Author

Arianna Vino

Max Planck Institute for Psycholinguistics

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

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Approach:statistical model· 2 Approach:benchmark study· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Research Focus:gene regulatory network inference· 1 Assay:proteomics· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Simon E. FisheriD· 2 shared Aglaia VignoliiD· 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 Bert B A De VriesiD· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetic & Genomic Medicine

Simon E. FisherORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

De novo protein-coding gene variants in developmental stuttering

Else Eising, Ivana Dzinovic, Arianna Vino, Lottie W. Stipdonk, Martin Pavlov, Juliane Winkelmann, Martin Sommer, Marie-Christine J. P. Franken, Konrad Oexle, Simon E. Fisher

The paper identifies de novo protein-coding gene variants in stuttering and highlights genetic links to neurodevelopmental disorders.

medRxiv · Nov 25, 2024 · PreprintGenetic & Genomic Medicine

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, Gökberk Alagöz, Michael S. Hildebrand, Christopher Barnett, Meghan Barnett, Alfredo Brusco, Diana Carli, Bert B A De Vries, Alexander J.M. Dingemans, Frances Elmslie, Giovanni Battista Ferrero, Nadieh A. Jansen, Ingrid M.B.H. van de Laar, , 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.

medRxiv · Mar 4, 2022 · PreprintGenetic & Genomic Medicine