The scientist’s investigation covers issues in Genetics, Molecular biology, Missense mutation, Corneal dystrophy and Haplotype. The concepts of his Molecular biology study are interwoven with issues in Retina, Biochemistry, Gene and Citric acid cycle. His Missense mutation research is multidisciplinary, incorporating perspectives in Frameshift mutation and Candidate gene.

In his work, Granular corneal dystrophy is strongly intertwined with TGFBI, which is a subfield of Corneal dystrophy. His Haplotype study combines topics in areas such as Dystrophy and Exon. His study in Programmed cell death is interdisciplinary in nature, drawing from both Cell culture, BECN1, Autolysosome, MAP1LC3B and Chaperone-mediated autophagy.