ORCA
Online Research @ CardiffÂ
Browse by All Cardiff Authors
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Up a levelNumber 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
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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
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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
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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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