Radha Ayyagari

A whole exome variant filtering software for identification of disease causing variants

Bruno Maranhao, John R. Heckenlively, Pooja Biswas, 2013 .

Mutations in GRM6 identified in consanguineous Pakistani families with congenital stationary night blindness

Tayyab Husnain, Radha Ayyagari, Shaheen N. Khan, 2015, Molecular vision.

Identification of a novel mutation in the CDHR1 gene in a family with recessive retinal degeneration.

Austin Roorda, Terry Gaasterland, Kavitha Ratnam, 2012, Archives of ophthalmology.

LONGITUDINAL STRUCTURAL CHANGES IN LATE-ONSET RETINAL DEGENERATION

Denise Cunningham, Radha Ayyagari, Paul A Sieving, 2016, Retina.

Loss of functional ELOVL4 depletes very long-chain fatty acids (≥C28) and the unique ω-O-acylceramides in skin leading to neonatal death

Radha Ayyagari, Peter M. Elias, P. Elias, 2007 .

Splice-site mutations identified in PDE6A responsible for retinitis pigmentosa in consanguineous Pakistani families

Shahbaz Ali, Tayyab Husnain, Radha Ayyagari, 2015, Molecular vision.