Thaddeus P. Dryja
Massachusetts Eye and Ear Infirmary(US)Harvard University(US)
Publications by Year
Research Areas
Retinal Development and Disorders, Photoreceptor and optogenetics research, Retinal Diseases and Treatments, Receptor Mechanisms and Signaling, Phosphodiesterase function and regulation
Most-Cited Works
- → Recessive mutations in the gene encoding the β–subunit of rod phosphodiesterase in patients with retinitis pigmentosa(1993)605 cited
- → Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness(1993)334 cited
- → Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness(1997)281 cited
- → Autosomal recessive retinitis pigmentosa caused by mutations in the α subunit of rod cGMP phosphodiesterase(1995)254 cited
- → Structure and partial genomic sequence of the human retinoblastoma susceptibility gene(1989)136 cited
- Mutations in ABCR (ABCA4) in patients with Stargardt macular degeneration or cone-rod degeneration.(2001)
- → Dominant Leber congenital amaurosis, cone-rod degeneration, and retinitis pigmentosa caused by mutant versions of the transcription factor CRX(2001)103 cited
- → Further Screening of the Rhodopsin Gene in Patients with Autosomal Dominant Retinitis Pigmentosa(1994)101 cited
- Clinical features and mutations in patients with dominant retinitis pigmentosa-1 (RP1).(2001)
- → Analysis of the DNA of patients with retinitis pigmentosa with a cellular retinaldehyde binding protein cDNA(1990)10 cited