Nancy J. Cox

According to our database1, Nancy J. Cox authored at least 20 papers between 2006 and 2023.

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Bibliography

2023
FAVOR: functional annotation of variants online resource and annotator for variation across the human genome.
Nucleic Acids Res., January, 2023

Interactive network-based clustering and investigation of multimorbidity association matrices with associationSubgraphs.
Bioinform., January, 2023

Author Correction: The high-dimensional space of human diseases built from diagnosis records and mapped to genetic loci.
Nat. Comput. Sci., 2023

The high-dimensional space of human diseases built from diagnosis records and mapped to genetic loci.
Nat. Comput. Sci., 2023

2021
A retrospective approach to evaluating potential adverse outcomes associated with delay of procedures for cardiovascular and cancer-related diagnoses in the context of COVID-19.
J. Biomed. Informatics, 2021

DDIWAS: High-throughput electronic health record-based screening of drug-drug interactions.
J. Am. Medical Informatics Assoc., 2021

Implications of Clinical Bias When Building Electronic Algorithms for Medical Record Phenotyping: Lessons from Type 2 Diabetes Mellitus.
Proceedings of the AMIA 2021, American Medical Informatics Association Annual Symposium, San Diego, CA, USA, October 30, 2021, 2021

2020
PheMap: a multi-resource knowledge base for high-throughput phenotyping within electronic health records.
J. Am. Medical Informatics Assoc., 2020

2019
De novo pattern discovery enables robust assessment of functional consequences of non-coding variants.
Bioinform., 2019

2017
The impact of rare variation on gene expression across tissues.
Nat., 2017

2016
Consistency in large pharmacogenomic studies.
Nat., 2016

STAMS: STRING-assisted module search for genome wide association studies and application to autism.
Bioinform., 2016

2015
Global circulation patterns of seasonal influenza viruses vary with antigenic drift.
Nat., 2015

Consensus Genotyper for Exome Sequencing (CGES): improving the quality of exome variant genotypes.
Bioinform., 2015

A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis.
Bioinform., 2015

SCAN database: facilitating integrative analyses of cytosine modification and expression QTL.
Database J. Biol. Databases Curation, 2015

2013
Research and applications: Network models of genome-wide association studies uncover the topological centrality of protein interactions in complex diseases.
J. Am. Medical Informatics Assoc., 2013

2012
Systems Pharmacogenomics-Bridging the Gap.
Proceedings of the Biocomputing 2012: Proceedings of the Pacific Symposium, 2012

2010
SCAN: SNP and copy number annotation.
Bioinform., 2010

2006
GEL: a novel genotype calling algorithm using empirical likelihood.
Bioinform., 2006


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