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ALEXANDRA BASSETT, D.M.D
D.M.D
Dentist
NPI: 1750770392Individual
Specialties, Licenses & Credentials
DentistPrimary
Dentist
Code: 122300000X
DEN.00202416(CO)
Research & Publications (20)
Voxel-based morphometry and automated lobar volumetry: the trade-off between spatial scale and statistical correction.
PMID 19619660·Neuroimage·2010
8-other
Identification of a schizophrenia-associated functional noncoding variant in NOS1AP.
PMID 19255043·Am J Psychiatry·2009
8-other
CpG oligodeoxynucleotides augment the murine immune response to the Yersinia pestis F1-V vaccine in bubonic and pneumonic models of plague.
PMID 19428836·Vaccine·2009
7-preclinical
Meta-analysis of 32 genome-wide linkage studies of schizophrenia.
PMID 19349958·Mol Psychiatry·2009
1-meta
Neuropathologic features in adults with 22q11.2 deletion syndrome.
PMID 18483005·Cereb Cortex·2009
5-case
Heritability of neurocognitive traits in familial schizophrenia.
PMID 19180565·Am J Med Genet B Neuropsychiatr Genet·2009
8-other
Highly specific gene silencing by artificial microRNAs in the unicellular alga Chlamydomonas reinhardtii.
PMID 19054357·Plant J·2009
8-other
The co-occurrence of early onset Parkinson disease and 22q11.2 deletion syndrome.
PMID 19208384·Am J Med Genet A·2009
5-case
Association of the PIK4CA schizophrenia-susceptibility gene in adults with the 22q11.2 deletion syndrome.
PMID 18646052·Am J Med Genet B Neuropsychiatr Genet·2009
8-other
Efficacy of oritavancin in a murine model of Bacillus anthracis spore inhalation anthrax.
PMID 18606841·Antimicrob Agents Chemother·2008
7-preclinical
Deubiquitylating enzyme UBP64 controls cell fate through stabilization of the transcriptional repressor tramtrack.
PMID 18160715·Mol Cell Biol·2008
7-preclinical
Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene.
PMID 18313022·Am J Hum Genet·2008
8-other
The chromatin remodelling factor dATRX is involved in heterochromatin formation.
PMID 18461125·PLoS One·2008
7-preclinical
Extracardiac features predicting 22q11.2 deletion syndrome in adult congenital heart disease.
PMID 18191243·Int J Cardiol·2008
4-observational
Phenotype matters: the case for careful characterization of relevant traits.
PMID 18765489·Am J Psychiatry·2008
8-other
Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome.
PMID 18806272·Hum Mol Genet·2008
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
- 677 S FEDERAL BLVD
DENVER, CO 80219 - Phone
- (303) 955-6079
Quick Facts
- NPI
- 1750770392
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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