Jukka S Moilanen

15PUBLICATIONS
60CO-AUTHORS
NeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Medical infection agents (incl. prions)Infant and child healthForensic epidemiology
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Publications (15)

|Oct 08, 2026
Genetic testing and counselling of patients with monogenic amyotrophic lateral sclerosis in Northern Finland: a retrospective, single-centre study.

|Oct 28, 2025
What is risk in clinical genetics? Designing and piloting tools to evaluate risk in clinical genetics using failure modes and effects analysis.

Deborah M Lambert, Helen Stewart, Mari Bandiola

|Aug 01, 2025
Cognitive impairment profile in patients with the m.3243A> G variant in mitochondrial DNA.

Satu Winqvist, Mikko Kärppä, Jukka S Moilanen

|May 06, 2025
Phenotypic Heterogeneity in Genetic and Acquired Pediatric Cerebellar Disorders.

Katariina Granath, Sanna Huhtaniska, Juulia Ellonen

|Jul 31, 2024
Brain MRI findings in paediatric genetic disorders associated with white matter abnormalities.

Jaakko H Oikarainen, Oula A Knuutinen, Salla M Kangas

|May 06, 2024
Clinical and genetic characteristics and natural history of Finnish families with familial exudative vitreoretinopathy due to pathogenic FZD4 variants.

Laura Lähteenoja, Tapani Palosaari, Timo Tiirikka

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Frequent Collaborators

5 joint publications

Elisa Rahikkala

3 joint publications

Päivi Vieira

2 joint publications

Aarno Palotie

2 joint publications

Johanna Uusimaa