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Internal Medicine Journal|May 24, 2023
Targeting the BRAF pathway in haematological diseasesMatthew J Rees, Michael Dickinson, James Paterson, et al.
Clinical Lymphoma, Myeloma & Leukemia|March 18, 2014
The choice of multiple myeloma induction therapy affects the frequency and severity of oral mucositis after melphalan-based autologous stem cell transplantationShaun Fleming, Simon J Harrison, Piers Blombery, et al.
Leukemia|February 24, 2023
Novel causative variants of VEXAS in UBA1 detected through whole genome transcriptome sequencing in a large cohort of hematological malignanciesMaki Sakuma, Piers Blombery, Manja Meggendorfer, et al.
BMC Bioinformatics|December 17, 2017
Canary: an atomic pipeline for clinical amplicon assaysKenneth D Doig, Jason Ellul, Andrew Fellowes, et al.
Pharmacogenomics and Personalized Medicine|July 7, 2023
Are We Ready for Whole Population Genomic Sequencing of Asymptomatic Newborns?Danya F Vears, Julian Savulescu, John Christodoulou, et al.
Journal of Clinical Pathology|August 13, 2017
Incidental detection of germline variants of potential clinical significance by massively parallel sequencing in haematological malignanciesCostas K Yannakou, Kate Jones, Georgina L Ryland, et al.
Histopathology|October 15, 2024
Closing the gap between biology and classification in splenic B-cell lymphomasPiers Blombery, Daphne de Jong, Judith A Ferry, et al.
British Journal of Haematology|December 15, 2023
Evaluation of T-cell clonality by anti-TRBC1 antibody-based flow cytometry and correlation with T-cell receptor sequencingPhillip C Nguyen, Tamia Nguyen, Clarissa Wilson, et al.
The Australasian Journal of Dermatology|October 5, 2022
VEXAS syndrome: A dermatological perspectiveJacqueline K Nguyen, David Routledge, Carrie van Der Weyden, et al.
Biodata Mining|October 30, 2025
Using artificial intelligence (AI) to model clinical variant reporting for next generation sequencing (NGS) oncology assaysKenneth D Doig, Rashindrie Perera, Yamuna Kankanige, et al.
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