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Blood|October 23, 2012
The clinical significance of NOTCH1 and SF3B1 mutations in the UK LRF CLL4 trialDavid G Oscier, Matthew J J Rose-Zerilli, Nils Winkelmann, et al.
American Journal of Human Genetics|August 5, 2005
A high-density SNP genomewide linkage scan for chronic lymphocytic leukemia-susceptibility lociGabrielle S Sellick, Emily L Webb, Ruth Allinson, et al.
Blood|November 26, 2010
Autologous hematopoietic stem cell transplantation in chronic lymphocytic leukemia: results of European intergroup randomized trial comparing autografting versus observationMauricette Michallet, Peter Dreger, Laurent Sutton, et al.
Haematologica|March 4, 2014
ATM mutation rather than BIRC3 deletion and/or mutation predicts reduced survival in 11q-deleted chronic lymphocytic leukemia: data from the UK LRF CLL4 trialMatthew J J Rose-Zerilli, Jade Forster, Helen Parker, et al.
British Journal of Haematology|May 11, 2011
Common genetic variation at 15q25.2 impacts on chronic lymphocytic leukaemia riskDalemari Crowther-Swanepoel, Maria Chiara Di Bernardo, Krzysztof Jamroziak, et al.
Blood|October 17, 2013
CYP2B6*6 is an independent determinant of inferior response to fludarabine plus cyclophosphamide in chronic lymphocytic leukemiaGillian G Johnson, Ke Lin, Trevor F Cox, et al.
Blood|March 16, 2018
iwCLL guidelines for diagnosis, indications for treatment, response assessment, and supportive management of CLLMichael Hallek, Bruce D Cheson, Daniel Catovsky, et al.
Blood|August 10, 2007
A high-density SNP genome-wide linkage search of 206 families identifies susceptibility loci for chronic lymphocytic leukemiaGabrielle S Sellick, Lynn R Goldin, Ruth W Wild, et al.
Cell Reports|August 16, 2016
Genetic Predisposition to Chronic Lymphocytic Leukemia Is Mediated by a BMF Super-Enhancer PolymorphismRadhika Kandaswamy, Georgina P Sava, Helen E Speedy, et al.
Nature Communications|August 11, 2019
Insight into genetic predisposition to chronic lymphocytic leukemia from integrative epigenomicsHelen E Speedy, Renée Beekman, Vicente Chapaprieta, et al.
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