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Search results (10)

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Individuals whose phenotype deviates from genetic expectation defined by common variation are enriched for rare damaging variants in genes that cause rare disease.

Baya NA. et al, (2025), medRxiv

Genome-wide associations spanning 194 in-hospital drug dosage change phenotypes highlight diverse genetic backgrounds in concurrent drug therapy.

Henriksen AP. et al, (2025), Comput Struct Biotechnol J, 28, 239 - 248

Genome-wide analysis identifies 66 variants underlying anatomical variation in human neuroendocrine structures and reveals links to testosterone

Currant H. et al, (2024)

Sub-cellular level resolution of common genetic variation in the photoreceptor layer identifies continuum between rare disease and common variation.

Currant H. et al, (2023), PLoS Genet, 19

Visualising disease trajectories from population-wide data.

Hjaltelin JX. et al, (2023), Front Bioinform, 3

Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images.

Currant H. et al, (2021), PLoS Genet, 17

Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries.

Gharahkhani P. et al, (2021), Nat Commun, 12

Comparison of Associations with Different Macular Inner Retinal Thickness Parameters in a Large Cohort: The UK Biobank.

Khawaja AP. et al, (2020), Ophthalmology, 127, 62 - 71

BayesPiles

Vogogias A. et al, (2019), ACM Transactions on Intelligent Systems and Technology, 10, 1 - 23

FFPred 3: feature-based function prediction for all Gene Ontology domains.

Cozzetto D. et al, (2016), Sci Rep, 6