Author

C. O’Donoghue

Trinity College DublinORCID 0000-0003-0728-6083Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Emrah KacariD· 2 shared Orla M. HardimaniD· 2 shared Ross Patrick ByrneiD· 2 shared Russell Lewis McLaughliniD· 2 shared Tomás DS GomesiD· 2 shared Colm PeeloiD· 1 shared Emmet CostelloiD· 1 shared Guste VenslovaiteiD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Emrah KacarORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintAug 21, 2026

Genome-wide analyses reveal shared and distinct genetic architecture linking amyotrophic lateral sclerosis, sporadic frontotemporal dementia and cognitive traits

Emrah Kacar, Tomás DS Gomes, C. O’Donoghue…·Ross Patrick Byrne

The paper identifies shared and distinct genetic loci linking ALS, sFTD, and cognitive traits using genome-wide association data.

DOI 10.64898/2026.08.17.26360494

humanGWAS summary statistics

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Genetic & Genomic MedicinemedRxivPreprintJun 10, 2026

Rare neurological and neurodevelopmental variants in ALS link to onset, survival and family history

C. O’Donoghue, Emrah Kacar, Tomás DS Gomes…·Ross Patrick Byrne

This study identifies rare neurological and neurodevelopmental variants in ALS patients, showing associations with onset, survival, and family history patterns across two cohorts.

DOI 10.64898/2026.06.09.26354977

humanwhole-genome sequencing

𝕏 PostBluesky