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BAHRAM YASHAR, D.O.
D.O.
Internal Medicine Physician
NPI: 1053349126Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
20A8818(CA)
Research & Publications (19)
Perceptions of licensure: a survey of Michigan genetic counselors.
PMID 19452266·J Genet Couns·2009
8-other
Molecular testing for hereditary retinal disease as part of clinical care.
PMID 17296903·Arch Ophthalmol·2007
5-case
An unusual X-linked retinoschisis phenotype and biochemical characterization of the W112C RS1 mutation.
PMID 16884758·Vision Res·2006
5-case
Meta-analysis of genome scans of age-related macular degeneration.
PMID 15987700·Hum Mol Genet·2005
1-meta
Toll-like receptor 4 variant D299G is associated with susceptibility to age-related macular degeneration.
PMID 15829498·Hum Mol Genet·2005
8-other
The interface between the practice of medical genetics and human genetic research: what every genetic counselor needs to know.
PMID 15604636·J Genet Couns·2004
8-other
Association of apolipoprotein E alleles with susceptibility to age-related macular degeneration in a large cohort from a single center.
PMID 15111581·Invest Ophthalmol Vis Sci·2004
8-other
Age-related macular degeneration: a high-resolution genome scan for susceptibility loci in a population enriched for late-stage disease.
PMID 14968411·Am J Hum Genet·2004
8-other
Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes.
PMID 14566651·Ophthalmic Genet·2003
8-other
Mutation screening of patients with Leber Congenital Amaurosis or the enhanced S-Cone Syndrome reveals a lack of sequence variations in the NRL gene.
PMID 12552256·Mol Vis·2003
8-other
DNA-sequence patenting: National Society of Genetic Counselors (NSGC) position paper.
PMID 12735296·J Genet Couns·2002
8-other
Retinal histopathology of an XLRP carrier with a mutation in the RPGR exon ORF15.
PMID 12387791·Exp Eye Res·2002
8-other
Microarray analysis of gene expression in the aging human retina.
PMID 12147584·Invest Ophthalmol Vis Sci·2002
8-other
A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosa.
PMID 11992260·Am J Hum Genet·2002
8-other
Treatment of erythromelalgia with a serotonin/noradrenaline reuptake inhibitor.
PMID 11903257·Br J Dermatol·2002
8-other
Evaluation of the ELOVL4 gene in patients with age-related macular degeneration.
PMID 11803489·Ophthalmic Genet·2001
8-other
Dual and opposing modulatory effects of serotonin on crayfish lateral giant escape command neurons.
PMID 11404440·J Neurosci·2001
7-preclinical
Uveitis associated with Mycoplasma pneumoniae meningitis.
PMID 11167302·Acta Ophthalmol Scand·2001
5-case
Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15.
PMID 10970770·Am J Hum Genet·2000
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
- 9808 VENICE BLVD STE 100
CULVER CITY, CA 90232 - Phone
- (832) 604-3771
Quick Facts
- NPI
- 1053349126
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 19
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