Search filters

List of works by Katariina Hannula-Jouppi

A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain

scientific article

Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia

scientific article published in November 2006

Altered Methylation of IGF2 Locus 20 Years after Preterm Birth at Very Low Birth Weight

scientific article

Clinically distinct epigenetic subgroups in Silver-Russell syndrome: the degree of H19 hypomethylation associates with phenotype severity and genital and skeletal anomalies

scientific article published on 18 November 2008

Differentially methylated regions in maternal and paternal uniparental disomy for chromosome 7.

scientific article

Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene

scientific article published on 6 March 2004

Genetic susceptibility to non-necrotizing erysipelas/cellulitis

scientific article

Hypomethylation of HOXA4 promoter is common in Silver-Russell syndrome and growth restriction and associates with stature in healthy children

scientific article published on 16 November 2017

The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia

scientific article published in October 2005

The mutation spectrum in RECQL4 diseases

scientific article

Paulina is supported by:

About Paulina

Help