-Thaddeus P Dryja Researcher Activity Profile

Research Author Detailed Information 

Thaddeus P Dryja Publication Rate By Year

Thaddeus P Dryja has published 1 paper(s) in 2006, 11 paper(s) in 2007, for a total of 12 research publications in total.

Thaddeus P Tp Dryja Author Information

LAST NAME: dryja

FIRST NAME: Thaddeus P

INITIALS: tp

AFFILIATION:

Papers

Thaddeus P Dryja's Publication Record

1. Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa. Year Published: 2007
Ocular Molecular Genetics Institute and the Berman-Gund Laboratory for the Study of Retinal Degenerations, Harvard Medical School, Massachusetts Eye and Ear Infirmary, Boston, MA 02114, USA.
2. Mutation screening of the peropsin gene, a retinal pigment epithelium specific rhodopsin homolog, in patients with retinitis pigmentosa and allied diseases. Year Published: 2006
Harvard Medical School, Massachusetts Eye and Ear Infirmary, Ocular Molecular Genetics Institute and The Berman-Gund Laboratory for the Study of Retinal Degenerations, Boston, MA, USA. carlo.rivolta@unil.ch
3. Solitary myofibroma of the sclera. Year Published: 2007
Cogan Eye Pathology Laboratory, Department of Ophthalmology, Massachusetts Eye and Ear Infirmary (MEEI), Boston, MA, USA.
4. Cigarette smoking, CFH, APOE, ELOVL4, and risk of neovascular age-related macular degeneration. Year Published: 2007
Department of Ophthalmology, Harvard Medical School, and Massachusetts Eye and Ear Infirmary, Boston, USA. margaret_deangelis@hms.harvard.edu
5. Disease course of patients with X-linked retinitis pigmentosa due to RPGR gene mutations. Year Published: 2007
Berman-Gund Laboratory for the Study of Retinal Degenerations, Harvard Medical School, Massachusetts Eye and Ear Infirmary, Boston, Massachusetts, USA. masandberg@aol.com
6. Fundus albipunctatus in a 6-year old girl due to compound heterozygous mutations in the RDH5 gene. Year Published: 2007
Retinal Degeneration and Ophthalmic Genetics Service, Hamilton Eye Institute, Department of Ophthalmology, University of Tennessee Health Science Center, 930 Madison Avenue, Suite 731, Memphis, TN, 38163, USA, iannacca@utmem.edu.
7. Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogram. Year Published: 2007
Ocular Molecular Genetics Institute, Harvard Medical School, Massachusetts Eye and Ear Infirmary, Boston, Massachusetts 02114, USA.
8. Fundus albipunctatus in a 6-year old girl due to compound heterozygous mutations in the RDH5 gene. Year Published: 2007
Retinal Degeneration and Ophthalmic Genetics Service, Hamilton Eye Institute, Department of Ophthalmology, University of Tennessee Health Science Center, 930 Madison Avenue, Suite 731, Memphis, TN 38163, USA. iannacca@utmem.edu
9. Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogram. Year Published: 2007
Ocular Molecular Genetics Institute, Harvard Medical School, Massachusetts Eye and Ear Infirmary, Boston, Massachusetts 02114, USA.
10. Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogram. Year Published: 2007
Ocular Molecular Genetics Institute, Harvard Medical School, Massachusetts Eye and Ear Infirmary, Boston, Massachusetts 02114, USA.
11. Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogram. Year Published: 2007
Ocular Molecular Genetics Institute, Harvard Medical School, Massachusetts Eye and Ear Infirmary, Boston, Massachusetts 02114, USA.
12. Fundus albipunctatus in a 6-year old girl due to compound heterozygous mutations in the RDH5 gene. Year Published: 2007
Retinal Degeneration and Ophthalmic Genetics Service, Hamilton Eye Institute, Department of Ophthalmology, University of Tennessee Health Science Center, 930 Madison Avenue, Suite 731, Memphis, TN 38163, USA. iannacca@utmem.edu