Ane-Marte Øye

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 · 65 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

CHD2 mutations in Lennox–Gastaut syndrome

Caroline Lund, Eylert Brodtkorb, Ane-Marte Øye et al. · Epilepsy & Behavior · 2014 · 64 citations

Life Sciences, Genetics, Molecular Genetics +5

Novel<i>UCHL1</i>mutations reveal new insights into ubiquitin processing

Siri Lynne Rydning, Paul Hoff Backe, Mirta Mittelstedt Leal de Sousa et al. · Human Molecular Genetics · 2016 · 33 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

Generalized epilepsy in a family with basal ganglia calcifications and mutations in SLC20A2 and CHRNB2

Eylert Brodtkorb, Ane-Marte Øye, Ying Sheng et al. · European Journal of Medical Genetics · 2015 · 28 citations

Life Sciences, Genetics, Neuroscience +12

A founder mutation p.H701P identified as a major cause of <scp>SPG</scp>7 in Norway

Siri Lynne Rydning, Iselin Marie Wedding, Jeanette Koht et al. · European Journal of Neurology · 2016 · 15 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17