Lista de obras - Kajsa Paulsson - Dominio Público Uruguay

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.

artículo científico publicado en 2006

A novel human in vitro papillomavirus type 16 positive tonsil cancer cell line with high sensitivity to radiation and cisplatin

scientific article published on 25 March 2019

A population-based single nucleotide polymorphism array analysis of genomic aberrations in younger adult acute lymphoblastic leukemia patients

artículo científico publicado en 2015

Allelic variants ofPRDM9associated with high hyperdiploid childhood acute lymphoblastic leukaemia

artículo científico publicado en 2014

Author Correction: Genetic and regulatory mechanism of susceptibility to high-hyperdiploid acute lymphoblastic leukaemia at 10q21.2.

artículo científico publicado en 2018

Characterisation of genomic translocation breakpoints and identification of an alternativeTCF3/PBX1fusion transcript in t(1;19)(q23;p13)-positive acute lymphoblastic leukaemias

artículo científico publicado en 2007

Chromosome gains drive childhood ALL.

artículo científico publicado en 2015

Clonal evolution through loss of chromosomes and subsequent polyploidization in chondrosarcoma

artículo científico publicado en 2011

Cooperative genetic changes in pediatric B-cell precursor acute lymphoblastic leukemia with deletions or mutations ofIKZF1

artículo científico publicado en 2015

Cytogenetic and molecular genetic characterization of the ‘high hyperdiploid’ B-cell precursor acute lymphoblastic leukaemia cell line MHH-CALL-2 reveals a near-haploid origin

artículo científico publicado en 2011

De novo activating mutations drive clonal evolution and enhance clonal fitness in KMT2A-rearranged leukemia.

artículo científico publicado en 2018

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

artículo científico publicado en 2015

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.

artículo científico publicado en 2013

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

artículo científico publicado en 2012

Evidence for a single-step mechanism in the origin of hyperdiploid childhood acute lymphoblastic leukemia.

artículo científico publicado en 2005

FLT3 mutations in a 10 year consecutive series of 177 childhood acute leukemias and their impact on global gene expression patterns

artículo científico publicado en 2008

Formation of der(19)t(1;19)(q23;p13) in acute lymphoblastic leukemia

artículo científico publicado en 2005

Formation of trisomies and their parental origin in hyperdiploid childhood acute lymphoblastic leukemia

scientific article published on 26 June 2003

Genetic and epigenetic characterization of hypodiploid acute lymphoblastic leukemia

artículo científico publicado en 2015

Genetic and regulatory mechanism of susceptibility to high-hyperdiploid acute lymphoblastic leukaemia at 10p21.2.

artículo científico publicado en 2017

Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia

artículo científico publicado en 2010

Genetic predisposition to B-cell acute lymphoblastic leukemia at 14q11.2 is mediated by a CEBPE promoter polymorphism

artículo científico publicado en 2018

Genomic complexity and targeted genes in anaplastic thyroid cancer cell lines.

artículo científico publicado en 2017

Genomic complexity and targeted genes in anaplastic thyroid cancer cell lines.

artículo científico publicado en 2017

Genomic heterogeneity in acute leukemia

artículo científico

Global RNA Expression and DNA Methylation Patterns in Primary Anaplastic Thyroid Cancer

scientific article published on 13 March 2020

High frequency of BTG1 deletions in acute lymphoblastic leukemia in children with down syndrome

artículo científico publicado en 2011

High hyperdiploid childhood acute lymphoblastic leukemia

artículo científico publicado en 2009

High hyperdiploid childhood acute lymphoblastic leukemia: Chromosomal gains as the main driver event

artículo científico publicado en 2015

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

artículo científico publicado en 2013

High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration

artículo científico publicado en 2006

Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia

artículo científico publicado en 2016

Identification of Targetable Lesions in Anaplastic Thyroid Cancer by Genome Profiling

artículo científico publicado en 2019

Identification of a commonly amplified 4.3 Mb region with overexpression of C8FW, but not MYC in MYC-containing double minutes in myeloid malignancies

artículo científico publicado en 2004

Identification of cryptic aberrations and characterization of translocation breakpoints using array CGH in high hyperdiploid childhood acute lymphoblastic leukemia

scientific article published on 14 September 2006

Improved cytogenetic characterization and risk stratification of pediatric acute lymphoblastic leukemia using single nucleotide polymorphism array analysis: A single center experience of 296 cases

scientific article published on 11 September 2018

Loss of chromosomes is the primary event in near-haploid and low-hypodiploid acute lymphoblastic leukemia

artículo científico publicado en 2012

MYC is not overexpressed in a case of chronic myelomonocytic leukemia with MYC-containing double minutes

artículo científico publicado en 2003

Methylation of tumour suppressor gene promoters in the presence and absence of transcriptional silencing in high hyperdiploid acute lymphoblastic leukaemia.

artículo científico publicado en 2008

Microdeletions are a general feature of adult and adolescent acute lymphoblastic leukemia: Unexpected similarities with pediatric disease

artículo científico publicado en 2008

Molecular characterisation of a recurrent, semi-cryptic RUNX1 translocation t(7;21) in myelodysplastic syndrome and acute myeloid leukaemia.

artículo científico publicado en 2010

Multicolor fluorescence in situ hybridization characterization of cytogenetically polyclonal hematologic malignancies.

artículo científico publicado en 2005

Mutation, methylation, and gene expression profiles in dup(1q)-positive pediatric B-cell precursor acute lymphoblastic leukemia.

artículo científico publicado en 2018

Mutations of FLT3, NRAS, KRAS, and PTPN11 are frequent and possibly mutually exclusive in high hyperdiploid childhood acute lymphoblastic leukemia.

artículo científico publicado en 2008

Near-haploid and low-hypodiploid acute lymphoblastic leukemia: two distinct subtypes with consistently poor prognosis

artículo científico publicado en 2016

Novel gene targets detected by genomic profiling in a consecutive series of 126 adults with acute lymphoblastic leukemia

artículo científico publicado en 2014

Outcome of Children With Hypodiploid Acute Lymphoblastic Leukemia: A Retrospective Multinational Study

scientific article published on 18 January 2019

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

artículo científico publicado en 2012

Patterns and frequencies of acquired and constitutional uniparental isodisomies in pediatric and adult B-cell precursor acute lymphoblastic leukemia.

artículo científico publicado en 2016

Proteogenomics and Hi-C reveal transcriptional dysregulation in high hyperdiploid childhood acute lymphoblastic leukemia

artículo científico publicado en 2019

Relapsed childhood high hyperdiploid acute lymphoblastic leukemia: presence of preleukemic ancestral clones and the secondary nature of microdeletions and RTK-RAS mutations.

artículo científico publicado en 2010

Retained heterodisomy is associated with high gene expression in hyperhaploid inflammatory leiomyosarcoma.

artículo científico publicado en 2012

Risk of RAS in relapsed childhood ALL.

artículo científico publicado en 2014

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 aberrations

artículo científico publicado en 2011

Searching for cryptic chromosomal aberrations in high hyperdiploid childhood acute lymphoblastic leukaemias

artículo científico publicado en 2006

Single nucleotide polymorphism array analysis of clonal evolution in younger adult acute lymphoblastic leukemia

scientific article published on 21 March 2016

Sister chromatid cohesion defects are associated with chromosomal copy number heterogeneity in high hyperdiploid childhood acute lymphoblastic leukemia

scientific article published on 23 December 2020

Substantial intrinsic variability in chemoradiosensitivity of newly established anaplastic thyroid cancer cell-lines

scientific article published on 10 January 2020

The clinical impact of IKZF1 deletions in paediatric B-cell precursor acute lymphoblastic leukaemia is independent of minimal residual disease stratification in Nordic Society for Paediatric Haematology and Oncology treatment protocols used between 1

artículo científico publicado en 2015

The genetic landscape of paediatric de novo acute myeloid leukaemia as defined by single nucleotide polymorphism array and exon sequencing of 100 candidate genes

artículo científico publicado en 2016

The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia

artículo científico publicado en 2015

The idic(X)(q13) in myeloid malignancies: breakpoint clustering in segmental duplications and association with TET2 mutations.

artículo científico publicado en 2010

The incidence of trisomy 8 as a sole chromosomal aberration in myeloid malignancies varies in relation to gender, age, prior iatrogenic genotoxic exposure, and morphology

artículo científico publicado en 2001

The insulin receptor substrate 4 gene (IRS4) is mutated in paediatric T-cell acute lymphoblastic leukaemia

article

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 overexpres

artículo científico publicado en 2007

Trisomy 8 as the sole chromosomal aberration in acute myeloid leukemia and myelodysplastic syndromes

artículo científico publicado en 2007

Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: a multicolor and locus-specific fluorescence in situ hybridization study

artículo científico

t(9;11)(p22;p15) [NUP98/PSIP1] is a poor prognostic marker associated with de novo acute myeloid leukaemia expressing both mature and immature surface antigens

artículo científico publicado en 2010

Lista de obras de Kajsa Paulsson

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.

A novel human in vitro papillomavirus type 16 positive tonsil cancer cell line with high sensitivity to radiation and cisplatin

A population-based single nucleotide polymorphism array analysis of genomic aberrations in younger adult acute lymphoblastic leukemia patients

Allelic variants ofPRDM9associated with high hyperdiploid childhood acute lymphoblastic leukaemia

Author Correction: Genetic and regulatory mechanism of susceptibility to high-hyperdiploid acute lymphoblastic leukaemia at 10q21.2.

Characterisation of genomic translocation breakpoints and identification of an alternativeTCF3/PBX1fusion transcript in t(1;19)(q23;p13)-positive acute lymphoblastic leukaemias

Chromosome gains drive childhood ALL.

Clonal evolution through loss of chromosomes and subsequent polyploidization in chondrosarcoma

Cooperative genetic changes in pediatric B-cell precursor acute lymphoblastic leukemia with deletions or mutations ofIKZF1

Cytogenetic and molecular genetic characterization of the ‘high hyperdiploid’ B-cell precursor acute lymphoblastic leukaemia cell line MHH-CALL-2 reveals a near-haploid origin

De novo activating mutations drive clonal evolution and enhance clonal fitness in KMT2A-rearranged 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 CDKN2A

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.

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

Evidence for a single-step mechanism in the origin of hyperdiploid childhood acute lymphoblastic leukemia.

FLT3 mutations in a 10 year consecutive series of 177 childhood acute leukemias and their impact on global gene expression patterns

Formation of der(19)t(1;19)(q23;p13) in acute lymphoblastic leukemia

Formation of trisomies and their parental origin in hyperdiploid childhood acute lymphoblastic leukemia

Genetic and epigenetic characterization of hypodiploid acute lymphoblastic leukemia

Genetic and regulatory mechanism of susceptibility to high-hyperdiploid acute lymphoblastic leukaemia at 10p21.2.

Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia

Genetic predisposition to B-cell acute lymphoblastic leukemia at 14q11.2 is mediated by a CEBPE promoter polymorphism

Genomic complexity and targeted genes in anaplastic thyroid cancer cell lines.

Genomic complexity and targeted genes in anaplastic thyroid cancer cell lines.

Genomic heterogeneity in acute leukemia

Global RNA Expression and DNA Methylation Patterns in Primary Anaplastic Thyroid Cancer

High frequency of BTG1 deletions in acute lymphoblastic leukemia in children with down syndrome

High hyperdiploid childhood acute lymphoblastic leukemia

High hyperdiploid childhood acute lymphoblastic leukemia: Chromosomal gains as the main driver event

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-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration

Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia

Identification of Targetable Lesions in Anaplastic Thyroid Cancer by Genome Profiling

Identification of a commonly amplified 4.3 Mb region with overexpression of C8FW, but not MYC in MYC-containing double minutes in myeloid malignancies

Identification of cryptic aberrations and characterization of translocation breakpoints using array CGH in high hyperdiploid childhood acute lymphoblastic leukemia

Improved cytogenetic characterization and risk stratification of pediatric acute lymphoblastic leukemia using single nucleotide polymorphism array analysis: A single center experience of 296 cases

Loss of chromosomes is the primary event in near-haploid and low-hypodiploid acute lymphoblastic leukemia

MYC is not overexpressed in a case of chronic myelomonocytic leukemia with MYC-containing double minutes

Methylation of tumour suppressor gene promoters in the presence and absence of transcriptional silencing in high hyperdiploid acute lymphoblastic leukaemia.

Microdeletions are a general feature of adult and adolescent acute lymphoblastic leukemia: Unexpected similarities with pediatric disease

Molecular characterisation of a recurrent, semi-cryptic RUNX1 translocation t(7;21) in myelodysplastic syndrome and acute myeloid leukaemia.

Multicolor fluorescence in situ hybridization characterization of cytogenetically polyclonal hematologic malignancies.

Mutation, methylation, and gene expression profiles in dup(1q)-positive pediatric B-cell precursor acute lymphoblastic leukemia.

Mutations of FLT3, NRAS, KRAS, and PTPN11 are frequent and possibly mutually exclusive in high hyperdiploid childhood acute lymphoblastic leukemia.

Near-haploid and low-hypodiploid acute lymphoblastic leukemia: two distinct subtypes with consistently poor prognosis

Novel gene targets detected by genomic profiling in a consecutive series of 126 adults with acute lymphoblastic leukemia

Outcome of Children With Hypodiploid Acute Lymphoblastic Leukemia: A Retrospective Multinational Study

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

Patterns and frequencies of acquired and constitutional uniparental isodisomies in pediatric and adult B-cell precursor acute lymphoblastic leukemia.

Proteogenomics and Hi-C reveal transcriptional dysregulation in high hyperdiploid childhood acute lymphoblastic leukemia

Relapsed childhood high hyperdiploid acute lymphoblastic leukemia: presence of preleukemic ancestral clones and the secondary nature of microdeletions and RTK-RAS mutations.

Retained heterodisomy is associated with high gene expression in hyperhaploid inflammatory leiomyosarcoma.

Risk of RAS in relapsed childhood ALL.

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 aberrations

Searching for cryptic chromosomal aberrations in high hyperdiploid childhood acute lymphoblastic leukaemias

Single nucleotide polymorphism array analysis of clonal evolution in younger adult acute lymphoblastic leukemia

Sister chromatid cohesion defects are associated with chromosomal copy number heterogeneity in high hyperdiploid childhood acute lymphoblastic leukemia

Substantial intrinsic variability in chemoradiosensitivity of newly established anaplastic thyroid cancer cell-lines

The clinical impact of IKZF1 deletions in paediatric B-cell precursor acute lymphoblastic leukaemia is independent of minimal residual disease stratification in Nordic Society for Paediatric Haematology and Oncology treatment protocols used between 1

The genetic landscape of paediatric de novo acute myeloid leukaemia as defined by single nucleotide polymorphism array and exon sequencing of 100 candidate genes

The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia

The idic(X)(q13) in myeloid malignancies: breakpoint clustering in segmental duplications and association with TET2 mutations.

The incidence of trisomy 8 as a sole chromosomal aberration in myeloid malignancies varies in relation to gender, age, prior iatrogenic genotoxic exposure, and morphology

The insulin receptor substrate 4 gene (IRS4) is mutated in paediatric T-cell acute lymphoblastic leukaemia

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 overexpres

Trisomy 8 as the sole chromosomal aberration in acute myeloid leukemia and myelodysplastic syndromes

Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: a multicolor and locus-specific fluorescence in situ hybridization study

t(9;11)(p22;p15) [NUP98/PSIP1] is a poor prognostic marker associated with de novo acute myeloid leukaemia expressing both mature and immature surface antigens