Author

Marta Vallverdú-Prats

Hospital del Mar Research InstituteORCID 0000-0002-5262-817XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:fine-mapping· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Israel Fernández‐CadenasiD· 2 shared Joan Jiménez-BaladóiD· 2 shared Jordi Jiménez-CondeiD· 2 shared Adekunle Gregory FakunleiD· 1 shared Aina Medina-DolsiD· 1 shared Alessandro PezziniiD· 1 shared Ana Rodríguez-CampelloiD· 1 shared Andrea Becerril‐GaitaniD· 1 shared

Activity by Year

2025-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Israel Fernández‐CadenasORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Rare Variant Association Analysis Uncovers Involvement of VNN2 in Stroke Outcome

Estefanía Alcaide-Consuegra, Marina Mola-Caminal, Geòrgia Escaramís, Uxue Lazcano, Isabel Fernández Pérez, Jaume Reig‐Palou, Joan Jiménez-Baladó, Eva Giralt Steinhauer, Elisa Cuadrado‐Godia, Ángel Ois, Ana Rodríguez-Campello, Marta Vallverdú-Prats, Aina Medina-Dols, Carmen Jiménez, Sílvia Tur, , Raquel Rabionet

This study identifies rare variants in VNN2 associated with improved stroke recovery using exome sequencing and structural analysis.

Stroke · Jun 11, 2025Peer-reviewedGenetic & Genomic Medicine

The Ethnic/Racial Variations of Intracerebral Hemorrhage Genetics (ERICH-GENE) Study Protocol

Guido J. Falcone, Stacey Q Wolfe, Marialuisa Zedde, Rosario Pascarella, Jordi Jiménez-Conde, Marta Vallverdú-Prats, Joan Jiménez-Baladó, Alessandro Pezzini, Sandra Rossi, Rustam Al‐Shahi Salman, Neshika Samarasekera, Ramin Zand, Jiaying Li, Christina Jern, Daniel Strbian, , the ERICH-Gene Investigators

ERICH-GENE collects and analyzes genomic and neuroimaging data from over 10,000 multi-ethnic ICH cases to identify genetic risk factors and trans-ethnic variation in ICH.

medRxiv · Jun 11, 2025 · PreprintGenetic & Genomic Medicine