Author

Ebrima Joof

University of LeicesterORCID 0000-0002-3367-0102Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Organism:human· 2 Approach:statistical model· 2

Frequent Co-Authors

Gisli R. JenkinsiD· 2 shared Louise V. WainiD· 2 shared Olivia C. LeavyiD· 2 shared Richard J. AlleniD· 2 shared Ritah NabunjeiD· 2 shared Tamara Hernández-BeeftinkiD· 2 shared Amaia Urrutia· 1 shared Beatriz Guillén‐GuíoiD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 42 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

2 shared papersGenetic & Genomic Medicine

Gisli R. JenkinsORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Genome-wide association studies to identify shared and distinct mechanisms of fibrosis across 12 organ-systems

Ebrima Joof, Tamara Hernández-Beeftink, Gina Parcesepe, Georgie May Massen, Ritah Nabunje, Hayley J Power, Ruby M Woodward, Feras Altunusi, Olivia C. Leavy, Hilary J Longhurst, Gisli R. Jenkins, Jennifer Kathleen Quint, Louise V. Wain, Richard J. Allen

BMJ connections. · Sep 1, 2026Peer-reviewedGenetic & Genomic Medicine

Cross-ancestry evaluation of idiopathic pulmonary fibrosis genetic risk variants

Ritah Nabunje, Beatriz Guillén‐Guío, Tamara Hernández-Beeftink, Ebrima Joof, Olivia C. Leavy, Toby M. Maher, Philip L. Molyneux, Justin M. Oldham, Imre Noth, Amaia Urrutia, Myriam Aburto, Carlos Flores, Gisli R. Jenkins, Louise V. Wain, Richard J. Allen

This study evaluates the genetic risk variants for idiopathic pulmonary fibrosis in non-European populations, finding partial replication and ancestry-specific effects, with rs35705950 as the most consistent signal.

medRxiv · Apr 25, 2026 · PreprintGenetic & Genomic Medicine