Kumaramanickavel G - Search Results

1

Gene symbol: CYP1B1. Disease: Primary congenital glaucoma. Accession #Hd0515.

Nirmaladevi J, Karthiyayini T, Kumaramanickavel G. Nirmaladevi J, et al. Among authors: kumaramanickavel g. Hum Genet. 2006 Feb;118(6):775. Hum Genet. 2006. PMID: 17297684 No abstract available.

2

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. Among authors: kumaramanickavel g. Ophthalmic Genet. 2007 Mar;28(1):17-24. doi: 10.1080/13816810701199449. Ophthalmic Genet. 2007. PMID: 17454743

3

Gene symbol: CYP1B1. Disease: Primary congenital glaucoma. Accession #Hm0544.

Nirmaladevi J, Karthiyayini T, Kumaramanickavel G. Nirmaladevi J, et al. Among authors: kumaramanickavel g. Hum Genet. 2006 Feb;118(6):779. Hum Genet. 2006. PMID: 17297699 No abstract available.

4

Biosynthetic and functional defects in newly identified SLC4A11 mutants and absence of COL8A2 mutations in Fuchs endothelial corneal dystrophy.

Soumittra N, Loganathan SK, Madhavan D, Ramprasad VL, Arokiasamy T, Sumathi S, Karthiyayini T, Rachapalli SR, Kumaramanickavel G, Casey JR, Rajagopal R. Soumittra N, et al. Among authors: kumaramanickavel g. J Hum Genet. 2014 Aug;59(8):444-53. doi: 10.1038/jhg.2014.55. Epub 2014 Jul 10. J Hum Genet. 2014. PMID: 25007886

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. Among authors: kumaramanickavel g. Mol Vis. 2006 Jul 24;12:816-20. Mol Vis. 2006. PMID: 16885925 Free article.

6

Transforming growth factor beta-1 -509C>T polymorphism in Indian patients with primary open angle glaucoma.

Sripriya S, George R, Arvind H, Baskaran M, Raju P, Ramesh SV, Karthiyayini T, Vijaya L, Kumaramanickavel G. Sripriya S, et al. Among authors: kumaramanickavel g. Mol Diagn Ther. 2007;11(3):151-4. doi: 10.1007/BF03256236. Mol Diagn Ther. 2007. PMID: 17570736

7

Gene symbol: PRPF31.

Mamatha G, Venkataramana A, Srilekha S, Kumaramanickavel G. Mamatha G, et al. Among authors: kumaramanickavel g. Hum Genet. 2007 Feb;120(6):908. Hum Genet. 2007. PMID: 17438597 No abstract available.

8

Gene symbol: RPE65. Disease: Leber's congenital amaurosis. Accession #Hm0548.

Gandra M, Sundaramurthy S, Kumaramanickavel G. Gandra M, et al. Among authors: kumaramanickavel g. Hum Genet. 2006 Feb;118(6):780. Hum Genet. 2006. PMID: 17297704 No abstract available.

9

Gene symbol: PRPF31. Disease: Retinitis pigmentosa. Accession #Hs0513.

Gandra M, Sundaramurthy S, Kumaramanickavel G. Gandra M, et al. Among authors: kumaramanickavel g. Hum Genet. 2006 Feb;118(6):784. Hum Genet. 2006. PMID: 17297719 No abstract available.

10

Gene symbol: PRPF31. Disease: Retinitis pigmentosa. Accession #Hs0514.

Gandra M, Sundaramurthy S, Kumaramanickavel G. Gandra M, et al. Among authors: kumaramanickavel g. Hum Genet. 2006 Feb;118(6):785. Hum Genet. 2006. PMID: 17297720 No abstract available.

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