S. Kandeeban

Genetic testing in four Indian families with suspected Stickler syndrome

S. Mathavan, M. Bhende, P. Bhende, 2022, Indian journal of ophthalmology.

High-throughput genetic analysis in a cohort of patients with Ocular Developmental Anomalies

K. Thirumalai, S. Sarangapani, Sumita Agarkar, 2017 .

Synthesis and pharmacological investigation of some novel 2-phenyl-3-(substituted methyl amino) quinazolin-4(3H)-ones as H1-receptor blockers.

S. Vijayakumar, V. Alagarsamy, R. Venkatesaperumal, 2002, Die Pharmazie.

An Overview on the Genetic Etiology, Testing, and Therapeutic Options for Retinitis Pigmentosa

S. Sripriya, S. Natarajan, Srilekha Sundaramurthy, 2022, Genetics of Ocular Diseases.

Mutation profile of Bardet‐Biedl syndrome patients from India: Implicative role of multiallelic rare variants and oligogenic inheritance pattern

M. Kabra, S. Sripriya, V. Khetan, 2023, Clinical genetics.

A Study on the Candidate Gene Association and Interaction with Measures of UV Exposure in Pseudoexfoliation Patients from India

S. Sripriya, R. George, R. Sharada, 2023, Current Eye Research.