| 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 | 204 | 2017 |
| 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 | 110 | 2018 |
| 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 | 102 | 2009 |
| 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 |
| 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 |
| 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 | 67 | 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 | 54 | 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, 1-8, 2008 | 49 | 2008 |
| Ataxia-pancytopenia syndrome with SAMD9L mutations S Gorcenco, J Komulainen-Ebrahim, K Nordborg, M Suo-Palosaari, ... Neurology: Genetics 3 (5), e183, 2017 | 37 | 2017 |
| 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 | 30 | 2008 |
| Constitutional trisomy 8 mosaicism as a model for epigenetic studies of aneuploidy J Davidsson, S Veerla, B Johansson Epigenetics & chromatin 6, 1-14, 2013 | 27 | 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 | 22 | 2010 |
| The epigenetic landscape of aneuploidy: constitutional mosaicism leading the way? J Davidsson Epigenomics 6 (1), 45-58, 2014 | 15 | 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 | 10 | 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), 2016 | 8 | 2016 |
| 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 | 5 | 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 | 5 | 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 | 5 | 2009 |
| 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 | 4 | 2008 |
| Searching for cryptic chromosomal aberrations in high hyperdiploid childhood acute lymphoblastic leukaemias. J Davidsson, K Paulsson, B Johansson European journal of haematology 76 (5), 449-450, 2006 | 2 | 2006 |
Srinivas Sunny VeerlaScientist, Lund UniversityBestätigte E-Mail-Adresse bei med.lu.se
