Physician-Scientist, Lund University
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Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptoms
B Tesi, J Davidsson, M Voss, E Rahikkala, TD Holmes, SCC Chiang, ...
Blood, The Journal of the American Society of Hematology 129 (16), 2266-2279, 2017
The DNA methylome of pediatric acute lymphoblastic leukemia
J Davidsson, H Lilljebjörn, A Andersson, S Veerla, J Heldrup, ...
Human molecular genetics 18 (21), 4054-4065, 2009
SAMD9 and SAMD9L in inherited predisposition to ataxia, pancytopenia, and myeloid malignancies
J Davidsson, A Puschmann, U Tedgård, D Bryder, L Nilsson, ...
Leukemia 32 (5), 1106-1115, 2018
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
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
The t (X; 7)(q22; q34) in paediatric T‐cell acute lymphoblastic leukaemia results in overexpression of the insulin receptor substrate 4 gene through illegitimate recombination …
K Karrman, E Kjeldsen, C Lassen, M Isaksson, J Davidsson, A Andersson, ...
British journal of haematology 144 (4), 546-551, 2009
Deletion of the SCN gene cluster on 2q24. 4 is associated with severe epilepsy: an array-based genotype–phenotype correlation and a comprehensive review of previously published …
J Davidsson, A Collin, ME Olsson, J Lundgren, M Soller
Epilepsy research 81 (1), 69-79, 2008
Array based characterization of a terminal deletion involving chromosome subband 15q26. 2: an emerging syndrome associated with growth retardation, cardiac defects and …
J Davidsson, A Collin, G Björkhem, M Soller
BMC Medical Genetics 9 (1), 1-8, 2008
BRAF mutations are very rare in B-and T-cell pediatric acute lymphoblastic leukemias
J Davidsson, H Lilljebjörn, I Panagopoulos, T Fioretos, B Johansson
Leukemia 22 (8), 1619-1621, 2008
Ataxia-pancytopenia syndrome with SAMD9L mutations
S Gorcenco, J Komulainen-Ebrahim, K Nordborg, M Suo-Palosaari, ...
Neurology Genetics 3 (5), 2017
Constitutional trisomy 8 mosaicism as a model for epigenetic studies of aneuploidy
J Davidsson, S Veerla, B Johansson
Epigenetics & chromatin 6 (1), 1-14, 2013
dup (19)(q12q13. 2): Array‐based Genotype–Phenotype Correlation of a New Possibly Obesity‐related Syndrome
J Davidsson, K Jahnke, M Forsgren, A Collin, M Soller
Obesity 18 (3), 580-587, 2010
The epigenetic landscape of aneuploidy: constitutional mosaicism leading the way?
J Davidsson
Epigenomics 6 (1), 45-58, 2014
Multicolor fluorescence in situ hybridization characterization of cytogenetically polyclonal hematologic malignancies
J Davidsson, K Paulsson, B Johansson
Cancer genetics and cytogenetics 163 (2), 180-183, 2005
Small molecule screen identifies differentiation‐promoting compounds targeting genetically diverse acute myeloid leukaemia
A Baudet, F Ek, J Davidsson, S Soneji, R Olsson, M Magnusson, ...
British Journal of Haematology 175 (2), 342-346, 2016
Tiling resolution array‐based comparative genomic hybridisation analyses of acute lymphoblastic leukaemias in children with Down syndrome reveal recurrent gain of 8q and …
C Lundin, J Davidsson, L Hjorth, M Behrendtz, B Johansson
British journal of haematology 146 (1), 113-115, 2009
Methylation patterns and chromatin accessibility in neuroendocrine lung cancer
E Arbajian, M Aine, A Karlsson, J Vallon-Christersson, H Brunnström, ...
Cancers 12 (8), 2003, 2020
Methylation and expression analyses of Pallister-Killian syndrome reveal partial dosage compensation of tetrasomy 12p and hypomethylation of gene-poor regions on 12p
J Davidsson, B Johansson
Epigenetics 11 (3), 194-204, 2016
Array‐based genotype–phenotype correlation in a case of supernumerary ring chromosome 12
J Davidsson, A Collin, M Oereberg, D Gisselsson
Clinical genetics 73 (1), 44-49, 2008
Array-based comparative genomic hybridization characterization of cytogenetically polyclonal myeloid malignancies
J Davidsson, M Heidenblad, Å Borg, B Johansson
Cancer genetics and cytogenetics 169 (2), 179-180, 2006
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