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THADDEUS DRYJA, MD
Ophthalmology Physician
NPI: 1619961968IndividualAccepts Medicare
Specialties, Licenses & Credentials
Ophthalmology PhysicianPrimary
Ophthalmology
Code: 207W00000X
41891(MA)
Clinical Pathology/Laboratory Medicine Physician
Pathology — Clinical Pathology/Laboratory Medicine
Code: 207ZP0105X
41891(MA)
Education
YALE UNIVERSITY SCHOOL OF MEDICINE
Class of 1976
Research & Publications (20)
Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6.
PMID 15781871·Proc Natl Acad Sci U S A·2005
8-other
Null RPGRIP1 alleles in patients with Leber congenital amaurosis.
PMID 11283794·Am J Hum Genet·2001
8-other
Novel rhodopsin mutations Gly114Val and Gln184Pro in dominant retinitis pigmentosa.
PMID 10967073·Invest Ophthalmol Vis Sci·2000
8-other
Molecular genetics of Oguchi disease, fundus albipunctatus, and other forms of stationary night blindness: LVII Edward Jackson Memorial Lecture.
PMID 11078833·Am J Ophthalmol·2000
8-other
Photoreceptor cell rescue in inherited and orphan retinal diseases: disease-specific requirements.
PMID 16374317·Retina·2005
6-review
Importance of genotyping in clinical trials of inherited and orphan retinal diseases.
PMID 16374348·Retina·2005
6-review
A homozygous missense mutation in the IRBP gene (RBP3) associated with autosomal recessive retinitis pigmentosa.
PMID 19074801·Invest Ophthalmol Vis Sci·2009
8-other
Search for a correlation between telomere length and severity of retinitis pigmentosa due to the dominant rhodopsin Pro23His mutation.
PMID 19325938·Mol Vis·2009
8-other
Diagnosis in a patient with fundus albipunctatus and atypical fundus changes.
PMID 18949499·Doc Ophthalmol·2009
5-case
Alleles in the HtrA serine peptidase 1 gene alter the risk of neovascular age-related macular degeneration.
PMID 18164066·Ophthalmology·2008
8-other
Insights from retinitis pigmentosa into the roles of isocitrate dehydrogenases in the Krebs cycle.
PMID 18806796·Nat Genet·2008
4-observational
Comprehensive analysis of CRP, CFH Y402H and environmental risk factors on risk of neovascular age-related macular degeneration.
PMID 18704199·Mol Vis·2008
8-other
Disease course in patients with autosomal recessive retinitis pigmentosa due to the USH2A gene.
PMID 18641288·Invest Ophthalmol Vis Sci·2008
8-other
Disease course of patients with X-linked retinitis pigmentosa due to RPGR gene mutations.
PMID 17325176·Invest Ophthalmol Vis Sci·2007
8-other
[Acute coronary syndrome with persistent ST-elevation and normal coronary angiography].
PMID 18181063·Kardiol Pol·2007
5-case
Cigarette smoking, CFH, APOE, ELOVL4, and risk of neovascular age-related macular degeneration.
PMID 17210851·Arch Ophthalmol·2007
8-other
Fundus albipunctatus in a 6-year old girl due to compound heterozygous mutations in the RDH5 gene.
PMID 17476461·Doc Ophthalmol·2007
5-case
Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa.
PMID 17438524·Mol Vis·2007
8-other
Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogram.
PMID 17896311·Ophthalmic Genet·2007
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 243 CHARLES ST
BOSTON, MA 02114 - Phone
- (617) 573-3319
Quick Facts
- NPI
- 1619961968
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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