Vitenskapelig artikkel

• Svalastoga, Pernille; Kaci, Alba; Molnes, Janne et al. (2023). Characterisation of HNF1A variants in paediatric diabetes in Norway using functional and clinical investigations to unmask phenotype and monogenic diabetes. (ekstern lenke)
• Tobias, Deirdre K.; Merino, Jordi; Ahmad, Abrar et al. (2023). Second international consensus report on gaps and opportunities for the clinical translation of precision diabetes medicine. (ekstern lenke)
• Svalastoga, Pernille; Sulen, Åsta Nordsveen; Fehn, Jarle Røneid et al. (2020). Intellectual disability in KATP channel neonatal diabetes. (ekstern lenke)
• Bowman, Pamela; Sulen, Åsta Nordsveen; Barbetti, Fabrizio et al. (2018). Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study. (ekstern lenke)

Vitenskapelig oversiktsartikkel/review

• Alam, Kazi Asraful; Svalastoga, Pernille; Martinez, Aurora et al. (2023). Potassium channels in behavioral brain disorders. Molecular mechanisms and therapeutic potential: A narrative review. (ekstern lenke)

Vitenskapelig foredrag

• Kaci, Alba; Aukrust, Ingvild; Njølstad, Pål Rasmus et al. (2019). Functional characterization of diabetes gene variants is important for precision medicine . (ekstern lenke)

Poster

• Kaci, Alba; Aukrust, Ingvild; Bjørkhaug, Lise et al. (2019). Functional characterization of HNF1A variants identified in Norwegian MODY diabetes registry can implement precision medicine in diabetes clinics. (ekstern lenke)

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