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DAVID ARNETT, M.D.
M.D.
Family Medicine Physician
NPI: 1730174871Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
20349(CO)
Research & Publications (20)
Genome-wide linkage analysis replicates susceptibility locus for fasting plasma triglycerides: NHLBI Family Heart Study.
PMID 15375693·Hum Genet·2004
8-other
Association between hyperuricemia and incident heart failure among older adults: a propensity-matched study.
PMID 19201041·Int J Cardiol·2010
8-other
The effect of a novel intergenic polymorphism (rs11774572) on HDL-cholesterol concentrations depends on TaqIB polymorphism in the cholesterol ester transfer protein gene.
PMID 19364639·Nutr Metab Cardiovasc Dis·2010
8-other
Value of orthopnea, paroxysmal nocturnal dyspnea, and medications in prospective population studies of incident heart failure.
PMID 19576357·Am J Cardiol·2009
8-other
Effect of sunlight exposure on cognitive function among depressed and non-depressed participants: a REGARDS cross-sectional study.
PMID 19638195·Environ Health·2009
8-other
Criteria for evaluation of novel markers of cardiovascular risk: a scientific statement from the American Heart Association.
PMID 19364974·Circulation·2009
8-other
Antihypertensive pharmacogenetic effect of fibrinogen-beta variant -455G>A on cardiovascular disease, end-stage renal disease, and mortality: the GenHAT study.
PMID 19352213·Pharmacogenet Genomics·2009
2-rct
Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study.
PMID 19454037·BMC Med Genet·2009
4-observational
Novel genetic variants contributing to left ventricular hypertrophy: the HyperGEN study.
PMID 19593212·J Hypertens·2009
8-other
Identification of a pleiotropic locus on chromosome 7q for a composite left ventricular wall thickness factor and body mass index: the HyperGEN Study.
PMID 19426520·BMC Med Genet·2009
8-other
Suggestion for linkage of chromosome 1p35.2 and 3q28 to plasma adiponectin concentrations in the GOLDN Study.
PMID 19426517·BMC Med Genet·2009
8-other
Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data.
PMID 19584346·JAMA·2009
1-meta
Admixture mapping of quantitative trait loci for BMI in African Americans: evidence for loci on chromosomes 3q, 5q, and 15q.
PMID 19584881·Obesity (Silver Spring)·2009
4-observational
Physical inactivity interacts with an endothelial lipase polymorphism to modulate high density lipoprotein cholesterol in the GOLDN study.
PMID 19380136·Atherosclerosis·2009
8-other
The effect of nine common polymorphisms in coagulation factor genes (F2, F5, F7, F12 and F13 ) on the effectiveness of statins: the GenHAT study.
PMID 19415820·Pharmacogenet Genomics·2009
4-observational
Has pharmacogenetics brought us closer to 'personalized medicine' for initial drug treatment of hypertension?
PMID 19509486·Curr Opin Cardiol·2009
6-review
Pharmacogenetics of antihypertensive treatment: detailing disciplinary dissonance.
PMID 19663674·Pharmacogenomics·2009
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
- 320 E 1ST ST
SALIDA, CO 81201 - Phone
- (719) 539-3583
Quick Facts
- NPI
- 1730174871
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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