Author

Malin Dewenter

Johannes Gutenberg University MainzORCID 0000-0001-8025-0736Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Pathology· 1

Signature Assays, Organisms & Methods

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Research Focus:genome assembly· 2 Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Assay:Hi-C· 1

Frequent Co-Authors

Alba Sanchis‐JuaniD· 1 shared Amélie PitoniD· 1 shared Amy McTagueiD· 1 shared Anne de Saint MartiniD· 1 shared Argirios DinopoulosiD· 1 shared Arthur J. CampbelliD· 1 shared Azza Soliman· 1 shared Damien LedereriD· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alba Sanchis‐JuanORCID

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2 papers

Recent·Most cited

PathologybioRxivPreprintMay 8, 2026

16p11.2 Copy Number Variation Alters Genome Architecture and Transcriptional Regulation During Neurodevelopment

Marco Bertin, Marcel Misak, Mohit Navandar…·Susann Schweiger

This study investigates how 16p11.2 copy number variations affect genome architecture and transcription during neurodevelopment, finding both local dosage effects and broader chromatin changes.

DOI 10.64898/2026.05.07.723480

humanbulk RNA-seq

𝕏 PostBluesky

Genetic & Genomic MedicineGenetics in MedicinePeer-reviewedDec 6, 2021

Structural mapping of GABRB3 variants reveals genotype-phenotype correlation

Katrine M. Johannesen, Sumaiya Iqbal, Milena Guazzi…·Elena Gardella

The paper analyzes GABRB3 variants in a cohort of 71 individuals to identify genotype-phenotype correlations, finding associations between variant locations and specific clinical features.

23 citations

humanstatistical model

𝕏 PostBluesky