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SHERRY WILTSHIRE, R.T.T., C.M.D
R.T.T., C.M.D
Radiation Therapy Radiologic Technologist
NPI: 1215344130Individual
Specialties, Licenses & Credentials
Radiation Therapy Radiologic TechnologistPrimary
Radiologic Technologist — Radiation Therapy
Code: 2471R0002X
Research & Publications (20)
Association of Interleukin-1 gene polymorphisms with central obesity and metabolic syndrome in a coronary heart disease population.
PMID 18716798·Hum Genet·2008
8-other
Investigating the association between K198N coding polymorphism in EDN1 and hypertension, lipoprotein levels, the metabolic syndrome and cardiovascular disease.
PMID 18288492·Hum Genet·2008
4-observational
Examining the statistical properties of fine-scale mapping in large-scale association studies.
PMID 18064636·Genet Epidemiol·2008
8-other
Association of PARL rs3732581 genetic variant with insulin levels, metabolic syndrome and coronary artery disease.
PMID 18758826·Hum Genet·2008
8-other
The apolipoprotein AII rs5082 variant is associated with reduced risk of coronary artery disease in an Australian male population.
PMID 18179799·Atherosclerosis·2008
8-other
Ovarian morphology is a marker of heritable biochemical traits in sisters with polycystic ovaries.
PMID 18559912·J Clin Endocrinol Metab·2008
8-other
Celestial3D: a novel method for 3D visualization of familial data.
PMID 18346980·Bioinformatics·2008
8-other
Comprehensive analysis of tagging sequence variants in DTNBP1 shows no association with schizophrenia or with its composite neurocognitive endophenotypes.
PMID 18314870·Am J Med Genet B Neuropsychiatr Genet·2008
8-other
Complex genetic control of host susceptibility to coxsackievirus B3-induced myocarditis.
PMID 17287827·Genes Immun·2007
7-preclinical
Examining the candidacy of ghrelin as a gene responsible for variation in adult stature in a United Kingdom population with type 2 diabetes.
PMID 17389697·J Clin Endocrinol Metab·2007
8-other
The value of gene-based selection of tag SNPs in genome-wide association studies.
PMID 16804554·Eur J Hum Genet·2006
4-observational
Association analysis of 6,736 U.K. subjects provides replication and confirms TCF7L2 as a type 2 diabetes susceptibility gene with a substantial effect on individual risk.
PMID 16936215·Diabetes·2006
8-other
Epistasis between type 2 diabetes susceptibility Loci on chromosomes 1q21-25 and 10q23-26 in northern Europeans.
PMID 17044847·Ann Hum Genet·2006
8-other
Significant linkage of BMI to chromosome 10p in the U.K. population and evaluation of GAD2 as a positional candidate.
PMID 16731858·Diabetes·2006
8-other
Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension.
PMID 16543358·Hum Mol Genet·2006
8-other
High-density haplotype structure and association testing of the insulin-degrading enzyme (IDE) gene with type 2 diabetes in 4,206 people.
PMID 16380485·Diabetes·2006
8-other
Detection of visible and latent fingerprints using micro-X-ray fluorescence elemental imaging.
PMID 16423224·J Forensic Sci·2006
8-other
High-throughput affinity ranking of antibodies using surface plasmon resonance microarrays.
PMID 16510109·Anal Biochem·2006
4-observational
Paraoxonase 2 (PON2) polymorphisms and development of renal dysfunction in type 2 diabetes: UKPDS 76.
PMID 17096118·Diabetologia·2006
4-observational
Ambivalence and uncertainty: experiences of and attitudes towards addiction and smoking cessation in the mid-to-late teens.
PMID 16107488·Health Educ Res·2006
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
- LAMONT STREET & VETERANS WAY
MOUNTAIN HOME, TN 37684 - Phone
- (423) 926-1171
Quick Facts
- NPI
- 1215344130
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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