Sreelatha Komatireddy

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

Subhabrata Chakrabarti, Kiranpreet Kaur, Sreelatha Komatireddy et al. · PubMed · 2005 · 58 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Glaucoma-Associated<i>CYP1B1</i>Mutations Share Similar Haplotype Backgrounds in POAG and PACG Phenotypes

Subhabrata Chakrabarti, Koilkonda R. Devi, Sreelatha Komatireddy et al. · Investigative Ophthalmology & Visual Science · 2007 · 57 citations

Life Sciences, Genetics, Ophthalmology +15

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

Sreelatha Komatireddy, Subhabrata Chakrabarti, Anil K. Mandal et al. · PubMed · 2003 · 50 citations

Medicine, Genetics, Ophthalmology +17

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

Arijit Mukhopadhyay, Sreelatha Komatireddy, Moulinath Acharya et al. · PubMed · 2005 · 42 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Complex phenotypes in an Indian family with homozygous SCA2 mutations

Mona Ragothaman, Nagaraja Sarangmath, Shashi Chaudhary et al. · Annals of Neurology · 2003 · 34 citations

Life Sciences, Genetics, Neurology +14