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Archives of Pathology & Laboratory Medicine|February 10, 2018
Sensitive NPM1 Mutation Quantitation in Acute Myeloid Leukemia Using Ultradeep Next-Generation Sequencing in the Diagnostic LaboratoryPiers Blombery, Kate Jones, Ken Doig, et al.
Molecular Cytogenetics|December 15, 2020
Detailed molecular cytogenetic characterisation of the myeloid cell line U937 reveals the fate of homologous chromosomes and shows that centromere capture is a feature of genome instabilityRuth N MacKinnon, Joanne Peverall, Lynda J Campbell, et al.
Cancer Genetics|May 4, 2011
A cryptic deletion in 5q31.2 provides further evidence for a minimally deleted region in myelodysplastic syndromesRuth N MacKinnon, George Kannourakis, Meaghan Wall, et al.
Annals of Hematology|February 6, 2017
Clinicopathological differences exist between CALR- and JAK2-mutated myeloproliferative neoplasms despite a similar molecular landscape: data from targeted next-generation sequencing in the diagnostic laboratoryRishu Agarwal, Piers Blombery, Michelle McBean, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 14, 2021
Newborn bloodspot screening in the time of COVID-19Ronda F Greaves, James Pitt, Candice McGregor, et al.
Cytogenetic and Genome Research|March 6, 2017
The Dicentric Chromosome dic(20;22) Is a Recurrent Abnormality in Myelodysplastic Syndromes and Is a Product of Telomere FusionRuth N MacKinnon, Hendrika M Duivenvoorden, Lynda J Campbell, et al.
Annals of Hematology|June 16, 2011
Prophylactic intravenous immunoglobulin during autologous haemopoietic stem cell transplantation for multiple myeloma is not associated with reduced infectious complicationsPiers Blombery, H Miles Prince, Leon J Worth, et al.
Nature Reviews. Clinical Oncology|July 9, 2026
CRISPR in clinical oncology: translational advances from molecular diagnostics to therapeuticsSamuel Grigg, Carolyn Shembrey, Mohamed Fareh, et al.
Genome Biology|January 7, 2022
JAFFAL: detecting fusion genes with long-read transcriptome sequencingNadia M Davidson, Ying Chen, Teresa Sadras, et al.
BMC Medical Genomics|March 29, 2022
Findings from precision oncology in the clinic: rare, novel variants are a significant contributor to scaling molecular diagnosticsKenneth D Doig, Christopher G Love, Thomas Conway, et al.
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