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Author Details
Full Name
Russell A Wilke
Affiliation
University of South Dakota Sanford School of Medicine
ORCID
Career Start Year
1989
Papers
114
H Index
39
Expertise
CM4AI Collaborator
Andrej Sali (CM4AI)
PMID
Paper Title
Journal Title
Published Year
36898195
Rural Land Management and Kidney Health.
S D Med
2023
37150941
Drug-Induced Liver Injury with Commonly Used Antibiotics in the All of Us Research Program.
Clin Pharmacol Ther
2023
35034348
SLCO1B1*5 Allele Is Associated With Atorvastatin Discontinuation and Adverse Muscle Symptoms in the Context of Routine Care.
Clin Pharmacol Ther
2022
36893027
Cytochrome P450 2D6 Genotyping for Post-Operative Opioids.
S D Med
2022
35152405
The Clinical Pharmacogenetics Implementation Consortium Guideline for SLCO1B1, ABCG2, and CYP2C9 genotypes and Statin-Associated Musculoskeletal Symptoms.
Clin Pharmacol Ther
2022
34343516
Air, Land, and Sea: Gene-Environment Interaction in Chronic Disease.
Am J Med
2021
34575630
Potential Use of Pharmacogenetics to Reduce Drug-Induced Syndrome of Inappropriate Antidiuretic Hormone (SIADH).
J Pers Med
2021
34449991
Relative Contribution of Genetic and Environmental Factors in CKD.
S D Med
2021
32723143
<i>CYP2C19</i> genotype-guided antiplatelet therapy: promises and pitfalls.
Pharmacogenomics
2020
30679510
Learning from Longitudinal Data in Electronic Health Record and Genetic Data to Improve Cardiovascular Event Prediction.
Sci Rep
2019
31453774
Implementation of wide-scale pharmacogenetic testing in primary care.
Pharmacogenomics
2019
30983508
<i>CYP2C19</i> genotype, physician prescribing pattern, and risk for long QT on serotonin selective reuptake inhibitors.
Pharmacogenomics
2019
30998912
Chronic Kidney Disease in Agricultural Communities.
Am J Med
2019
29102571
Multisite Investigation of Outcomes With Implementation of CYP2C19 Genotype-Guided Antiplatelet Therapy After Percutaneous Coronary Intervention.
JACC Cardiovasc Interv
2018
29634825
Fracking and Climate Change-Reply.
JAMA
2018
29703846
LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins.
Circulation
2018
29280137
Multisite Investigation of Strategies for the Implementation of CYP2C19 Genotype-Guided Antiplatelet Therapy.
Clin Pharmacol Ther
2018
28532511
Challenges and strategies for implementing genomic services in diverse settings: experiences from the Implementing GeNomics In pracTicE (IGNITE) network.
BMC Med Genomics
2017
28294551
The IGNITE Pharmacogenetics Working Group: An Opportunity for Building Evidence with Pharmacogenetic Implementation in a Real-World Setting.
Clin Transl Sci
2017
29334439
Pharmacogenetics - The Year in Review.
S D Med
2017
29049815
Potential Health Implications Related to Fracking.
JAMA
2017
28813770
Point-Counterpoint: SLCO1B1 Genotyping for Statins.
S D Med
2017
27023676
Navigating pleiotropy in precision medicine: pharmacogenes from trauma to behavioral health.
Pharmacogenomics
2016
27587472
Meta-analysis of genome-wide association studies of HDL cholesterol response to statins.
J Med Genet
2016
27320715
The Reply.
Am J Med
2016
26709912
PharmGKB summary: very important pharmacogene information for RYR1.
Pharmacogenet Genomics
2016
26031886
Integration of Genomics in Primary Care.
Am J Med
2015
24096969
Characterization of statin dose response in electronic medical records.
Clin Pharmacol Ther
2014
25717410
Creation and Validation of an EMR-based Algorithm for Identifying Major Adverse Cardiac Events while on Statins.
AMIA Jt Summits Transl Sci Proc
2014
25493567
Genetic variation in the UGT1A locus is associated with simvastatin efficacy in a clinical practice setting.
Pharmacogenomics
2014
25352737
Electronic medical records and genomics (eMERGE) network exploration in cataract: several new potential susceptibility loci.
Mol Vis
2014
25350695
Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins.
Nat Commun
2014
24918167
The clinical pharmacogenetics implementation consortium guideline for SLCO1B1 and simvastatin-induced myopathy: 2014 update.
Clin Pharmacol Ther
2014
24297552
Utilization of an EMR-biorepository to identify the genetic predictors of calcineurin-inhibitor toxicity in heart transplant recipients.
Pac Symp Biocomput
2014
21912424
CYP4A11 variant is associated with high-density lipoprotein cholesterol in women.
Pharmacogenomics J
2013
23829686
Rank-based genome-wide analysis reveals the association of ryanodine receptor-2 gene variants with childhood asthma among human populations.
Hum Genomics
2013
23876492
Clinical and pharmacogenetic predictors of circulating atorvastatin and rosuvastatin concentrations in routine clinical care.
Circ Cardiovasc Genet
2013
23995691
A statin-dependent QTL for GATM expression is associated with statin-induced myopathy.
Nature
2013
23651022
Assessment of a pharmacogenomic marker panel in a polypharmacy population identified from electronic medical records.
Pharmacogenomics
2013
23748922
A common functional promoter variant links CNR1 gene expression to HDL cholesterol level.
Nat Commun
2013
23267855
The effect of novel promoter variants in MATE1 and MATE2 on the pharmacokinetics and pharmacodynamics of metformin.
Clin Pharmacol Ther
2013
22060278
Lack of association between polymorphisms in the prostaglandin F2α receptor and solute carrier organic anion transporter family 2A1 genes and intraocular pressure response to prostaglandin analogs.
Ophthalmic Genet
2012
23067351
High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOE.
Clin Transl Sci
2012
22739144
Optimizing drug outcomes through pharmacogenetics: a case for preemptive genotyping.
Clin Pharmacol Ther
2012
22534870
Electronic medical records as a tool in clinical pharmacology: opportunities and challenges.
Clin Pharmacol Ther
2012
22462750
Individualized risk for statin-induced myopathy: current knowledge, emerging challenges and potential solutions.
Pharmacogenomics
2012
22588608
Operational implementation of prospective genotyping for personalized medicine: the design of the Vanderbilt PREDICT project.
Clin Pharmacol Ther
2012
22617227
The clinical pharmacogenomics implementation consortium: CPIC guideline for SLCO1B1 and simvastatin-induced myopathy.
Clin Pharmacol Ther
2012
22567136
CNR1 genotype influences HDL-cholesterol response to change in dietary fat intake.
PLoS One
2012
22319176
Importance of multi-modal approaches to effectively identify cataract cases from electronic health records.
J Am Med Inform Assoc
2012
1 - 50 of 114
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