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Publications

Combining evidence from human genetic and functional screens to identify pathways altering obesity and fat distribution

Baya NA. et al, (2024)

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

Currant H. et al, (2024)

Enhancing cross-institute generalisation of GNNs in histopathology through multiple embedding graph augmentation (MEGA)

Campbell J. et al, (2024), Proceedings of the 28th Conference on Medical Image Understanding and Analysis (MIUA 2024), 270 - 284

Characterising the genetic architecture of changes in adiposity during adulthood using electronic health records.

Venkatesh SS. et al, (2024), Nat Commun, 15

Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK Biobank.

Lassen FH. et al, (2024), Cell Genom

Mapping cell-to-tissue graphs across human placenta histology whole slide images using deep learning with HAPPY.

Vanea C. et al, (2024), Nat Commun, 15

Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

Suzuki K. et al, (2024), Nature

Enhancing Cross-Institute Generalisation of GNNs in Histopathology Through Multiple Embedding Graph Augmentation (MEGA)

Campbell J. et al, (2024), Medical Image Understanding and Analysis, 270 - 284

Genic constraint against nonsynonymous variation across the mouse genome.

Powell G. et al, (2023), BMC Genomics, 24

Association between maternal haemoglobin concentrations and maternal and neonatal outcomes: the prospective, observational, multinational, INTERBIO-21st fetal study.

Ohuma EO. et al, (2023), Lancet Haematol, 10, e756 - e766

Discovering cellular programs of intrinsic and extrinsic drivers of metabolic traits using LipocyteProfiler.

Laber S. et al, (2023), Cell Genom, 3

Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK Biobank

Lassen FH. et al, (2023)

Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake.

Williamson A. et al, (2023), Nat Genet, 55, 973 - 983

A non-coding variant linked to metabolic obesity with normal weight affects actin remodelling in subcutaneous adipocytes.

Glunk V. et al, (2023), Nat Metab, 5, 861 - 879

The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions

Rahmioglu N. et al, (2023), Nature Genetics

Loci for insulin processing and secretion provide insight into type 2 diabetes risk.

Broadaway KA. et al, (2023), Am J Hum Genet

Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts

Wang Y. et al, (2023), Cell Genomics, 3

The genetic architecture of changes in adiposity during adulthood

Venkatesh SS. et al, (2023)

Meta-analysis fine-mapping is often miscalibrated at single-variant resolution

Kanai M. et al, (2022), Cell Genomics, 2

A saturated map of common genetic variants associated with human height.

Yengo L. et al, (2022), Nature

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