Anshuman Verma

VST Centre For Glaucoma Care
Hyderabad, TG, India

Last Updated: 09/26/2026

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Found 13 publications

ASPH-related ectopia lentis revisited: genetic variability, clinical diversity, and evolving therapeutic approaches.

ASPH-related ectopia lentis revisited: genetic variability, clinical diversity, and evolving therapeutic approaches.

Journal: Ophthalmic genetics

Published: March 23, 2026

Ocular Manifestations and Genetic Spectrum of Xeroderma Pigmentosum: Insights From an Indian Cohort in a Global Context.

Ocular Manifestations and Genetic Spectrum of Xeroderma Pigmentosum: Insights From an Indian Cohort in a Global Context.

Journal: Cornea

Published: May 06, 2025

LTBP2 variants in childhood glaucoma: Phenotypic expansion and clinical experience.

LTBP2 variants in childhood glaucoma: Phenotypic expansion and clinical experience.

Journal: Molecular vision

Published: August 25, 2024

GAPO syndrome: a novel variant in ANTXR1 gene.

GAPO syndrome: a novel variant in ANTXR1 gene.

Journal: Ophthalmic genetics

Published: May 01, 2024

Band-shaped keratopathy in HNF4A-related Fanconi syndrome: a case report and review of the literature.

Band-shaped keratopathy in HNF4A-related Fanconi syndrome: a case report and review of the literature.

Journal: Ophthalmic genetics

Published: November 24, 2023

Updates on congenital hereditary endothelial dystrophy.

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.

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

Commentary: Genomic testing is a powerful tool in diagnosing and managing anterior segment dysgenesis.

Commentary: Genomic testing is a powerful tool in diagnosing and managing anterior segment dysgenesis.

Journal: Indian journal of ophthalmology

Published: July 06, 2022

Identification and in silico analysis of a spectrum of SLC4A11 variations in Indian familial and sporadic cases of congenital hereditary endothelial dystrophy.

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: May 06, 2022

New Frontier in the Management of Corneal Dystrophies: Basics, Development, and Challenges in Corneal Gene Therapy and Gene Editing.

New Frontier in the Management of Corneal Dystrophies: Basics, Development, and Challenges in Corneal Gene Therapy and Gene Editing.

Journal: Asia-Pacific journal of ophthalmology (Philadelphia, Pa.)

Published: June 21, 2021

Association study in a South Indian population supports rs1015213 as a risk factor for primary angle closure.

Association study in a South Indian population supports rs1015213 as a risk factor for primary angle closure.

Journal: Investigative ophthalmology & visual science

Published: July 13, 2013

Mutational screening of LCA genes emphasizing RPE65 in South Indian cohort of patients.

Mutational screening of LCA genes emphasizing RPE65 in South Indian cohort of patients.

Journal: PloS one

Published: January 29, 2013

Showing 1-12 of 13

Last Updated: 09/26/2026