Genetic and epigenetic studies of pediatric leukemia
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- 2024
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Clinical and genetic analyses of a Swedish patient series diagnosed with ataxia
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- Contribution to journal › Article
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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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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 › Letter
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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 › Letter
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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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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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Clonal origin and development of high hyperdiploidy in childhood acute lymphoblastic leukaemia
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- Contribution to journal › Article
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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
- 2021
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Evolution of P-wave indices during long-term follow-up as markers of atrial substrate progression in arrhythmogenic right ventricular cardiomyopathy
2021) In Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 23(1). p.29-37(
- Contribution to journal › Article
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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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HUGO Gene Nomenclature Committee (HGNC) recommendations for the designation of gene fusions
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- Contribution to journal › Debate/Note/Editorial
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Single base substitution mutational signatures in pediatric acute myeloid leukemia based on whole genome sequencing
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- Contribution to journal › Letter
- 2020
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Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
2020) In Genetics in Medicine(
- Contribution to journal › Article
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Genomic arrays identify high-risk chronic lymphocytic leukemia with genomic complexity : A multi-center study
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- Contribution to journal › Article
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Parental origin of monosomic chromosomes in near-haploid acute lymphoblastic leukemia
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- Contribution to journal › Letter
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SFPQ-ABL1-positive B-cell precursor acute lymphoblastic leukemias
2020) In Genes, Chromosomes and Cancer(
- Contribution to journal › Letter
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Frequent false-negative FIP1L1-PDGFRA FISH analyses of bone marrow samples from clonal eosinophilia at diagnosis
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- Contribution to journal › Letter
- 2019
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Mark
Cancer chromosome breakpoints cluster in gene-rich genomic regions
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- Contribution to journal › Article
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Proteogenomics and Hi-C reveal transcriptional dysregulation in high hyperdiploid childhood acute lymphoblastic leukemia
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- Contribution to journal › Article