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Hanne Sagsveen Hjorthaug

Oslo University Hospital

13

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209

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0.01

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A novel somatic mutation in GNB2 provides new insights to the pathogenesis of Sturge-weber syndrome.

2021 Human Molecular Genetics
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Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis

2019 Brain
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Neuronal and glial DNA methylation and gene expression changes in early epileptogenesis.

2019 PLOS ONE
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A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegia

2018 European Journal of Neurology
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Exploring the influence from whole blood DNA extraction methods on Infinium 450K DNA methylation

2018 PLOS ONE
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Additional file 2: Figure S2. of Intra-individual changes in DNA methylation not mediated by cell-type composition are correlated with aging during childhood

2016
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Additional file 1: Figure S1. of Intra-individual changes in DNA methylation not mediated by cell-type composition are correlated with aging during childhood

2016
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Intra-individual changes in DNA methylation not mediated by cell-type composition are correlated with aging during childhood

2016 Clinical Epigenetics
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Additional file 3: Figure S3. of Intra-individual changes in DNA methylation not mediated by cell-type composition are correlated with aging during childhood

2016
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Pet keeping and tobacco exposure influence CD14 methylation in childhood.

2012 Pediatric Allergy and Immunology
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Citations (23)