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

Genomic considerations for FHIR®; eMERGE implementation lessons.
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

User-Centered Design of a Collaborative Genetic Variant Interpretation Tool.
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


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


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