Balasubramanian D - Search Results

1

Allelic heterogeneity of the carbohydrate sulfotransferase-6 gene in patients with macular corneal dystrophy.

Sultana A, Sridhar MS, Klintworth GK, Balasubramanian D, Kannabiran C. Sultana A, et al. Among authors: balasubramanian d. Clin Genet. 2005 Nov;68(5):454-60. doi: 10.1111/j.1399-0004.2005.00517.x. Clin Genet. 2005. PMID: 16207214

2

Novel mutations of the carbohydrate sulfotransferase-6 (CHST6) gene causing macular corneal dystrophy in India.

Sultana A, Sridhar MS, Jagannathan A, Balasubramanian D, Kannabiran C, Klintworth GK. Sultana A, et al. Among authors: balasubramanian d. Mol Vis. 2003 Dec 22;9:730-4. Mol Vis. 2003. PMID: 14735064 Free article.

3

Molecular genetics of cataract.

Kannabiran C, Balasubramanian D. Kannabiran C, et al. Among authors: balasubramanian d. Indian J Ophthalmol. 2000 Mar;48(1):5-13. Indian J Ophthalmol. 2000. PMID: 11271936 Free article. Review.

4

Identification of Key Genes and Pathways in Persistent Hyperplastic Primary Vitreous of the Eye Using Bioinformatic Analysis.

Thomas DM, Kannabiran C, Balasubramanian D. Thomas DM, et al. Among authors: balasubramanian d. Front Med (Lausanne). 2021 Aug 13;8:690594. doi: 10.3389/fmed.2021.690594. eCollection 2021. Front Med (Lausanne). 2021. PMID: 34485332 Free PMC article.

5

Myocilin gene implicated in primary congenital glaucoma.

Kaur K, Reddy AB, Mukhopadhyay A, Mandal AK, Hasnain SE, Ray K, Thomas R, Balasubramanian D, Chakrabarti S. Kaur K, et al. Among authors: balasubramanian d. Clin Genet. 2005 Apr;67(4):335-40. doi: 10.1111/j.1399-0004.2005.00411.x. Clin Genet. 2005. PMID: 15733270

6

Mutation spectrum of the CYP1B1 gene in Indian primary congenital glaucoma patients.

Reddy AB, Kaur K, Mandal AK, Panicker SG, Thomas R, Hasnain SE, Balasubramanian D, Chakrabarti S. Reddy AB, et al. Among authors: balasubramanian d. Mol Vis. 2004 Sep 30;10:696-702. Mol Vis. 2004. PMID: 15475877 Free article.

7

Identification of novel mutations causing familial primary congenital glaucoma in Indian pedigrees.

Panicker SG, Reddy AB, Mandal AK, Ahmed N, Nagarajaram HA, Hasnain SE, Balasubramanian D. Panicker SG, et al. Among authors: balasubramanian d. Invest Ophthalmol Vis Sci. 2002 May;43(5):1358-66. Invest Ophthalmol Vis Sci. 2002. PMID: 11980847

8

Mutation spectrum of FOXC1 and clinical genetic heterogeneity of Axenfeld-Rieger anomaly in India.

Komatireddy S, Chakrabarti S, Mandal AK, Reddy AB, Sampath S, Panicker SG, Balasubramanian D. Komatireddy S, et al. Among authors: balasubramanian d. Mol Vis. 2003 Feb 18;9:43-8. Mol Vis. 2003. PMID: 12592227 Free article.

9

Gene symbol: MY0C (GLC1A). Disease: glaucoma 1, open angle.

Chakrabarti S, Komatireddy S, Mandal AK, Balasubramanian D. Chakrabarti S, et al. Among authors: balasubramanian d. Hum Genet. 2003 Nov;113(6):557. Hum Genet. 2003. PMID: 14640116 No abstract available.

10

Identification of R368H as a predominant CYP1B1 allele causing primary congenital glaucoma in Indian patients.

Reddy AB, Panicker SG, Mandal AK, Hasnain SE, Balasubramanian D. Reddy AB, et al. Among authors: balasubramanian d. Invest Ophthalmol Vis Sci. 2003 Oct;44(10):4200-3. doi: 10.1167/iovs.02-0945. Invest Ophthalmol Vis Sci. 2003. PMID: 14507861

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