Cross-ancestry evaluation of idiopathic pulmonary fibrosis genetic risk variants

promoter variant rs35705950 emerged as the dominant and most consistent signal across ancestries. Our findings highlight the need for larger, well-characterised studies in understudied populations to support robust discovery and translation.

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Publication Details

Journal
medRxiv
Published
2026-04-25
DOI
https://doi.org/10.64898/2026.04.17.26349970
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
Field-Weighted Citation Impact
0.00
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article

Cross-ancestry evaluation of idiopathic pulmonary fibrosis genetic risk variants

Ritah Nabunje, C Flores, Tamara Hernández-Beeftink, Toby M. Maher et al.
medRxiv
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
article

Cross-ancestry evaluation of idiopathic pulmonary fibrosis genetic risk variants

Ritah Nabunje, C Flores, Tamara Hernández-Beeftink, Toby M. Maher, Myriam Aburto, Ebrima Joof, Olivia C. Leavy, Phil Molyneux, RJ Allen, Amaia Urrutia, Louise V Wain, Beatriz Guillen-Guio, Imre Noth, R Gisli Jenkins
article en

Abstract

promoter variant rs35705950 emerged as the dominant and most consistent signal across ancestries. Our findings highlight the need for larger, well-characterised studies in understudied populations to support robust discovery and translation.

medRxiv
University of Southern California (US), University of Leicester (GB), University of Michigan (US), Instituto de Salud Carlos III (ES), University Hospitals of Leicester NHS Trust (GB), Hospital Universitario Nuestra Señora de Candelaria (ES), Universidad Fernando Pessoa Canarias (ES), Centro de Investigación Biomédica en Red de Enfermedades Respiratorias (ES), Instituto Tecnológico y de Energías Renovables (ES), NIHR Imperial Biomedical Research Centre (GB), Hospital de Galdakao (ES), Hospital de Cruces (ES), NIHR Leicester Biomedical Research Centre (GB), Imperial College London (GB), University of Virginia (US)
Openalex Percentile: Top 13%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
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