Nutland, Sarah
University of Cambridge · Breakthrough T1D UK · Addenbrooke's Hospital · Wellcome Trust
5 papers on CoChat
Most cited papers
- Verified
Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease
Ueda, H., Howson, J. M. M., Esposito, L., Heward, J., Snook, Chamberlain, G., Rainbow, D. B., Hunter, K. M. D., Smith, A. N., Di Genova, G., et al. (2003) · Nature
Diabetes and associated disordersGenetic Associations and Epidemiology
Cited by 2,175
- Verified
Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes
Finland, G. O. T. 1. D. I., Todd, J. A., the Wellcome Trust Case Control Consortium, Walker, N. M., Cooper, J. D., Smyth, D. J., Downes, K., Plagnol, V., Bailey, R., Nejentsev, S., et al. (2007) · Nature Genetics
Diabetes and associated disordersGenetic Associations and Epidemiology
Cited by 1,456
- Verified
Haplotype tagging for the identification of common disease genes
Johnson, G. C. L., Esposito, L., Barratt, B. J., Smith, A. N., Heward, J., Di Genova, G., Ueda, H., Cordell, H. J., Eaves, I. A., Dudbridge, F., et al. (2001) · Nature Genetics
Genetic Associations and EpidemiologyForensic and Genetic Research
Cited by 1,174
- Verified
Population structure, differential bias and genomic control in a large-scale, case-control association study
Clayton, D. G., Walker, N. M., Smyth, D. J., Pask, R., Cooper, J. D., Maier, L. M., Smink, L. J., Lam, A. C., Ovington, N. R., Stevens, H. E., et al. (2005) · Nature Genetics
Genetic Associations and EpidemiologyForensic and Genetic Research
Cited by 526
- Verified
Cell-specific protein phenotypes for the autoimmune locus IL2RA using a genotype-selectable human bioresource
Dendrou, C. A., Plagnol, V., Fung, E., Yang, J. H. M., Downes, K., Cooper, J. D., Nutland, S., Coleman, G., Himsworth, M., Hardy, M., et al. (2009) · Nature Genetics
Genetic Associations and EpidemiologyDiabetes and associated disorders
Cited by 274
Go further with a free account
Verify every reference, keep papers in a library, and ask questions across them.
Sign up - it is free