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NHS gene

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A novel approach to defining progression in MDS and precursor myeloid conditions in the MDS Natural History Study.
NHS
Somatic and germline genetic testing pathways in haematological malignancies: Best practice consensus guidelines from the 2025 national meeting organised by UK Cancer Genetics Group (UKCGG), CanGene-CanVar and the NHS England Haematological Oncology Working Group.
NHS
Heteroaggregation of Wild-Type and ALS Mutant SOD1.
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Experimental Cancer Medicine Centre (ECMC) network proposal for a consensus gene panel for pan-cancer sequencing: a Delphi methodology.
NHS
Implementation and Audit of Mainstream Genetic Testing Within a High-Volume UK Breast Unit for Pathogenic Variations Associated With Breast Cancer Using the R208 and R444.1 National Test Directory Criterion.
NHS
ADVANTAGE: Advanced discovery of visceral analgesics by neuroimmune targets and the genetics of extreme human phenotype, a study protocol.
NHS
Performance of international phenotypic criteria for prenatal exome sequencing: systematic review and comparative diagnostic accuracy study using historical individual participant data.
NHS
Validating data from multiplex assays of variant effect: A CanVIG-UK national survey of NHS clinical scientists.
NHS
Clinical Impact of Constitutional Genomic Testing on Current Breast Cancer Care.
NHS
Developing a Paired Whole Genome Sequencing Service for Children With Cancer.
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