Author

Guillermo Rocamora Perez

Aligning Science Across Parkinson'sORCID 0000-0002-4795-3648Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 3

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 3 Research Focus:differential expression· 3 Organism:human· 3 Approach:statistical model· 3 Research Focus:cell type annotation· 2 Research Focus:gene regulatory network inference· 1 Assay:scRNA-seq· 1 Research Focus:spatial domain detection· 1

Frequent Co-Authors

Aine Fairbrother-BrowneiD· 3 shared Amy R. HicksiD· 3 shared Emil Karl GustavssoniD· 3 shared John HardyiD· 3 shared Jonathan BrentoniD· 3 shared Kylie MontgomeryiD· 3 shared Melissa Grant‐PetersiD· 3 shared Mina RyteniD· 3 shared

Activity by Year

2025-2025 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersNeuroscience

Aine Fairbrother-BrowneORCID

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3 papers

Recent·Most cited

NeurosciencebioRxivPreprintSep 4, 2025

TDP-43 loss of function drives aberrant splicing in Parkinson's disease

Jonathan Brenton, Jordan Follett, Raja Sekhar Nirujogi…·Mina Ryten

The paper identifies splicing dysregulation in Parkinson's disease linked to TDP-43 loss of function and shows its association with genetic mutations and cellular models.

1 citation

humanbulk RNA-seq

𝕏 PostBluesky

NeurosciencebioRxivPreprintMar 17, 2025

17q21.31 locus regulates Parkinson's disease relevant pathways through KANSL1 activity

Amy R. Hicks, Benjamin J. O’Callaghan, Jonathan Brenton…·Mina Ryten

The paper investigates how the 17q21.31 locus influences Parkinson's disease through KANSL1 activity, showing haplotype-specific effects on key biological processes.

DOI 10.1101/2025.03.17.641409

humanbulk RNA-seq

𝕏 PostBluesky

NeurosciencebioRxivPreprintJan 3, 2025

Transcriptomic analysis of repeat expansion-ataxias uncovers distinct non-neuronal cell type-specific signatures of disease across the human brain

Zhongbo Chen, Amy R. Hicks, Jonathan Brenton…·Mina Ryten

This study uses bulk and single nuclear RNA-sequencing to analyze transcriptomic changes in repeat expansion ataxias, revealing distinct non-neuronal cell type-specific disease signatures across the human brain.

2 citations

humanbulk RNA-seq

𝕏 PostBluesky