Author

Sarah C. Hanks

University of MichiganORCID 0000-0003-2978-5289Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:ATAC-seq· 1 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:GWAS / association mapping· 1 Assay:scRNA-seq· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Francis S. CollinsiD· 2 shared Heather M. StringhamiD· 2 shared Heikki A. KoistineniD· 2 shared Karen L. MohlkeiD· 2 shared Lori L. BonnycastleiD· 2 shared Markku LaaksoiD· 2 shared Adolfo CorreaiD· 1 shared Alanna C. MorrisoniD· 1 shared

Activity by Year

2018-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenomics

Francis S. CollinsORCID

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2 papers

Recent·Most cited

GenomicsbioRxivPreprintOct 27, 2025

Inverse directions of association of higher physical activity and higher insulin resistance with human skeletal muscle cell type abundance and fiber type-level gene expression

Dan L. Ciotlos, Sarah C. Hanks, Arushi Varshney…·Laura J. Scott

The paper examines how physical activity and insulin resistance relate to skeletal muscle cell type abundance and gene expression in humans, finding inverse associations with specific cell types and gene expression patterns.

DOI 10.1101/2025.10.27.683567

humanscRNA-seq

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GeneticsbioRxivPreprintJul 31, 2018

Genetic discovery and translational decision support from exome sequencing of 20,791 type 2 diabetes cases and 24,440 controls from five ancestries

Jason A. Flannick, Josep Maria Mercader, Christian Fuchsberger…·Markku Laakso

This study identifies rare genetic variants associated with type 2 diabetes using exome sequencing of 20,791 cases and 24,440 controls, and provides a Bayesian framework to improve variant prioritization.

3 citations

humanwhole-exome sequencing

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