| Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia H Lilljebjörn, R Henningsson, A Hyrenius-Wittsten, L Olsson, ... Nature communications 7 (1), 11790, 2016 | 302 | 2016 |
| High hyperdiploid childhood acute lymphoblastic leukemia K Paulsson, B Johansson Genes, Chromosomes and Cancer 48 (8), 637-660, 2009 | 261 | 2009 |
| The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia K Paulsson, H Lilljebjörn, A Biloglav, L Olsson, M Rissler, A Castor, ... Nature genetics 47 (6), 672-676, 2015 | 215 | 2015 |
| Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia K Paulsson, E Forestier, H Lilljebjörn, J Heldrup, M Behrendtz, BD Young, ... Proceedings of the National Academy of Sciences 107 (50), 21719-21724, 2010 | 191 | 2010 |
| Mutations of FLT3, NRAS, KRAS, and PTPN11 are frequent and possibly mutually exclusive in high hyperdiploid childhood acute lymphoblastic leukemia K Paulsson, A Horvat, B Strömbeck, F Nilsson, J Heldrup, M Behrendtz, ... Genes, Chromosomes and Cancer 47 (1), 26-33, 2008 | 133 | 2008 |
| Trisomy 8 as the sole chromosomal aberration in acute myeloid leukemia and myelodysplastic syndromes K Paulsson, B Johansson Pathologie Biologie 55 (1), 37-48, 2007 | 133 | 2007 |
| 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 … L Olsson, A Castor, M Behrendtz, A Biloglav, E Forestier, K Paulsson, ... Leukemia 28 (2), 302-310, 2014 | 126 | 2014 |
| Microdeletions are a general feature of adult and adolescent acute lymphoblastic leukemia: Unexpected similarities with pediatric disease K Paulsson, JB Cazier, F MacDougall, J Stevens, I Stasevich, N Vrcelj, ... Proceedings of the National Academy of Sciences 105 (18), 6708-6713, 2008 | 126 | 2008 |
| Near-haploid and low-hypodiploid acute lymphoblastic leukemia: two distinct subtypes with consistently poor prognosis S Safavi, K Paulsson Blood, The Journal of the American Society of Hematology 129 (4), 420-423, 2017 | 113 | 2017 |
| High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration K Paulsson, M Heidenblad, B Strömbeck, J Staaf, G Jönsson, Å Borg, ... Leukemia 20 (5), 840-846, 2006 | 94 | 2006 |
| A novel and cytogenetically cryptic t (7; 21)(p22; q22) in acute myeloid leukemia results in fusion of RUNX1 with the ubiquitin-specific protease gene USP42 K Paulsson, AN Bekassy, T Olofsson, F Mitelman, B Johansson, ... Leukemia 20 (2), 224-229, 2006 | 87 | 2006 |
| Evidence for a single‐step mechanism in the origin of hyperdiploid childhood acute lymphoblastic leukemia K Paulsson, H Mörse, T Fioretos, M Behrendtz, B Strömbeck, ... Genes, Chromosomes and Cancer 44 (2), 113-122, 2005 | 83 | 2005 |
| The incidence of trisomy 8 as a sole chromosomal aberration in myeloid malignancies varies in relation to gender, age, prior iatrogenic genotoxic exposure, and morphology K Paulsson, T Säll, T Fioretos, F Mitelman, B Johansson Cancer genetics and cytogenetics 130 (2), 160-165, 2001 | 83 | 2001 |
| Outcome of children with hypodiploid acute lymphoblastic leukemia: a retrospective multinational study CH Pui, P Rebora, M Schrappe, A Attarbaschi, A Baruchel, G Basso, ... Journal of Clinical Oncology 37 (10), 770-779, 2019 | 82 | 2019 |
| Proteogenomics and Hi-C reveal transcriptional dysregulation in high hyperdiploid childhood acute lymphoblastic leukemia M Yang, M Vesterlund, I Siavelis, LH Moura-Castro, A Castor, T Fioretos, ... Nature communications 10 (1), 1519, 2019 | 78 | 2019 |
| Relapsed childhood high hyperdiploid acute lymphoblastic leukemia: presence of preleukemic ancestral clones and the secondary nature of microdeletions and RTK-RAS mutations J Davidsson, K Paulsson, D Lindgren, H Lilljebjörn, T Chaplin, E Forestier, ... Leukemia 24 (5), 924-931, 2010 | 74 | 2010 |
| High modal number and triple trisomies are highly correlated favorable factors in childhood B-cell precursor high hyperdiploid acute lymphoblastic leukemia treated according to … K Paulsson, E Forestier, MK Andersen, K Autio, G Barbany, G Borgström, ... haematologica 98 (9), 1424, 2013 | 70 | 2013 |
| Identification of a commonly amplified 4.3 Mb region with overexpression of C8FW , but not MYC in MYC -containing … CT Storlazzi, T Fioretos, K Paulsson, B Strömbeck, C Lassen, T Ahlgren, ... Human molecular genetics 13 (14), 1479-1485, 2004 | 70 | 2004 |
| Loss of chromosomes is the primary event in near-haploid and low-hypodiploid acute lymphoblastic leukemia S Safavi, E Forestier, I Golovleva, G Barbany, KH Nord, AV Moorman, ... Leukemia 27 (1), 248-250, 2013 | 69 | 2013 |
| Tiling resolution array comparative genomic hybridization, expression and methylation analyses of dup (1q) in Burkitt lymphomas and pediatric high hyperdiploid acute … J Davidsson, A Andersson, K Paulsson, M Heidenblad, M Isaksson, ... Human molecular genetics 16 (18), 2215-2225, 2007 | 68 | 2007 |
