|The CLIPMERGE PGx Program: clinical implementation of personalized medicine through electronic health records and genomics–pharmacogenomics|
O Gottesman, SA Scott, SB Ellis, CL Overby, A Ludtke, JS Hulot, J Hall, ...
Clinical Pharmacology & Therapeutics 94 (2), 214-217, 2013
|Implementation of pharmacogenetics: The University of Maryland personalized anti‐platelet pharmacogenetics program|
AR Shuldiner, K Palmer, RE Pakyz, TD Alestock, KA Maloney, C O'Neill, ...
American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2014
|Usability evaluation of pharmacogenomics clinical decision support aids and clinical knowledge resources in a computerized provider order entry system: a mixed methods approach|
EB Devine, CJ Lee, CL Overby, N Abernethy, J McCune, JW Smith, ...
International journal of medical informatics 83 (7), 473-483, 2014
|CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record|
BH Shirts, JS Salama, SJ Aronson, WK Chung, SW Gray, LA Hindorff, ...
Journal of the American Medical Informatics Association 22 (6), 1231-1242, 2015
|Opportunities for genomic clinical decision support interventions|
CL Overby, I Kohane, JL Kannry, MS Williams, J Starren, E Bottinger, ...
GeNetiCS in meDiCiNe 15 (10), 817-823, 2013
|A collaborative approach to developing an electronic health record phenotyping algorithm for drug-induced liver injury|
CL Overby, J Pathak, O Gottesman, K Haerian, A Perotte, S Murphy, ...
Journal of the American Medical Informatics Association 20 (e2), e243-e252, 2013
|Feasibility of incorporating genomic knowledge into electronic medical records for pharmacogenomic clinical decision support|
CL Overby, P Tarczy-Hornoch, JI Hoath, IJ Kalet, DL Veenstra
BMC bioinformatics 11 (S9), S10, 2010
|Personalized medicine: challenges and opportunities for translational bioinformatics|
CL Overby, P Tarczy-Hornoch
Personalized medicine 10 (5), 453-462, 2013
|Practical considerations in genomic decision support: The eMERGE experience|
TM Herr, SJ Bielinski, E Bottinger, A Brautbar, M Brilliant, CG Chute, ...
Journal of pathology informatics 6, 2015
|Disseminating context-specific access to online knowledge resources within electronic health record systems|
G Del Fiol, C Curtis, JJ Cimino, A Iskander, ASD Kalluri, X Jing, NC Hulse, ...
Studies in health technology and informatics 192, 672, 2013
|Physician attitudes toward adopting genome-guided prescribing through clinical decision support|
CL Overby, AL Erwin, NS Abul-Husn, SB Ellis, SA Scott, AO Obeng, ...
Journal of personalized medicine 4 (1), 35-49, 2014
|Making pharmacogenomic-based prescribing alerts more effective: a scenario-based pilot study with physicians|
CL Overby, EB Devine, N Abernethy, JS McCune, P Tarczy-Hornoch
Journal of biomedical informatics 55, 249-259, 2015
|Developing a prototype system for integrating pharmacogenomics findings into clinical practice|
CL Overby, P Tarczy-Hornoch, IJ Kalet, KE Thummel, JW Smith, GD Fiol, ...
Journal of personalized medicine 2 (4), 241-256, 2012
|Practical considerations for implementing genomic information resources: experiences from eMERGE and CSER|
LV Rasmussen, CL Overby, J Connolly, CG Chute, JC Denny, ...
Applied clinical informatics 7 (3), 870, 2016
|Integrating genomic resources with electronic health records using the HL7 Infobutton standard|
BSE Heale, CL Overby, G Del Fiol, WS Rubinstein, DR Maglott, ...
Applied clinical informatics 7 (3), 817, 2016
|User-centered design of multi-gene sequencing panel reports for clinicians|
E Cutting, M Banchero, AL Beitelshees, JJ Cimino, G Del Fiol, AP Gurses, ...
Journal of biomedical informatics 63, 1-10, 2016
|A template for authoring and adapting genomic medicine content in the eMERGE infobutton project|
CL Overby, LV Rasmussen, A Hartzler, JJ Connolly, JF Peterson, ...
AMIA annual symposium proceedings 2014, 944, 2014
|Practical choices for infobutton customization: experience from four sites|
JJ Cimino, CL Overby, EB Devine, NC Hulse, X Jing, SM Maviglia, ...
AMIA Annual Symposium Proceedings 2013, 236, 2013
|Harmonizing clinical sequencing and interpretation for the eMERGE III network|
H Zouk, E Venner, NJ Lennon, DM Muzny, D Abrams, S Adunyah, ...
The American Journal of Human Genetics 105 (3), 588-605, 2019
|Providing access to genomic variant knowledge in a healthcare setting: a vision for the ClinGen Electronic Health Records Workgroup|
CL Overby, B Heale, S Aronson, JM Cherry, S Dwight, A Milosavljevic, ...
Clinical Pharmacology & Therapeutics 99 (2), 157-160, 2016