Kaarlo Mikko Kallela

Person

Latest publications

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

    Hiekkala, M. E., Vuola, P., Artto, V., Häppölä, P., Häppölä, E., Vepsäläinen, S., Cuenca-Leon, E., Lal, D., Gormley, P., Hämäläinen, E., Ilmavirta, M., Nissilä, M., Säkö, E., Sumelahti, M-L., Harno, H., Havanka, H., Keski-Säntti, P., Färkkilä, M., Palotie, A., Wessman, M. & 2 othersKaunisto, M. A. & Kallela, M., Oct 2018, In : Cephalalgia. 38, 12, p. 1849-1863 15 p.

    Research output: Contribution to journalArticleScientificpeer-review

  2. Molecular genetic overlap between migraine and major depressive disorder

    Int Headache Genetics Consortium, Aug 2018, In : European Journal of Human Genetics. 26, 8, p. 1202-1216 15 p.

    Research output: Contribution to journalArticleScientificpeer-review

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

    23me Res Team & Int Headache Genetics Consortium, 16 May 2018, In : Neuron. 98, 4, p. 743-+ 15 p.

    Research output: Contribution to journalArticleScientificpeer-review

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