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TYLER MCGEE, MD
MD
Orthopaedic Surgery Physician
NPI: 1588368567Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Orthopaedic Surgery PhysicianPrimary
Orthopaedic Surgery
Code: 207X00000X
T-4926(MS)
Research & Publications (20)
A homozygous missense mutation in the IRBP gene (RBP3) associated with autosomal recessive retinitis pigmentosa.
PMID 19074801·Invest Ophthalmol Vis Sci·2009
8-other
Early pubertal maturation in the prediction of early adult substance use: a prospective study.
PMID 18983626·Addiction·2009
8-other
Search for a correlation between telomere length and severity of retinitis pigmentosa due to the dominant rhodopsin Pro23His mutation.
PMID 19325938·Mol Vis·2009
8-other
A single-base substitution within an intronic repetitive element causes dominant retinitis pigmentosa with reduced penetrance.
PMID 19618371·Hum Mutat·2009
8-other
Disease course in patients with autosomal recessive retinitis pigmentosa due to the USH2A gene.
PMID 18641288·Invest Ophthalmol Vis Sci·2008
8-other
Insights from retinitis pigmentosa into the roles of isocitrate dehydrogenases in the Krebs cycle.
PMID 18806796·Nat Genet·2008
4-observational
Preliminary molecular dynamic simulations of the estrogen receptor alpha ligand binding domain from antagonist to apo.
PMID 18678925·Int J Environ Res Public Health·2008
8-other
Decrease of D2 receptor binding but increase in D2-stimulated G-protein activation, dopamine transporter binding and behavioural sensitization in brains of mice treated with a chronic escalating dose 'binge' cocaine administration paradigm.
PMID 18671743·Eur J Neurosci·2008
7-preclinical
Child and adolescent externalizing behavior and cannabis use disorders in early adulthood: an Australian prospective birth cohort study.
PMID 17996381·Addict Behav·2008
8-other
Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogram.
PMID 17896311·Ophthalmic Genet·2007
8-other
Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa.
PMID 17438524·Mol Vis·2007
8-other
A screen for mutations in the transducin gene GNB1 in patients with autosomal dominant retinitis pigmentosa.
PMID 17167406·Mol Vis·2006
8-other
Characterization of a novel calcium phosphate composite bone cement: flow, setting, and aging properties.
PMID 17122927·J Mater Sci Mater Med·2006
8-other
Variation in retinitis pigmentosa-11 (PRPF31 or RP11) gene expression between symptomatic and asymptomatic patients with dominant RP11 mutations.
PMID 16708387·Hum Mutat·2006
4-observational
Screen of the IMPDH1 gene among patients with dominant retinitis pigmentosa and clinical features associated with the most common mutation, Asp226Asn.
PMID 15851576·Invest Ophthalmol Vis Sci·2005
8-other
Clinical phenotype in a Swedish family with a mutation in the IMPDH1 gene.
PMID 16272056·Ophthalmic Genet·2005
8-other
Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6.
PMID 15781871·Proc Natl Acad Sci U S A·2005
8-other
Early risk factors for adolescent antisocial behaviour: an Australian longitudinal study.
PMID 15144516·Aust N Z J Psychiatry·2004
8-other
Review of ozone and temperature lidar validations performed within the framework of the Network for the Detection of Stratospheric Change.
PMID 15346175·J Environ Monit·2004
6-review
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2500 N STATE ST
JACKSON, MS 39216 - Phone
- (601) 984-1000
Quick Facts
- NPI
- 1588368567
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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