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Author Details
Full Name
Erica Bowton
Affiliation
Institute for Clinical and Translational Research, Vanderbilt University
ORCID
Career Start Year
2006
Papers
35
H Index
25
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
28542097
Genome-wide association and pathway analysis of left ventricular function after anthracycline exposure in adults.
Pharmacogenet Genomics
2017
27632229
Genetic determinants of variability in warfarin response after the dose-titration phase.
Pharmacogenet Genomics
2016
26628336
A prognostic model based on readily available clinical data enriched a pre-emptive pharmacogenetic testing program.
J Clin Epidemiol
2016
25410959
Examining 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 Genet
2015
26265699
Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemia.
Blood
2015
26110578
Phenotype-Driven Plasma Biobanking Strategies and Methods.
J Pers Med
2015
26083494
Deciphering Signaling Pathway Networks to Understand the Molecular Mechanisms of Metformin Action.
PLoS Comput Biol
2015
26030142
Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy.
PLoS One
2015
25503805
A genome-wide association study of heparin-induced thrombocytopenia using an electronic medical record.
Thromb Haemost
2015
24253661
Clinically actionable genotypes among 10,000 patients with preemptive pharmacogenomic testing.
Clin Pharmacol Ther
2014
25521356
Genotype and risk of major bleeding during warfarin treatment.
Pharmacogenomics
2014
25313507
SLC6A3 coding variant Ala559Val found in two autism probands alters dopamine transporter function and trafficking.
Transl Psychiatry
2014
24786321
Biobanks and electronic medical records: enabling cost-effective research.
Sci Transl Med
2014
24297552
Utilization of an EMR-biorepository to identify the genetic predictors of calcineurin-inhibitor toxicity in heart transplant recipients.
Pac Symp Biocomput
2014
24319008
Using systems approaches to address challenges for clinical implementation of pharmacogenomics.
Wiley Interdiscip Rev Syst Biol Med
2014
23281421
Inclusion of pediatric samples in an opt-out biorepository linking DNA to de-identified medical records: pediatric BioVU.
Clin Pharmacol Ther
2013
24270849
Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data.
Nat Biotechnol
2013
23886923
Ethical and practical challenges to studying patients who opt out of large-scale biorepository research.
J Am Med Inform Assoc
2013
24009000
Electronic health record design and implementation for pharmacogenomics: a local perspective.
Genet Med
2013
24030437
Stakeholder engagement: a key component of integrating genomic information into electronic health records.
Genet Med
2013
23651022
Assessment of a pharmacogenomic marker panel in a polypharmacy population identified from electronic medical records.
Pharmacogenomics
2013
23588301
The Pharmacogenomics Research Network Translational Pharmacogenetics Program: overcoming challenges of real-world implementation.
Clin Pharmacol Ther
2013
22190063
Predicting clopidogrel response using DNA samples linked to an electronic health record.
Clin Pharmacol Ther
2012
23304330
A study of transportability of an existing smoking status detection module across institutions.
AMIA Annu Symp Proc
2012
22739144
Optimizing drug outcomes through pharmacogenetics: a case for preemptive genotyping.
Clin Pharmacol Ther
2012
22514303
Attention deficit/hyperactivity disorder-derived coding variation in the dopamine transporter disrupts microdomain targeting and trafficking regulation.
J Neurosci
2012
22588608
Operational implementation of prospective genotyping for personalized medicine: the design of the Vanderbilt PREDICT project.
Clin Pharmacol Ther
2012
22329724
Predicting warfarin dosage in European-Americans and African-Americans using DNA samples linked to an electronic health record.
Pharmacogenomics
2012
21399631
Flotillin-1 is essential for PKC-triggered endocytosis and membrane microdomain localization of DAT.
Nat Neurosci
2011
21672908
Facilitating pharmacogenetic studies using electronic health records and natural-language processing: a case study of warfarin.
J Am Med Inform Assoc
2011
20427663
Dysregulation of dopamine transporters via dopamine D2 autoreceptors triggers anomalous dopamine efflux associated with attention-deficit hyperactivity disorder.
J Neurosci
2010
19098122
A juxtamembrane mutation in the N terminus of the dopamine transporter induces preference for an inward-facing conformation.
Mol Pharmacol
2009
18614672
Anomalous dopamine release associated with a human dopamine transporter coding variant.
J Neurosci
2008
18617632
Syntaxin 1A interaction with the dopamine transporter promotes amphetamine-induced dopamine efflux.
Mol Pharmacol
2008
16908408
Calmodulin kinase II interacts with the dopamine transporter C terminus to regulate amphetamine-induced reverse transport.
Neuron
2006
1 - 35 of 35
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Christian M Shaffer
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Co-authored papers
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Marylyn D Ritchie
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Peter Weeke
Rigshospitalet, University of Copenhagen
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Jessica T Delaney
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Jonathan D Mosley
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Julie R Field
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Yaping Shi
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