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Lista de obras de Kristina Gervin

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

artículo científico publicado en 2012

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

artículo científico publicado en 2016

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

artículo científico publicado en 2012

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

artículo científico publicado en 2016

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

artículo científico publicado en 2011

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

artículo científico publicado en 2015

Limitations and possibilities of low cell number ChIP-seq.

artículo científico publicado en 2012

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

artículo científico

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

artículo científico publicado en 2011

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

artículo científico publicado en 2008

Pet keeping and tobacco exposure influence CD14 methylation in childhood

artículo científico publicado en 2012

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

artículo científico publicado en 2012

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

artículo científico publicado en 2009

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