Prediction of periventricular leukomalacia. Part I: Selection of hemodynamic features using logistic regression and decision tree algorithms. - Biswanath Samanta; Geoffrey L. Bird; Marijn Kuijpers; Robert A. Zimmerman; Gail P. Jarvik; Gil Wernovsky; Robert R. Clancy; Daniel J. Licht; J. William Gaynor; Chandrasekhar Nataraj (Artif. Intell. Medicine, 2009)

Prediction of periventricular leukomalacia. Part II: Selection of hemodynamic features using computational intelligence. - Biswanath Samanta; Geoffrey L. Bird; Marijn Kuijpers; Robert A. Zimmerman; Gail P. Jarvik; Gil Wernovsky; Robert R. Clancy; Daniel J. Licht; J. William Gaynor; Chandrasekhar Nataraj (Artif. Intell. Medicine, 2009)

Using Electronic Health Records to Identify Heart Failure Cohorts with Differentiation for Preserved and Reduced Ejection Fraction. - Suzette J. Bielinski; Jyotishman Pathak; Hongfang Liu; Sunghwan Sohn; Gail P. Jarvik; David Carrell; Naveen Pereira; Véronique L. Roger (AMIA, 2012)

Using PheWAS to Assess Pleiotropy of Genetic Risk Scores for Rheumatoid Arthritis and Coronary Artery Disease in the eMERGE Network. - Robert J. Carroll; Katherine P. Liao; Anne E. Eyler; Lisa Bastarache; Dana C. Crawford; Peggy L. Peissig; Jyotishman Pathak; David Carrell; Abel N. Kho; Rongling Li; Daniel R. Masys; Gail P. Jarvik; et al. (AMIA, 2012)

Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study. - Abel N. Kho; M. Geoffrey Hayes; Laura Rasmussen-Torvik; Jennifer A. Pacheco; William K. Thompson; Loren L. Armstrong; Joshua C. Denny; Peggy L. Peissig; Aaron W. Miller; Wei-Qi Wei; Suzette J. Bielinski; Christopher G. Chute; et al. (J. Am. Medical Informatics Assoc., 2012)

Technical desiderata for the integration of genomic data into Electronic Health Records. - Daniel R. Masys; Gail P. Jarvik; Neil F. Abernethy; Nicholas R. Anderson 001; George J. Papanicolaou; Dina N. Paltoo; Mark A. Hoffman; Isaac S. Kohane; Howard P. Levy (J. Biomed. Informatics, 2012)

A Template for Authoring and Adapting Genomic Medicine Content in the eMERGE Infobutton Project. - Casey L. Overby; Luke V. Rasmussen; Andrea L. Hartzler; John J. Connolly; Josh F. Peterson; RoseMary Hedberg; Robert R. Freimuth; Brian H. Shirts; Joshua C. Denny; Eric B. Larson; Christopher G. Chute; Gail P. Jarvik; et al. (AMIA, 2014)

Replication of SCN5A Associations with Electrocardiographic Traits in African Americans from Clinical and Epidemiologic Studies. - Janina M. Jeff; Kristin Brown-Gentry; Robert J. Goodloe; Marylyn D. Ritchie; Joshua C. Denny; Abel N. Kho; Loren L. Armstrong; Bob McClellan Jr.; Ping Mayo; Melissa Allen; Hailing Jin; Niloufar B. Gillani; et al. (EvoApplications, 2014)

Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR). - Rishika De; Shefali S. Verma; Fotios Drenos; Emily Rose Holzinger; Michael Holmes; Molly A. Hall; David R. Crosslin; David Carrell; Hakon Hakonarson; Gail P. Jarvik; Eric B. Larson; Jennifer A. Pacheco; et al. (BioData Min., 2015)

Desiderata for computable representations of electronic health records-driven phenotype algorithms. - Huan Mo; William K. Thompson; Luke V. Rasmussen; Jennifer A. Pacheco; Guoqian Jiang; Richard C. Kiefer; Qian Zhu 003; Jie Xu 011; Enid N. H. Montague; David S. Carrell; Todd Lingren; Frank D. Mentch; et al. (J. Am. Medical Informatics Assoc., 2015)

CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record. - Brian H. Shirts; Joseph S. Salama; Samuel J. Aronson; Wendy K. Chung; Stacy W. Gray; Lucia A. Hindorff; Gail P. Jarvik; Sharon E. Plon; Elena M. Stoffel; Peter Tarczy-Hornoch; Eliezer M. Van Allen; Karen E. Weck; et al. (J. Am. Medical Informatics Assoc., 2015)

User-Centered Design of a Collaborative Genetic Variant Interpretation Tool. - Wayne H. Liang; Bas de Veer; Diane M. Korngiebel; Annie T. Chen; Gail P. Jarvik; Peter Tarczy-Hornoch; David R. Crosslin (AMIA, 2017)

Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals. - Emily Rose Holzinger; Shefali S. Verma; Carrie Colleen Buchanan Moore; Molly A. Hall; Rishika De; Diane Gilbert-Diamond; Matthew B. Lanktree; Nathan Pankratz; Antoinette Amuzu; Amber Burt; Caroline Dale; Scott M. Dudek; et al. (BioData Min., 2017)

Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43, 870 individuals from the eMERGE network. - Xinyuan Zhang 003; Yogasudha Veturi; Shefali Setia Verma; William Bone; Anurag Verma; Anastasia Lucas; Scott J. Hebbring; Joshua C. Denny; Ian B. Stanaway; Gail P. Jarvik; David R. Crosslin; Eric B. Larson; et al. (PSB, 2019)

Enrichment sampling for a multi-site patient survey using electronic health records and census data. - Nathaniel D. Mercaldo; Kyle B. Brothers; David S. Carrell; Ellen Wright Clayton; John J. Connolly; Ingrid A. Holm; Carol R. Horowitz; Gail P. Jarvik; Terrie E. Kitchner; Rongling Li; Catherine A. McCarty; Jennifer B. McCormick; et al. (J. Am. Medical Informatics Assoc., 2019)

Implementation matters: How patient experiences differ when genetic counseling accompanies the return of genetic variants of uncertain significance. - Harsh V. Patel; Nora Henrikson; James D. Ralston; Kathleen A. Leppig; Aaron Scrol; Gail P. Jarvik; Shannon DeVange; Eric Larson; Andrea L. Hartzler (AMIA, 2021)

Genomic considerations for FHIR®; eMERGE implementation lessons. - Mullai Murugan; Lawrence J. Babb; Casey Overby Taylor; Luke V. Rasmussen; Robert R. Freimuth; Eric Venner; Fei Yan; Victoria Yi; Stephen J. Granite; Hana Zouk; Samuel J. Aronson; Kevin Power; et al. (J. Biomed. Informatics, 2021)

Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies. - Ning Shang; Atlas Khan; Fernanda Polubriaginof; Francesca Zanoni; Karla Mehl; David Fasel; Paul E. Drawz; Robert J. Carroll; Joshua C. Denny; Matthew A. Hathcock; Adelaide M. Arruda-Olson; Peggy L. Peissig; et al. (npj Digit. Medicine, 2021)

A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources. - Ken Wiley; Laura Findley; Madison Goldrich; Tejinder K. Rakhra-Burris; Ana Stevens; Pamela Williams; Carol J. Bult; Rex L. Chisholm; Patricia Deverka; Geoffrey S. Ginsburg; Eric D. Green; Gail P. Jarvik; et al. (J. Am. Medical Informatics Assoc., 2022)

Enriched phenotypes in rare variant carriers suggest pathogenic mechanisms in rare disease patients. - Lane Fitzsimmons; Maria T. Acosta; David R. Adams; Ben Afzali; Ali Al-Beshri; Eric Allenspach; Aimee Allworth; Raquel L. Alvarez; Justin Alvey; Ashley Andrews; Euan A. Ashley; Carlos A. Bacino; et al. (BioData Min., 2025)