Brian H. Shirts

发表

An interlaboratory study of complex variant detection

Marc L. Salit, Eric W. Klee, Nazneen Rahman, 2017, bioRxiv.

Pragmatic and Ethical Challenges of Incorporating the Genome into the Electronic Health Record

Peter Tarczy-Hornoch, Brian H. Shirts, Adam A. Nishimura, 2014, Current Genetic Medicine Reports.

A Template for Authoring and Adapting Genomic Medicine Content in the eMERGE Infobutton Project

Christopher G. Chute, Joshua C. Denny, Marc S. Williams, 2014, AMIA.

Clinical laboratory analytics: Challenges and promise for an emerging discipline

Brian R. Jackson, Enrique Terrazas, Brian H. Shirts, 2015, Journal of pathology informatics.

The genomic CDS sandbox: An assessment among domain experts

Kensaku Kawamoto, Karen Eilbeck, Marc S. Williams, 2016, J. Biomed. Informatics.

Modeling the costs of clinical decision support for genomic precision medicine

Peter Tarczy-Hornoch, Brian H. Shirts, Patrick C. Mathias, 2016, AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science.

Physician perspectives of CYP2C19 and clopidogrel drug-gene interaction active clinical decision support alerts

Peter Tarczy-Hornoch, Emily Beth Devine, Brian H. Shirts, 2016, Int. J. Medical Informatics.

CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record

Christopher G. Chute, Marc S. Williams, Peggy L. Peissig, 2015, J. Am. Medical Informatics Assoc..

Utilization and utility of clinical laboratory reports with graphical elements

Brian R. Jackson, Brian H. Shirts, Nichole Larsen, 2012, Journal of pathology informatics.

The 2013 symposium on pathology data integration and clinical decision support and the current state of field

Ramy Arnaout, John R. Gilbertson, Alexis B. Carter, 2014, Journal of pathology informatics.

Using Patients Like My Patient for Clinical Decision Support: Institution-Specific Probability of Celiac Disease Diagnosis Using Simplified Near-Neighbor Classification

Brian R. Jackson, Brian H. Shirts, Sterling T. Bennett, 2013, Journal of general internal medicine.

Erratum: Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine (American Journal of Human Genetics (2016) 98(6) (1067–1076) (S0002929716301069) (10.1016/j.ajhg.2016.04.011))

Sara Chandros Hull, Robert C. Green, Sean D. Mooney, 2016 .

Power of pedigree likelihood analysis in extended pedigrees to classify rare variants of uncertain significance in cancer risk genes

Brian H. Shirts, Elisabeth A. Rosenthal, B. Shirts, 2017, Familial Cancer.

Large numbers of individuals are required to classify and define risk for rare variants in known cancer risk genes

Gail P. Jarvik, Brian L. Browning, Brian H. Shirts, 2013, Genetics in Medicine.