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European Journal of Haematology|June 4, 2023
Impact of 1q gains on treatment outcomes of patients with newly diagnosed multiple myeloma in a real-world Swedish population receiving modern treatmentKonstantinos Lemonakis, Linda Olsson-Arvidsson, Conny Karlsson, et al.Genes, Chromosomes & Cancer|August 6, 2024
TLE3 Is a Novel Fusion Partner of JAK2 in Myeloid/Lymphoid Neoplasm With Eosinophilia Responding to JAK2 InhibitionVladimir Lazarevic, Henrik Lilljebjörn, Linda Olsson-Arvidsson, et al.Genes, Chromosomes & Cancer|April 20, 2020
SFPQ-ABL1-positive B-cell precursor acute lymphoblastic leukemiasAndrea Biloglav, Linda Olsson-Arvidsson, Johan Theander, et al.Journal of Medical Economics|August 5, 2024
Micro-costing of genetic diagnostics in acute leukemia in Sweden: from standard-of-care to whole-genome sequencingTharshini Thangavelu, Valtteri Wirta, Christina Orsmark-Pietras, et al.Blood|May 9, 2020
13q12.2 deletions in acute lymphoblastic leukemia lead to upregulation of FLT3 through enhancer hijackingMinjun Yang, Setareh Safavi, Eleanor L Woodward, et al.Genes, Chromosomes & Cancer|May 13, 2024
Constitutional and acquired genetic variants in ARID5B in pediatric B-cell precursor acute lymphoblastic leukemiaCharlotte Ragnarsson, Minjun Yang, Larissa Helena Moura-Castro, et al.Nature Communications|March 25, 2023
Clonal origin and development of high hyperdiploidy in childhood acute lymphoblastic leukaemiaEleanor L Woodward, Minjun Yang, Larissa H Moura-Castro, et al.Frontiers in Oncology|September 4, 2023
Feasibility to use whole-genome sequencing as a sole diagnostic method to detect genomic aberrations in pediatric B-cell acute lymphoblastic leukemiaFatemah Rezayee, Jesper Eisfeldt, Aron Skaftason, et al.Pageof 1