Author

Niall P Pender

Trinity College DublinORCID 0000-0002-4172-0704Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

C. O’DonoghueiD· 1 shared Colm PeeloiD· 1 shared Emmet CostelloiD· 1 shared Emrah KacariD· 1 shared Marie RyaniD· 1 shared Mark HeveriniD· 1 shared Orla M. HardimaniD· 1 shared Peter BedeiD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenetic & Genomic Medicine

C. O’DonoghueORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

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

C. O’Donoghue, Emrah Kacar, Tomás DS Gomes, Emmet Costello, Niall P Pender, Colm Peelo, Marie Ryan, Mark Heverin, Susan Byrne, Peter Bede, Orla M. Hardiman, Russell Lewis McLaughlin, 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.

medRxiv · Jun 10, 2026 · PreprintGenetic & Genomic Medicine