Gail P. Jarvik
According to our database1,
Gail P. Jarvik
authored at least 19 papers
between 2009 and 2022.
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Bibliography
2022
A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources.
J. Am. Medical Informatics Assoc., 2022
2021
Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies.
npj Digit. Medicine, 2021
J. Biomed. Informatics, 2021
Implementation matters: How patient experiences differ when genetic counseling accompanies the return of genetic variants of uncertain significance.
Proceedings of the AMIA 2021, American Medical Informatics Association Annual Symposium, San Diego, CA, USA, October 30, 2021, 2021
2019
Enrichment sampling for a multi-site patient survey using electronic health records and census data.
J. Am. Medical Informatics Assoc., 2019
Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43, 870 individuals from the eMERGE network.
Proceedings of the Biocomputing 2019: Proceedings of the Pacific Symposium, 2019
2017
Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals.
BioData Min., 2017
Proceedings of the AMIA 2017, 2017
2015
CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record.
J. Am. Medical Informatics Assoc., 2015
Desiderata for computable representations of electronic health records-driven phenotype algorithms.
J. Am. Medical Informatics Assoc., 2015
Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR).
BioData Min., 2015
2014
Replication of SCN5A Associations with Electrocardiographic Traits in African Americans from Clinical and Epidemiologic Studies.
Proceedings of the Applications of Evolutionary Computation - 17th European Conference, 2014
A Template for Authoring and Adapting Genomic Medicine Content in the eMERGE Infobutton Project.
Proceedings of the AMIA 2014, 2014
2012
Technical desiderata for the integration of genomic data into Electronic Health Records.
J. Biomed. Informatics, 2012
Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study.
J. Am. Medical Informatics Assoc., 2012
Using PheWAS to Assess Pleiotropy of Genetic Risk Scores for Rheumatoid Arthritis and Coronary Artery Disease in the eMERGE Network.
Proceedings of the AMIA 2012, 2012
Using Electronic Health Records to Identify Heart Failure Cohorts with Differentiation for Preserved and Reduced Ejection Fraction.
Proceedings of the AMIA 2012, 2012
2009
Prediction of periventricular leukomalacia. Part II: Selection of hemodynamic features using computational intelligence.
Artif. Intell. Medicine, 2009
Prediction of periventricular leukomalacia. Part I: Selection of hemodynamic features using logistic regression and decision tree algorithms.
Artif. Intell. Medicine, 2009