Latest papers

Parent-of-origin effects at the major histocompatibility complex in multiple sclerosis.

Atypical Silver-Russell phenotype resulting from maternal uniparental disomy of chromosome 7.

Developmental biology. Which parental gene gets the upper hand?

Sex-specific parent-of-origin allelic expression in the mouse brain.

Differential methylation as a cause of allele dropout at the imprinted GNAS locus.

[Imprinting genes and it's expression in Arabidopsis].

The imprinted gene neuronatin is regulated by metabolic status and associated with obesity.

How genome-wide approaches can be used to unravel the remaining secrets of the imprintome.

Mechanisms and evolution of genomic imprinting in plants.

Quantitative 1-step DNA methylation analysis with native genomic DNA as template.

Brain function and chromatin plasticity.

Sex bias in trials and treatment must end.

ARHI (DIRAS3), an imprinted tumour suppressor gene, binds to importins and blocks nuclear import of cargo proteins.

Loss of imprinting of IGF2 characterises high IGF2 mRNA-expressing type of fibroblast-like synoviocytes in rheumatoid arthritis.

The X-linked imprinted gene family Fthl17 shows predominantly female expression following the two-cell stage in mouse embryos.

Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction.

Chromosomal networks as mediators of epigenetic states: the maternal genome connection.

Atp10a, a gene adjacent to the PWS/AS gene cluster, is not imprinted in mouse and is insensitive to the PWS-IC.

[Evolution of genomic imprinting in mammals: what a zoo!].

Phenotypic heterogeneity and parental origin of extra chromosome 21 in Down syndrome.