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MICHAEL GORIN, MD
MD
Ophthalmology Physician
NPI: 1457323123Individual
Specialties, Licenses & Credentials
Ophthalmology PhysicianPrimary
Ophthalmology
Code: 207W00000X
00G342310(CA)
Research & Publications (20)
A clinician's view of the molecular genetics of age-related maculopathy.
PMID 17210848·Arch Ophthalmol·2007
6-review
Interpretation of genetic association studies: markers with replicated highly significant odds ratios may be poor classifiers.
PMID 19197355·PLoS Genet·2009
8-other
Protein kinase C epsilon: an oncogene and emerging tumor biomarker.
PMID 19228372·Mol Cancer·2009
6-review
Optimization of total hip arthroplasty implantation: is the anterior pelvic plane concept valid?
PMID 18977114·J Arthroplasty·2009
8-other
Pharmacotherapy of head and neck squamous cell carcinoma.
PMID 19663637·Expert Opin Pharmacother·2009
6-review
Exclusion of positional candidate gene coding region mutations in the common posterior polymorphous corneal dystrophy 1 candidate gene interval.
PMID 19574904·Cornea·2009
8-other
Preclinical development of a bifunctional cancer cell homing, PKCepsilon inhibitory peptide for the treatment of head and neck cancer.
PMID 19567682·Cancer Res·2009
7-preclinical
C2 and CFB genes in age-related maculopathy and joint action with CFH and LOC387715 genes.
PMID 18493315·PLoS One·2008
8-other
A reliable behavioral assay for the assessment of sustained photophobia in mice.
PMID 18568886·Curr Eye Res·2008
7-preclinical
Acetazolamide in the treatment of X-linked retinoschisis maculopathy.
PMID 17420384·Arch Ophthalmol·2007
5-case
IDOCS: intelligent distributed ontology consensus system--the use of machine learning in retinal drusen phenotyping.
PMID 17460291·Invest Ophthalmol Vis Sci·2007
8-other
Identification of mutations in UBIAD1 following exclusion of coding mutations in the chromosome 1p36 locus for Schnyder crystalline corneal dystrophy.
PMID 17960116·Mol Vis·2007
8-other
Apolipoprotein e gene and age-related maculopathy in older individuals: the cardiovascular health study.
PMID 17210854·Arch Ophthalmol·2007
8-other
High-density genome array is superior to fluorescence in-situ hybridization analysis of monosomy 3 in choroidal melanoma fine needle aspiration biopsy.
PMID 18199974·Mol Vis·2007
4-observational
Proximal renal tubular acidosis and ocular pathology: a novel missense mutation in the gene (SLC4A4) for sodium bicarbonate cotransporter protein (NBCe1).
PMID 16636648·Mol Vis·2006
5-case
A novel RPGR exon ORF15 mutation in a family with X-linked retinitis pigmentosa and Coats'-like exudative vasculopathy.
PMID 16387007·Am J Ophthalmol·2006
5-case
BRCA1 mutation analysis of 41 human breast cancer cell lines reveals three new deleterious mutants.
PMID 16397213·Cancer Res·2006
8-other
CFH, ELOVL4, PLEKHA1 and LOC387715 genes and susceptibility to age-related maculopathy: AREDS and CHS cohorts and meta-analyses.
PMID 17000705·Hum Mol Genet·2006
1-meta
Susceptibility genes for age-related maculopathy on chromosome 10q26.
PMID 16080115·Am J Hum Genet·2005
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 501 S SHORE CTR W, SUITE 103B
ALAMEDA, CA 94501 - Phone
- (510) 521-6510
Quick Facts
- NPI
- 1457323123
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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