List of works - Chitra Kannabiran

A Fluorescent Quantitative Multiplex PCR Method to Detect Copy Number Changes in the RB1 Gene

scientific article published in 2018

A comprehensive, sensitive and economical approach for the detection of mutations in the RB1 gene in retinoblastoma.

scientific article

A missense mutation in ASRGL1 is involved in causing autosomal recessive retinal degeneration.

scientific article

Allelic heterogeneity of the carbohydrate sulfotransferase-6 gene in patients with macular corneal dystrophy

scientific article published on 20 September 2005

Association of Human Leukocyte Antigen Class 1 genes with Stevens Johnson Syndrome with severe ocular complications in an Indian population.

scientific article published on 21 November 2017

Bilateral granular dystrophy: A clinicopathogenetic correlation after alcohol assisted debridement with phototherapeutic keratectomy.

scientific article published on 29 November 2012

Coexistence of Congenital Hereditary Endothelial Dystrophy and Fuchs Endothelial Corneal Dystrophy Associated With SLC4A11 Mutations in Affected Families

scientific article published on 01 March 2020

Genetic analysis of Indian families with autosomal recessive retinitis pigmentosa by homozygosity screening

scientific article published on April 2009

Genotype-phenotype correlation in 2 Indian families with severe granular corneal dystrophy.

scientific article

Homozygous Null Mutations in the ABCA4 Gene in Two Families With Autosomal Recessive Retinal Dystrophy

scientific article published in May 2006

Identification of Key Genes and Pathways in Persistent Hyperplastic Primary Vitreous of the Eye Using Bioinformatic Analysis

scientific article published on 13 August 2021

Mapping of locus for autosomal dominant retinitis pigmentosa on chromosome 6q23

scientific article published on 15 November 2011

Mutation of the gap junction protein alpha 8 (GJA8) gene causes autosomal recessive cataract

scientific article published in July 2007

Mutational screening of the RB1 gene in Indian patients with retinoblastoma reveals eight novel and several recurrent mutations

scientific article published on 29 August 2003

NMNAT1 mutations cause Leber congenital amaurosis

scientific article

Phenotypic characterization of retinoblastoma for the presence of putative cancer stem-like cell markers by flow cytometry.

scientific article published on 21 November 2008

Posterior microphthalmos pigmentary retinopathy syndrome

scientific article published on 18 March 2011

Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degeneration

scientific article

RB1 gene mutations in retinoblastoma and its clinical correlation

scientific article

Reliability of nested polymerase chain reaction in the diagnosis of bacterial endophthalmitis.

scientific article published in January 2002

Screening for homozygosity by descent in families with autosomal recessive retinitis pigmentosa

scientific article published in August 2002

Share, learn and get together: knowledge and information interactions at the XLV International Symposium of ISCEV - Hyderabad, India, 25-29 August 2007.

scientific article published in July 2007

Splicing aberrations caused by constitutional RB1 gene mutations in retinoblastoma

scientific article published in June 2011

Stevens-Johnson syndrome: The role of an ophthalmologist.

scientific article published on 29 January 2016

TGFBI gene mutations in corneal dystrophies.

scientific article

Therapeutic avenues for hereditary forms of retinal blindness

scientific article published on 20 January 2018

Trans-ethnic study confirmed independent associations of HLA-A02:06 and HLA-B44:03 with cold medicine-related Stevens-Johnson syndrome with severe ocular surface complications.

scientific article

List of works by Chitra Kannabiran

A Fluorescent Quantitative Multiplex PCR Method to Detect Copy Number Changes in the RB1 Gene

A comprehensive, sensitive and economical approach for the detection of mutations in the RB1 gene in retinoblastoma.

A missense mutation in ASRGL1 is involved in causing autosomal recessive retinal degeneration.

Allelic heterogeneity of the carbohydrate sulfotransferase-6 gene in patients with macular corneal dystrophy

Association of Human Leukocyte Antigen Class 1 genes with Stevens Johnson Syndrome with severe ocular complications in an Indian population.

Bilateral granular dystrophy: A clinicopathogenetic correlation after alcohol assisted debridement with phototherapeutic keratectomy.

Coexistence of Congenital Hereditary Endothelial Dystrophy and Fuchs Endothelial Corneal Dystrophy Associated With SLC4A11 Mutations in Affected Families

Genetic analysis of Indian families with autosomal recessive retinitis pigmentosa by homozygosity screening

Genotype-phenotype correlation in 2 Indian families with severe granular corneal dystrophy.

Homozygous Null Mutations in the ABCA4 Gene in Two Families With Autosomal Recessive Retinal Dystrophy

Identification of Key Genes and Pathways in Persistent Hyperplastic Primary Vitreous of the Eye Using Bioinformatic Analysis

Mapping of locus for autosomal dominant retinitis pigmentosa on chromosome 6q23

Mutation of the gap junction protein alpha 8 (GJA8) gene causes autosomal recessive cataract

Mutational screening of the RB1 gene in Indian patients with retinoblastoma reveals eight novel and several recurrent mutations

NMNAT1 mutations cause Leber congenital amaurosis

Phenotypic characterization of retinoblastoma for the presence of putative cancer stem-like cell markers by flow cytometry.

Posterior microphthalmos pigmentary retinopathy syndrome

Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degeneration

RB1 gene mutations in retinoblastoma and its clinical correlation

Reliability of nested polymerase chain reaction in the diagnosis of bacterial endophthalmitis.

Screening for homozygosity by descent in families with autosomal recessive retinitis pigmentosa

Share, learn and get together: knowledge and information interactions at the XLV International Symposium of ISCEV - Hyderabad, India, 25-29 August 2007.

Splicing aberrations caused by constitutional RB1 gene mutations in retinoblastoma

Stevens-Johnson syndrome: The role of an ophthalmologist.

TGFBI gene mutations in corneal dystrophies.

Therapeutic avenues for hereditary forms of retinal blindness

Trans-ethnic study confirmed independent associations of HLA-A*02:06 and HLA-B*44:03 with cold medicine-related Stevens-Johnson syndrome with severe ocular surface complications.

Trans-ethnic study confirmed independent associations of HLA-A02:06 and HLA-B44:03 with cold medicine-related Stevens-Johnson syndrome with severe ocular surface complications.