Genetic and epigenetic studies of pediatric leukemia
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- 2024
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Mark
Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4 : A poly-glycine disease
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- Contribution to journal › Article
- 2023
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Mark
A cloud-based resource for genome coordinate-based exploration and large-scale analysis of chromosome aberrations and gene fusions in cancer
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- Contribution to journal › Article
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Feasibility to use whole-genome sequencing as a sole diagnostic method to detect genomic aberrations in pediatric B-cell acute lymphoblastic leukemia
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- Contribution to journal › Article
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Mark
Acquired uniparental isodisomies involving chromosome 12 in paediatric B-cell precursor acute lymphoblastic leukaemia : Associations with chromosome 21 gains and SH2B3 mutations
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- Contribution to journal › Article
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Mark
Clonal origin and development of high hyperdiploidy in childhood acute lymphoblastic leukaemia
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- Contribution to journal › Article
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Mark
Impact of 1q gains on treatment outcomes of patients with newly diagnosed multiple myeloma in a real-world Swedish population receiving modern treatment
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- Contribution to journal › Article
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The Prognostic Effect of IKZF1 Deletions in ETV6:: RUNX1 and High Hyperdiploid Childhood Acute Lymphoblastic Leukemia
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- Contribution to journal › Article
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Genetic Subtypes and Outcome of Patients Aged 1 to 45 Years Old with Acute Lymphoblastic Leukemia in the NOPHO ALL2008 Trial
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- Contribution to journal › Article
- 2021
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Mark
Parental origin of monosomy 7 in acute leukaemia
2021) In British Journal of Haematology(
- Contribution to journal › Letter
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Mark
HUGO Gene Nomenclature Committee (HGNC) recommendations for the designation of gene fusions
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- Contribution to journal › Debate/Note/Editorial