Frederick E. Dewey

发表

Integrating Clinical Laboratory Measures and ICD-9 Code Diagnoses in Phenome-Wide Association Studies

Marylyn D. Ritchie, Shefali S. Verma, Anurag Verma, 2016, PSB.

Identifying Genetic Associations with Variability in Metabolic Health and Blood Count Laboratory Values: Diving into the Quantitative Traits by Leveraging Longitudinal Data from an EHR

Marylyn D. Ritchie, Shefali S. Verma, Joseph B. Leader, 2017, PSB.

CLAMMS: a scalable algorithm for calling common and rare copy number variants from exome sequencing data

Frederick E. Dewey, Alexander E. Lopez, John D. Overton, 2015, Bioinform..

Genetic identification of familial hypercholesterolemia within a single U.S. health care system

Marylyn D. Ritchie, Alan R. Shuldiner, Laney K. Jones, 2016, Science.

Sequence to Medical Phenotypes: A Framework for Interpretation of Human Whole Genome DNA Sequence Data

Russ B. Altman, Matthew Wheeler, Teri E. Klein, 2015, PLoS genetics.

KaryoScan: abnormal karyotype detection from whole-exome sequence

Jeffrey Staples, Frederick E. Dewey, Alexander E. Lopez, 2017 .

Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study

Marylyn D. Ritchie, Scott Mellis, Alan R. Shuldiner, 2016, Science.

Systems-Based Approaches to Cardiovascular Biomarker Discovery

Francisco Azuaje, Euan A. Ashley, Frederick E. Dewey, 2012, Circulation. Cardiovascular genetics.

Profiling copy number variation and disease associations from 50,726 DiscovEHR Study exomes

Marylyn D. Ritchie, Alan R. Shuldiner, Jeffrey Staples, 2017, bioRxiv.

Gene Coexpression Network Topology of Cardiac Development, Hypertrophy, and Failure

Euan A. Ashley, Sridhar Hannenhalli, Frederick E. Dewey, 2011, Circulation. Cardiovascular genetics.

MAPPIN: a method for annotating, predicting pathogenicity and mode of inheritance for nonsynonymous variants

Frederick E. Dewey, Suganthi Balasubramanian, Nehal Gosalia, 2017, Nucleic acids research.