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Search results (415)

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RAB3GAP2 is a regulator of skeletal muscle endothelial cell proliferation and associated with capillary-to-fiber ratio.

Ström K. et al, (2026), Cell reports, 45

Individuals whose phenotype deviates from genetic expectation defined by common variation are enriched for rare damaging variants in genes that cause rare disease

Baya NA. et al, (2025)

Biologically Inspired Digital Histology for Deep Phenotyping of Placental Composition Changes Across Major Lesion Types

Walker EC. et al, (2025)

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

Baya NA. et al, (2025), The American Journal of Human Genetics, 112, 2316 - 2337

Genome-wide analyses identify 25 infertility loci and relationships with reproductive traits across the allele frequency spectrum

Venkatesh SS. et al, (2025), Nature Genetics, 57, 1107 - 1118

Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes.

Henry A. et al, (2025), Nature genetics, 57, 815 - 828

Altered Hormone and Bioactive Lipid Plasma Profile in Rodent Models of Polycystic Ovarian Syndrome Revealed by Targeted Mass Spectrometry

Scott HC. et al, (2025), Journal of Endocrinology and Metabolism, 15, 1 - 14

Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy.

Zheng SL. et al, (2024), Nature genetics, 56, 2646 - 2658

Altered Hormone and Bioactive Lipid Plasma Profile in Rodent Models of Polycystic Ovarian Syndrome Revealed by Targeted Mass Spectrometry

Scott HC. et al, (2024)

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)

Genome-wide association meta-analysis identifies five loci associated with postpartum hemorrhage.

Westergaard D. et al, (2024), Nature genetics, 56, 1597 - 1603

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

Lassen FH. et al, (2024), Cell genomics, 4

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

Venkatesh SS. et al, (2024), Nature communications, 15

Genetic drivers of heterogeneity in type 2 diabetes pathophysiology.

Suzuki K. et al, (2024), Nature, 627, 347 - 357

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