1. Survey of patients with granular, lattice, avellino, and Reis-Bucklers corneal dystrophies for mutations in the BIGH3 and gelsolin genes;Afshari;Arch. Ophthalmol.,2001
2. Atypical asymmetric lattice corneal dystrophy associated with a novel homozygous mutation (Val624Met) in the TGFBI gene;Afshari;Mol. Vis.,2008
3. Initial suppression of transforming growth factor-beta signaling and loss of TGFBI causes early alveolar structural defects resulting in bronchopulmonary dysplasia;Ahlfeld;Am. J. Pathol.,2016
4. Unilateral lattice corneal dystrophy associated with the novel His572del mutation in the TGFBI gene;Aldave;Mol. Vis.,2006
5. A clinical and histopathologic examination of accelerated TGFBIp deposition after LASIK in combined granular-lattice corneal dystrophy;Aldave;Am. J. Ophthalmol.,2007