Kajsa Paulsson - Dissemin

All papers authored by Kajsa Paulsson

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2023 Eleanor L. Woodward, Minjun Yang

, Larissa H. Moura-Castro

, Hilda van den Bos, Rebeqa Gunnarsson, Linda Olsson-Arvidsson, Diana C. J. Spierings

, Anders Castor, Nicolas Duployez, Marketa Zaliova

, Jan Zuna

, Bertil Johansson

, Floris Foijer

, Kajsa Paulsson

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

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2020 Sigurdur Gretarsson, Alexander Nygren, Ann H. Rosendahl, Nektaria Mylona, Elisabeth Kjellén, Yuesheng Jin, Kajsa Paulsson

, Åke Borg

, Eva Brun, Jan Tennvall, Anders Bergenfelz

, Lennart Greiff, Johan Wennerberg, Lars Ekblad

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

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2017 Eleanor L. Woodward, Andrea Biloglav, Naveen Ravi, Minjun Yang, Lars Ekblad, Johan Wennerberg, Kajsa Paulsson

Genomic complexity and targeted genes in anaplastic thyroid cancer cell lines

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2016 Henrik Lilljebjörn, Rasmus Henningsson, Axel Hyrenius-Wittsten, Linda Olsson, Christina Orsmark-Pietras, Sofia von Palffy, Maria Askmyr, Marianne Rissler, Martin Schrappe, Gunnar Cario, Anders Castor, Cornelis J. H. Pronk, Mikael Behrendtz, Felix Mitelman

, Bertil Johansson and 4 other authors

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

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Linda Olsson, Sofia Zettermark

, Andrea Biloglav, Anders Castor, Mikael Behrendtz, Erik Forestier, Kajsa Paulsson

, Bertil Johansson

The genetic landscape of paediatricde novoacute myeloid leukaemia as defined by single nucleotide polymorphism array and exon sequencing of 100 candidate genes

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Vaidas Dirse, Egle Gineikiene, Tadas Zvirblis, Ruta Bertasiute, Kajsa Paulsson

, Laimonas Griskevicius

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

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2015 Kajsa Paulsson

Chromosome gains drive childhood ALL

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Linda Olsson, Ingegerd Ivanov Öfverholm, Ulrika Norén-Nyström, Vasilios Zachariadis, Jessica Nordlund, Helene Sjögren, Irina Golovleva, Ann Nordgren, Kajsa Paulsson

, Mats Heyman, Gisela Barbany, Bertil Johansson

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 a

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Kristina Karrman

, Anders Castor, Mikael Behrendtz, Erik Forestier, Linda Olsson, Mats Ehinger, Andrea Biloglav, Thoas Fioretos, Kajsa Paulsson

, Bertil Johansson

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

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Vaidas Dirse, Agne Bertasiute, Egle Gineikiene, Tadas Zvirblis, Ruta Dambrauskiene, Rolandas Gerbutavicius, Elona Juozaityte, Ligita Malciute, Kajsa Paulsson

, Laimonas Griskevicius

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

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2014 Setareh Safavi, Markus Hansson, Karin Karlsson, Andrea Biloglav, Bertil Johansson, Kajsa Paulsson

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

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Eleanor L. Woodward, Martin L. Olsson, Bertil Johansson, Kajsa Paulsson

Allelic variants ofPRDM9associated with high hyperdiploid childhood acute lymphoblastic leukaemia

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2013 Linda Olsson, Anders Castor, M. Behrendtz, Andrea Biloglav, E. Forestier, Kajsa Paulsson

, Bertil Johansson

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.

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Kajsa Paulsson

, Erik Forestier, Mette K. Andersen, Kirsi Autio, Gisela Barbany, Georg Borgstrom, Lucia Cavelier, Irina Golovleva, Sverre Heim, Kristiina Heinonen, Randi Hovland, Johann H. Johannsson, Eigil Kjeldsen, Ann Nordgren, Lars Palmqvist and 1 other authors

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

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K. Paulsson

Genomic Heterogeneity in Acute Leukemia

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2012 K. Paulsson

, C. J. Harrison, M. K. Andersen, L. Chilton

, A. Nordgren, A. V. Moorman, B. Johansson

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

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Karolin H. Nord, Kajsa Paulsson

, Srinivas Veerla, Johan Wejde, Otte Brosjö, Nils Mandahl, Fredrik Mertens

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

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Setareh Safavi, E. Forestier, I. Golovleva, G. Barbany, Karolin Hansén Nord, K. H. Nord, A. V. Moorman, C. J. Harrison, Bertil Johansson, Kajsa Paulsson

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

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E. Herou, A. Biloglav, B. Johansson, K. Paulsson

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

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2011 Catarina Lundin, Lars Hjorth, Mikael Behrendtz, Ann Nordgren, Lars Palmqvist, Mette Klarskov Andersen, Andrea Biloglav, Erik Forestier, Kajsa Paulsson

, Bertil Johansson

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

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All papers authored by Kajsa Paulsson