Jyoti Shetty

Role of CYP1B1, MYOC, OPTN, and OPTC genes in adult-onset primary open-angle glaucoma: predominance of CYP1B1 mutations in Indian patients.

Arun Kumar, Manjunath G Basavaraj, Santosh K. Gupta et al. · PubMed · 2007 · 84 citations

A homozygous mutation in LTBP2 causes isolated microspherophakia

Arun Kumar, Maheswara R. Duvvari, Venkatesh C. Prabhakaran et al. · Human Genetics · 2010 · 77 citations

Mendelian Disorder, Genetic Disorder, Genetics +4

Whole exome sequencing identifies a novel splice-site mutation in ADAMTS17 in an Indian family with Weill-Marchesani syndrome.

Mohd Hussain Shah, Vishwanath Kumble Bhat, Jyoti Shetty et al. · PubMed · 2014 · 33 citations · Full text

The Pattern of Childhood Blindness in Karnataka, South India

Parikshit Gogate, H Kishore, Kuldeep Dole et al. · Ophthalmic Epidemiology · 2009 · 29 citations · Full text

Confirmation of linkage and refinement of the RP28 locus for autosomal recessive retinitis pigmentosa on chromosome 2p14-p15 in an Indian family.

Arun Kumar, Jyoti Shetty, Bharath Kumar et al. · PubMed · 2004 · 18 citations