Jukka S Moilanen
14PUBLICATIONS
59CO-AUTHORS
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Publications (14)
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|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
|Mar 12, 2024
Evidence for the additivity of rare and common variant burden throughout the spectrum of intellectual disability.Lea Urpa, Mitja I Kurki, Elisa Rahikkala
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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
2 joint publications
Tytti Pokka
2 joint publications
Maria Suo-Palosaari
2 joint publications
Katri Pylkäs
2 joint publications
Reetta M Hinttala
2 joint publications
Salla M Kangas
2 joint publications
Lea Urpa
