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ANDRE SINGLETON, LDO
LDO
Optician
NPI: 1457839847Individual
Specialties, Licenses & Credentials
OpticianPrimary
Technician/Technologist — Optician
Code: 156FX1800X
DO6854(FL)
Research & Publications (20)
Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP.
PMID 18667258·Neurobiol Aging·2010
8-other
Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations.
PMID 19205068·Mov Disord·2009
8-other
The TOR1A polymorphism rs1182 and the risk of spread in primary blepharospasm.
PMID 19202559·Mov Disord·2009
8-other
Cardiac rhythm disturbance in a depressed patient after implantation with a vagus nerve stimulator.
PMID 19384253·J ECT·2009
5-case
A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease.
PMID 19375058·Am J Hum Genet·2009
8-other
Parkin and PINK1 mutations in early-onset Parkinson's disease: comprehensive screening in publicly available cases and control.
PMID 19351622·J Med Genet·2009
8-other
Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations.
PMID 19303062·Am J Hum Genet·2009
8-other
Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease.
PMID 19286695·Brain·2009
4-observational
Measures of autozygosity in decline: globalization, urbanization, and its implications for medical genetics.
PMID 19282984·PLoS Genet·2009
8-other
Extended tracts of homozygosity identify novel candidate genes associated with late-onset Alzheimer's disease.
PMID 19271249·Neurogenetics·2009
8-other
Genotype-imputation accuracy across worldwide human populations.
PMID 19215730·Am J Hum Genet·2009
8-other
Meta-analysis of genome-wide association data identifies two loci influencing age at menarche.
PMID 19448620·Nat Genet·2009
8-other
Common lipid-altering gene variants are associated with therapeutic intervention thresholds of lipid levels in older people.
PMID 19435741·Eur Heart J·2009
4-observational
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis.
PMID 19193627·Hum Mol Genet·2009
8-other
Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study.
PMID 19185284·Am J Hum Genet·2009
8-other
Meeting report: consensus statement-Parkinson's disease and the environment: collaborative on health and the environment and Parkinson's Action Network (CHE PAN) conference 26-28 June 2007.
PMID 19165397·Environ Health Perspect·2009
8-other
Parkinson's disease and low frequency alleles found together throughout LRRK2.
PMID 19489756·Ann Hum Genet·2009
8-other
SNCA variants are associated with increased risk for multiple system atrophy.
PMID 19475667·Ann Neurol·2009
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
- 35170 US HIGHWAY 19 N
PALM HARBOR, FL 34684 - Phone
- (727) 789-5333
Quick Facts
- NPI
- 1457839847
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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