Author

Rustam Al‐Shahi Salman

University of EdinburghORCID 0000-0002-2108-9222Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:fine-mapping· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Neshika SamarasekeraiD· 2 shared Adekunle Gregory FakunleiD· 1 shared Alessandro PezziniiD· 1 shared Andrea Becerril‐GaitaniD· 1 shared Aniket MishraiD· 1 shared Barry W. McColliD· 1 shared Bethany GearyiD· 1 shared Bradford B. WorralliD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersNeuroscience

Neshika SamarasekeraORCID

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2 papers

Recent·Most cited

Mononuclear myeloid cells mount an adaptive protective response to intracerebral haemorrhage by activation of NRF2

James JM Loan, Jing Qiu, Jack Barrington, Paul S. Baxter, Sean McKay, Caoimhe Kirby, Xin He, Christine Lerpiniere, Karina McDade, Meryam Beniazza, Jamie McQueen, Friederike Schaper, Yihui Cheng, Bethany Geary, Owen Dando, , Giles E. Hardingham

The paper identifies NRF2 activation in mononuclear myeloid cells as a protective response to intracerebral haemorrhage, showing its therapeutic potential through modulation of interferon pathways.

bioRxiv · May 20, 2026 · PreprintNeuroscience

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