David S. Carrell

发表

Automatic Text De-Identification: How and When is it Acceptable?

Stéphane M. Meystre, Lynette Hirschman, John S. Aberdeen, 2018, American Medical Informatics Association Annual Symposium.

Facilitating phenotype transfer using a common data model

George Hripcsak, Chunhua Weng, Joshua C. Denny, 2019, J. Biomed. Informatics.

Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals

Jason H. Moore, Gerard Tromp, Marylyn D. Ritchie, 2017, BioData Mining.

Is an Algorithm Just an Algorithm? How to Define Clinical Concepts for Use in Comparative Safety and Effectiveness Distributed Research Networks

Keith Marsolo, Leonard W. D'Avolio, Jeffrey S. Brown, 2017, CRI.

PS1-17: Organization-wide Collaboration to Convert Binary Clinical Notes to Research-ready Text

Roy Pardee, Roger Wong, Carolyn M. Rutter, 2014, Clinical Medicine & Research.

Challenges in adapting existing clinical natural language processing systems to multiple, diverse health care settings

Sherri Rose, Robert E. Schoen, Ateev Mehrotra, 2017, J. Am. Medical Informatics Assoc..

Using natural language processing to identify problem usage of prescription opioids

David Cronkite, David S. Carrell, Roy E. Palmer, 2015, Int. J. Medical Informatics.

Desiderata for computable representations of electronic health records-driven phenotype algorithms

Paul A. Harris, Gerard Tromp, Jie Xu, 2015, J. Am. Medical Informatics Assoc..

Enrichment sampling for a multi-site patient survey using electronic health records and census data

Sarah C. Stallings, Jonathan S. Schildcrout, Gail P. Jarvik, 2019, J. Am. Medical Informatics Assoc..

Facilitating Self-reflection about Values and Self-care Among Individuals with Chronic Conditions

Tad Hirsch, James D. Ralston, David S. Carrell, 2019, CHI.

Prospective participant selection and ranking to maximize actionable pharmacogenetic variants and discovery in the eMERGE Network

Marylyn D. Ritchie, Andrea Hartzler, James Ralston, 2015, Genome Medicine.

Detecting the Presence of an Individual in Phenotypic Summary Data

Murat Kantarcioglu, Yevgeniy Vorobeychik, Bradley Malin, 2018, AMIA.

C3-4: An Algorithm to Combine Machine Learning and Structured Data to Automate De-identification of Clinical Text

David S. Carrell, Scott Halgrim, Diem-Thy Tran, 2014, Clinical Medicine & Research.

PheKB: a catalog and workflow for creating electronic phenotype algorithms for transportability

Paul A. Harris, Gerard Tromp, Joshua C. Denny, 2016, J. Am. Medical Informatics Assoc..

ePhenotyping for Abdominal Aortic Aneurysm in the Electronic Medical Records and Genomics (eMERGE) Network: Algorithm Development and Konstanz Information Miner Workflow

Jyotishman Pathak, Joshua C Denny, Peggy L Peissig, 2015, International journal of biomedical data mining.

Making work visible for electronic phenotype implementation: Lessons learned from the eMERGE network

Joshua C. Denny, Chunhua Weng, Wei-Qi Wei, 2019, J. Biomed. Informatics.

Identification of Four Novel Loci in Asthma in European American and African American Populations

Peggy L. Peissig, Jennifer A. Pacheco, Iftikhar J. Kullo, 2017, American journal of respiratory and critical care medicine.

Mechanistic Phenotypes: An Aggregative Phenotyping Strategy to Identify Disease Mechanisms Using GWAS Data

Gerard Tromp, Yan Guo, Marylyn D. Ritchie, 2013, PloS one.

Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.

Jonathan S. Schildcrout, Stephanie M. Fullerton, Gail P. Jarvik, 2017, American journal of human genetics.

The phenotypic legacy of admixture between modern humans and Neandertals

Gerard Tromp, Marylyn D. Ritchie, Joshua C. Denny, 2016, Science.

Design and Anticipated Outcomes of the eMERGE-PGx Project: A Multi-Center Pilot for Pre-Emptive Pharmacogenomics in Electronic Health Record Systems

Suzette J. Bielinski, Christopher G. Chute, Marylyn D. Ritchie, 2014, Clinical pharmacology and therapeutics.

Identifying gene–gene interactions that are highly associated with four quantitative lipid traits across multiple cohorts

Gerard Tromp, Marylyn D. Ritchie, Shefali S. Verma, 2016, Human Genetics.

Practice of Epidemiology Using Natural Language Processing to Improve Efficiency of Manual Chart Abstraction in Research : The Case of Breast Cancer Recurrence

Wendy W. Chapman, Scott R. Halgrim, Guergana Savova, 2014 .

Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index

Suzette J. Bielinski, Gerard Tromp, Christopher G. Chute, 2014, Front. Genet..

Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci

Gerard Tromp, Marylyn D. Ritchie, Dana C. Crawford, 2017, Circulation research.