A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2

Overview of attention for article published in neurogenetics, May 2004

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Astrocytes in Atp1a2‐deficient heterozygous mice exhibit hyperactivity after induction of cortical spreading depression

Article in FEBS Open Bio (April 2020)

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

Article in Neuron (May 2018)

The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families

Article in Cephalalgia (February 2018)

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