Jyoti S. Shetty

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

V. Bhat, Arun Kumar, M. H. Shah, 2014, Molecular vision.

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

S. Dorairaj, A. Ali, Arun Kumar, 2007, Molecular vision.

A homozygous mutation in LTBP2 causes isolated microspherophakia

S. Blanton, M. R. Duvvari, G. Murthy, 2010, Human Genetics.

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

S. Blanton, Arun Kumar, Jyoti S. Shetty, 2004, Molecular vision.

Genetic analysis of an Indian family with members affected with juvenile-onset primary open-angle glaucoma

S. Dorairaj, A. Kumar, Arun Kumar, 2004, Ophthalmic genetics.