Juvenile retinoschisis: a model for molecular diagnostic testing of X-linked ophthalmic disease.

Por Sieving, P A, Yashar, B M, Ayyagari, R
Publicado em 1999

eyeGENE®: a vision community resource facilitating patient care and paving the path for research through molecular diagnostic testing

Por Blain, D, Goetz, KE, Ayyagari, R, Tumminia, SJ
Publicado em 2013

Mutations in yeast proliferating cell nuclear antigen define distinct sites for interaction with DNA polymerase delta and DNA polymerase epsilon.

Por Eissenberg, J C, Ayyagari, R, Gomes, X V, Burgers, P M
Publicado em 1997

A mutational analysis of the yeast proliferating cell nuclear antigen indicates distinct roles in DNA replication and DNA repair.

Por Ayyagari, R, Impellizzeri, K J, Yoder, B L, Gary, S L, Burgers, P M
Publicado em 1995

Autosomal dominant zonular cataract with sutural opacities localized to chromosome 17q11-12.

Por Padma, T, Ayyagari, R, Murty, J S, Basti, S, Fletcher, T, Rao, G N, Kaiser-Kupfer, M, Hejtmancik, J F
Publicado em 1995

exomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease causing SNVs/indels

Por Maranhao, B., Biswas, P., Duncan, J.L., Branham, K.E., Silva, G.A., Naeem, M.A., Khan, S.N., Riazuddin, S., Hejtmancik, J.F., Heckenlively, J.R., Riazuddin, S.A., Lee, P.L., Ayyagari, R.
Publicado em 2014