Lilljebjörn H - Search Results

1

Clinical and genomic characterization of patients diagnosed with the provisional entity acute myeloid leukemia with BCR-ABL1, a Swedish population-based study.

Orsmark-Pietras C, Landberg N, Lorenz F, Uggla B, Höglund M, Lehmann S, Derolf Å, Deneberg S, Antunovic P, Cammenga J, Möllgård L, Wennström L, Lilljebjörn H, Rissler M, Fioretos T, Lazarevic VL. Orsmark-Pietras C, et al. Among authors: lilljebjorn h. Genes Chromosomes Cancer. 2021 Jun;60(6):426-433. doi: 10.1002/gcc.22936. Epub 2021 Jan 22. Genes Chromosomes Cancer. 2021. PMID: 33433047 Free article.

2

Fusion gene-mediated truncation of RUNX1 as a potential mechanism underlying disease progression in the 8p11 myeloproliferative syndrome.

Agerstam H, Lilljebjörn H, Lassen C, Swedin A, Richter J, Vandenberghe P, Johansson B, Fioretos T. Agerstam H, et al. Among authors: lilljebjorn h. Genes Chromosomes Cancer. 2007 Jul;46(7):635-43. doi: 10.1002/gcc.20442. Genes Chromosomes Cancer. 2007. PMID: 17394134

3

Combined high-resolution array-based comparative genomic hybridization and expression profiling of ETV6/RUNX1-positive acute lymphoblastic leukemias reveal a high incidence of cryptic Xq duplications and identify several putative target genes within the commonly gained region.

Lilljebjörn H, Heidenblad M, Nilsson B, Lassen C, Horvat A, Heldrup J, Behrendtz M, Johansson B, Andersson A, Fioretos T. Lilljebjörn H, et al. Leukemia. 2007 Oct;21(10):2137-44. doi: 10.1038/sj.leu.2404879. Epub 2007 Aug 9. Leukemia. 2007. PMID: 17690704

4

FLT3 mutations in a 10 year consecutive series of 177 childhood acute leukemias and their impact on global gene expression patterns.

Andersson A, Paulsson K, Lilljebjörn H, Lassen C, Strömbeck B, Heldrup J, Behrendtz M, Johansson B, Fioretos T. Andersson A, et al. Among authors: lilljebjorn h. Genes Chromosomes Cancer. 2008 Jan;47(1):64-70. doi: 10.1002/gcc.20508. Genes Chromosomes Cancer. 2008. PMID: 17943971

5

The DNA methylome of pediatric acute lymphoblastic leukemia.

Davidsson J, Lilljebjörn H, Andersson A, Veerla S, Heldrup J, Behrendtz M, Fioretos T, Johansson B. Davidsson J, et al. Among authors: lilljebjorn h. Hum Mol Genet. 2009 Nov 1;18(21):4054-65. doi: 10.1093/hmg/ddp354. Epub 2009 Aug 13. Hum Mol Genet. 2009. PMID: 19679565

6

Relapsed childhood high hyperdiploid acute lymphoblastic leukemia: presence of preleukemic ancestral clones and the secondary nature of microdeletions and RTK-RAS mutations.

Davidsson J, Paulsson K, Lindgren D, Lilljebjörn H, Chaplin T, Forestier E, Andersen MK, Nordgren A, Rosenquist R, Fioretos T, Young BD, Johansson B. Davidsson J, et al. Among authors: lilljebjorn h. Leukemia. 2010 May;24(5):924-31. doi: 10.1038/leu.2010.39. Epub 2010 Mar 18. Leukemia. 2010. PMID: 20237506

7

Integrative analysis of gene expression and copy number alterations using canonical correlation analysis.

Soneson C, Lilljebjörn H, Fioretos T, Fontes M. Soneson C, et al. Among authors: lilljebjorn h. BMC Bioinformatics. 2010 Apr 15;11:191. doi: 10.1186/1471-2105-11-191. BMC Bioinformatics. 2010. PMID: 20398334 Free PMC article.

8

Genetic analysis of dasatinib-treated chronic myeloid leukemia rapidly developing into acute myeloid leukemia with monosomy 7 in Philadelphia-negative cells.

Larsson N, Billström R, Lilljebjörn H, Lassen C, Richter J, Ekblom M, Fioretos T. Larsson N, et al. Among authors: lilljebjorn h. Cancer Genet Cytogenet. 2010 Jun;199(2):89-95. doi: 10.1016/j.cancergencyto.2010.02.005. Cancer Genet Cytogenet. 2010. PMID: 20471511

9

The correlation pattern of acquired copy number changes in 164 ETV6/RUNX1-positive childhood acute lymphoblastic leukemias.

Lilljebjörn H, Soneson C, Andersson A, Heldrup J, Behrendtz M, Kawamata N, Ogawa S, Koeffler HP, Mitelman F, Johansson B, Fontes M, Fioretos T. Lilljebjörn H, et al. Hum Mol Genet. 2010 Aug 15;19(16):3150-8. doi: 10.1093/hmg/ddq224. Epub 2010 May 31. Hum Mol Genet. 2010. PMID: 20513752 Free PMC article.

10

Myeloid malignancies with acquired trisomy 21 as the sole cytogenetic change are clinically highly variable and display a heterogeneous pattern of copy number alterations and mutations.

Larsson N, Lilljebjörn H, Lassen C, Johansson B, Fioretos T. Larsson N, et al. Among authors: lilljebjorn h. Eur J Haematol. 2012 Feb;88(2):136-43. doi: 10.1111/j.1600-0609.2011.01710.x. Epub 2011 Nov 17. Eur J Haematol. 2012. PMID: 21933280

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