Author

Aglaia Vignoli

University of MilanORCID 0000-0003-4638-4663Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Assay:DNA methylation· 1 Organism:Drosophila· 1 Approach:experimental assay· 1 Organism:human· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

Alessandro MineoiD· 1 shared Alexander J.M. DingemansiD· 1 shared Alfredo BruscoiD· 1 shared Alice MoroniiD· 1 shared Angela PeroniD· 1 shared Angela Tamsin MorganiD· 1 shared Antonio GaleoneiD· 1 shared Arianna Vino· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetics

Alessandro MineoORCID

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2 papers

Recent·Most cited

GeneticsbioRxivPreprintDec 18, 2025

Mesodermal-specific MECP2 expression in Drosophila induces visceral and skeletal muscle defects rescued by butyrate supplementation

Gaia Consonni, Mustafa Kaan Kozluca, Maria Cristina Gagliani…·Thomas Vaccari

This study shows that mesodermal-specific MECP2 overexpression in Drosophila causes muscle and gut defects, which are rescued by butyrate and valproate.

DOI 10.64898/2025.12.16.694631

Drosophilaexperimental assay

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintMar 4, 2022

SETBP1 variants outside the degron disrupt DNA-binding and transcription independent of protein abundance to cause a heterogeneous neurodevelopmental disorder

Maggie M. K. Wong, Rosalie A. Kampen, Ruth O. Braden…·Simon E. Fisher

The paper investigates SETBP1 variants outside the degron, showing they cause a heterogeneous neurodevelopmental disorder through loss-of-function mechanisms independent of protein abundance.

6 citations

humanDNA methylation

𝕏 PostBluesky