Author

Francesc Valldeoriola

Biomedical Research Networking Center on Neurodegenerative DiseasesORCID 0000-0002-8680-4274Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:GWAS / association mapping· 2 Research Focus:differential expression· 1 Research Focus:fine-mapping· 1 Assay:GWAS summary statistics· 1 Approach:machine learning (classical)· 1 Assay:proteomics· 1

Frequent Co-Authors

Esteban MuñoziD· 3 shared Marı́a José Martı́iD· 3 shared Yaroslau ComptaiD· 3 shared Ana CámaraiD· 2 shared Cèlia PainousiD· 2 shared Dolores Buiza‐RuedaiD· 2 shared Jaime KulisevskyiD· 2 shared Javier PagonabarragaiD· 2 shared

Activity by Year

2019-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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

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3 shared papersNeuroscience

Esteban MuñozORCID

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Author profile →

3 papers

Recent·Most cited

Phospho-signalling deregulation of the mTOR pathway in fibroblasts from LRRK2 Parkinson s patients

Rodolfo Alejandro, Joaquín Fernández‐Irigoyen, Pares Guillem, Adriana Cortés, Enrique Santamaría, Manel Fernández, Esteban Muñoz, Almudena Sánchez‐Gómez, Cèlia Painous, Ana Cámara, Francesc Valldeoriola, Yaroslau Compta, Eduardo Tolosa, Alícia Garrido, Marı́a José Martı́, , Mario Ezquerra

This study identifies mTOR pathway deregulation in fibroblasts from LRRK2 Parkinson's patients through proteomic and phospho-proteomic analysis.

bioRxiv · Dec 9, 2025 · PreprintNeuroscience

A Novel Susceptibility Locus in NFASC Highlights Oligodendrocytes and Myelination in Progressive Supranuclear Palsy Pathology

Pablo García‐González, Héctor Rodrigo Lara, Yaroslau Compta, Manuel Fernandez, Sven J. van der Lee, Itziar de Rojas, Laura Saiz-Aúz, Cèlia Painous, Ana Camara, Esteban Muñoz, Marı́a José Martı́, Francesc Valldeoriola, Raquel Puerta, Ignacio Illán‐Gala, Javier Pagonabarraga, , Agustı́n Ruiz

The paper performs a GWAS on PSP in the Iberian population, replicates known risk variants, and identifies a novel locus in NFASC/CNTN2 associated with oligodendrocyte and myelination processes.

medRxiv · Jun 21, 2024 · PreprintGenetic & Genomic Medicine

The genetic architecture of Parkinson disease in Spain: characterizing population-specific risk, differential haplotype structures, and providing etiologic insight

Sara Bandrés‐Ciga, Sarah Ahmed, Marya S. Sabir, Cornelis Blauwendraat, Astrid Daniela Adarmes-Gómez, Inmaculada Bernal‐Bernal, Marta Bonilla‐Toribio, Dolores Buiza‐Rueda, Fátima Carrillo, Mario Carrión‐Claro, Pilar Gómez‐Garre, Silvia Jesús, Miguel Ángel Labrador‐Espinosa, Daniel Macías, Carlota Méndez‐del‐Barrio, , Andrew Singleton

This study conducts a GWAS of Parkinson disease in Spain, identifies a novel population-specific signal at PARK2 associated with age-at-onset, and highlights genetic substructure for future fine-mapping.

Movement Disorders · Oct 29, 2019Peer-reviewedNeuroscience