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Author Details

Erica Bowton
Institute for Clinical and Translational Research, Vanderbilt University
2006
35
25
PMIDPaper TitleJournal TitlePublished Year
28542097Genome-wide association and pathway analysis of left ventricular function after anthracycline exposure in adults.Pharmacogenet Genomics2017
27632229Genetic determinants of variability in warfarin response after the dose-titration phase.Pharmacogenet Genomics2016
26628336A prognostic model based on readily available clinical data enriched a pre-emptive pharmacogenetic testing program.J Clin Epidemiol2016
25410959Examining rare and low-frequency genetic variants previously associated with lone or familial forms of atrial fibrillation in an electronic medical record system: a cautionary note.Circ Cardiovasc Genet2015
26265699Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemia.Blood2015
26110578Phenotype-Driven Plasma Biobanking Strategies and Methods.J Pers Med2015
26083494Deciphering Signaling Pathway Networks to Understand the Molecular Mechanisms of Metformin Action.PLoS Comput Biol2015
26030142Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy.PLoS One2015
25503805A genome-wide association study of heparin-induced thrombocytopenia using an electronic medical record.Thromb Haemost2015
24253661Clinically actionable genotypes among 10,000 patients with preemptive pharmacogenomic testing.Clin Pharmacol Ther2014
25521356Genotype and risk of major bleeding during warfarin treatment.Pharmacogenomics2014
25313507SLC6A3 coding variant Ala559Val found in two autism probands alters dopamine transporter function and trafficking.Transl Psychiatry2014
24786321Biobanks and electronic medical records: enabling cost-effective research.Sci Transl Med2014
24297552Utilization of an EMR-biorepository to identify the genetic predictors of calcineurin-inhibitor toxicity in heart transplant recipients.Pac Symp Biocomput2014
24319008Using systems approaches to address challenges for clinical implementation of pharmacogenomics.Wiley Interdiscip Rev Syst Biol Med2014
23281421Inclusion of pediatric samples in an opt-out biorepository linking DNA to de-identified medical records: pediatric BioVU.Clin Pharmacol Ther2013
24270849Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data.Nat Biotechnol2013
23886923Ethical and practical challenges to studying patients who opt out of large-scale biorepository research.J Am Med Inform Assoc2013
24009000Electronic health record design and implementation for pharmacogenomics: a local perspective.Genet Med2013
24030437Stakeholder engagement: a key component of integrating genomic information into electronic health records.Genet Med2013
23651022Assessment of a pharmacogenomic marker panel in a polypharmacy population identified from electronic medical records.Pharmacogenomics2013
23588301The Pharmacogenomics Research Network Translational Pharmacogenetics Program: overcoming challenges of real-world implementation.Clin Pharmacol Ther2013
22190063Predicting clopidogrel response using DNA samples linked to an electronic health record.Clin Pharmacol Ther2012
23304330A study of transportability of an existing smoking status detection module across institutions.AMIA Annu Symp Proc2012
22739144Optimizing drug outcomes through pharmacogenetics: a case for preemptive genotyping.Clin Pharmacol Ther2012
22514303Attention deficit/hyperactivity disorder-derived coding variation in the dopamine transporter disrupts microdomain targeting and trafficking regulation.J Neurosci2012
22588608Operational implementation of prospective genotyping for personalized medicine: the design of the Vanderbilt PREDICT project.Clin Pharmacol Ther2012
22329724Predicting warfarin dosage in European-Americans and African-Americans using DNA samples linked to an electronic health record.Pharmacogenomics2012
21399631Flotillin-1 is essential for PKC-triggered endocytosis and membrane microdomain localization of DAT.Nat Neurosci2011
21672908Facilitating pharmacogenetic studies using electronic health records and natural-language processing: a case study of warfarin.J Am Med Inform Assoc2011
20427663Dysregulation of dopamine transporters via dopamine D2 autoreceptors triggers anomalous dopamine efflux associated with attention-deficit hyperactivity disorder.J Neurosci2010
19098122A juxtamembrane mutation in the N terminus of the dopamine transporter induces preference for an inward-facing conformation.Mol Pharmacol2009
18614672Anomalous dopamine release associated with a human dopamine transporter coding variant.J Neurosci2008
18617632Syntaxin 1A interaction with the dopamine transporter promotes amphetamine-induced dopamine efflux.Mol Pharmacol2008
16908408Calmodulin kinase II interacts with the dopamine transporter C terminus to regulate amphetamine-induced reverse transport.Neuron2006
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Collaborators

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University of Washington School of Medicine.
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Center for Systems Genomics, Pennsylvania State University, University Park
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Rigshospitalet, University of Copenhagen
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Co-authored papers 5
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Co-authored papers 5
Vanderbilt Institute for Clinical and Translational Research
Co-authored papers 5
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Co-authored papers 5
The University of Texas Health Science Center at Houston
Co-authored papers 4
University of South Dakota Sanford School of Medicine
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Norton Children's Research Institute Affiliated with the University of Louisville
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Harvard Medical School, Vanderbilt University, Yale University Yale Law School
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