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VAIBHAV RAMPRASAD, M.D.
M.D.
Otolaryngology Physician
NPI: 1265967905IndividualAccepts Medicare
Specialties, Licenses & Credentials
Sleep Medicine (Otolaryngology) Physician
Otolaryngology — Sleep Medicine
Code: 207YS0012X
35.148701(OH)
Otolaryngology PhysicianPrimary
Otolaryngology
Code: 207Y00000X
35.148701(OH)
CMS Specialties
PrimaryOTOLARYNGOLOGY
Education
DUKE UNIVERSITY SCHOOL OF MEDICINE
Class of 2017
Research & Publications (12)
CERKL mutations cause an autosomal recessive cone-rod dystrophy with inner retinopathy.
PMID 19578027·Invest Ophthalmol Vis Sci·2009
8-other
A missense mutation in the nuclear localization signal sequence of CERKL (p.R106S) causes autosomal recessive retinal degeneration.
PMID 18978954·Mol Vis·2008
8-other
Identification of a novel splice-site mutation in the Lebercilin (LCA5) gene causing Leber congenital amaurosis.
PMID 18334959·Mol Vis·2008
5-case
Association of non-synonymous single nucleotide polymorphisms in the LOXL1 gene with pseudoexfoliation syndrome in India.
PMID 18334947·Mol Vis·2008
8-other
SLC4A11 mutations in Fuchs endothelial corneal dystrophy.
PMID 18024964·Hum Mol Genet·2008
4-observational
Molecular genetic analysis of a consanguineous south Indian family with congenital glaucoma: relevance of genetic testing and counseling.
PMID 17454743·Ophthalmic Genet·2007
8-other
Novel SLC4A11 mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2). Mutation in brief #958. Online.
PMID 17397048·Hum Mutat·2007
8-other
Retinoblastoma in India : microsatellite analysis and its application in genetic counseling.
PMID 17286451·Mol Diagn Ther·2007
8-other
Genetic homogeneity for inherited congenital microcoria loci in an Asian Indian pedigree.
PMID 16288197·Mol Vis·2005
8-other
Truncating mutation in the NHS gene: phenotypic heterogeneity of Nance-Horan syndrome in an asian Indian family.
PMID 15623749·Invest Ophthalmol Vis Sci·2005
8-other
Z-2 aldose reductase allele and diabetic retinopathy in India.
PMID 12660865·Ophthalmic Genet·2003
4-observational
Inducible nitric oxide synthase gene and diabetic retinopathy in Asian Indian patients.
PMID 12081717·Clin Genet·2002
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 3 locations total
- Address
- 9500 EUCLID AVE # A71
CLEVELAND, OH 44195 - Phone
- (216) 444-1948
Quick Facts
- NPI
- 1265967905
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 3
- Years in Practice
- 9
- Publications
- 12
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