The relationship between Graves’ ophthalmopathy and dry eye syndrome

Por Selter, Jessica H, Gire, Anisa I, Sikder, Shameema
Publicado no Clin Ophthalmol (2014)

MUTATIONS IN KNOWN GENES ACCOUNT FOR 58% OF AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA (adRP)

Por Daiger, Stephen P., Sullivan, Lori S., Gire, Anisa I., Birch, David G., Heckenlively, John R., Bowne, Sara J.
Publicado em 2008

Mutations in the TOPORS gene cause 1% of autosomal dominant retinitis pigmentosa

Por Bowne, Sara J., Sullivan, Lori. S., Gire, Anisa I., Birch, David G., Hughbanks-Wheaton, Dianna, Heckenlively, John R., Daiger, Stephen P.
Publicado em 2008

Phenotypic Characterization of a Large Family With RP10 Autosomal-Dominant Retinitis Pigmentosa: An Asp226Asn Mutation in the IMPDH1 Gene

Por KOZMA, PETRA, HUGHBANKS-WHEATON, DIANNA K., LOCKE, KIRSTEN G., FISH, GARRY E., GIRE, ANISA I., SPELLICY, CATHERINE J., SULLIVAN, LORI S., BOWNE, SARA J., DAIGER, STEPHEN P., BIRCH, DAVID G.
Publicado em 2005

Spectrum and Frequency of Mutations in IMPDH1 Associated with Autosomal Dominant Retinitis Pigmentosa and Leber Congenital Amaurosis

Por Bowne, Sara J., Sullivan, Lori S., Mortimer, Sarah E., Hedstrom, Lizbeth, Zhu, Jingya, Spellicy, Catherine J., Gire, Anisa I., Hughbanks-Wheaton, Dianna, Birch, David G., Lewis, Richard A., Heckenlively, John R., Daiger, Stephen P.
Publicado em 2006

Prevalence of Disease-Causing Mutations in Families with Autosomal Dominant Retinitis Pigmentosa: A Screen of Known Genes in 200 Families

Por Sullivan, Lori S., Bowne, Sara J., Birch, David G., Hughbanks-Wheaton, Dianna, Heckenlively, John R., Lewis, Richard Alan, Garcia, Charles A., Ruiz, Richard S., Blanton, Susan H., Northrup, Hope, Gire, Anisa I., Seaman, Robyn, Duzkale, Hatice, Spellicy, Catherine J., Zhu, Jingya, Shankar, Suma P., Daiger, Stephen P.
Publicado em 2006