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Aramati B. M. Reddy

L V Prasad Eye Institute

12

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490

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Disease-causing mutations in proteins: structural analysis of the CYP1B1 mutations causing primary congenital glaucoma in humans.

2006 Biophysical Journal
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Myocilin gene implicated in primary congenital glaucoma

2005 Clinical Genetics
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Correlations of genotype with phenotype in Indian patients with primary congenital glaucoma

2004 Investigative Ophthalmology & Visual Science
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A STUDY OF CYP1B1 SNPs IN PRIMARY CONGENITAL GLAUCOMA CASES FROM INDIA

2004 Investigative Ophthalmology & Visual Science
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Mutation spectrum of the CYP1B1 gene in Indian primary congenital glaucoma patients.

2004 Molecular Vision
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Identification of a Predominant cyp1b1 Gene Mutation in Indian Primary Congenital Glaucoma Patients - Implications for Genetic Testing

2003 Investigative Ophthalmology & Visual Science
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Congenital glaucoma associated with 22p+ variant in a dysmorphic child

2003 Indian Journal of Ophthalmology
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PAX6 gene mutations and genotype-phenotype correlations in sporadic cases of aniridia from India.

2003 Ophthalmic Genetics
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Identification of R368H as a Predominant CYP1B1 Allele Causing Primary Congenital Glaucoma in Indian Patients

2003 Investigative Ophthalmology & Visual Science
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Mutation spectrum of FOXC1 and clinical genetic heterogeneity of Axenfeld-Rieger anomaly in India.

2003 Molecular Vision
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Citations (44)