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RUSSELL WILKE, MD
MD
Internal Medicine Physician
NPI: 1811007966Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
38145(WI)45694(TN)42291(MN)12805(ND)9764(SD)
Research & Publications (20)
Estrogen receptor genotype is associated with risk of venous thromboembolism during tamoxifen therapy.
PMID 19082882·Breast Cancer Res Treat·2009
8-other
Use of an electronic medical record to characterize cases of intermediate statin-induced muscle toxicity.
PMID 19476582·Prev Cardiol·2009
4-observational
An epidemiological approach for the estimation of disease onset in Central Europe in central and peripheral monogenic retinal dystrophies.
PMID 19277693·Graefes Arch Clin Exp Ophthalmol·2009
8-other
P-type Cu--Ti--O nanotube arrays and their use in self-biased heterojunction photoelectrochemical diodes for hydrogen generation.
PMID 18540655·Nano Lett·2008
8-other
Genetic variation in cannabinoid receptor 1 (CNR1) is associated with derangements in lipid homeostasis, independent of body mass index.
PMID 19018721·Pharmacogenomics·2008
8-other
The Pathway Less Traveled: Moving from Candidate Genes to Candidate Pathways in the Analysis of Genome-Wide Data from Large Scale Pharmacogenetic Association Studies.
PMID 19421424·Curr Pharmacogenomics Person Med·2008
8-other
Extraocular surgery for implantation of an active subretinal visual prosthesis with external connections: feasibility and outcome in seven patients.
PMID 18662916·Br J Ophthalmol·2008
8-other
Intraocular pressure response to topical beta-blockers associated with an ADRB2 single-nucleotide polymorphism.
PMID 18625943·Arch Ophthalmol·2008
8-other
Molecular analysis of ABCA4 and CRB1 genes in a Spanish family segregating both Stargardt disease and autosomal recessive retinitis pigmentosa.
PMID 18334942·Mol Vis·2008
5-case
CERKL mutations and associated phenotypes in seven Spanish families with autosomal recessive retinitis pigmentosa.
PMID 18515597·Invest Ophthalmol Vis Sci·2008
8-other
Mutation analysis identifies GUCY2D as the major gene responsible for autosomal dominant progressive cone degeneration.
PMID 18487367·Invest Ophthalmol Vis Sci·2008
4-observational
Enhancement of the response of poly(dimethylsiloxane) hollow prisms through air mirrors for absorbance-based sensing.
PMID 18371909·Talanta·2008
8-other
Characterization of low-density lipoprotein cholesterol-lowering efficacy for atorvastatin in a population-based DNA biorepository.
PMID 18834356·Basic Clin Pharmacol Toxicol·2008
8-other
Intraocular pressure response to medication in a clinical setting: the Marshfield Clinic Personalized Medicine Research Project.
PMID 18703947·J Glaucoma·2008
8-other
Multiple internal reflection poly(dimethylsiloxane) systems for optical sensing.
PMID 17960286·Lab Chip·2007
8-other
Identifying genetic risk factors for serious adverse drug reactions: current progress and challenges.
PMID 17971785·Nat Rev Drug Discov·2007
6-review
The atmospheric background of perfluorocarbon compounds used as tracers.
PMID 17993127·Environ Sci Technol·2007
8-other
Mutation screening of 299 Spanish families with retinal dystrophies by Leber congenital amaurosis genotyping microarray.
PMID 18055816·Invest Ophthalmol Vis Sci·2007
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
- 1205 S GRANGE AVE, STE 510
SIOUX FALLS, SD 57105 - Phone
- (605) 328-7500
Quick Facts
- NPI
- 1811007966
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 5
- Locations
- 1
- Publications
- 20
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