Author

Gerardo Gutiérrez‐Gutiérrez

Hospital Universitario Infanta SofíaORCID 0000-0003-1391-754XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Organism:Drosophila· 1 Approach:experimental assay· 1 Approach:statistical model· 1

Frequent Co-Authors

Adolfo López de MunaíniD· 1 shared Adrian M. IsaacsiD· 1 shared Agustín Martínez· 1 shared Ahmet HökeiD· 1 shared Alessandro Bertini· 1 shared Amets SáenziD· 1 shared Amy R. HicksiD· 1 shared Andrea CorteseiD· 1 shared

Activity by Year

2023-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 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 paperGenetic & Genomic Medicine

Adolfo López de MunaínORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

NeurosciencebioRxivPreprintNov 18, 2025

CANVAS causing AAGGG repeat expansions cause tissue-specific reduction in RFC1 expression and increase sensitivity to DNA damage

Riccardo Curró, Natalia Dominik, Stefano Facchini…·Andrea Cortese

DOI 10.1101/2025.11.18.688292

Drosophilahuman

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintJul 19, 2023

The in-frame p.Lys254del-CAPN3 deletion is not sufficient to cause late-onset camptocormia in dominantly inherited calpainopathy

Andrea Valls, Gerardo Gutiérrez‐Gutiérrez, Agustín Martínez…·Amets Sáenz

The study shows that the p.Lys254del-CAPN3 mutation is not sufficient to cause late-onset camptocormia in dominant calpainopathy.

DOI 10.1101/2023.07.19.23292361

humanDNA methylation

𝕏 PostBluesky