Chitra Kannabiran
Hyderabad, TG, India
Last Updated: 09/26/2026
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Found 39 publications
Generation and validation of a Leber Congenital Amaurosis, Type 12 patient-specific iPSC line (LVPEIi006-B) with a splice-site mutation in RD3 and an isogenic mutation-corrected iPSC line (LVPEIi006-B-1).
Journal: Stem cell research
Published: March 01, 2025
BEST1 associated bestrophinopathies with angle closure and post-surgical malignant glaucoma.
Journal: Ophthalmic genetics
Published: September 11, 2024
Generation and characterization of a Stargardt's disease-specific induced pluripotent stem cell line (LVPEIi008-A) with a homozygous nonsense mutation in exon 44 of ABCA4.
Journal: Stem cell research
Published: March 25, 2024
Leber congenital amaurosis: A clinical and genetic study from a tertiary eye care center.
Journal: Indian journal of ophthalmology
Published: February 29, 2024
RPE65 mutations in Leber congenital amaurosis, early-onset severe retinal dystrophy, and retinitis pigmentosa from a tertiary eye care center in India.
Journal: Ophthalmic genetics
Published: February 07, 2024
Generation of two induced pluripotent stem cell lines (LVPEIi007-B, LVPEIi008-B) from patients harboring homozygous mutation in ABCA4 (c.6088C>T) using non-integrative Sendai virus-based approach.
Journal: Stem cell research
Published: February 01, 2024
Generation of Leber congenital amaurosis, type 12 patient-specific induced pluripotent stem cell line (LVPEIi006-A), harboring a homozygous mutation in RD3.
Journal: Stem cell research
Published: January 29, 2024
Generation of two induced pluripotent stem cell lines (LVPEIi004-A and LVPEIi005-A) from probands with Leber Congenital Amaurosis 2 (LCA2) and harboring mutations in RPE65.
Journal: Stem cell research
Published: January 29, 2024
Updates on congenital hereditary endothelial dystrophy.
Journal: Taiwan journal of ophthalmology
Published: September 11, 2023
Correction to: identification and in silico analysis of a spectrum of SLC4A11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy.
Journal: Orphanet journal of rare diseases
Published: June 29, 2023
Update on the genetics of corneal endothelial dystrophies.
Journal: Indian journal of ophthalmology
Published: July 06, 2022
Commentary: Decoding genetic retinal diseases research in India.
Journal: Indian journal of ophthalmology
Published: July 06, 2022
Last Updated: 09/26/2026