Physician
Ophthalmology
Dr. Thaddeus P. Dryja, MD
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Thaddeus Dryja works in the field of Ophthalmology. He studied medicine at Yale University School of Medicine. Yale University School of Medicine is a one of the best medicals schools. Yale University School of Medicine is ranked 7/57 in Research/PrimaryCare. He over the years received 1 awards: "Fellow (FAAO)". Doctor Thaddeus P. Dryja, MD is a published doctor and has 43 publications published. The lastest was: 'Reliability of the mouse model of choroidal neovascularization induced by laser photocoagulation.' Thaddeus P. Dryja accepts Medicare.
Publications
- Reliability of the mouse model of choroidal neovascularization induced by laser photocoagulation.
- Interview with thaddeus p. Dryja, MD.
- A homozygous missense mutation in the IRBP gene (RBP3) associated with autosomal recessive retinitis pigmentosa.
- Search for a correlation between telomere length and severity of retinitis pigmentosa due to the dominant rhodopsin Pro23His mutation.
- Disease course in patients with autosomal recessive retinitis pigmentosa due to the USH2A gene.
- Insights from retinitis pigmentosa into the roles of isocitrate dehydrogenases in the Krebs cycle.
- Alleles in the HtrA serine peptidase 1 gene alter the risk of neovascular age-related macular degeneration.
- Comprehensive analysis of CRP, CFH Y402H and environmental risk factors on risk of neovascular age-related macular degeneration.
- Disease course of patients with X-linked retinitis pigmentosa due to RPGR gene mutations.
- Solitary myofibroma of the sclera.
- Cigarette smoking, CFH, APOE, ELOVL4, and risk of neovascular age-related macular degeneration.
- Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa.
- Variation in retinitis pigmentosa-11 (PRPF31 or RP11) gene expression between symptomatic and asymptomatic patients with dominant RP11 mutations.
- Case records of the Massachusetts General Hospital. Case 5-2006. An 11-year-old girl with loss of vision in the right eye.
- Melanocytoma of the optic nerve associated with sound-induced phosphenes.
- A screen for mutations in the transducin gene GNB1 in patients with autosomal dominant retinitis pigmentosa.
- Mutation screening of the peropsin gene, a retinal pigment epithelium specific rhodopsin homolog, in patients with retinitis pigmentosa and allied diseases.
- Photoreceptor cell rescue in inherited and orphan retinal diseases: disease-specific requirements.
- Importance of genotyping in clinical trials of inherited and orphan retinal diseases.
- Screen of the IMPDH1 gene among patients with dominant retinitis pigmentosa and clinical features associated with the most common mutation, Asp226Asn.
- Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6.
- Cone cGMP-gated channel mutations and clinical findings in patients with achromatopsia, macular degeneration, and other hereditary cone diseases.
- Recessive NRL mutations in patients with clumped pigmentary retinal degeneration and relative preservation of blue cone function.
- A novel mutation (I143NT) in guanylate cyclase-activating protein 1 (GCAP1) associated with autosomal dominant cone degeneration.
- A "negative" temporal artery biopsy, positive for arteritis.
- Extremely discordant sib-pair study design to determine risk factors for neovascular age-related macular degeneration.
- Cutaneous benign mixed tumor (chondroid syringoma) of the eyelid: clinical presentation and management.
- Mutation screening of the phosducin gene PDC in patients with retinitis pigmentosa and allied diseases.
- Novel mutations in the cellular retinaldehyde-binding protein gene (RLBP1) associated with retinitis punctata albescens: evidence of interfamilial genetic heterogeneit...
- RP2 and RPGR mutations and clinical correlations in patients with X-linked retinitis pigmentosa.
- Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration.
- Clinicopathologic reports, case reports, and small case series: surgical removal and histopathologic findings of a subfoveal neovascular membrane associated with choro...
- Barrier to autointegration factor interacts with the cone-rod homeobox and represses its transactivation function.
- Paternal uniparental heterodisomy with partial isodisomy of chromosome 1 in a patient with retinitis pigmentosa without hearing loss and a missense mutation in the Ush...
- High-grade uveal B-cell lymphoma as the initial feature in Richter syndrome.
- Disease progression in patients with dominant retinitis pigmentosa and rhodopsin mutations.
- Histopathologic study of variation in severity of retinitis pigmentosa due to the dominant rhodopsin mutation Pro23His.
- Mutated alleles of the rod and cone Na-Ca+K-exchanger genes in patients with retinal diseases.
- Ocular findings in spinocerebellar ataxia 7.
- Novel mutations in the NRL gene and associated clinical findings in patients with dominant retinitis pigmentosa.
- Understanding the etiology of Stargardt's disease.
- Profile of the genes expressed in the human peripheral retina, macula, and retinal pigment epithelium determined through serial analysis of gene expression (SAGE).
Schools
Yale University
Waterbury Hospital
Mass Ee Infirm
Chldrns Hospital
Doctors Specialties
- Clinical Molecular Genetics
- Ophthalmology
Accepted Insurances
- Blue Card PPO
- BlueConnect HMO
- Blue with Managed Care Behavioral Health HMO
- Preferred Blue PPO
- Cigna HMO
- Cigna PPO
- Great West Healthcare-Cigna PPO
- LocalPlus
- Open Access Plus
- Commercial Insurance Company
- GHI PPO
- First Health (Coventry Health Care) PPO
- Harvard Pilgrim Health Care PPO
- Medicare MCR
- MultiPlan PPO
- PHCS Network PPO
- Choice Plus POS
- Navigate HMO
- Navigate POS
- Options PPO
- United Healthcare
Awards
- Fellow (FAAO)
Education
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Yale University School of Medicine
Hospital
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Massachusetts General Hospital -
Massachusetts Eye and Ear Infirmary
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1619961968 |
| Last Name Of The Provider | DRYJA |
| First Name Of The Provider | THADDEUS |
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