Irene Soler-Sáez

The paper analyzes single-cell data from multiple sclerosis patients to identify sex-specific molecular differences in brain and immune cells across disease progression.

This study identifies consistent sex differences in gut microbiota of MS patients across multiple cohorts, highlighting the importance of sex as a variable in microbiome research.

The paper analyzes transposable elements in Parkinson Disease datasets to build a cell-type specific atlas and explore their role in sex differences.

This study shows that MCT2 is essential for oligodendrocyte myelin maintenance and axonal support, and its loss leads to myelin and axonal damage, which can be mitigated by a ketogenic diet.

This study identifies sex differences in gene expression, cell-cell communication, and pathway activation in Parkinson's Disease through meta-analysis of single-cell transcriptomic data.

The paper identifies shared transcriptomic features between melanoma brain metastases and neurodegenerative diseases, highlighting key genes and providing an open-source tool for analysis.

This paper identifies sex-specific genes, transcription factors, and pathways in Alzheimer's disease using meta-analyses of transcriptomic data from the cerebral cortex and hippocampus.

This paper identifies sex-specific miRNA expression differences in Alzheimer's disease patients through meta-analysis of blood and brain samples, revealing distinct biological process associations in each sex.

This study identifies miRNA signatures associated with melanoma progression and prognosis by integrating transcriptomic data and analyzing miRNA-mRNA interactions.

This study identifies sex-based molecular differences in multiple sclerosis through transcriptomic meta-analysis, revealing tissue-specific gene expression patterns and functional immune pathway alterations.

This study identifies sex-based differences in Parkinson's disease transcriptomics through meta-analysis of 267 samples across three brain regions, revealing sex-specific gene expression and pathway alterations.