Chakrabarti S - Search Results

1

Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil.

de Melo MB, Mandal AK, Tavares IM, Ali MH, Kabra M, de Vasconcellos JP, Senthil S, Sallum JM, Kaur I, Betinjane AJ, Moura CR, Paula JS, Costa KA, Sarfarazi M, Paolera MD, Finzi S, Ferraz VE, Costa VP, Belfort R Jr, Chakrabarti S. de Melo MB, et al. Among authors: chakrabarti s. PLoS One. 2015 May 15;10(5):e0127147. doi: 10.1371/journal.pone.0127147. eCollection 2015. PLoS One. 2015. PMID: 25978063 Free PMC article.

2

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: chakrabarti s. Mol Vis. 2003 Feb 18;9:43-8. Mol Vis. 2003. PMID: 12592227 Free article.

3

Genomic diversities and affinities among four endogamous groups of Punjab (India) based on autosomal and mitochondrial DNA polymorphisms.

Kaur I, Roy S, Chakrabarti S, Sarhadi VK, Majumder PP, Bhanwer AJ, Singh JR. Kaur I, et al. Among authors: chakrabarti s. Hum Biol. 2002 Dec;74(6):819-36. doi: 10.1353/hub.2003.0007. Hum Biol. 2002. PMID: 12617491

4

PAX6 gene mutations and genotype-phenotype correlations in sporadic cases of aniridia from India.

Dharmaraj N, Reddy A, Kiran V, Mandal A, Panicker S, Chakrabarti S. Dharmaraj N, et al. Among authors: chakrabarti s. Ophthalmic Genet. 2003 Sep;24(3):161-5. doi: 10.1076/opge.24.3.161.15607. Ophthalmic Genet. 2003. PMID: 12868034

5

Gene symbol: CYP1B1. Disease: glaucoma, primary congenital.

Chakrabarti S, Komatireddy S, Mandal AK, Balasubramanian D. Chakrabarti S, et al. Hum Genet. 2003 Nov;113(6):556. Hum Genet. 2003. PMID: 14640114 No abstract available.

6

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

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

7

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: chakrabarti s. Mol Vis. 2004 Sep 30;10:696-702. Mol Vis. 2004. PMID: 15475877 Free article.

8

Gln48His is the prevalent myocilin mutation in primary open angle and primary congenital glaucoma phenotypes in India.

Chakrabarti S, Kaur K, Komatireddy S, Acharya M, Devi KR, Mukhopadhyay A, Mandal AK, Hasnain SE, Chandrasekhar G, Thomas R, Ray K. Chakrabarti S, et al. Mol Vis. 2005 Feb 4;11:111-3. Mol Vis. 2005. PMID: 15723004 Free article.

9

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: chakrabarti s. Clin Genet. 2005 Apr;67(4):335-40. doi: 10.1111/j.1399-0004.2005.00411.x. Clin Genet. 2005. PMID: 15733270

10

Evaluation of Optineurin as a candidate gene in Indian patients with primary open angle glaucoma.

Mukhopadhyay A, Komatireddy S, Acharya M, Bhattacharjee A, Mandal AK, Thakur SK, Chandrasekhar G, Banerjee A, Thomas R, Chakrabarti S, Ray K. Mukhopadhyay A, et al. Among authors: chakrabarti s. Mol Vis. 2005 Sep 23;11:792-7. Mol Vis. 2005. PMID: 16205626 Free article.

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