Author

Anette S. B. Wolff

Haukeland University HospitalORCID 0000-0002-8485-2248Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Research Focus:differential expression· 2 Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Assay:bulk RNA-seq· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Stefan JohanssoniD· 3 shared Eirik BratlandiD· 2 shared Ellen Christine RøyrvikiD· 2 shared Haydeé ArtazaiD· 2 shared Ksenia Lavrichenko· 2 shared Marc VaudeliD· 2 shared Amund Holte BergeriD· 1 shared Bente Berg JohanssoniD· 1 shared

Activity by Year

2024-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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3 shared papersGenomics

Stefan JohanssonORCID

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3 papers

Recent·Most cited

High-Resolution Transcriptional Impact of AIRE: Effects of Pathogenic Variants p.Arg257Ter, p.Cys311Tyr, and Polygenic Risk Variant p.Arg471Cys

Amund Holte Berger, Bergithe Eikeland Oftedal, Anette S. B. Wolff, Eystein S. Husebye, Per Morten Knappskog, Eirik Bratland, Stefan Johansson

The paper evaluates the transcriptional impact of three AIRE variants using a cell system, showing different functional effects on gene expression.

Frontiers in Immunology · Apr 22, 2025Peer-reviewedGenomics

Contribution of Rare Large High-Penetrance CNVs to Pediatric and MODY Diabetes in Norway

Haydeé Artaza, Divya Sri Priyanka Tallapragada, Janne Molnes, Ksenia Lavrichenko, Anette S. B. Wolff, Ellen Christine Røyrvik, Torild Skrivarhaug, Marc Vaudel, Eirik Bratland, Bente Berg Johansson, Pål R. Njølstad, Stefan Johansson

The paper identifies rare, large, high-penetrance CNVs in Norwegian pediatric diabetes and MODY patients, finding 0.63% and 0.09% of cases attributable to pathogenic deletions, with some undetected by standard methods.

medRxiv · Feb 25, 2025 · PreprintGenetic & Genomic Medicine

Rare Copy Number Variant analysis in case-control studies using SNP Array Data: a scalable and automated data analysis pipeline

Haydeé Artaza, Ksenia Lavrichenko, Anette S. B. Wolff, Ellen Christine Røyrvik, Marc Vaudel, Stefan Johansson

This paper presents a scalable and automated pipeline for analyzing rare copy number variants in case-control studies using SNP array data, enabling efficient CNV detection, quality control, and impact assessment.

BMC Bioinformatics · Nov 15, 2024Peer-reviewedBioinformatics