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Publications

The genetic architecture of changes in adiposity during adulthood

Venkatesh S. 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

Correction: Obesity and risk of female reproductive conditions: A Mendelian randomisation study.

Venkatesh SS. et al, (2022), PLoS medicine, 19

Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes.

Pervjakova N. et al, (2022), Human molecular genetics, 31, 3377 - 3391

Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies.

Gorski M. et al, (2022), Kidney international

Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.

Winkler TW. et al, (2022), Communications biology, 5

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

Temprano-Sagrera G. et al, (2022), Journal of thrombosis and haemostasis : JTH, 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), Nature genetics, 54, 560 - 572

Transcriptome and fatty-acid signatures of adipocyte hypertrophy and its non-invasive MR-based characterization in human adipose tissue.

Honecker J. et al, (2022), EBioMedicine, 79

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

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

Modelling the genetic aetiology of complex disease: human-mouse conservation of noncoding features and disease-associated loci.

Powell G. et al, (2022), Biol Lett, 18

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

Obesity and risk of female reproductive conditions: A Mendelian randomisation study

Venkatesh SS. et al, (2022), PLOS Medicine, 19, e1003679 - e1003679

Broad-Spectrum Antidote Discovery by Untangling the Reactivation Mechanism of Nerve-Agent-Inhibited Acetylcholinesterase

Lindgren C. et al, (2022), Chemistry - A European Journal

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

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

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

Long HS. et al, (2022), Epigenetics & chromatin, 15

Response to comment on "Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics".

Bovijn J. et al, (2021), Science translational medicine, 13

Evidence From Men for Ovary-independent Effects of Genetic Risk Factors for Polycystic Ovary Syndrome.

Zhu J. et al, (2021), The Journal of clinical endocrinology and metabolism

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