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Proceedings of the National Academy of Sciences of the United States of America|November 25, 2010
Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemiaKajsa Paulsson, Erik Forestier, Henrik Lilljebjörn, et al.
Genes, Chromosomes & Cancer|April 30, 2002
Detailed genomic mapping and expression analyses of 12p amplifications in pancreatic carcinomas reveal a 3.5-Mb target region for amplificationMarkus Heidenblad, Tord Jonson, Eija H Mahlamäki, et al.
British Journal of Haematology|August 4, 2004
High frequencies of chromosomal aberrations in multiple myeloma and monoclonal gammopathy of undetermined significance in direct chromosome preparationTherese Nilsson, Stig Lenhoff, Lars Rylander, et al.
British Journal of Haematology|March 22, 2003
A pooled analysis of karyotypic patterns, breakpoints and imbalances in 783 cytogenetically abnormal multiple myelomas reveals frequently involved chromosome segments as well as significant age- and sex-related differencesThérèse Nilsson, Mattias Höglund, Stig Lenhoff, et al.
British Journal of Haematology|June 26, 2003
Clinical and genetic studies of ETV6/ABL1-positive chronic myeloid leukaemia in blast crisis treated with imatinib mesylateAikaterini Barbouti, Tomas Ahlgren, Bertil Johansson, et al.
Genes, Chromosomes & Cancer|August 31, 2004
Structural integrity and expression of the L3MBTL gene in normal and malignant hematopoietic cellsDonal MacGrogan, Nagesh Kalakonda, Sara Alvarez, et al.
Scientific Reports|October 5, 2024
Characterizing the allele-specific gene expression landscape in high hyperdiploid acute lymphoblastic leukemia with BASEJonas Andersson, Efe Aydın, Rebeqa Gunnarsson, et al.
Genes, Chromosomes & Cancer|March 31, 2007
Fusion gene-mediated truncation of RUNX1 as a potential mechanism underlying disease progression in the 8p11 myeloproliferative syndromeHelena Agerstam, Henrik Lilljebjörn, Carin Lassen, et al.
Human Molecular Genetics|January 23, 2010
The idic(X)(q13) in myeloid malignancies: breakpoint clustering in segmental duplications and association with TET2 mutationsKajsa Paulsson, Claudia Haferlach, Christa Fonatsch, et al.
British Journal of Haematology|March 30, 2016
The genetic landscape of paediatric de novo acute myeloid leukaemia as defined by single nucleotide polymorphism array and exon sequencing of 100 candidate genesLinda Olsson, Sofia Zettermark, Andrea Biloglav, et al.
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