Author

Joan Jiménez-Baladó

Hospital del Mar Research InstituteORCID 0000-0003-4125-9134Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Research Focus:fine-mapping· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1

Frequent Co-Authors

Israel Fernández‐CadenasiD· 3 shared Jordi Jiménez-CondeiD· 3 shared Jara Cárcel‐MárqueziD· 2 shared Marta Vallverdú-PratsiD· 2 shared Adekunle Gregory FakunleiD· 1 shared Aina Medina-DolsiD· 1 shared Alessandro PezziniiD· 1 shared Ana Aguilera‐SimóniD· 1 shared

Activity by Year

2025-2025 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Israel Fernández‐CadenasORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

NeurosciencebioRxivPreprintOct 1, 2025

Biological age acceleration is more prevalent in men than in women at time of spontaneous intracerebral hemorrhage

Cristina Gallego-Fábrega, Joan Jiménez-Baladó, Natàlia Cullell…·Israel Fernández‐Cadenas

The paper compares epigenetic age acceleration between men and women with spontaneous intracerebral hemorrhage, finding men show greater acceleration than women.

DOI 10.1101/2025.10.01.679916

humanDNA methylation

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Genetic & Genomic MedicineStrokePeer-reviewedJun 11, 2025

Rare Variant Association Analysis Uncovers Involvement of VNN2 in Stroke Outcome

Estefanía Alcaide-Consuegra, Marina Mola-Caminal, Geòrgia Escaramís…·Raquel Rabionet

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

DOI 10.1161/strokeaha.124.049365

humanwhole-exome sequencing

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Genetic & Genomic MedicinemedRxivPreprintJun 11, 2025

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

Guido J. Falcone, Stacey Q Wolfe, Marialuisa Zedde…·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.

1 citation

humanwhole-genome sequencing

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