Panos Deloukas

Publisher Correction: Multi-ancestry genome-wide association study of severe pregnancy nausea and vomiting.

The contribution of Apoliproprotein E genetic variation to dementia risk in British South Asians

Multi-ancestry genome-wide association study of severe pregnancy nausea and vomiting.

Fejzo M, Wang X, Tan Q et al. (2026) . Publisher Correction: Multi-ancestry genome-wide association study of severe pregnancy nausea and vomiting . nameOfConference

Jacobs BM, Chandra A, Foote IF et al. (2026) . The contribution of apolipoprotein E genetic variation to dementia risk in British South Asians . nameOfConference

Fejzo M, Wang X, Tan Q et al. (2026) . Multi-ancestry genome-wide association study of severe pregnancy nausea and vomiting . nameOfConference

Polygenic prediction of body mass index and obesity through the life course and across ancestries.

Inherited predisposition to pneumothorax: estimating the frequency of Birt-Hogg-Dubé syndrome from genomics and population cohorts.

Understanding the potential contribution of polygenic risk scores to the prediction of gestational and type 2 diabetes in women from British Pakistani and Bangladeshi groups: a cohort study in Genes and Health.

XBP1 expression in pancreatic islet cells is associated with poor glycaemic control especially in young non-obese onset diabetes across ancestries

Insights from the largest diverse ancestry sex-specific disease map for genetically predicted height.

A genes and health recall study of intrahepatic cholestasis of pregnancy and cholestatic liver disease.

Smit RAJ, Wade KH, Hui Q et al. (2025) . Polygenic prediction of body mass index and obesity through the life course and across ancestries . nameOfConference

Yngvadottir B, Richman L, Andreou A et al. (2025) . Inherited predisposition to pneumothorax: estimating the frequency of Birt-Hogg-Dubé syndrome from genomics and population cohorts . nameOfConference

Zöllner J, Orazumbekova B, Hodgson S et al. (2025) . Understanding the potential contribution of polygenic risk scores to the prediction of gestational and type 2 diabetes in women from British Pakistani and Bangladeshi groups: a cohort study in Genes and Health . nameOfConference

Genetic basis of early onset and progression of type 2 diabetes in South Asians

Genetic architecture of routinely acquired blood tests in a British South Asian cohort

Prediction of atrial fibrillation and stroke using machine learning models in UK Biobank.

Author Correction: The power of genetic diversity in genome-wide association studies of lipids

Height, Autoimmune Thyroid Disease, and Thyroid Cancer: A Mendelian Randomization Study.

Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

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

DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases

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

DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases.

Genetically Determined Reproductive Aging and Coronary Heart Disease: A Bidirectional 2-sample Mendelian Randomization

Thyroid function, pernicious anemia and erythropoiesis: a two-sample Mendelian randomization study.

Genetically Determined Reproductive Aging and Coronary Heart Disease: A Bidirectional 2-sample Mendelian Randomization.

A Saturated Map of Common Genetic Variants Associated with Human Height from 5.4 Million Individuals of Diverse Ancestries

The power of genetic diversity in genome-wide association studies of lipids