Sripriya S - Search Results

1

Mutation spectrum in BBS genes guided by homozygosity mapping in an Indian cohort.

Sathya Priya C, Sen P, Umashankar V, Gupta N, Kabra M, Kumaramanickavel G, Stoetzel C, Dollfus H, Sripriya S. Sathya Priya C, et al. Among authors: sripriya s. Clin Genet. 2015 Feb;87(2):161-6. doi: 10.1111/cge.12342. Epub 2014 Feb 18. Clin Genet. 2015. PMID: 24400638

2

Tumor necrosis factor allelic polymorphism with diabetic retinopathy in India.

Kumaramanickavel G, Sripriya S, Vellanki RN, Upadyay NK, Badrinath SS, Arokiasamy T, Sukumar B, Vidhya A, Joseph B, Sharma T, Gopal L. Kumaramanickavel G, et al. Among authors: sripriya s. Diabetes Res Clin Pract. 2001 Nov;54(2):89-94. doi: 10.1016/s0168-8227(01)00269-8. Diabetes Res Clin Pract. 2001. PMID: 11640992

3

Inducible nitric oxide synthase gene and diabetic retinopathy in Asian Indian patients.

Kumaramanickavel G, Sripriya S, Vellanki RN, Upadyay NK, Badrinath SS, Rajendran V, Sukumar B, Ramprasad VL, Sharma T. Kumaramanickavel G, et al. Among authors: sripriya s. Clin Genet. 2002 May;61(5):344-8. doi: 10.1046/j.0009-9163.2002.00251.x. Clin Genet. 2002. PMID: 12081717

4

Low frequency of myocilin mutations in Indian primary open-angle glaucoma patients.

Sripriya S, Uthra S, Sangeetha R, George RJ, Hemamalini A, Paul PG, Amali J, Vijaya L, Kumaramanickavel G. Sripriya S, et al. Clin Genet. 2004 Apr;65(4):333-7. doi: 10.1111/j.1399-0004.2004.00232.x. Clin Genet. 2004. PMID: 15025728

5

OPTN gene: profile of patients with glaucoma from India.

Sripriya S, Nirmaladevi J, George R, Hemamalini A, Baskaran M, Prema R, Ve Ramesh S, Karthiyayini T, Amali J, Job S, Vijaya L, Kumaramanickavel G. Sripriya S, et al. Mol Vis. 2006 Jul 24;12:816-20. Mol Vis. 2006. PMID: 16885925 Free article.

6

Next-generation sequencing-based method shows increased mutation detection sensitivity in an Indian retinoblastoma cohort.

Singh J, Mishra A, Pandian AJ, Mallipatna AC, Khetan V, Sripriya S, Kapoor S, Agarwal S, Sankaran S, Katragadda S, Veeramachaneni V, Hariharan R, Subramanian K, Mannan AU. Singh J, et al. Among authors: sripriya s. Mol Vis. 2016 Aug 16;22:1036-47. eCollection 2016. Mol Vis. 2016. PMID: 27582626 Free PMC article.

7

Bardet-Biedl syndrome: Genetics, molecular pathophysiology, and disease management.

Priya S, Nampoothiri S, Sen P, Sripriya S. Priya S, et al. Among authors: sripriya s. Indian J Ophthalmol. 2016 Sep;64(9):620-627. doi: 10.4103/0301-4738.194328. Indian J Ophthalmol. 2016. PMID: 27853007 Free PMC article. Review.

8

CERKL mutation causing retinitis pigmentosa(RP) in Indian population - a genotype and phenotype correlation study.

Sen P, Maitra P, Natarajan S, Sripriya S, Mathavan S, Bhende M, Manchegowda PT. Sen P, et al. Among authors: sripriya s. Ophthalmic Genet. 2020 Dec;41(6):570-578. doi: 10.1080/13816810.2020.1814347. Epub 2020 Aug 31. Ophthalmic Genet. 2020. PMID: 32865075

9

Prenatal genetic diagnosis of retinoblastoma and report of RB1 gene mutation from India.

Shah PK, Sripriya S, Narendran V, Pandian AJ. Shah PK, et al. Among authors: sripriya s. Ophthalmic Genet. 2016 Dec;37(4):430-433. doi: 10.3109/13816810.2015.1107595. Epub 2016 Feb 25. Ophthalmic Genet. 2016. PMID: 26914665

10

Strategies for Gene Mapping in Inherited Ophthalmic Diseases.

Srilekha S, Rao B, Rao DM, Sudha D, Chandrasekar SP, Pandian AJ, Soumittra N, Sripriya S. Srilekha S, et al. Among authors: sripriya s. Asia Pac J Ophthalmol (Phila). 2016 Jul-Aug;5(4):282-92. doi: 10.1097/APO.0000000000000228. Asia Pac J Ophthalmol (Phila). 2016. PMID: 27488070 Free article. Review.

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