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British Journal of Haematology|March 3, 2025
Heterozygous germline TET2 loss-of-function variants associated with an ALPS-like phenotypeSean Harrop, Joshua Casan, Hannah Rose, et al.
Scientific Reports|May 9, 2019
Hemopoietic Cell Kinase amplification with Protein Tyrosine Phosphatase Receptor T depletion leads to polycythemia, aberrant marrow erythoid maturation, and splenomegalyMatthew Ku, Ruth N MacKinnon, Meaghan Wall, et al.
Oncotarget|December 15, 2018
Frequent activating STAT3 mutations and novel recurrent genomic abnormalities detected in breast implant-associated anaplastic large cell lymphomaPiers Blombery, Ella Thompson, Georgina L Ryland, et al.
Blood Advances|July 28, 2022
Enrichment of BTK Leu528Trp mutations in patients with CLL on zanubrutinib: potential for pirtobrutinib cross-resistancePiers Blombery, Ella R Thompson, Thomas E Lew, et al.
Ejhaem|May 19, 2023
Biallelic deleterious germline SH2B3 variants cause a novel syndrome of myeloproliferation and multi-organ autoimmunityPiers Blombery, Vahid Pazhakh, Adriana S Albuquerque, et al.
Leukemia & Lymphoma|June 6, 2014
Src family kinases and their role in hematological malignanciesMatthew Ku, Meaghan Wall, Ruth N MacKinnon, et al.
Cancer|March 20, 2014
Underestimation of myelodysplastic syndrome incidence by cancer registries: Results from a population-based data linkage studyZoe K McQuilten, Erica M Wood, Mark N Polizzotto, et al.
Blood Advances|December 3, 2021
Single-cell sequencing demonstrates complex resistance landscape in CLL and MCL treated with BTK and BCL2 inhibitorsElla R Thompson, Tamia Nguyen, Yamuna Kankanige, et al.
Scientific Reports|April 25, 2019
CNspector: a web-based tool for visualisation and clinical diagnosis of copy number variation from next generation sequencingJohn F Markham, Satwica Yerneni, Georgina L Ryland, et al.
Scientific Reports|June 25, 2020
Publisher Correction: CNspector: a web-based tool for visualisation and clinical diagnosis of copy number variation from next generation sequencingJohn F Markham, Satwica Yerneni, Georgina L Ryland, et al.
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