Chakrabarti S - Search Results

1

Regional variation in the incidence of pseudo-exfoliation in the Andhra Pradesh Eye Disease Study (APEDS).

Choudhari NS, Khanna RC, Marmamula S, Mettla AL, Giridhar P, Banerjee S, Shekhar K, Chakrabarti S, Murthy GVS, Gilbert C, Rao GN; Andhra Pradesh Eye Disease Study Group. Choudhari NS, et al. Among authors: chakrabarti s. Eye (Lond). 2023 Jun;37(8):1704-1710. doi: 10.1038/s41433-022-02226-9. Epub 2022 Sep 9. Eye (Lond). 2023. PMID: 36085361 Free PMC article.

2

Globally, CYP1B1 mutations in primary congenital glaucoma are strongly structured by geographic and haplotype backgrounds.

Chakrabarti S, Kaur K, Kaur I, Mandal AK, Parikh RS, Thomas R, Majumder PP. Chakrabarti S, et al. Invest Ophthalmol Vis Sci. 2006 Jan;47(1):43-7. doi: 10.1167/iovs.05-0912. Invest Ophthalmol Vis Sci. 2006. PMID: 16384942

3

The LOXL1 gene variations are not associated with primary open-angle and primary angle-closure glaucomas.

Chakrabarti S, Rao KN, Kaur I, Parikh RS, Mandal AK, Chandrasekhar G, Thomas R. Chakrabarti S, et al. Invest Ophthalmol Vis Sci. 2008 Jun;49(6):2343-7. doi: 10.1167/iovs.07-1557. Epub 2008 Jan 25. Invest Ophthalmol Vis Sci. 2008. PMID: 18223248

4

Variants in the 10q26 gene cluster (LOC387715 and HTRA1) exhibit enhanced risk of age-related macular degeneration along with CFH in Indian patients.

Kaur I, Katta S, Hussain A, Hussain N, Mathai A, Narayanan R, Hussain A, Reddy RK, Majji AB, Das T, Chakrabarti S. Kaur I, et al. Among authors: chakrabarti s. Invest Ophthalmol Vis Sci. 2008 May;49(5):1771-6. doi: 10.1167/iovs.07-0560. Invest Ophthalmol Vis Sci. 2008. PMID: 18436811

5

Exfoliation syndrome and exfoliation glaucoma-associated LOXL1 variations are not involved in pigment dispersion syndrome and pigmentary glaucoma.

Rao KN, Ritch R, Dorairaj SK, Kaur I, Liebmann JM, Thomas R, Chakrabarti S. Rao KN, et al. Among authors: chakrabarti s. Mol Vis. 2008 Jul 9;14:1254-62. Mol Vis. 2008. PMID: 18618003 Free PMC article.

6

The transcription factor gene FOXC1 exhibits a limited role in primary congenital glaucoma.

Chakrabarti S, Kaur K, Rao KN, Mandal AK, Kaur I, Parikh RS, Thomas R. Chakrabarti S, et al. Invest Ophthalmol Vis Sci. 2009 Jan;50(1):75-83. doi: 10.1167/iovs.08-2253. Epub 2008 Aug 15. Invest Ophthalmol Vis Sci. 2009. PMID: 18708620

7

The involvement of complement factor B and complement component C2 in an Indian cohort with age-related macular degeneration.

Kaur I, Katta S, Reddy RK, Narayanan R, Mathai A, Majji AB, Chakrabarti S. Kaur I, et al. Among authors: chakrabarti s. Invest Ophthalmol Vis Sci. 2010 Jan;51(1):59-63. doi: 10.1167/iovs.09-4135. Epub 2009 Aug 20. Invest Ophthalmol Vis Sci. 2010. PMID: 19696172

8

Lack of association of three primary open-angle glaucoma-susceptible loci with primary glaucomas in an Indian population.

Rao KN, Kaur I, Chakrabarti S. Rao KN, et al. Among authors: chakrabarti s. Proc Natl Acad Sci U S A. 2009 Nov 3;106(44):E125-6; author reply E127. doi: 10.1073/pnas.0910416106. Epub 2009 Oct 21. Proc Natl Acad Sci U S A. 2009. PMID: 19846772 Free PMC article. No abstract available.

9

The molecular genetic basis of age-related macular degeneration: an overview.

Katta S, Kaur I, Chakrabarti S. Katta S, et al. Among authors: chakrabarti s. J Genet. 2009 Dec;88(4):425-49. doi: 10.1007/s12041-009-0064-4. J Genet. 2009. PMID: 20090206 Review.

10

Variations in NTF4, VAV2, and VAV3 genes are not involved with primary open-angle and primary angle-closure glaucomas in an indian population.

Rao KN, Kaur I, Parikh RS, Mandal AK, Chandrasekhar G, Thomas R, Chakrabarti S. Rao KN, et al. Among authors: chakrabarti s. Invest Ophthalmol Vis Sci. 2010 Oct;51(10):4937-41. doi: 10.1167/iovs.10-5553. Epub 2010 May 12. Invest Ophthalmol Vis Sci. 2010. PMID: 20463313

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