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Number of items: 6.

Zhang, Lei ORCID: https://orcid.org/0000-0003-3536-8692, Evans, Anna ORCID: https://orcid.org/0000-0002-2430-811X, von Ruhland, Chris, Draman, Mohd Shazli, Edkins, Sarah ORCID: https://orcid.org/0000-0003-0717-1972, Vincent, Amy E., Berlinguer-Palmini, Rolando, Rees, D. Aled ORCID: https://orcid.org/0000-0002-1165-9092, Haridas, Anjana S, Morris, Dan, Tee, Andrew R. ORCID: https://orcid.org/0000-0002-5577-4631, Ludgate, Marian, Turnbull, Doug M., Karpe, Fredrik and Dayan, Colin M. ORCID: https://orcid.org/0000-0002-6557-3462 2020. Distinctive features of orbital adipose tissue (OAT) in Graves' orbitopathy. International Journal of Molecular Sciences 21 (23) , 9145. 10.3390/ijms21239145
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Richards, Alexander, Leonenko, Ganna M ORCID: https://orcid.org/0000-0001-8025-661X, Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053, Kavanagh, D, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Evans, Anna ORCID: https://orcid.org/0000-0002-2430-811X, Chambert, K. D., Moran, J. L., Goldstein, J., Neale, B. M., McCarroll, S. A., Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2016. Exome arrays capture polygenic rare variant contributions to schizophrenia. Human Molecular Genetics 25 (5) , pp. 1001-1007. 10.1093/hmg/ddv620
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Ostronoff, F., Othus, M., Lazenby, Michelle, Estey, E., Appelbaum, F. R., Evans, Anna ORCID: https://orcid.org/0000-0002-2430-811X, Godwin, J., Gilkes, Amanda F., Kopecky, K. J., Burnett, Alan, List, A. F., Fang, M., Oehler, V. G., Petersdorf, S. H., Pogosova-Agadjanyan, E. L., Radich, J. P., Willman, C. L., Meshinchi, S. and Stirewalt, D. L. 2015. Prognostic significance of NPM1 mutations in the absence of FLT3-internal tandem duplication in older patients with acute myeloid leukemia: A SWOG and UK National Cancer Research Institute/Medical Research Council report. Journal of Clinical Oncology 33 (10) , pp. 1157-1164. 10.1200/JCO.2014.58.0571

Walter, R. B., Othus, M., Burnett, A. K., Löwenberg, B., Kantarjian, H. M., Ossenkoppele, G. J., Hills, R. K. ORCID: https://orcid.org/0000-0003-0166-0062, Ravandi, F., Pabst, T., Evans, A. ORCID: https://orcid.org/0000-0002-2430-811X, Pierce, S. R., Vekemans, M-C, Appelbaum, F. R. and Estey, E. H. 2015. Resistance prediction in AML: analysis of 4601 patients from MRC/NCRI, HOVON/SAKK, SWOG and MD Anderson Cancer Center. Leukemia 29 (2) , pp. 312-320. 10.1038/leu.2014.242

Lazenby, Michelle, Gilkes, Amanda, Marrin, C., Evans, Anna ORCID: https://orcid.org/0000-0002-2430-811X, Hills, Robert Kerrin ORCID: https://orcid.org/0000-0003-0166-0062 and Burnett, A. K. 2014. The prognostic relevance of flt3 and npm1 mutations on older patients treated intensively or non-intensively: a study of 1312 patients in the UK NCRI AML16 trial. Leukemia 28 , pp. 1953-1959. 10.1038/leu.2014.90

Walter, R. B., Othus, M., Burnett, Alan K., Lowenberg, B., Kantarjian, H. M., Ossenkoppele, G. J., Hills, Robert Kerrin ORCID: https://orcid.org/0000-0003-0166-0062, van Montfort, K. G. M., Ravandi, F., Evans, Anna ORCID: https://orcid.org/0000-0002-2430-811X, Pierce, S. R., Appelbaum, F. R. and Estey, E. H. 2013. Significance of FAB subclassification of "acute myeloid leukemia, NOS" in the 2008 WHO classification: analysis of 5848 newly diagnosed patients. Blood 121 (13) , p. 2424. 10.1182/blood-2012-10-462440

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