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- Clinical genomics in the world of the electronic health record.Genet Med. 2013; 15: 786-791
- Adoption factors of the electronic health record: a systematic review.JMIR Med Inform. 2016; 4: e19
- Future of electronic health records: implications for decision support.Mt Sinai J Med. 2012; 79: 757-768
- Translational bioinformatics: past, present, and future.Genomics Proteomics Bioinformatics. 2016; 14: 31-41
- Towards precision medicine.Nat Rev Genet. 2016; 17: 507-522
- A new initiative on precision medicine.N Engl J Med. 2015; 372: 793-795
- Predictive, personalized, preventive, participatory (P4) cancer medicine.Nat Rev Clin Oncol. 2011; 8: 184-187
- A 2014 medical informatics perspective on clinical decision support systems: do we hit the ceiling of effectiveness?.Yearb Med Inform. 2014; 9: 163-166
- A roadmap for national action on clinical decision support.J Am Med Inform Assoc. 2007; 14: 141-145
- Personalized medicine: hope or hype?.Eur Heart J. 2012; 33: 1564-1570
- Effects of computerized clinical decision support systems on practitioner performance and patient outcomes: a systematic review.JAMA. 2005; 293: 1223-1238
- Medication-related clinical decision support in computerized provider order entry systems: a review.J Am Med Inform Assoc. 2007; 14: 29-40
- Clinical decision support and appropriateness of antimicrobial prescribing: a randomized trial.JAMA. 2005; 294: 2305-2314
- CPIC: clinical pharmacogenetics implementation consortium of the pharmacogenomics research network.Clin Pharmacol Ther. 2011; 89: 464-467
- Development and use of active clinical decision support for preemptive pharmacogenomics.J Am Med Inform Assoc. 2014; 21: e93-e99
- Feasibility of incorporating genomic knowledge into electronic medical records for pharmacogenomic clinical decision support.BMC Bioinformatics. 2010; 11: S10
- Electronic health records (EHRs): supporting ASCO's vision of cancer care.Am Soc Clin Oncol Educ Book. 2014; 34: 225-231
- Workflow-driven clinical decision support for personalized oncology.BMC Med Inform Decis Mak. 2016; 16: 147
- Can computerized clinical decision support systems improve practitioners' diagnostic test ordering behavior? A decision-maker-researcher partnership systematic review.Implement Sci. 2011; 6: 88
- Improving the value of costly genetic reference laboratory testing with active utilization management.Arch Pathol Lab Med. 2014; 138: 110-113
- Clinical decision support systems for the practice of evidence-based medicine.J Am Med Inform Assoc. 2001; 8: 527-534
- Clinical decision support for genetically guided personalized medicine: a systematic review.J Am Med Inform Assoc. 2013; 20: 388-400
- Clinical decision support systems for improving diagnostic accuracy and achieving precision medicine.J Clin Bioinforma. 2015; 5: 4
- Changing interpretations, stable genes: responsibilities of patients, professionals, and policy makers in the clinical interpretation of complex genetic information.Genet Med. 2008; 10: 778-783
- Clinical decision support systems.in: Berner E.S. Springer, New York2006https://doi.org/10.1007/978-0-387-38319-4
- Design recommendations for pharmacogenomics clinical decision support systems.AMIA Jt Summits Transl Sci Proc. 2017; 2017: 237-246
- The pharmacogenetics and pharmacogenomics knowledge base: accentuating the knowledge.Nucleic Acids Res. 2007; 36: D913-D918
- Genetics aware clinical decision support.in: Genomic and precision medicine. Academic Press, 2016: 205-215
- Optimization of infobutton design and Implementation: a systematic review.J Biomed Inform. 2017; 74: 10-19
- Online Mendelian Inheritance in man, OMIM®.(Available at:) (Accessed October 15, 2018)
- Clinical analysis and interpretation of cancer genome data.J Clin Oncol. 2013; 31: 1825-1833
- A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health record.Genet Med. 2013; 15: 824-832
- Ten commandments for effective clinical decision support: making the practice of evidence-based medicine a reality.J Am Med Inform Assoc. 2003; 10: 523-530
- The genome-enabled electronic medical record.J Biomed Inform. 2007; 40: 44-46
- Technical desiderata for the integration of genomic data into electronic health records.J Biomed Inform. 2012; 45: 419-422
- Technical desiderata for the integration of genomic data with clinical decision support.J Biomed Inform. 2014; 51: 3-7
- Improving performance of healthcare systems with service oriented architecture.InfoQ, 2008 (Available at:) (Accessed October 15, 2018)
- Practical challenges in integrating genomic data into the electronic health record.Genet Med. 2013; 15: 772-778
- Empowering Mayo Clinic individualized medicine with genomic data warehousing.J Pers Med. 2017; 7: 7
- CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record.J Am Med Inform Assoc. 2015; 22: 1231-1242
- The real cost of sequencing: scaling computation to keep pace with data generation.Genome Biol. 2016; 17: 4731
- Comparison of high-throughput sequencing data compression tools.Nat Methods. 2016; 13: 1005-1008
- Raw genomic data: storage, access, and sharing.Trends Genet. 2018; 34: 8-10
- Cloud computing for genomic data analysis and collaboration.Nat Rev Genet. 2018; 19: 208-219
- Genomic cloud computing: legal and ethical points to consider.Eur J Hum Genet. 2015; 23: 1271-1278
- Facilitating a culture of responsible and effective sharing of cancer genome data.Nat Med. 2016; 22: 464-471
- SMART on FHIR Genomics: facilitating standardized clinico-genomic apps.J Am Med Inform Assoc. 2015; 22: 1173-1178
- SMART on FHIR: a standards-based, interoperable apps platform for electronic health records.J Am Med Inform Assoc. 2016; 23: 899-908
- Integrating cancer genomic data into electronic health records.Genome Med. 2016; 8: 113
McGowan-Jordan J, Schmid M, Simons A. Iscn 2016. 2016.
- HGVS recommendations for the description of sequence variants: 2016 update.Hum Mutat. 2016; 37: 564-569
- Supporting interoperability of genetic data with LOINC.J Am Med Inform Assoc. 2015; 22: 621-627
- The variant call format and VCFtools.Bioinformatics. 2011; 27: 2156-2158
- GT2RDF: semantic representation of genetic testing data.AMIA Annu Symp Proc. 2016; 2016: 1060-1069
- CDS-Hooks.(Available at:)
- The personal and clinical utility of polygenic risk scores.Nat Rev Genet. 2018; 19: 581-590
- Modeling the costs of clinical decision support for genomic precision medicine.AMIA Jt Summits Transl Sci Proc. 2016; 2016: 60-64
- Analysis of protein-coding genetic variation in 60,706 humans.Nature. 2016; 536: 285-291
- Family-specific variants and the limits of human genetics.Trends Mol Med. 2016; 22: 925-934
- Knowledge for precision medicine: mechanistic reasoning and methodological pluralism.JAMA. 2017; 318: 1649
- Finding the missing heritability of complex diseases.Nature. 2009; 461: 747-753
- Advances in sharing multi-sourced health data on decision support science 2016-2017.Yearb Med Inform. 2018; 27: 16-24
- Genetic data sharing and privacy.Neuroinformatics. 2015; 13: 1-6
- Clinical decision support capabilities of commercially-available clinical information systems.J Am Med Inform Assoc. 2009; 16: 637-644
- Formative evaluation of clinician experience with integrating family history-based clinical decision support into clinical practice.J Pers Med. 2014; 4: 115-136
- Family health history: the case for better tools.JAMA. 2015; 313: 1711-1712
- An assessment of family history information captured in an electronic health record.AMIA Annu Symp Proc. 2015; 2015: 2035-2042
Coalition’s reactions to public comments on the voluntary industry guidelines. cdscoalition.org. Available at: http://cdscoalition.org/wp-content/uploads/2017/08/CDS-3060-Guidelines-Final-2.pdf. Accessed October 15, 2018.
- Clinical decision support and malpractice risk.JAMA. 2011; 306: 90-91
- Clinical decision support systems: a discussion of quality, safety and legal liability issues.Proc AMIA Symp. 2002; : 265-269
- Key principles for a national clinical decision support knowledge sharing framework: synthesis of insights from leading subject matter experts.J Am Med Inform Assoc. 2013; 20: 199-207
Clinical and patient decision support software. fda.gov. Available at: https://www.fda.gov/downloads/medicaldevices/deviceregulationandguidance/guidancedocuments/ucm587819.pdf. Accessed October 15, 2018.
- Overcoming the Reimbursement barriers for clinical sequencing.JAMA. 2014; 312: 1857-1858
- Communicating new knowledge on previously reported genetic variants.Genet Med. 2012; 14: 713-719
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Disclosure Statement: Dr N. Krumm and Dr B.H. Shirts are funded by the University of Washington, Department of Laboratory Medicine. Dr B.H. Shirts also receives funds from the Damon Runyon Cancer Research Foundation (DRR-33-15) and the Fred Hutch/University of Washington Cancer Consortium (NCI 5P30 CA015704-39).