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ALLEN BURT, PH.D.
PH.D.
Clinical Psychologist
NPI: 1720091226Individual
Specialties, Licenses & Credentials
Clinical PsychologistPrimary
Psychologist — Clinical
Code: 103TC0700X
1567(TN)
Research & Publications (20)
Family physicians' satisfaction with current practice: what is the role of their interactions with specialists?
PMID 19377349·Healthc Policy·2009
8-other
How to obtain excellent response rates when surveying physicians.
PMID 19074758·Fam Pract·2009
8-other
A mechanistic explanation of popularity: genes, rule breaking, and evocative gene-environment correlations.
PMID 19309202·J Pers Soc Psychol·2009
8-other
The vasa regulatory region mediates germline expression and maternal transmission of proteins in the malaria mosquito Anopheles gambiae: a versatile tool for genetic control strategies.
PMID 19573226·BMC Mol Biol·2009
7-preclinical
Selection of natural health products for clinical trials: a preclinical template.
PMID 19448735·Can J Physiol Pharmacol·2009
7-preclinical
Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate.
PMID 18716610·Eur J Hum Genet·2009
8-other
Who delivers preventive care as recommended?: Analysis of physician and practice characteristics.
PMID 19005132·Can Fam Physician·2008
8-other
Population genomics of the wild yeast Saccharomyces paradoxus: Quantifying the life cycle.
PMID 18344325·Proc Natl Acad Sci U S A·2008
8-other
Fibrosis and cirrhosis reversibility - molecular mechanisms.
PMID 18984474·Clin Liver Dis·2008
6-review
Fatigue in non-alcoholic fatty liver disease (NAFLD) is significant and associates with inactivity and excessive daytime sleepiness but not with liver disease severity or insulin resistance.
PMID 18270241·Gut·2008
8-other
The specificity of liver inflammation in mouse models of primary biliary cirrhosis.
PMID 18792128·Hepatology·2008
7-preclinical
Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate.
PMID 18413325·Hum Mol Genet·2008
8-other
Mutations in CHD7 in patients with CHARGE syndrome cause T-B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndrome.
PMID 18505430·Clin Exp Immunol·2008
5-case
Kinetics of monoclonal anti-epidermal growth factor receptor antibody (IOR EGF/r3)-induced apoptosis in human carcinoma bearing nude mice.
PMID 18450231·P R Health Sci J·2008
7-preclinical
Epithelial to mesenchymal transition in primary sclerosing cholangitis.
PMID 18783551·Liver Int·2008
8-other
The population genetics of using homing endonuclease genes in vector and pest management.
PMID 18660532·Genetics·2008
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 6025 BROOKVALE LN, SUITE 205
KNOXVILLE, TN 37919 - Phone
- (865) 766-0075
Quick Facts
- NPI
- 1720091226
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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