Ramprasad VL - Search Results

1

ABCC5, a gene that influences the anterior chamber depth, is associated with primary angle closure glaucoma.

Nongpiur ME, Khor CC, Jia H, Cornes BK, Chen LJ, Qiao C, Nair KS, Cheng CY, Xu L, George R, Tan D, Abu-Amero K, Perera SA, Ozaki M, Mizoguchi T, Kurimoto Y, Low S, Tajudin LS, Ho CL, Tham CC, Soto I, Chew PT, Wong HT, Shantha B, Kuroda M, Osman EA, Tang G, Fan S, Meng H, Wang H, Feng B, Yong VH, Ting SM, Li Y, Wang YX, Li Z, Lavanya R, Wu RY, Zheng YF, Su DH, Loon SC, Yong VK, Allingham RR, Hauser MA, Soumittra N, Ramprasad VL, Waseem N, Yaakub A, Chia KS, Kumaramanickavel G, Wong TT, How AC, Chau TN, Simmons CP, Bei JX, Zeng YX, Bhattacharya SS, Zhang M, Tan DT, Teo YY, Al-Obeidan SA, Hon DN, Tai ES, Saw SM, Foster PJ, Vijaya L, Jonas JB, Wong TY, John SW, Pang CP, Vithana EN, Wang N, Aung T. Nongpiur ME, et al. Among authors: ramprasad vl. PLoS Genet. 2014 Mar 6;10(3):e1004089. doi: 10.1371/journal.pgen.1004089. eCollection 2014 Mar. PLoS Genet. 2014. PMID: 24603532 Free PMC article.

2

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: ramprasad vl. Clin Genet. 2002 May;61(5):344-8. doi: 10.1046/j.0009-9163.2002.00251.x. Clin Genet. 2002. PMID: 12081717

3

Association of Gly82Ser polymorphism in the RAGE gene with diabetic retinopathy in type II diabetic Asian Indian patients.

Kumaramanickavel G, Ramprasad VL, Sripriya S, Upadyay NK, Paul PG, Sharma T. Kumaramanickavel G, et al. Among authors: ramprasad vl. J Diabetes Complications. 2002 Nov-Dec;16(6):391-4. doi: 10.1016/s1056-8727(02)00187-3. J Diabetes Complications. 2002. PMID: 12477623

4

Z-2 aldose reductase allele and diabetic retinopathy in India.

Kumaramanickavel G, Sripriya S, Ramprasad VL, Upadyay NK, Paul PG, Sharma T. Kumaramanickavel G, et al. Among authors: ramprasad vl. Ophthalmic Genet. 2003 Mar;24(1):41-8. doi: 10.1076/opge.24.1.41.13889. Ophthalmic Genet. 2003. PMID: 12660865

5

Truncating mutation in the NHS gene: phenotypic heterogeneity of Nance-Horan syndrome in an asian Indian family.

Ramprasad VL, Thool A, Murugan S, Nancarrow D, Vyas P, Rao SK, Vidhya A, Ravishankar K, Kumaramanickavel G. Ramprasad VL, et al. Invest Ophthalmol Vis Sci. 2005 Jan;46(1):17-23. doi: 10.1167/iovs.04-0477. Invest Ophthalmol Vis Sci. 2005. PMID: 15623749

6

Genetic homogeneity for inherited congenital microcoria loci in an Asian Indian pedigree.

Ramprasad VL, Sripriya S, Ronnie G, Nancarrow D, Saxena S, Hemamalini A, Kumar D, Vijaya L, Kumaramanickavel G. Ramprasad VL, et al. Mol Vis. 2005 Nov 3;11:934-40. Mol Vis. 2005. PMID: 16288197 Free article.

7

Retinoblastoma in India : microsatellite analysis and its application in genetic counseling.

Ramprasad VL, Madhavan J, Murugan S, Sujatha J, Suresh S, Sharma T, Kumaramanickavel G. Ramprasad VL, et al. Mol Diagn Ther. 2007;11(1):63-70. doi: 10.1007/BF03256223. Mol Diagn Ther. 2007. PMID: 17286451

8

Novel SLC4A11 mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2). Mutation in brief #958. Online.

Ramprasad VL, Ebenezer ND, Aung T, Rajagopal R, Yong VH, Tuft SJ, Viswanathan D, El-Ashry MF, Liskova P, Tan DT, Bhattacharya SS, Kumaramanickavel G, Vithana EN. Ramprasad VL, et al. Hum Mutat. 2007 May;28(5):522-3. doi: 10.1002/humu.9487. Hum Mutat. 2007. PMID: 17397048

9

Molecular genetic analysis of a consanguineous south Indian family with congenital glaucoma: relevance of genetic testing and counseling.

Ramprasad VL, George RJ, Sripriya S, Nirmaladevi J, Vijaya L, Kumaramanickavel G. Ramprasad VL, et al. Ophthalmic Genet. 2007 Mar;28(1):17-24. doi: 10.1080/13816810701199449. Ophthalmic Genet. 2007. PMID: 17454743

10

SLC4A11 mutations in Fuchs endothelial corneal dystrophy.

Vithana EN, Morgan PE, Ramprasad V, Tan DT, Yong VH, Venkataraman D, Venkatraman A, Yam GH, Nagasamy S, Law RW, Rajagopal R, Pang CP, Kumaramanickevel G, Casey JR, Aung T. Vithana EN, et al. Hum Mol Genet. 2008 Mar 1;17(5):656-66. doi: 10.1093/hmg/ddm337. Epub 2007 Nov 16. Hum Mol Genet. 2008. PMID: 18024964

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

70 results

Search Page

Filters