Ben Burkley

Ben Burkley,

Regulatory Research Manager

Department: Shared Service Center
Business Phone: (352) 273-5283
Business Email: burkley@cop.ufl.edu

Publications

2018
Implementation of Standardized Clinical Processes for TPMT Testing in a Diverse Multidisciplinary Population: Challenges and Lessons Learned.
Clinical and translational science. 11(2):175-181 [DOI] 10.1111/cts.12533. [PMID] 29351371.
2016
CYP2C19 and CES1 polymorphisms and efficacy of clopidogrel and aspirin dual antiplatelet therapy in patients with symptomatic intracranial atherosclerotic disease.
Journal of neurosurgery. 124(6):1746-51 [DOI] 10.3171/2015.6.JNS15795. [PMID] 26587656.
2016
Effects of Using Personal Genotype Data on Student Learning and Attitudes in a Pharmacogenomics Course.
American journal of pharmaceutical education. 80(7) [PMID] 27756930.
View on: PubMed
2014
Clinical pharmacogenetics implementation: approaches, successes, and challenges.
American journal of medical genetics. Part C, Seminars in medical genetics. 166C(1):56-67 [DOI] 10.1002/ajmg.c.31390. [PMID] 24616371.
2014
Genetic variant in folate homeostasis is associated with lower warfarin dose in African Americans.
Blood. 124(14):2298-305 [DOI] 10.1182/blood-2014-04-568436. [PMID] 25079360.
2014
Impact of CYP2D6 polymorphisms on clinical efficacy and tolerability of metoprolol tartrate.
Clinical pharmacology and therapeutics. 96(2):175-81 [DOI] 10.1038/clpt.2014.62. [PMID] 24637943.
2013
Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study.
Lancet (London, England). 382(9894):790-6 [DOI] 10.1016/S0140-6736(13)60681-9. [PMID] 23755828.
2013
Loci influencing blood pressure identified using a cardiovascular gene-centric array.
Human molecular genetics. 22(8):1663-78 [DOI] 10.1093/hmg/dds555. [PMID] 23303523.
2013
Pharmacogenomic association of nonsynonymous SNPs in SIGLEC12, A1BG, and the selectin region and cardiovascular outcomes.
Hypertension (Dallas, Tex. : 1979). 62(1):48-54 [DOI] 10.1161/HYPERTENSIONAHA.111.00823. [PMID] 23690342.
2013
The Pharmacogenomics Research Network Translational Pharmacogenetics Program: overcoming challenges of real-world implementation.
Clinical pharmacology and therapeutics. 94(2):207-10 [DOI] 10.1038/clpt.2013.59. [PMID] 23588301.
2012
Association of Fto With Hydrochlorothiazide (Hctz)-Induced Elevation in Uric Acid (Ua) in African American (Aa) Hypertensives in the Pharmacogenomic Evaluation of Antihypertensive Response (Pear) Study.
Clinical Pharmacology & Therapeutics. 91:S59-S60
2012
Chronic pain, perceived stress, and cellular aging: an exploratory study.
Molecular pain. 8 [DOI] 10.1186/1744-8069-8-12. [PMID] 22325162.
2012
Effects of genetic variation in H3K79 methylation regulatory genes on clinical blood pressure and blood pressure response to hydrochlorothiazide.
Journal of translational medicine. 10 [DOI] 10.1186/1479-5876-10-56. [PMID] 22440088.
2012
Implementing personalized medicine: development of a cost-effective customized pharmacogenetics genotyping array.
Clinical pharmacology and therapeutics. 92(4):437-9 [DOI] 10.1038/clpt.2012.125. [PMID] 22910441.
2012
Non-Synonymous Snps in Sele, Selp, and Siglec12 Associate With Cardiovascular (Cv) Outcomes in the International Verapamil Sr-Trandol-April Study Genetic Substudy (Invest-Genes)
Clinical Pharmacology & Therapeutics. 91:S20-S21
2011
Genetic polymorphisms and other risk factors associated with bisphosphonate induced osteonecrosis of the jaw.
International journal of oral and maxillofacial surgery. 40(6):605-11 [DOI] 10.1016/j.ijom.2011.02.002. [PMID] 21396799.
2010
New-Onset Diabetes Risk Associated With Antihypertensive Therapy in Hypertensive Coronary Artery Disease Patients Is Modified By a Single Nucleotide Polymorphism (Snp) in the L-Type Calcium Channel (Ltcc)
Clinical Pharmacology & Therapeutics. 87
2006
Genetic variation at the mitochondrial DNA 9-bp repeat locus in the Sakha of Siberia.
Human biology. 78(2):179-98 [PMID] 17036925.
View on: PubMed

Contact Details

Phones:
Business:
(352) 273-5283
Emails: