Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Publications

Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

CHEN Z. et al, (2024), Nature

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

ZONDERVAN K. and RAHMIOGLU N., (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

Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease

Zhou W. et al, (2022), Cell Genomics, 2

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

Yengo L. et al, (2022), Nature, 610, 704 - 712

Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations.

Temprano-Sagrera G. et al, (2022), J Thromb Haemost, 20, 1331 - 1349

Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.

Mahajan A. et al, (2022), Nat Genet, 54, 560 - 572

Genetic architecture of longitudinal obesity trajectories in primary care electronic health records

Venkatesh SS. et al, (2022), HUMAN HEREDITY, VOL., 21 - 22

USP19 Inhibition Affects Adipogenesis, Reflecting a Novel Target in Obesity and Female-Specific Cardiometabolic Traits

O'Brien DP. et al, (2022), REPRODUCTIVE SCIENCES, 29, 239 - 239

Making sense of the linear genome, gene function and TADs.

Long HS. et al, (2022), Epigenetics Chromatin, 15

Genetic variation influencing DNA methylation provides insights into molecular mechanisms regulating genomic function

Hawe JS. et al, (2022), Nature Genetics

Load More

Include forthcoming?