The clinical utility of C-peptide measurement in the care of patients with diabetes

by Jones, A G, Hattersley, A T
Published 2013

The development and validation of a clinical prediction model to determine the probability of MODY in patients with young-onset diabetes

by Shields, B. M., McDonald, T. J., Ellard, S., Campbell, M. J., Hyde, C., Hattersley, A. T.
Published 2012

Analysis of cell‐free fetal DNA for non‐invasive prenatal diagnosis in a family with neonatal diabetes

by De Franco, E., Caswell, R., Houghton, J. A. L., Iotova, V., Hattersley, A. T., Ellard, S.
Published 2016

RET gene mutations are not a common cause of congenital solitary functioning kidney in adults

by Oram, Richard A., Edghill, Emma L., Woolf, Adrian S., Hennekam, R. C., Ellard, Sian, Hattersley, A. T., Bingham, Coralie
Published 2009

Biallelic PDX1 (insulin promoter factor 1) mutations causing neonatal diabetes without exocrine pancreatic insufficiency

by De Franco, E, Shaw-Smith, C, Flanagan, S E, Edghill, E L, Wolf, J, Otte, V, Ebinger, F, Varthakavi, P, Vasanthi, T, Edvardsson, S, Hattersley, A T, Ellard, S
Published 2013

Improved genetic testing for monogenic diabetes using targeted next-generation sequencing

by Ellard, S., Lango Allen, H., De Franco, E., Flanagan, S. E., Hysenaj, G., Colclough, K., Houghton, J. A. L., Shepherd, M., Hattersley, A. T., Weedon, M. N., Caswell, R.
Published 2013

Sequencing PDX1 (insulin promoter factor 1) in 1788 UK individuals found 5% had a low frequency coding variant, but these variants are not associated with Type 2 diabetes

by Edghill, E L, Khamis, A, Weedon, M N, Walker, M, Hitman, G A, McCarthy, M I, Owen, K R, Ellard, S, T Hattersley, A, Frayling, T M
Published 2011

Psychiatric morbidity in children with KCNJ11 neonatal diabetes

by Bowman, P., Broadbridge, E., Knight, B. A., Pettit, L., Flanagan, S. E., Reville, M., Tonks, J., Shepherd, M. H., Ford, T. J., Hattersley, A. T.
Published 2016

Urinary C‐peptide creatinine ratio detects absolute insulin deficiency in Type 2 diabetes

by Hope, S. V., Jones, A. G., Goodchild, E., Shepherd, M., Besser, R. E. J., Shields, B., McDonald, T., Knight, B. A., Hattersley, A.
Published 2013

Expanding the Clinical Spectrum Associated With GLIS3 Mutations

by Dimitri, P., Habeb, A. M., Garbuz, F., Millward, A., Wallis, S., Moussa, K., Akcay, T., Taha, D., Hogue, J., Slavotinek, A., Wales, J. K. H., Shetty, A., Hawkes, D., Hattersley, A. T., Ellard, S., De Franco, E.
Published 2015

Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes

by Albrechtsen, A., Grarup, N., Li, Y., Sparsø, T., Tian, G., Cao, H., Jiang, T., Kim, S. Y., Korneliussen, T., Li, Q., Nie, C., Wu, R., Skotte, L., Morris, A. P., Ladenvall, C., Cauchi, S., Stančáková, A., Andersen, G., Astrup, A., Banasik, K., Bennett, A. J., Bolund, L., Charpentier, G., Chen, Y., Dekker, J. M., Doney, A. S. F., Dorkhan, M., Forsen, T., Frayling, T. M., Groves, C. J., Gui, Y., Hallmans, G., Hattersley, A. T., He, K., Hitman, G. A., Holmkvist, J., Huang, S., Jiang, H., Jin, X., Justesen, J. M., Kristiansen, K., Kuusisto, J., Lajer, M., Lantieri, O., Li, W., Liang, H., Liao, Q., Liu, X., Ma, T., Ma, X., Manijak, M. P., Marre, M., Mokrosiński, J., Morris, A. D., Mu, B., Nielsen, A. A., Nijpels, G., Nilsson, P., Palmer, C. N. A., Rayner, N. W., Renström, F., Ribel-Madsen, R., Robertson, N., Rolandsson, O., Rossing, P., Schwartz, T. W., Slagboom, P. E., Sterner, M., Tang, M., Tarnow, L., Tuomi, T., van’t Riet, E., van Leeuwen, N., Varga, T. V., Vestmar, M. A., Walker, M., Wang, B., Wang, Y., Wu, H., Xi, F., Yengo, L., Yu, C., Zhang, X., Zhang, J., Zhang, Q., Zhang, W., Zheng, H., Zhou, Y., Altshuler, D., ‘t Hart, L. M., Franks, P. W., Balkau, B., Froguel, P., McCarthy, M. I., Laakso, M., Groop, L., Christensen, C., Brandslund, I., Lauritzen, T., Witte, D. R., Linneberg, A., Jørgensen, T., Hansen, T., Wang, J., Nielsen, R., Pedersen, O.
Published 2012