David R. Crosslin

发表

Controlling for population structure and genotyping platform bias in the eMERGE multi-institutional biobank linked to electronic health records

Marylyn D. Ritchie, Dana C. Crawford, Shefali S. Verma, 2014, Front. Genet..

Automatic Identification of Lifestyle and Environmental Factors from Social History in Clinical Text

Lucy Vanderwende, Meliha Yetisgen-Yildiz, David R. Crosslin, 2016, CRI.

Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network.

Robert C. Green, Keith Marsolo, Casey Overby Taylor, 2019, American journal of human genetics.

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.

A Randomized Trial of Population-Based Clinical Decision Support to Manage Health and Resource Use for Medicaid Beneficiaries

Kensaku Kawamoto, Janese M. Willis, Jessica Simo, 2013, Journal of Medical Systems.

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.

Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR)

Jason H. Moore, Marylyn D. Ritchie, Shefali S. Verma, 2015, BioData Mining.

Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study

Suzette J. Bielinski, Christopher G. Chute, Joshua C. Denny, 2012, J. Am. Medical Informatics Assoc..

User-Centered Design of a Collaborative Genetic Variant Interpretation Tool

Annie T. Chen, Wayne H. Liang, Peter Tarczy-Hornoch, 2017, AMIA.

Assessing the Potential Economic Value of Health Information Technology Interventions in a Community-Based Health Network

Kensaku Kawamoto, Jennifer M. Macri, Kevin J. Anstrom, 2005, AMIA.

Assessing the Quality of Medical Information Technology Economic Evaluations: Room for Improvement

Kevin J. Anstrom, David F. Lobach, Eric L. Eisenstein, 2006, AMIA.

Copy number variation analysis in the context of electronic medical records and large-scale genomics consortium efforts

David R. Crosslin, Gail P. Jarvik, Berta Almoguera, 2014, Front. Genet..

Developing a Framework for Conducting Economic Evaluations of Community-Based Health Information Technology Interventions

Kensaku Kawamoto, Jennifer M. Macri, Kevin J. Anstrom, 2005, AMIA.

Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43,870 individuals from the eMERGE network

Xinyuan Zhang, Marylyn D. Ritchie, Chunhua Weng, 2018, PSB.

GWASTools: an R/Bioconductor package for quality control and analysis of genome-wide association studies

David Levine, Xiuwen Zheng, Thomas Lumley, 2012, Bioinform..

Economic Evaluation in Medical Information Technology: Why the Numbers Don't Add Up

Kevin J. Anstrom, David F. Lobach, Eric L. Eisenstein, 2006, AMIA.

Detectable clonal mosaicism from birth to old age and its relationship to cancer

Ingo Ruczinski, Li-e Wang, William L. Lowe, 2012, Nature Genetics.

LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins

George Hripcsak, Joshua C. Denny, Peggy L. Peissig, 2018, Circulation.

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

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

The phenotypic legacy of admixture between modern humans and Neandertals

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

Genetic Variants Associated with Serum Thyroid Stimulating Hormone (TSH) Levels in European Americans and African Americans from the eMERGE Network

Suzette J. Bielinski, Christopher G. Chute, Marylyn D. Ritchie, 2014, PloS one.

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.

A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects

Christopher G. Chute, Marylyn D. Ritchie, Joshua C. Denny, 2013, Human Genetics.

Electronic medical records and genomics (eMERGE) network exploration in cataract: Several new potential susceptibility loci

Marylyn D. Ritchie, Joshua C. Denny, Shefali S. Verma, 2014, Molecular vision.

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.

eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants

Suzette J. Bielinski, Gerard Tromp, Marylyn D. Ritchie, 2016, BMC Medical Genomics.

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 .

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.

Confirmation of the Reported Association of Clonal Chromosomal Mosaicism with an Increased Risk of Incident Hematologic Cancer

Alex P. Reiner, David R. Crosslin, Gail P. Jarvik, 2013, PloS one.