Author

Päivi Auvinen

University of Eastern FinlandORCID 0000-0002-2392-9395Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Andreas HadjisavvasiD· 1 shared Anna González‐NeiraiD· 1 shared Anna JakubowskaiD· 1 shared Annika LindblomiD· 1 shared Anthony HowelliD· 1 shared Antoinette HollestelleiD· 1 shared Archie I CampbelliD· 1 shared Artitaya LophatananoniD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Andreas HadjisavvasORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicineGenome MedicinePeer-reviewedMay 18, 2022

Breast cancer risks associated with missense variants in breast cancer susceptibility genes

Leila Dorling, Sara Carvalho, Jamie Allen…·Javier J. Benitez

The paper assesses breast cancer risks linked to rare missense variants in five susceptibility genes using logistic and mixture models, finding varying risk contributions across genes.

55 citationstop 2%

humanbulk RNA-seq

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