Linda Arvidsson-Olsson

Lund, M, Sweden

Last Updated: 09/26/2026

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Found 13 publications

Mutational signatures and kataegis in pediatric B-cell precursor acute lymphoblastic leukemia.

Mutational signatures and kataegis in pediatric B-cell precursor acute lymphoblastic leukemia.

Journal: HemaSphere

Published: February 14, 2025

Micro-costing of genetic diagnostics in acute leukemia in Sweden: from standard-of-care to whole-genome sequencing.

Micro-costing of genetic diagnostics in acute leukemia in Sweden: from standard-of-care to whole-genome sequencing.

Journal: Journal of medical economics

Published: August 05, 2024

TLE3 Is a Novel Fusion Partner of JAK2 in Myeloid/Lymphoid Neoplasm With Eosinophilia Responding to JAK2 Inhibition.

TLE3 Is a Novel Fusion Partner of JAK2 in Myeloid/Lymphoid Neoplasm With Eosinophilia Responding to JAK2 Inhibition.

Journal: Genes, chromosomes & cancer

Published: April 28, 2024

Constitutional and acquired genetic variants in ARID5B in pediatric B-cell precursor acute lymphoblastic leukemia.

Constitutional and acquired genetic variants in ARID5B in pediatric B-cell precursor acute lymphoblastic leukemia.

Journal: Genes, chromosomes & cancer

Published: February 27, 2024

Feasibility to use whole-genome sequencing as a sole diagnostic method to detect genomic aberrations in pediatric B-cell acute lymphoblastic leukemia.

Feasibility to use whole-genome sequencing as a sole diagnostic method to detect genomic aberrations in pediatric B-cell acute lymphoblastic leukemia.

Journal: Frontiers in oncology

Published: May 05, 2023

Impact of 1q gains on treatment outcomes of patients with newly diagnosed multiple myeloma in a real-world Swedish population receiving modern treatment.

Impact of 1q gains on treatment outcomes of patients with newly diagnosed multiple myeloma in a real-world Swedish population receiving modern treatment.

Journal: European journal of haematology

Published: February 27, 2023

Acquired uniparental isodisomies involving chromosome 12 in paediatric B-cell precursor acute lymphoblastic leukaemia: Associations with chromosome 21 gains and SH2B3 mutations.

Acquired uniparental isodisomies involving chromosome 12 in paediatric B-cell precursor acute lymphoblastic leukaemia: Associations with chromosome 21 gains and SH2B3 mutations.

Journal: British journal of haematology

Published: February 06, 2023

Clonal origin and development of high hyperdiploidy in childhood acute lymphoblastic leukaemia.

Clonal origin and development of high hyperdiploidy in childhood acute lymphoblastic leukaemia.

Journal: Nature communications

Published: April 19, 2022

Single base substitution mutational signatures in pediatric acute myeloid leukemia based on whole genome sequencing.

Single base substitution mutational signatures in pediatric acute myeloid leukemia based on whole genome sequencing.

Journal: Leukemia

Published: October 05, 2020

Parental origin of monosomic chromosomes in near-haploid acute lymphoblastic leukemia.

Parental origin of monosomic chromosomes in near-haploid acute lymphoblastic leukemia.

Journal: Blood cancer journal

Published: March 09, 2020

13q12.2 deletions in acute lymphoblastic leukemia lead to upregulation of FLT3 through enhancer hijacking.

13q12.2 deletions in acute lymphoblastic leukemia lead to upregulation of FLT3 through enhancer hijacking.

Journal: Blood

Published: December 23, 2019

Frequent false-negative FIP1L1-PDGFRA FISH analyses of bone marrow samples from clonal eosinophilia at diagnosis.

Frequent false-negative FIP1L1-PDGFRA FISH analyses of bone marrow samples from clonal eosinophilia at diagnosis.

Journal: British journal of haematology

Published: December 20, 2019

Showing 1-12 of 13

Last Updated: 09/26/2026