Novel mutations in BBS5 highlight the importance of this gene in non-Caucasian Bardet–Biedl syndrome patients

od Hjortshøj, Tina Duelund, Grønskov, Karen, Philp, Alisdair R, Nishimura, Darryl Y, Adeyemo, Adebowale, Rotimi, Charles N, Sheffield, Val C, Rosenberg, Thomas, Brøndum-Nielsen, Karen
Izdano 2008

Identical Mutation in a Novel Retinal Gene Causes Progressive Rod-Cone Degeneration (prcd) in Dogs and Retinitis Pigmentosa in Man

od Zangerl, Barbara, Goldstein, Orly, Philp, Alisdair R., Lindauer, Sarah J.P., Pearce-Kelling, Susan E., Mullins, Robert F., Graphodatsky, Alexander S., Ripoll, Daniel, Felix, Jeanette S., Stone, Edwin M., Acland, Gregory M., Aguirre, Gustavo D.
Izdano 2006

Visual Impairment in the Absence of Dystroglycan

od Satz, Jakob S., Philp, Alisdair R., Nguyen, Huy, Kusano, Hajime, Lee, Jane, Turk, Rolf, Riker, Megan J., Hernández, Jasmine, Weiss, Robert M., Anderson, Michael G., Mullins, Robert F., Moore, Steven A., Stone, Edwin M., Campbell, Kevin P.
Izdano 2009

Regulation of gene expression in the mammalian eye and its relevance to eye disease

od Scheetz, Todd E., Kim, Kwang-Youn A., Swiderski, Ruth E., Philp, Alisdair R., Braun, Terry A., Knudtson, Kevin L., Dorrance, Anne M., DiBona, Gerald F., Huang, Jian, Casavant, Thomas L., Sheffield, Val C., Stone, Edwin M.
Izdano 2006

A knockin mouse model of the Bardet–Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesity

od Davis, Roger E., Swiderski, Ruth E., Rahmouni, Kamal, Nishimura, Darryl Y., Mullins, Robert F., Agassandian, Khristofor, Philp, Alisdair R., Searby, Charles C., Andrews, Michael P., Thompson, Stewart, Berry, Christopher J., Thedens, Daniel R., Yang, Baoli, Weiss, Robert M., Cassell, Martin D., Stone, Edwin M., Sheffield, Val C.
Izdano 2007