations in Asian Indian Children with Congenital Hyperinsulinemic Hypoglycemia. (September 2014) Authors: Jahnavi, Suresh; Poovazhagi, Varadarajan; Kanthimathi, Sekar; Balamurugan, Kandasamy; Bodhini, Dhanasekaran; Yadav, Jaivinder; Jain, Vandana; Khadgawat, Rajesh; Sikdar, Mahuya; Bhavatharini, Ayurchelvan; Das, Ashok Kumar; Kaur, Tanvir; Mohan, Viswanathan; Radha, Venkatesan Journal: Annals of human genetics Issue: Volume 78:Number 5(2014:Sep.) Page Start: 311 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗