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Genetic testing in four Indian families with suspected Stickler syndrome.
Indian J Ophthalmol. 2022 Jul;70(7):2578-2583. doi: 10.4103/ijo.IJO_1833_21.
Indian J Ophthalmol. 2022.
PMID: 35791160
Free PMC article.
Mutation profile of Bardet-Biedl syndrome patients from India: Implicative role of multiallelic rare variants and oligogenic inheritance pattern.
Gnanasekaran H, Chandrasekhar SP, Kandeeban S, Periyasamy P, Bhende M, Khetan V, Gupta N, Kabra M, Namboothri S, Sen P, Sripriya S.
Gnanasekaran H, et al. Among authors: kandeeban s.
Clin Genet. 2023 Oct;104(4):443-460. doi: 10.1111/cge.14398. Epub 2023 Jul 11.
Clin Genet. 2023.
PMID: 37431782
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A Study on the Candidate Gene Association and Interaction with Measures of UV Exposure in Pseudoexfoliation Patients from India.
Kandeeban S, Ishwarya S, Nareshkumar RN, Gunalan V, Porkodi P, Shyam Sundar J, Asokan R, Sharada R, Sripriya K, George R, Sripriya S.
Kandeeban S, et al.
Curr Eye Res. 2023 Dec;48(12):1144-1152. doi: 10.1080/02713683.2023.2246689. Epub 2023 Aug 14.
Curr Eye Res. 2023.
PMID: 37556844
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Synthesis and pharmacological investigation of some novel 2-phenyl-3-(substituted methyl amino) quinazolin-4(3H)-ones as H1-receptor blockers.
Alagarsamy V, Venkatesaperumal R, Vijayakumar S, Angayarkanni T, Pounammal P, Senthilganesh S, Kandeeban S.
Alagarsamy V, et al. Among authors: kandeeban s.
Pharmazie. 2002 May;57(5):306-7.
Pharmazie. 2002.
PMID: 12061252
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