Author

Alexa Anderson

Renown Health

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

Alexandre BolzeiD· 1 shared Anna A. BakhtinaiD· 1 shared Anna Jacobsen· 1 shared Caiyi C. Li· 1 shared Catherine A. HajekiD· 1 shared Christos P. KyriakopoulosiD· 1 shared Clint Gwynn· 1 shared Daniel KiseriD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alexandre BolzeORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Cardiomyocyte-specific loss of Smyd5 leads to a robust activation of inflammatory signaling and heart failure in mice.

Ryan D. Bia, Samuel M. Hickenlooper, Mickey R. Miller, Caiyi C. Li, Emilee Horiuchi, Anna A. Bakhtina, Li Wang, Steven Valdez, Kathryn Davis, Alexa Anderson, June Garcia-Llana, Ludovica Farese, Sean O’Very, Nicholas Santa Ana, Anna Jacobsen, , Sarah Franklin

This study shows that loss of Smyd5 in cardiomyocytes causes inflammation and heart failure in mice by reducing H4K20me3 and increasing Il-6 expression.

bioRxiv · Sep 3, 2026 · PreprintMolecular Biology

Combining rare and common genetic variants improves population risk stratification for breast cancer

Alexandre Bolze, Daniel Kiser, Kelly M. Schiabor Barrett, Gai Elhanan, Jamie M. Schnell Blitstein, Iva Neveux, Shaun Dabe, Harry Reed, Alexa Anderson, William J. Metcalf, Ekaterina Orlova, Ildiko Thibodeau, Natalie Telis, Ruomu Jiang, Nicole L. Washington, , Joseph J. Grzymski

This study evaluates genetic screening approaches for breast cancer risk, finding that combining rare and common variants improves risk stratification.

Genetics in Medicine Open · Jan 1, 2024Peer-reviewedGenetic & Genomic Medicine