about
Trisomy 8 as the sole chromosomal aberration in acute myeloid leukemia and myelodysplastic syndromesClonal evolution through loss of chromosomes and subsequent polyploidization in chondrosarcoma.Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia.Tiling resolution array comparative genomic hybridization, expression and methylation analyses of dup(1q) in Burkitt lymphomas and pediatric high hyperdiploid acute lymphoblastic leukemias reveal clustered near-centromeric breakpoints and overexpresNovel gene targets detected by genomic profiling in a consecutive series of 126 adults with acute lymphoblastic leukemia.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 CDKN2ARetained heterodisomy is associated with high gene expression in hyperhaploid inflammatory leiomyosarcoma.Genetic and regulatory mechanism of susceptibility to high-hyperdiploid acute lymphoblastic leukaemia at 10p21.2.Genetic and epigenetic characterization of hypodiploid acute lymphoblastic leukemia.Microdeletions are a general feature of adult and adolescent acute lymphoblastic leukemia: Unexpected similarities with pediatric disease.Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia.High modal number and triple trisomies are highly correlated favorable factors in childhood B-cell precursor high hyperdiploid acute lymphoblastic leukemia treated according to the NOPHO ALL 1992/2000 protocols.High hyperdiploid childhood acute lymphoblastic leukemia.Genomic heterogeneity in acute leukemia.Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: a multicolor and locus-specific fluorescence in situ hybridization study.Genomic complexity and targeted genes in anaplastic thyroid cancer cell lines.Near-haploid and low-hypodiploid acute lymphoblastic leukemia: two distinct subtypes with consistently poor prognosis.The genetic landscape of paediatric de novo acute myeloid leukaemia as defined by single nucleotide polymorphism array and exon sequencing of 100 candidate genes.A novel and cytogenetically cryptic t(7;21)(p22;q22) in acute myeloid leukemia results in fusion of RUNX1 with the ubiquitin-specific protease gene USP42.High hyperdiploid childhood acute lymphoblastic leukemia: Chromosomal gains as the main driver event.A population-based single nucleotide polymorphism array analysis of genomic aberrations in younger adult acute lymphoblastic leukemia patients.Chromosome gains drive childhood ALL.Partial 17q gain resulting from isochromosomes, unbalanced translocations and complex rearrangements is associated with gene overexpression, older age and shorter overall survival in high hyperdiploid childhood acute lymphoblastic leukemia.Loss of chromosomes is the primary event in near-haploid and low-hypodiploid acute lymphoblastic leukemia.Distinct patterns of gained chromosomes in high hyperdiploid acute lymphoblastic leukemia with t(1;19)(q23;p13), t(9;22)(q34;q22) or MLL rearrangements.FLT3 mutations in a 10 year consecutive series of 177 childhood acute leukemias and their impact on global gene expression patterns.Mutations of FLT3, NRAS, KRAS, and PTPN11 are frequent and possibly mutually exclusive in high hyperdiploid childhood acute lymphoblastic leukemia.Identification of a commonly amplified 4.3 Mb region with overexpression of C8FW, but not MYC in MYC-containing double minutes in myeloid malignancies.The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia.Risk of RAS in relapsed childhood ALL.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.Genomic complexity and targeted genes in anaplastic thyroid cancer cell lines.De novo activating mutations drive clonal evolution and enhance clonal fitness in KMT2A-rearranged leukemia.Mutation, methylation, and gene expression profiles in dup(1q)-positive pediatric B-cell precursor acute lymphoblastic leukemia.Patterns and frequencies of acquired and constitutional uniparental isodisomies in pediatric and adult B-cell precursor acute lymphoblastic leukemia.The idic(X)(q13) in myeloid malignancies: breakpoint clustering in segmental duplications and association with TET2 mutations.SNP array analysis of leukemic relapse samples after allogeneic hematopoietic stem cell transplantation with a sibling donor identifies meiotic recombination spots and reveals possible correlation with the breakpoints of acquired genetic aberrationsMolecular characterisation of a recurrent, semi-cryptic RUNX1 translocation t(7;21) in myelodysplastic syndrome and acute myeloid leukaemia.Methylation of tumour suppressor gene promoters in the presence and absence of transcriptional silencing in high hyperdiploid acute lymphoblastic leukaemia.Evidence for a single-step mechanism in the origin of hyperdiploid childhood acute lymphoblastic leukemia.
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description
Zweeds onderzoekster
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hulumtuese
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researcher
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taighdeoir
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հետազոտող
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name
Kajsa Paulsson
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Kajsa Paulsson
@en
Kajsa Paulsson
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Kajsa Paulsson
@ga
Kajsa Paulsson
@nl
Kajsa Paulsson
@sl
Kajsa Paulsson
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type
label
Kajsa Paulsson
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Kajsa Paulsson
@en
Kajsa Paulsson
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Kajsa Paulsson
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Kajsa Paulsson
@nl
Kajsa Paulsson
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Kajsa Paulsson
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prefLabel
Kajsa Paulsson
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Kajsa Paulsson
@en
Kajsa Paulsson
@es
Kajsa Paulsson
@ga
Kajsa Paulsson
@nl
Kajsa Paulsson
@sl
Kajsa Paulsson
@sq
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0000-0001-7950-222X