Beer, Nicola L.
University of Oxford · Oxford Centre for Diabetes, Endocrinology and Metabolism
4 papers on CoChatORCID 0000-0002-4964-7150
Most cited papers
- Verified
The genetic architecture of type 2 diabetes
Fuchsberger, C., Flannick, J., Teslovich, T. M., Mahajan, A., Agarwala, V., Gaulton, K. J., Ma, C., Fontanillas, P., Moutsianas, L., McCarthy, D. J., et al. (2016) · Nature
Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals
Cited by 1,051
- Verified
Loss-of-function mutations in SLC30A8 protect against type 2 diabetes
Go-T2D Consortium, Flannick, J., T2D-GENES Consortium, Thorleifsson, G., Beer, N. L., Jacobs, S. B. R., Grarup, N., Burtt, N. P., Mahajan, A., Fuchsberger, C., et al. (2014) · Nature Genetics
Genetic Associations and EpidemiologyDiabetes and associated disorders
Cited by 492
- Verified
The P446L variant in GCKR associated with fasting plasma glucose and triglyceride levels exerts its effect through increased glucokinase activity in liver
Beer, N. L., Tribble, N. D., McCulloch, L. J., Roos, C., Johnson, P. R. V., Orho-Melander, M., & Gloyn, A. L. (2009) · Human Molecular Genetics
Pancreatic function and diabetesGenetic Associations and Epidemiology
Cited by 401
- Verified
Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes
Flannick, J., Beer, N. L., Bick, A. G., Agarwala, V., Molnes, J., Gupta, N., Burtt, N. P., Florez, J. C., Meigs, J. B., Taylor, H., et al. (2013) · Nature Genetics
Genomics and Rare DiseasesGenetic Associations and Epidemiology
Cited by 136
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