Päivi Vieira

7PUBLICATIONS
31CO-AUTHORS
Fairness, accountability, transparency, trust and ethics of computer systemsInformation systems development methodologies and practiceInfant and child healthGene expression (incl. microarray and other genome-wide approaches)Genetic immunology
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Publications (7)

|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

|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

|Oct 08, 2021
Cytosolic phosphoenolpyruvate carboxykinase deficiency: Expanding the clinical phenotype and novel laboratory findings.

Päivi Vieira, Irina I Nagy, Elisa Rahikkala

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