Achary, M.S. and Reddy, A.B.M. and Chakrabarti, S. and Panicker, S.G. and Mandal, A.K. and Ahmed, N. and Balasubramanian, D. and Hasnain, S.E. and Nagarajaram, H.A. (2006) Disease-Causing Mutations in Proteins: Structural Analysis of the CYP1b1 Mutations Causing Primary Congenital Glaucoma in Humans. Biophysical Journal, 91 (12). pp. 4329-4339. ISSN 0006-3495

Kaur, K. and Reddy, A.B.M. and Mukhopadhyay, A. and Mandal, A.K. and Hasnain, S.E. and Ray, K. and Thomas, R. and Balasubramanian, D. and Chakrabarti, S. (2005) Myocilin gene implicated in primary congenital glaucoma. Clinical Genetics, 67 (4). pp. 335-340. ISSN 0009-9163

Chakrabarti, S. and Kaur, K. and Sreelatha, K. and Acharya, M. and Devi, K.R. and Mukhopadhyay, A. and Mandal, A.K. and Hasnain, S.E. and Chandrasekhar, G. and Thomas, R. and Ray, K. (2005) Gln48His is the prevalent myocilin mutation in primary open angle and primary congenital glaucoma phenotypes in India. Molecular Vision, 11. pp. 111-3. ISSN 1090-0535

Reddy, A.B.M. and Kaur, K. and Mandal, A.K. and Panicker, S.G. and Thomas, R. and Hasnain, S.E. and Balasubramanian, D. and Chakrabarti, S. (2004) Mutation spectrum of the CYP1B1 gene in Indian primary congenital glaucoma patients. Molecular vision, 10. pp. 696-702. ISSN 1090-0535

Panicker, S.G. and Mandal, A.K. and Reddy, A.B.M. and Gothwal, V.K. and Hasnain, S.E. (2004) Correlations of Genotype with Phenotype in Indian Patients with Primary Congenital Glaucoma. Investigative Opthalmology & Visual Science, 45 (4). pp. 1149-1156. ISSN 1552-5783

Mandal, A.K. and Prabhakara, K. and Reddy, A.B.M. and Radha Rama Devi, A. and Panicker, S.G. (2003) Congenital glaucoma associated with 22p+ variant in a dysmorphic child. Indian Journal of Ophthalmology, 51 (4). pp. 355-7. ISSN 0301-4738

Reddy, A.B.M. and Panicker, S.G. and Mandal, A.K. and Hasnain, S.E. and Balasubramanian, D. (2003) Identification of R368H as a PredominantCYP1B1Allele Causing Primary Congenital Glaucoma in Indian Patients. Investigative Opthalmology & Visual Science, 44 (10). p. 4200. ISSN 1552-5783

Panicker, S.G. and Sampath, S. and Mandal, A.K. and Reddy, A.B.M. and Ahmed, N. and Hasnain, S.E. (2002) Novel mutation in FOXC1 wing region causing Axenfeld-Rieger anomaly. Investigative Ophthalmology & Visual Science, 43 (12). pp. 3613-3616. ISSN 0146-0404

Panicker, S.G. and Reddy, A.B.M. and Mandal, A.K. and Ahmed, N. and Nagarajaram, H.A. and Hasnain, S.E. and Balasubramanian, D. (2002) Identification of novel mutations causing familial primary congenital glaucoma in Indian pedigrees. Investigative Ophthalmology & Visual Science, 43 (5). pp. 1358-66. ISSN 0146-0404