Myelodysplastic Syndromes (MDS) Group

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Research Output

Correct application of variant classification guidelines in germline RUNX1 mutated disorders to assist clinical diagnosis

Brown, A. L., Hahn, C., Hiwase, D., Godley, L. A. & Scott, H. S., 2 Jan 2020, In : Leukemia and Lymphoma. 61, 1, p. 246-247 2 p.

Research output: Contribution to journalLetter

RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML

Brown, A. L., Arts, P., Carmichael, C. L., Babic, M., Dobbins, J., Chong, C. E., Schreiber, A. W., Feng, J., Phillips, K., Wang, P. P. S., Ha, T., Homan, C. C., King-Smith, S. L., Rawlings, L., Vakulin, C., Dubowsky, A., Burdett, J., Moore, S., McKavanagh, G., Henry, D. & 39 others, Wells, A., Mercorella, B., Nicola, M., Suttle, J., Wilkins, E., Li, X. C., Michaud, J., Brautigan, P., Cannon, P., Altree, M., Jaensch, L., Fine, M., Butcher, C., D'Andrea, R. J., Lewis, I. D., Hiwase, D. K., Papaemmanuil, E., Horwitz, M. S., Natsoulis, G., Rienhoff, H. Y., Patton, N., Mapp, S., Susman, R., Morgan, S., Cooney, J., Currie, M., Popat, U., Bochtler, T., Izraeli, S., Bradstock, K., Godley, L. A., Kr¨amer, A., Fröhling, S., Wei, A. H., Forsyth, C., Fan, H. M., Poplawski, N. K., Hahn, C. N. & Scott, H. S., 24 Mar 2020, In : Blood Advances. 4, 6, p. 1131-1144 14 p.

Research output: Contribution to journalArticle

Screening for deficits using the G8 and VES-13 in older patients with Myelodysplastic syndromes

Molga, A., Wall, M., Wee, L. Y., Chhetri, R., Singhal, D., Singhal, N., To, L. B., Shakib, S., To, T. & Hiwase, D., 1 Jan 2020, In : Journal of Geriatric Oncology. 11, 1, p. 128-130 3 p.

Research output: Contribution to journalLetter

1 Citation (Scopus)