Josef Davidsson (Former)
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- 2020
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Mark
Methylation patterns and chromatin accessibility in neuroendocrine lung cancer
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- Contribution to journal › Article
- 2018
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Mark
SAMD9 and SAMD9L in inherited predisposition to ataxia, pancytopenia, and myeloid malignancies
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- Contribution to journal › Article
- 2017
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Mark
Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS and neurological symptoms
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- Contribution to journal › Article
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Mark
Ataxia-pancytopenia syndrome with SAMD9L mutations
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- Contribution to journal › Article
- 2016
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Mark
Methylation and expression analyses of Pallister-Killian syndrome reveal partial dosage compensation of tetrasomy 12p and hypomethylation of gene-poor regions on 12p.
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- Contribution to journal › Article
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Mark
Small molecule screen identifies differentiation-promoting compounds targeting genetically diverse acute myeloid leukaemia.
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- Contribution to journal › Article
- 2014
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Mark
The epigenetic landscape of aneuploidy: constitutional mosaicism leading the way?
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- Contribution to journal › Article
- 2013
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Mark
Constitutional trisomy 8 mosaicism as a model for epigenetic studies of aneuploidy.
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- Contribution to journal › Article
- 2010
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Mark
dup(19)(q12q13.2): Array-based Genotype-Phenotype Correlation of a New Possibly Obesity-related Syndrome.
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- Contribution to journal › Article
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Mark
Relapsed childhood high hyperdiploid acute lymphoblastic leukemia: presence of preleukemic ancestral clones and the secondary nature of microdeletions and RTK-RAS mutations.
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- Contribution to journal › Article
- 2009
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Mark
Relapsed Childhood High Hyperdiploid Acute Lymphoblastic Leukemia: Genome-Wide Screening Reveals the Presence of Preleukemic Ancestral Clones and the Secondary Nature of Microdeletions and RTK-RAS Mutations
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- Contribution to journal › Published meeting abstract
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Mark
Genetic and epigenetic characterization of pediatric high hyperdiploid acute lymphoblastic leukemia
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- Thesis › Doctoral thesis (compilation)
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Mark
The DNA methylome of pediatric acute lymphoblastic leukemia.
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- Contribution to journal › Article
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Mark
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 with the T-cell receptor beta locus.
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- Contribution to journal › Article
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Mark
Tiling resolution array-based comparative genomic hybridisation analyses of acute lymphoblastic leukaemias in children with Down syndrome reveal recurrent gain of 8q and deletions of 7p and 9p.
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- Contribution to journal › Article
- 2008
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Mark
Array-based genotype-phenotype correlation in a case of supernumerary ring chromosome 12
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- Contribution to journal › Article
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Mark
The hypermethylome of pediatric acute lymphoblastic leukemia
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- Contribution to journal › Published meeting abstract
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Mark
Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delay.
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- Contribution to journal › Article
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Mark
BRAF mutations are very rare in B- and T-cell pediatric acute lymphoblastic leukemias.
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- Contribution to journal › Article
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Mark
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 cases.
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- Contribution to journal › Article
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Mark
Delection 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 area
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- Contribution to journal › Article
- 2007
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Mark
Tiling resolution array comparative genomic hybridization, expression and methylation analyses of dup(1q) in Burkitt lymphomas and pediatric high hyperdiploid acute lymphoblastic leukemias reveal clustered near-centromeric breakpoints and overexpression of genes in 1q22-32.3
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- Contribution to journal › Article
- 2006
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Mark
Searching for cryptic chromosomal aberrations in high hyperdiploid childhood acute lymphoblastic leukaemias
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- Contribution to journal › Letter
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Mark
Array-based comparative genomic hybridization characterization of cytogenetically polyclonal myeloid malignancies.
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- Contribution to journal › Letter
- 2005
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Mark
Multicolor fluorescence in situ hybridization characterization of cytogenetically polyclonal hematologic malignancies.
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- Contribution to journal › Article