Hanne Sagsveen Hjorthaug

Limitations and possibilities of low cell number ChIP-seq

Gregor D. Gilfillan, Timothy Hughes, Ying Sheng et al. · BMC Genomics · 2012 · 89 citations · Full text

A novel somatic mutation in<i>GNB2</i>provides new insights to the pathogenesis of Sturge–Weber syndrome

Roar Fjær, Katarzyna Marciniak, Olav Sundnes et al. · Human Molecular Genetics · 2021 · 63 citations · Full text

Sturge–weber Syndrome, Somatic Mutation, Somatic Variant +15

CD14 polymorphisms and serum CD14 levels through childhood: A role for gene methylation?

Monica Cheng Munthe‐Kaas, Tale Mæhre Torjussen, Kristina Gervin et al. · Journal of Allergy and Clinical Immunology · 2010 · 42 citations

Cd14 Levels, Autoimmune Disease, Genetic Disorder +10

A novel heterozygous variant in <i>ERLIN2</i> causes autosomal dominant pure hereditary spastic paraplegia

Siri Lynne Rydning, Aleš Dudešek, Florian Rimmele et al. · European Journal of Neurology · 2018 · 42 citations

Ephrin‐A1 stimulates migration of CD8⁺CCR7⁺ T lymphocytes

Hanne Sagsveen Hjorthaug, Hans‐Christian Aasheim · European Journal of Immunology · 2007 · 40 citations · Full text