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List of works by Kristina Gervin

A conserved eEF2 coding variant in SCA26 leads to loss of translational fidelity and increased susceptibility to proteostatic insult

scientific article

Cell type specific DNA methylation in cord blood: A 450K-reference data set and cell count-based validation of estimated cell type composition

scientific article

DNA methylation and gene expression changes in monozygotic twins discordant for psoriasis: identification of epigenetically dysregulated genes

scientific article

Differentially Methylated DNA Regions in Monozygotic Twin Pairs Discordant for Rheumatoid Arthritis: An Epigenome-Wide Study.

scientific article

Extensive variation and low heritability of DNA methylation identified in a twin study

scientific article

Genome-wide blood DNA methylation alterations at regulatory elements and heterochromatic regions in monozygotic twins discordant for obesity and liver fat.

scientific article

Limitations and possibilities of low cell number ChIP-seq.

scientific article

Long-term prenatal exposure to paracetamol is associated with DNA methylation differences in children diagnosed with ADHD.

scientific article published on 02 August 2017

Multiple loci in the HLA complex are associated with Addison's disease

scientific article published on 03 August 2011

Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease

scientific article

Pet keeping and tobacco exposure influence CD14 methylation in childhood

scientific article

Rapid and efficient FBN1 mutation detection using automated sample preparation and direct sequencing as the primary strategy

scientific article published on 01 January 2006

Systematic evaluation and validation of reference and library selection methods for deconvolution of cord blood DNA methylation data

scientific article published on 27 August 2019

The Norwegian Twin Registry from a public health perspective: a research update

scientific article published on 28 November 2012

X-linked congenital adrenal hypoplasia with hypogonadotropic hypogonadism caused by an inversion disrupting a conserved noncoding element upstream of the NR0B1 (DAX1) gene

scientific article published on 22 September 2009

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