Jordi Jiménez-Conde

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

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

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.

This study identifies eight new genetic loci associated with cardioembolic stroke using multitrait analysis of GWAS data, revealing distinct genetic pathways from atrial fibrillation.

This paper identifies seven genome-wide significant loci associated with early neurological instability after acute ischemic stroke, linking excitotoxic genes to poor outcomes.

The paper identifies genetic variants influencing DNA methylation in blood and shows their associations with complex traits and diseases, but finds limited direct causality.

This paper develops a radiomic signature from T2-FLAIR MRI images to predict white matter hyperintensities burden and links it to clinical phenotypes.

This study identifies sex-specific lesion patterns in acute ischemic stroke that correlate with stroke severity, highlighting differences in lesion distribution between men and women.

This study identifies 20 novel loci associated with ischemic stroke through an epigenome-wide association study, highlighting methylation changes in pathways like inflammation and lipid metabolism.

The paper identifies subtype-specific genetic loci associated with stroke subtypes and finds heterogeneity in their effects across different stroke types.

The paper presents an automated pipeline for quantifying white matter hyperintensity in acute ischemic stroke cohorts, showing improved accuracy and enabling large-scale analysis.