Josef Davidsson

Medicon Village
Lund, M 22381, Sweden

Last Updated: 09/26/2026

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Found 16 publications

Methylation Patterns and Chromatin Accessibility in Neuroendocrine Lung Cancer.

Methylation Patterns and Chromatin Accessibility in Neuroendocrine Lung Cancer.

Journal: Cancers
Published: May 04, 2020

SAMD9 and SAMD9L in inherited predisposition to ataxia, pancytopenia, and myeloid malignancies.

SAMD9 and SAMD9L in inherited predisposition to ataxia, pancytopenia, and myeloid malignancies.

Journal: Leukemia
Published: October 17, 2017

Ataxia-pancytopenia syndrome with SAMD9L mutations.

Ataxia-pancytopenia syndrome with SAMD9L mutations.

Journal: Neurology. Genetics
Published: May 02, 2017

Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptoms.

Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptoms.

Journal: Blood
Published: October 03, 2016

Methylation and expression analyses of Pallister-Killian syndrome reveal partial dosage compensation of tetrasomy 12p and hypomethylation of gene-poor regions on 12p.

Methylation and expression analyses of Pallister-Killian syndrome reveal partial dosage compensation of tetrasomy 12p and hypomethylation of gene-poor regions on 12p.

Journal: Epigenetics
Published: February 19, 2016

Small molecule screen identifies differentiation-promoting compounds targeting genetically diverse acute myeloid leukaemia.

Small molecule screen identifies differentiation-promoting compounds targeting genetically diverse acute myeloid leukaemia.

Journal: British journal of haematology
Published: November 17, 2015

The epigenetic landscape of aneuploidy: constitutional mosaicism leading the way?

The epigenetic landscape of aneuploidy: constitutional mosaicism leading the way?

Journal: Epigenomics
Published: March 04, 2014

Constitutional trisomy 8 mosaicism as a model for epigenetic studies of aneuploidy.

Constitutional trisomy 8 mosaicism as a model for epigenetic studies of aneuploidy.

Journal: Epigenetics & chromatin
Published: January 20, 2013

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

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

Journal: Leukemia
Published: March 19, 2010

dup(19)(q12q13.2): array-based genotype-phenotype correlation of a new possibly obesity-related syndrome.

dup(19)(q12q13.2): array-based genotype-phenotype correlation of a new possibly obesity-related syndrome.

Journal: Obesity (Silver Spring, Md.)
Published: September 19, 2009

The DNA methylome of pediatric acute lymphoblastic leukemia.

The DNA methylome of pediatric acute lymphoblastic leukemia.

Journal: Human molecular genetics
Published: August 15, 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 cases.

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.

Journal: Epilepsy research
Published: December 17, 2007
Showing 1-12 of 16

Last Updated: 09/26/2026