Sundaresan P - Search Results

1

Evaluation of Primary Angle-Closure Glaucoma Susceptibility Loci in Patients with Early Stages of Angle-Closure Disease.

Nongpiur ME, Cheng CY, Duvesh R, Vijayan S, Baskaran M, Khor CC, Allen J, Kavitha S, Venkatesh R, Goh D, Husain R, Boey PY, Quek D, Ho CL, Wong TT, Perera S, Wong TY, Krishnadas SR, Sundaresan P, Aung T, Vithana EN. Nongpiur ME, et al. Among authors: sundaresan p. Ophthalmology. 2018 May;125(5):664-670. doi: 10.1016/j.ophtha.2017.11.016. Epub 2018 Jan 6. Ophthalmology. 2018. PMID: 29310965

2

A novel PAX6 gene mutation in an Indian aniridia patient.

Neethirajan G, Hanson IM, Krishnadas SR, Vijayalakshmi P, Anupkumar K, Sundaresan P. Neethirajan G, et al. Among authors: sundaresan p. Mol Vis. 2003 May 29;9:205-9. Mol Vis. 2003. PMID: 12789139 Free article.

3

Evaluation and understanding of myocilin mutations in Indian primary open angle glaucoma patients.

Kanagavalli J, Krishnadas SR, Pandaranayaka E, Krishnaswamy S, Sundaresan P. Kanagavalli J, et al. Among authors: sundaresan p. Mol Vis. 2003 Nov 14;9:606-14. Mol Vis. 2003. PMID: 14627955 Free article.

4

A review of genetic and structural understanding of the role of myocilin in primary open angle glaucoma.

Kanagavalli J, Pandaranayaka E, Krishnadas SR, Krishnaswamy S, Sundaresan P. Kanagavalli J, et al. Among authors: sundaresan p. Indian J Ophthalmol. 2004 Dec;52(4):271-80. Indian J Ophthalmol. 2004. PMID: 15693317 Free article. Review.

5

Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2).

Vithana EN, Morgan P, Sundaresan P, Ebenezer ND, Tan DT, Mohamed MD, Anand S, Khine KO, Venkataraman D, Yong VH, Salto-Tellez M, Venkatraman A, Guo K, Hemadevi B, Srinivasan M, Prajna V, Khine M, Casey JR, Inglehearn CF, Aung T. Vithana EN, et al. Among authors: sundaresan p. Nat Genet. 2006 Jul;38(7):755-7. doi: 10.1038/ng1824. Epub 2006 Jun 11. Nat Genet. 2006. PMID: 16767101

6

Absence of phenotype-genotype correlation of patients expressing mutations in the SLC4A11 gene.

Mehta JS, Hemadevi B, Vithana EN, Arunkumar J, Srinivasan M, Prajna V, Tan DT, Aung T, Sundaresan P. Mehta JS, et al. Among authors: sundaresan p. Cornea. 2010 Mar;29(3):302-6. doi: 10.1097/ICO.0b013e3181ae9038. Cornea. 2010. PMID: 20118786

7

Polymorphisms in an intronic region of the myocilin gene associated with primary open-angle glaucoma--a possible role for alternate splicing.

Pandaranayaka PJ, Prasanthi N, Kannabiran N, Rangachari K, Dhivya M, Krishnadas SR, Sundaresan P, Krishnaswamy S. Pandaranayaka PJ, et al. Among authors: sundaresan p. Mol Vis. 2010 Dec 29;16:2891-902. Mol Vis. 2010. PMID: 21203411 Free PMC article.

8

Evaluation of SNPs on chromosome 2p with primary open angle glaucoma in the South Indian cohort.

Balasubbu S, Krishnadas SR, Jiao X, Hejtmancik JF, Sundaresan P. Balasubbu S, et al. Among authors: sundaresan p. Invest Ophthalmol Vis Sci. 2012 Apr 6;53(4):1861-4. doi: 10.1167/iovs.11-8602. Invest Ophthalmol Vis Sci. 2012. PMID: 22410552

9

Polymorphisms in ARMS2/HTRA1 and complement genes and age-related macular degeneration in India: findings from the INDEYE study.

Sundaresan P, Vashist P, Ravindran RD, Shanker A, Nitsch D, Nonyane BA, Smeeth L, Chakravarthy U, Fletcher AE. Sundaresan P, et al. Invest Ophthalmol Vis Sci. 2012 Nov 1;53(12):7492-7. doi: 10.1167/iovs.12-10073. Invest Ophthalmol Vis Sci. 2012. PMID: 23060141 Free PMC article.

10

Association study in a South Indian population supports rs1015213 as a risk factor for primary angle closure.

Duvesh R, Verma A, Venkatesh R, Kavitha S, Ramulu PY, Wojciechowski R, Sundaresan P. Duvesh R, et al. Among authors: sundaresan p. Invest Ophthalmol Vis Sci. 2013 Aug 19;54(8):5624-8. doi: 10.1167/iovs.13-12186. Invest Ophthalmol Vis Sci. 2013. PMID: 23847314 Free PMC article.

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