Copy number loss in <i>SFMBT1</i> is common among Finnish and Norwegian patients with iNPHVille E. Korhonen, Ville Leinonen, Kimmo Lönnrot et al.|Neurology Genetics|2018Cited by 26
Risk Variants Associated With Normal Pressure HydrocephalusJoel Räsänen, Ville Leinonen, Sami Heikkinen et al.|Neurology|2024Cited by 24
Low prevalence of CWH43 variants among Finnish and Norwegian idiopathic normal pressure hydrocephalus patients: a cohort-based observational studyJoel Räsänen, Anssi Lipponen, Seppo Helisalmi et al.|Fluids and Barriers of the CNS|2025Cited by 4