| Whole-genome sequencing analysis of anthropometric traits in 672,976 individuals reveals convergence between rare and common genetic associations | Nature communications |  | | 2026 | 10 | 13 |
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| Genetic and epidemiological evidence linking respiratory and musculoskeletal diseases: shared risk factors and intervention windows | Respiratory research | | | 2026 | 11 | 7 |
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| Genetics identifies obesity as a shared risk factor for co-occurring multiple long-term conditions | Communications medicine | | | 2026 | 3 | 2 |
|
| Polygenic prediction of body mass index and obesity through the life course and across ancestries | Nature medicine | | | 2025 | 26 | 308 |
|
| A systematic analysis of the contribution of genetics to multimorbidity and comparisons with primary care data | EBioMedicine | | | 2025 | 15 | 171 |
|
| Whole-genome sequencing analysis identifies rare, large-effect noncoding variants and regulatory regions associated with circulating protein levels | Nature genetics | | | 2025 | 23 | 84 |
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| Using clustering of genetic variants in Mendelian randomization to interrogate the causal pathways underlying multimorbidity from a common risk factor | Genetic epidemiology | | | 2025 | 3 | 5 |
|
| Effects of childhood and adult height on later life cardiovascular disease risk estimated through Mendelian randomization | European journal of epidemiology | | | 2025 | 17 | 187 |
|
| Weight Management in a Patient With Smith-Magenis Syndrome : The Role of GLP-1 Receptor Agonists | JCEM case reports | | | 2025 | 77 | 448 |
|
| Getting to GRIPS with MR-Egger : Modelling directional pleiotropy independently of allele coding | PLOS genetics | | | 2025 | 3 | 2 |
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| Clinical utility of self-reported sleep duration and insomnia symptoms in type 2 diabetes prediction | Diabetologia | | | 2025 | 18 | 69 |
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