Was the Human Genome Project Worth the Effort?

od Daiger, Stephen P.
Izdano 2005

Identifying retinal disease genes: how far have we come, how far do we have to go?

od Daiger, Stephen P.
Izdano 2004

Mutations in Linkage Disequilibrium With Putative Disease-Causing Mutations

od Daiger, Stephen P.
izdano v Invest Ophthalmol Vis Sci (2016)

The Role of X-Chromosome Inactivation in Retinal Development and Disease

od Fahim, Abigail T., Daiger, Stephen P.
izdano v Adv Exp Med Biol (2016)

Understanding the genetic architecture of human retinal degenerations

od Hejtmancik, J. Fielding, Daiger, Stephen P.
izdano v Proc Natl Acad Sci U S A (2020)

Perspective on Genes and Mutations Causing Retinitis Pigmentosa

od Daiger, Stephen P., Bowne, Sara J., Sullivan, Lori S.
Izdano 2007

Genes and Mutations Causing Autosomal Dominant Retinitis Pigmentosa

od Daiger, Stephen P., Bowne, Sara J., Sullivan, Lori S.
izdano v Cold Spring Harb Perspect Med (2015)

PCR detection of the BgIII RFLP at the RBP3 locus

od Rodriguez, Joseph A., Liou, Greg I., Daiger, Stephen P.
Izdano 1990

Reply to Inglehearn and Hardcastle: The Map Is Not the Territory

od Daiger, Stephen P., McGuire, Rachel E., Heckenlively, John R.
Izdano 1996

Identifying and mapping novel retinal-expressed ESTs from humans

od Malone, Kimberly, Sohocki, Melanie M., Sullivan, Lori S., Daiger, Stephen P.
Izdano 1999

Comparative analysis of aryl-hydrocarbon receptor interacting protein-like 1 (Aipl1), a gene associated with inherited retinal disease in humans

od Sohocki, Melanie M., Sullivan, Lori S., Tirpak, Dayna L., Daiger, Stephen P.
Izdano 2001

Reply to Farrall et al

od Hecht, Jacqueline T., Wang, Yaping, Blanton, Susan H., Michels, Virginia V., Daiger, Stephen P.
Izdano 1993

Retinal Isoforms of Inosine 5′-Monophosphate Dehydrogenase Type I Are Poor Nucleic Acid Binding Proteins

od Xu, Dong, Cobb, Garrett C., Spellicy, Catherine J., Bowne, Sara J., Daiger, Stephen P., Hedstrom, Lizbeth
Izdano 2008

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

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

Investigating the Mechanism of Disease in the RP10 Form of Retinitis Pigmentosa

od Spellicy, Catherine J., Xu, Dong, Cobb, Garrett, Hedstrom, Lizbeth, Bowne, Sara J., Sullivan, Lori S., Daiger, Stephen P.
Izdano 2010

Molecular Defects of the Disease-Causing Human Arrestin-1 C147F Mutant

od Vishnivetskiy, Sergey A., Sullivan, Lori S., Bowne, Sara J., Daiger, Stephen P., Gurevich, Eugenia V., Gurevich, Vsevolod V.
izdano v Invest Ophthalmol Vis Sci (2018)

Time Course of Disease Progression of PRPF31-mediated Retinitis Pigmentosa

od Kiser, Kelly, Webb-Jones, Kaylie D., Bowne, Sara J., Sullivan, Lori S., Daiger, Stephen P., Birch, David G.
izdano v Am J Ophthalmol (2018)

ON THE ROLE OF IMPDH1 IN RETINAL DEGENERATION

od Kennan, Avril, Aherne, Aileen, Bowne, Sara J., Daiger, Stephen P., Jane Farrar, G., Kenna, Paul F., Humphries, Pete
Izdano 2003

IDENTIFICATION OF THE RP1 AND RP10 (IMPDH1) GENES CAUSING AUTOSOMAL DOMINANT RP

od Daiger, Stephen P., Sullivan, Lori S., Bowne, Sara J., Kennan, Avril, Humphries, Peter, Birch, David G., Heckenlively, John R.
Izdano 2003

PITPNM3 is an uncommon cause of cone and cone-rod dystrophies

od Köhn, Linda, Kohl, Susanne, Bowne, Sara J, Sullivan, Lori S, Kellner, Ulrich, Daiger, Stephen P, Sandgren, Ola, Golovleva, Irina
Izdano 2010