S. Jahnavi

Glucokinase gene mutations (MODY 2) in Asian Indians.

V. Mohan, V. Radha, S. Chowdhury, 2014, Diabetes technology & therapeutics.

Fine needle aspiration cytology findings in human immunodeficiency virus lymphadenopathy.

S. M. Nyasavajjala, S. Jahnavi, 2010, Indian journal of pathology & microbiology.

Comprehensive genomic analysis identifies pathogenic variants in maturity-onset diabetes of the young (MODY) patients in South India

Leonard D. Goldstein, V. Mohan, V. Gayathri, 2018, BMC Medical Genetics.

Clinical and molecular characterization of neonatal diabetes and monogenic syndromic diabetes in Asian Indian children

V. Mohan, V. Radha, R. Unnikrishnan, 2013, Clinical genetics.

Clinical profile and outcome of infantile onset diabetes mellitus in southern India

V. Mohan, V. Radha, S. Senniappan, 2013, Indian Pediatrics.

Novel ABCC8 (SUR1) Gene Mutations in Asian Indian Children with Congenital Hyperinsulinemic Hypoglycemia

V. Mohan, V. Radha, A. Das, 2014, Annals of human genetics.

EIF2AK3 mutations in South Indian children with permanent neonatal diabetes mellitus associated with Wolcott–Rallison syndrome

V. Mohan, V. Gayathri, V. Radha, 2014, Pediatric diabetes.

Berardinelli Seip congenital lipodystrophy presenting with neonatal diabetes mellitus due to a mutation in the AGPAT2 gene

V. Mohan, V. Radha, V. Poovazhagi, 2012, International Journal of Diabetes in Developing Countries.

Clinical Presentation and Long Term Outcome of 40 children with Infantile Onset Diabetes Mellitus in South India

Mohan, Radha, S. Senniappan, 2013 .