Professor, Ophthalmology, Harvard Medical School
Ophthalmology
Dr. Eliot L. Berson, MD
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Eliot Berson practices Ophthalmology. He went to Harvard Medical School. Harvard Medical School is one of the top medical schools in the US. Harvard Medical School is ranked 1 in research and 12 in primary care medicine He has 2 awards "Fellow (FAAO)" and "Whos Who in Medicine and Healthcare". Eliot L. Berson, MD has written publications. He has 52 publications published with PubMed. The lastest paper is: 'Photoreceptor rescue by an abbreviated human RPGR gene in a murine model of X-linked retinitis pigmentosa.' Dr. Eliot L. Berson is registered with Medicare.
Publications
- Targeted exon sequencing in Usher syndrome type I.
- The Relationship of Central Foveal Thickness to Urinary Iodine Concentration in Retinitis Pigmentosa With or Without Cystoid Macular Edema.
- Spinocerebellar ataxia type 7: clinical course, phenotype-genotype correlations, and neuropathology.
- Disease Course of Patients with Unilateral Pigmentary Retinopathy.
- Histopathology and functional correlations in a patient with a mutation in RPE65, the gene for retinol isomerase.
- Molecular analysis of Bardet-Biedl syndrome families: report of 21 novel mutations in 10 genes.
- Next generation sequencing of pooled samples reveals new SNRNP200 mutations associated with retinitis pigmentosa.
- A Missense Mutation in PRPF6 Causes Impairment of pre-mRNA Splicing and Autosomal-Dominant Retinitis Pigmentosa.
- Letter From the DSMC Regarding a Clinical Trial of Lutein in Patients With Retinitis Pigmentosa--Reply.
- Replacement gene therapy with a human RPGRIP1 sequence slows photoreceptor Degeneration in a murine model of Leber congenital amaurosis.
- Clinical trial of lutein in patients with retinitis pigmentosa receiving vitamin A.
- The relationship of Macular pigment optical density to serum lutein in retinitis pigmentosa.
- A single-base substitution within an intronic repetitive element causes dominant retinitis pigmentosa with reduced penetrance.
- 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.
- Visual acuity is related to parafoveal retinal thickness in patients with retinitis pigmentosa and Macular cysts.
- Premature termination codons in PRPF31 cause retinitis pigmentosa via haploinsufficiency due to nonsense-mediated mRNA decay.
- Retinal Degenerations: planning for the future.
- Disease course of patients with X-linked retinitis pigmentosa due to RPGR gene mutations.
- Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa.
- Rod and cone opsin mislocalization in an autopsy eye from a carrier of X-linked retinitis pigmentosa with a Gly436Asp mutation in the RPGR gene.
- Variation in retinitis pigmentosa-11 (PRPF31 or RP11) gene expression between symptomatic and asymptomatic patients with dominant RP11 mutations.
- Natural course of ocular function in pigmented paravenous retinoChoroidal atrophy.
- Mutation screening of the peropsin gene, a retinal pigment epithelium specific rhodopsin homolog, in patients with retinitis pigmentosa and allied diseases.
- A screen for mutations in the transducin gene GNB1 in patients with autosomal dominant retinitis pigmentosa.
- The association between visual acuity and central retinal thickness in retinitis pigmentosa.
- Disease course of patients with pericentral retinitis pigmentosa.
- 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.
- Further evaluation of docosahexaenoic acid in patients with retinitis pigmentosa receiving vitamin A treatment: subgroup analyses.
- Clinical trial of docosahexaenoic acid in patients with retinitis pigmentosa receiving vitamin A treatment.
- Histologic study of retinitis pigmentosa due to a mutation in the RP13 gene (PRPC8): comparison with rhodopsin Pro23His, Cys110Arg, and Glu181Lys.
- Mutation screening of the phosducin gene PDC in patients with retinitis pigmentosa and allied diseases.
- 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.
- Evaluation of the ELOVL4 gene in patients with autosomal recessive retinitis pigmentosa and Leber congenital amaurosis.
- 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...
- Lymphoma-associated Retinopathy.
- 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.
- Absence of photoreceptor rescue with D-cis-diltiazem in the rd mouse.
- Novel mutations in the NRL gene and associated clinical findings in patients with dominant retinitis pigmentosa.
- Molecular Genetics of FAM161A in North American Patients with Early-Onset Retinitis Pigmentosa.
- Photoreceptor rescue by an abbreviated human RPGR gene in a murine model of X-linked retinitis pigmentosa.
Schools
Harvard Medical School
Uc San Francisco Hosps
Barnes McMillan Hospital
Conditions Treated
- Age-Related Macular Degeneration
- Astigmatism
- Benign Neoplasm of Choroid
- Benign Neoplasm of Eye
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Doctors Specialties
- Ophthalmology
Accepted Insurances
Awards
- Fellow (FAAO)
- Whos Who in Medicine and Healthcare
Education
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Washington University - Barnes-Jewish Hospital -
UCSF -
Harvard Medical School
Hospital
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Massachusetts General Hospital -
Massachusetts Eye and Ear Infirmary
Drug Facts
| NPI NUMBER | 1700877560 | |
| NPPES Provider LastName | BERSON | |
| NPPES Provider FirstName | ELIOT | |
| NPPES Provider ZIPCode | 021143002 | |
| NPPES Provider State | MA | |
| Specialty Description | Ophthalmology | |
| Total Claim Count | 72.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1700877560 |
| Last Name Of The Provider | BERSON |
| First Name Of The Provider | ELIOT |
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