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

Journal article

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

Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability

Journal article

Lagou V. et al, (2021), Nature Communications, 12

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

Journal article

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

The genomics of heart failure: design and rationale of the HERMES consortium.

Journal article

Lumbers RT. et al, (2021), ESC Heart Fail

Investigating causality of risk factors for miscarriage - a Mendelian randomization analysis

Conference paper

Painter J. et al, (2021), HUMAN REPRODUCTION, 36, 306 - 307

Colocalization analysis of polycystic ovary syndrome to identify potential disease-mediating genes and proteins.

Journal article

Censin JC. et al, (2021), European journal of human genetics : EJHG

A regulatory variant at 3q21.1 confers an increased pleiotropic risk for hyperglycemia and altered bone mineral density

Journal article

Sinnott-Armstrong N. et al, (2021), Cell Metabolism, 33, 615 - 628.e13

Genome-wide association study identifies 48 common genetic variants associated with handedness

Journal article

Cuellar-Partida G. et al, (2021), Nature Human Behaviour, 5, 59 - 70

The genetic architecture of sporadic and multiple consecutive miscarriage.

Journal article

Laisk T. et al, (2020), Nature communications, 11

Genetic variants mimicking therapeutic inhibition of IL-6 receptor signaling and risk of COVID-19.

Journal article

Bovijn J. et al, (2020), The Lancet Rheumatology, 2, e658 - e659

Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.

Journal article

Folkersen L. et al, (2020), Nature metabolism, 2, 1135 - 1148

Genome-wide Study Identifies Association between HLA-B∗55:01 and Self-Reported Penicillin Allergy

Journal article

Krebs K. et al, (2020), The American Journal of Human Genetics, 107, 612 - 621

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