Author

Andrea Prunotto

University of FreiburgORCID 0000-0003-1235-1740Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Approach:statistical model· 2 Research Focus:cell-cell communication· 1 Research Focus:differential expression· 1 Assay:proteomics· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Akira MurakamiiD· 1 shared Atta Ur RehmaniD· 1 shared Bettina Liebowitz Knapp· 1 shared Carlo RivoltaiD· 1 shared Carsten SchwaniD· 1 shared Chikashi C. TeraoiD· 1 shared Frans P.M. CremersiD· 1 shared Friedel DrepperiD· 1 shared

Activity by Year

2019-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 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

1 shared paperGenomics

Akira MurakamiORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Molecular BiologyCell ReportsPeer-reviewedApr 25, 2025

TAF2 condensation in nuclear speckles links basal transcription factor TFIID to RNA splicing

Tanja Bhuiyan, Niccolò Arecco, Paulina Karen Mendoza Sanchez…·Sebastian J. Arnold

This study shows TAF2's intrinsically disordered region drives condensation in nuclear speckles, recruiting SRRM2 to TFIID and affecting alternative splicing.

5 citations

humanproteomics

𝕏 PostBluesky

GenomicsNature CommunicationsPeer-reviewedJun 28, 2019

A frequent variant in the Japanese population determines quasi-Mendelian inheritance of rare retinal ciliopathy

Konstantinos Nikopoulos, Katarina Vizar Cisarova, Mathieu Quinodoz…·Carlo Rivolta

The paper identifies a common variant in the Japanese population that shows quasi-Mendelian inheritance patterns in rare retinal ciliopathy.

41 citations

humanwhole-exome sequencing

𝕏 PostBluesky