Genetic and epigenetic studies of pediatric leukemia
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- 2024
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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
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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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Constitutional and acquired genetic variants in ARID5B in pediatric B-cell precursor acute lymphoblastic leukemia
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- Contribution to journal › Article
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Postnatal origin of the chromosomal gains in older patients with high hyperdiploid acute lymphoblastic leukemia
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- Contribution to journal › Letter
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Drug-resilient Cancer Cell Phenotype Is Acquired via Polyploidization Associated with Early Stress Response Coupled to HIF2α Transcriptional Regulation
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- Contribution to journal › Article
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TLE3 Is a Novel Fusion Partner of JAK2 in Myeloid/Lymphoid Neoplasm With Eosinophilia Responding to JAK2 Inhibition
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- Contribution to journal › Article
- 2023
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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
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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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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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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
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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
- 2021
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Parental origin of monosomy 7 in acute leukaemia
2021) In British Journal of Haematology(
- Contribution to journal › Letter
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Mark
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
Single base substitution mutational signatures in pediatric acute myeloid leukemia based on whole genome sequencing
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- 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
- 2020
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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
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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
- 2019
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Cancer chromosome breakpoints cluster in gene-rich genomic regions
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- Contribution to journal › Article
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Idiopathic ventricular fibrillation – Long term prognosis in relation to clinical findings and ECG patterns in a Swedish cohort
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- Contribution to journal › Article
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Most gene fusions in cancer are stochastic events
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- Contribution to journal › Article
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Danon disease presenting with early onset of hypertrophic cardiomyopathy and peripheral pigmentary retinal dystrophy in a female with a de novo novel mosaic mutation in the LAMP2 gene
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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
- 2018
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Transcriptional landscape of B cell precursor acute lymphoblastic leukemia based on an international study of 1,223 cases
2018) In Proceedings of the National Academy of Sciences of the United States of America 115(50). p.11711-11720(
- Contribution to journal › Article
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Mark
Improved cytogenetic characterization and risk stratification of pediatric acute lymphoblastic leukemia using single nucleotide polymorphism array analysis : A single center experience of 296 cases
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- Contribution to journal › Article
- 2017
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Mark
Pediatric T-cell acute lymphoblastic leukemia
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- Contribution to journal › Scientific review
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Genomic complexity and targeted genes in anaplastic thyroid cancer cell lines
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- Contribution to journal › Article
- 2016
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Rare novel variants in the ZIC3 gene cause X-linked heterotaxy
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- Contribution to journal › Article
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The genetic landscape of paediatric de novo acute myeloid leukaemia as defined by single nucleotide polymorphism array and exon sequencing of 100 candidate genes
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- Contribution to journal › Article
- 2015
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The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia.
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- Contribution to journal › Article
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Deep sequencing and SNP array analyses of pediatric T-cell acute lymphoblastic leukemia reveal NOTCH1 mutations in minor subclones and a high incidence of uniparental isodisomies affecting CDKN2A.
(
- Contribution to journal › Article
- 2014
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Mark
Clinical and genetic features of pediatric acute lymphoblastic leukemia in Down syndrome in the Nordic countries
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- Contribution to journal › Article
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Deletions of IKZF1 and SPRED1 are associated with poor prognosis in a population-based series of pediatric B-cell precursor acute lymphoblastic leukemia diagnosed between 1992 and 2011.
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- Contribution to journal › Article
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Mark
Comprehensive genetic characterization of pediatric T-cell acute lymphoblastic leukemia
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- Contribution to journal › Published meeting abstract
- 2010
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Mark
Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia.
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- Contribution to journal › Article
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Relapsed childhood high hyperdiploid acute lymphoblastic leukemia: presence of preleukemic ancestral clones and the secondary nature of microdeletions and RTK-RAS mutations.
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- Contribution to journal › Article
- 2008
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Cytogenetic features of acute lymphoblastic and myeloid leukemias in pediatric patients with Down syndrome: an iBFM-SG study
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- Contribution to journal › Article
- 2003
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Mark
Formation of trisomies and their parental origin in hyperdiploid childhood acute lymphoblastic leukemia.
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- Contribution to journal › Article
- 1997
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Mark
A breakpoint map of recurrent chromosomal rearrangements in human neoplasia
(
- Contribution to journal › Article