Author

Andrea N. Burnett‐Hartman

Kaiser PermanenteORCID 0000-0003-4009-0680Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:statistical model· 4 Organism:human· 3 Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Research Focus:benchmarking· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Stephen Jacob ChanockiD· 3 shared Andrea GsuriD· 2 shared Andrew Tan ChaniD· 2 shared Annika LindblomiD· 2 shared Conghui QuiD· 2 shared Daniel D. BuchananiD· 2 shared David Timothy BishopiD· 2 shared David V. ContiiD· 2 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Stephen Jacob ChanockORCID

Mutual co-authors in cluster

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4 papers

Recent·Most cited

Genetic & Genomic MedicineGenetics in MedicinePeer-reviewedJun 28, 2024

Using Coincidence Analysis to Identify Causal Chains of Factors Associated with Implementation and Optimization of Lynch Syndrome Tumor Screening Across Multiple Health care Systems

Deborah L. Cragun, Zachary M. Salvati, Jennifer L. Schneider…·Alanna Kulchak Rahm

This paper identifies causal chains affecting Lynch syndrome tumor screening implementation across healthcare systems using coincidence analysis of stakeholder interviews.

6 citations

statistical modelbenchmarking

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintJan 19, 2023

Combining Asian-European Genome-Wide Association Studies of Colorectal Cancer Improves Risk Prediction Across Race and Ethnicity

Minta Thomas, Yu‐Ru Su, Elisabeth A. Rosenthal…·Taiki Yamaji

This study improves polygenic risk scores for colorectal cancer by combining Asian and European ancestry data, enhancing risk prediction across diverse racial and ethnic groups.

1 citation

humanGWAS summary statistics

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Genetic & Genomic MedicineNature GeneticsPeer-reviewedJul 14, 2022

Genetic regulation of OAS1 nonsense-mediated decay underlies association with risk of severe COVID-19

Abdul Rouf Banday, Megan Lynn Stanifer, Oscar Flórez-Vargas…·Ludmila Prokunina‐Olsson

The paper identifies a Neandertal introgressed haplotype in the OAS1 gene associated with increased risk of severe COVID-19 and shows it impairs SARS-CoV-2 clearance through genetic regulation of OAS1 expression.

130 citationstop 1%

humanwhole-genome sequencing

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Genetic & Genomic MedicineGutPeer-reviewedFeb 25, 2021

Genetic architectures of proximal and distal colorectal cancer are partly distinct

Jeroen R. Huyghe, Tabitha A. Harrison, Stephanie A. Bien…·Rachel Pearlman

This study identifies 13 new genetic loci specific to proximal or distal colorectal cancer subtypes, revealing partly distinct genetic architectures for these tumor locations.

80 citations

humanGWAS summary statistics

𝕏 PostBluesky