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Human Molecular Genetics|April 14, 2011
Analysis of a breakpoint cluster reveals insight into the mechanism of intrachromosomal amplification in a lymphoid malignancyPaul B Sinclair, Helen Parker, Qian An, et al.
Immunological Reviews|September 30, 2024
Fc gamma receptors: Their evolution, genomic architecture, genetic variation, and impact on human diseaseSarah Frampton, Rosanna Smith, Lili Ferson, et al.
Nature Communications|June 28, 2016
Chromatin accessibility maps of chronic lymphocytic leukaemia identify subtype-specific epigenome signatures and transcription regulatory networksAndré F Rendeiro, Christian Schmidl, Jonathan C Strefford, et al.
British Journal of Haematology|February 6, 2016
The outcome of Chronic lymphocytic leukaemia patients with 97% IGHV gene identity to germline is distinct from cases with <97% identity and similar to those with 98% identityZadie Davis, Francesco Forconi, Anton Parker, et al.
Immunological Reviews|October 27, 2015
Fcγ receptors: genetic variation, function, and diseaseChantal E Hargreaves, Matthew J J Rose-Zerilli, Lee R Machado, et al.
Exploration of Targeted Anti-Tumor Therapy|September 16, 2024
The genomic and molecular landscape of splenic marginal zone lymphoma, biological and clinical implicationsAmatta Mirandari, Helen Parker, Margaret Ashton-Key, et al.
Molecular & Cellular Proteomics : MCP|January 26, 2018
Proteomics Profiling of CLL Versus Healthy B-cells Identifies Putative Therapeutic Targets and a Subtype-independent Signature of Spliceosome DysregulationHarvey E Johnston, Matthew J Carter, Marta Larrayoz, et al.
Briefings in Bioinformatics|August 30, 2014
Exome sequence read depth methods for identifying copy number changesLatha Kadalayil, Sajjad Rafiq, Matthew J J Rose-Zerilli, et al.
Journal of Medicinal Chemistry|August 9, 2024
Exploring 2-Sulfonylpyrimidine Warheads as Acrylamide Surrogates for Targeted Covalent Inhibition: A BTK StoryRuxandra Moraru, Beatriz Valle-Argos, Annabel Minton, et al.
Plos One|December 19, 2013
Whole exome sequencing identifies novel recurrently mutated genes in patients with splenic marginal zone lymphomaMarina Parry, Matthew J J Rose-Zerilli, Jane Gibson, et al.
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