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- 2024
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Mark
Constitutional and acquired genetic variants in ARID5B in pediatric B-cell precursor acute lymphoblastic leukemia
(
- Contribution to journal › Article
-
Mark
Postnatal origin of the chromosomal gains in older patients with high hyperdiploid acute lymphoblastic leukemia
(
- Contribution to journal › Letter
-
Mark
Drug-resilient Cancer Cell Phenotype Is Acquired via Polyploidization Associated with Early Stress Response Coupled to HIF2α Transcriptional Regulation
(
- Contribution to journal › Article
- 2023
-
Mark
A cloud-based resource for genome coordinate-based exploration and large-scale analysis of chromosome aberrations and gene fusions in cancer
(
- Contribution to journal › Article
-
Mark
Clonal origin and development of high hyperdiploidy in childhood acute lymphoblastic leukaemia
(
- Contribution to journal › Article
-
Mark
Acquired uniparental isodisomies involving chromosome 12 in paediatric B-cell precursor acute lymphoblastic leukaemia : Associations with chromosome 21 gains and SH2B3 mutations
(
- Contribution to journal › Article
-
Mark
The Prognostic Effect of IKZF1 Deletions in ETV6:: RUNX1 and High Hyperdiploid Childhood Acute Lymphoblastic Leukemia
(
- Contribution to journal › Article
-
Mark
Genetic Subtypes and Outcome of Patients Aged 1 to 45 Years Old with Acute Lymphoblastic Leukemia in the NOPHO ALL2008 Trial
(
- Contribution to journal › Article
-
Mark
Impact of 1q gains on treatment outcomes of patients with newly diagnosed multiple myeloma in a real-world Swedish population receiving modern treatment
(
- Contribution to journal › Article
-
Mark
Feasibility to use whole-genome sequencing as a sole diagnostic method to detect genomic aberrations in pediatric B-cell acute lymphoblastic leukemia
(
- Contribution to journal › Article
- 2022
-
Mark
Single base substitution and insertion/deletion mutational signatures in adult core binding factor acute myeloid leukemia
2022) In Leukemia(
- Contribution to journal › Letter
- 2021
-
Mark
Parental origin of monosomy 7 in acute leukaemia
2021) In British Journal of Haematology(
- Contribution to journal › Letter
-
Mark
Single base substitution mutational signatures in pediatric acute myeloid leukemia based on whole genome sequencing
(
- Contribution to journal › Letter
-
Mark
HUGO Gene Nomenclature Committee (HGNC) recommendations for the designation of gene fusions
(
- Contribution to journal › Debate/Note/Editorial
- 2020
-
Mark
Frequent false-negative FIP1L1-PDGFRA FISH analyses of bone marrow samples from clonal eosinophilia at diagnosis
(
- Contribution to journal › Letter
-
Mark
Why classical cytogenetics still matters in acute myeloid leukemia
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
13q12.2 deletions in acute lymphoblastic leukemia lead to upregulation of FLT3 through enhancer hijacking
(
- Contribution to journal › Article
-
Mark
Parental origin of monosomic chromosomes in near-haploid acute lymphoblastic leukemia
(
- Contribution to journal › Letter
-
Mark
SFPQ-ABL1-positive B-cell precursor acute lymphoblastic leukemias
2020) In Genes, Chromosomes and Cancer(
- Contribution to journal › Letter
- 2019
-
Mark
Cancer chromosome breakpoints cluster in gene-rich genomic regions
(
- Contribution to journal › Article
-
Mark
Most gene fusions in cancer are stochastic events
(
- Contribution to journal › Article
- 2018
-
Mark
Mutation, methylation, and gene expression profiles in dup(1q)-positive pediatric B-cell precursor acute lymphoblastic leukemia
(
- Contribution to journal › Article
-
Mark
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
-
Mark
Whole-exome sequencing exploration of acquired uniparental disomies in B-cell precursor acute lymphoblastic leukemia
(
- Contribution to journal › Article
-
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
(
- Contribution to journal › Article
- 2017
-
Mark
Incidence and prognostic significance of isolated trisomies in adult acute myeloid leukemia : A population-based study from the Swedish AML registry
(
- Contribution to journal › Article
-
Mark
Pediatric T-cell acute lymphoblastic leukemia
(
- Contribution to journal › Scientific review
- 2016
-
Mark
Methylation and expression analyses of Pallister-Killian syndrome reveal partial dosage compensation of tetrasomy 12p and hypomethylation of gene-poor regions on 12p.
(
- Contribution to journal › Article
-
Mark
Patterns and Frequencies of Acquired and Constitutional Uniparental Isodisomies in Pediatric and Adult B-Cell Precursor Acute Lymphoblastic Leukemia.
(
- Contribution to journal › Article
-
Mark
Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia
(
- Contribution to journal › Article
-
Mark
Detailed gene dose analysis reveals recurrent focal gene deletions in pediatric B-cell precursor acute lymphoblastic leukemia
(
- Contribution to journal › Article
-
Mark
The genetic landscape of paediatric de novo acute myeloid leukaemia as defined by single nucleotide polymorphism array and exon sequencing of 100 candidate genes
(
- Contribution to journal › Article
- 2015
-
Mark
Novel gene targets detected by genomic profiling in a consecutive series of 126 adults with acute lymphoblastic leukemia
(
- Contribution to journal › Article
-
Mark
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 1992 and 2013.
(
- Contribution to journal › Article
-
Mark
The emerging complexity of gene fusions in cancer.
(
- Contribution to journal › Scientific review
-
Mark
The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia.
(
- Contribution to journal › Article
-
Mark
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
-
Mark
Prognostic significance of high hyperdiploid and tri-/tetraploid adult acute myeloid leukemia.
(
- Contribution to journal › Article
-
Mark
Failure matters: unsuccessful cytogenetics and unperformed cytogenetics are associated with a poor prognosis in a population-based series of acute myeloid leukaemia.
(
- Contribution to journal › Article
-
Mark
Ikaros and leukaemia.
(
- Contribution to journal › Scientific review
-
Mark
Cooperative genetic changes in pediatric B-cell precursor acute lymphoblastic leukemia with deletions or mutations of IKZF1.
(
- Contribution to journal › Article
-
Mark
Genetic and epigenetic characterization of hypodiploid acute lymphoblastic leukemia.
(
- Contribution to journal › Article
-
Mark
Acute lymphoblastic leukemia
2015) p.198-251(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Acute myeloid leukemia
2015) p.62-125(
- Chapter in Book/Report/Conference proceeding › Book chapter
- 2014
-
Mark
t(6;9)(p22; q34)/DEK-NUP214-rearranged pediatric myeloid leukemia: an international study of 62 patients
(
- Contribution to journal › Article
-
Mark
Detecting dic(9;20)(p13.2;p11.2)-positive B-cell precursor acute lymphoblastic leukemia in a clinical setting using fluorescence in situ hybridization
(
- Contribution to journal › Letter
-
Mark
Clinical and genetic features of pediatric acute lymphoblastic leukemia in Down syndrome in the Nordic countries
(
- Contribution to journal › Article
-
Mark
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.
(
- Contribution to journal › Article
-
Mark
Incidence and prognostic significance of karyotypic subgroups in older patients with acute myeloid leukemia: the Swedish population-based experience.
(
- Contribution to journal › Article
-
Mark
Normal karyotype is a poor prognostic factor in myeloid leukemia of Down syndrome: a retrospective, international study
(
- Contribution to journal › Article
-
Mark
Allelic variants of PRDM9 associated with high hyperdiploid childhood acute lymphoblastic leukaemia.
(
- Contribution to journal › Letter
-
Mark
Prognostic Implications of Mutations in NOTCH1 and FBXW7 in Childhood T-ALL Treated According to the NOPHO ALL-1992 and ALL-2000 Protocols
(
- Contribution to journal › Article
-
Mark
Comprehensive genetic characterization of pediatric T-cell acute lymphoblastic leukemia
(
- Contribution to journal › Published meeting abstract
- 2013
-
Mark
Loss of chromosomes is the primary event in near-haploid and low hypodiploid acute lymphoblastic leukemia.
(
- Contribution to journal › Article
-
Mark
Constitutional trisomy 8 mosaicism as a model for epigenetic studies of aneuploidy.
(
- Contribution to journal › Article
-
Mark
Submicroscopic genomic imbalances in burkitt lymphomas/leukemias: Association with age and further evidence that 8q24/MYC translocations are not sufficient for leukemogenesis.
(
- Contribution to journal › Article
-
Mark
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
(
- Contribution to journal › Article
- 2012
-
Mark
Whole-exome sequencing of pediatric acute lymphoblastic leukemia.
(
- Contribution to journal › Article
-
Mark
Additional aberrations of the ETV6 and RUNX1 genes have no prognostic impact in 229 t(12;21)(p13;q22)-positive B-cell precursor acute lymphoblastic leukaemias treated according to the NOPHO-ALL-2000 protocol
(
- Contribution to journal › Letter
-
Mark
Homozygous deletions of CDKN2A are present in all dic(9;20)(p13.2;q11.2)-positive B-cell precursor acute lymphoblastic leukaemias and may be important for leukaemic transformation
(
- Contribution to journal › Letter
-
Mark
Myeloid malignancies with acquired trisomy 21 as the sole cytogenetic change are clinically highly variable and display a heterogeneous pattern of copy number alterations and mutations(a).
(
- Contribution to journal › Article
-
Mark
Disease-associated patterns of disomic chromosomes in hyperhaploid neoplasms.
(
- Contribution to journal › Article
-
Mark
High frequency of BTG1 deletions in acute lymphoblastic leukemia in children with down syndrome.
(
- Contribution to journal › Article
- 2011
-
Mark
The frequency and prognostic impact of dic(9;20)(p13.2;q11.2) in childhood B-cell precursor acute lymphoblastic leukemia: results from the NOPHO ALL-2000 trial
(
- Contribution to journal › Article
-
Mark
Amplification of the G allele at SNP rs6983267 in 8q24 amplicons in myeloid malignancies as cause of the lack of MYC overexpression?
(
- Contribution to journal › Letter
-
Mark
Paediatric B-cell precursor acute lymphoblastic leukaemia with t(1;19)(q23;p13): clinical and cytogenetic characteristics of 47 cases from the Nordic countries treated according to NOPHO protocols.
(
- Contribution to journal › Article
-
Mark
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.
(
- Contribution to journal › Letter
-
Mark
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.
(
- Contribution to journal › Article
-
Mark
The insulin receptor substrate 4 gene (IRS4) is mutated in paediatric T-cell acute lymphoblastic leukaemia.
(
- Contribution to journal › Letter
-
Mark
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.
(
- Contribution to journal › Letter
- 2010
-
Mark
Myeloid Leukemia of Down Syndrome The Results of An International Retrospective Study
(
- Contribution to journal › Published meeting abstract
-
Mark
The correlation pattern of acquired copy number changes in 164 ETV6/RUNX1-positive childhood acute lymphoblastic leukemias
(
- Contribution to journal › Article
-
Mark
Unrelated clones in AML/MDS - characterisation and prognostic relevance
(
- Contribution to journal › Published meeting abstract
-
Mark
Unrelated Clones In Myelodysplastic Syndromes and Acute Myeloid Leukemia Characterization and Prognostic Relevance
(
- Contribution to journal › Published meeting abstract
-
Mark
The idic(X)(q13) in myeloid malignancies: breakpoint clustering in segmental duplications and association with TET2 mutations.
(
- Contribution to journal › Article
-
Mark
Persistent malignant stem cells in del(5q) myelodysplasia in remission.
(
- Contribution to journal › Article
-
Mark
Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia.
(
- Contribution to journal › Article
-
Mark
Relapsed childhood high hyperdiploid acute lymphoblastic leukemia: presence of preleukemic ancestral clones and the secondary nature of microdeletions and RTK-RAS mutations.
(
- Contribution to journal › Article
- 2009
-
Mark
Relapsed Childhood High Hyperdiploid Acute Lymphoblastic Leukemia: Genome-Wide Screening Reveals the Presence of Preleukemic Ancestral Clones and the Secondary Nature of Microdeletions and RTK-RAS Mutations
(
- Contribution to journal › Published meeting abstract
-
Mark
The DNA methylome of pediatric acute lymphoblastic leukemia.
(
- Contribution to journal › Article
-
Mark
The t(X;7)(q22;q34) in paediatric T-cell acute lymphoblastic leukaemia results in overexpression of the insulin receptor substrate 4 gene through illegitimate recombination with the T-cell receptor beta locus.
(
- Contribution to journal › Article
-
Mark
Smoking as a risk factor for myelodysplastic syndromes and acute myeloid leukemia and its relation to cytogenetic findings: A case-control study.
2009) In Leukemia Research: A Forum for Studies on Leukemia and Normal Hemopoiesis Nov 17. p.788-791(
- Contribution to journal › Article
-
Mark
Clinical and cytogenetic features of a population-based consecutive series of 285 pediatric T-cell acute lymphoblastic leukemias: Rare T-cell receptor gene rearrangements are associated with poor outcome.
(
- Contribution to journal › Article
-
Mark
High hyperdiploid childhood acute lymphoblastic leukemia.
(
- Contribution to journal › Article
-
Mark
Tiling resolution array-based comparative genomic hybridisation analyses of acute lymphoblastic leukaemias in children with Down syndrome reveal recurrent gain of 8q and deletions of 7p and 9p.
(
- Contribution to journal › Article
-
Mark
B-cell precursor t(8;14)(q11;q32)-positive acute lymphoblastic leukemia in children is strongly associated with Down syndrome or with a concomitant Philadelphia chromosome.
(
- Contribution to journal › Article
- 2008
-
Mark
Cytogenetic features of acute lymphoblastic and myeloid leukemias in pediatric patients with Down syndrome: an iBFM-SG study
(
- Contribution to journal › Article
-
Mark
Outcome of ETV6/RUNX1-positive childhood acute lymphoblastic leukaemia in the NOPHO-ALL-1992 protocol: frequent late relapses but good overall survival
(
- Contribution to journal › Article
-
Mark
Mutations of FLT3, NRAS, KRAS, and PTPN11 are frequent and possibly mutually exclusive in high hyperdiploid childhood acute lymphoblastic leukemia
(
- Contribution to journal › Article
-
Mark
The hypermethylome of pediatric acute lymphoblastic leukemia
(
- Contribution to journal › Published meeting abstract
-
Mark
Clinical and cytogenetic features of pediatric dic(9;20)(p13.2;q11.2)-positive B-Cell precursor acute lymphoblastic leukemias: A nordic series of 24 cases and review of the literature
(
- Contribution to journal › Scientific review
-
Mark
BRAF mutations are very rare in B- and T-cell pediatric acute lymphoblastic leukemias.
(
- Contribution to journal › Article
-
Mark
FLT3 mutations in a 10 year consecutive series of 177 childhood acute leukemias and their impact on global gene expression patterns.
(
- Contribution to journal › Article
-
Mark
Exit of pediatric pre-B acute lymphoblastic leukaemia cells from the bone marrow to the peripheral blood is not associated with cell maturation or alterations in gene expression.
(
- Contribution to journal › Article
- 2007
-
Mark
Fusion of NUP98 and the SET binding protein 1 (SETBP1) gene in a paediatric acute T cell lymphoblastic leukaemia with t(11;18)(p15;q12).
(
- Contribution to journal › Article
-
Mark
Fusion gene-mediated truncation of RUNX1 as a potential mechanism underlying disease progression in the 8p11 myeloproliferative syndrome.
(
- Contribution to journal › Article
-
Mark
The molecular signature of MDS stem cells supports a stem-cell origin of 5q - myelodysplastic syndromes
(
- Contribution to journal › Article
-
Mark
Cytogenetic evolution patterns in CML post-SCT.
(
- Contribution to journal › Article
-
Mark
Characterisation of genomic translocation breakpoints and identification of an alternative TCF3/PBX1 fusion transcript in t(1;19)(q23;p13)-positive acute lymphoblastic leukaemias.
(
- Contribution to journal › Article
-
Mark
Proposals for standardized Protocols for cytogenetic analyses of acute leukemias, chronic lymphocytic leukemia, chronic myeloid leukemia, chronic myeloproliferative disorders, and myelodysplastic syndromes
(
- Contribution to journal › Article