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Eija Inkeri Hämäläinen

  • PL 20 (Tukholmankatu 8)

    00014

    Finland

19942018
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International and National Collaboration Publications and projects within past five years.

Publications 1994 2018

Analysis of shared heritability in common disorders of the brain

Brainstorm Consortium, Anttila, V., Bulik-Sullivan, B., Finucane, H. K., Walters, R. K., Bras, J., Duncan, L., Escott-Price, V., Falcone, G. J., Gormley, P., Malik, R., Patsopoulos, N. A., Ripke, S., Wei, Z., Yu, D., Lee, P. H., Turley, P., Grenier-Boley, B., Chouraki, V., Kamatani, Y. & 33 othersBerr, C., Letenneur, L., Hannequin, D., Amouyel, P., Boland, A., Deleuze, J-F., Duron, E., Vardarajan, B. N., Reitz, C., Goate, A. M., Huentelman, M. J., Kamboh, M. I., Larson, E. B., Rogaeva, E., St George-Hyslop, P., Hakonarson, H., Kukull, W. A., Palta, P., Wedenoja, J., Artto, V., Kaunisto, M., Vepsäläinen, S., Kurki, M. I., Hämäläinen, E., Kaprio, J., Metspalu, A., Keski-Rahkonen, A., Raevuori, A., Ripatti, S., Lönnqvist, J., Daly, M., Palotie, A. & Neale, B. M., 22 Jun 2018, In : Science. 360, 6395, p. 1313-+ 13 p., 8757.

Research output: Contribution to journalArticleScientificpeer-review

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

23 Me Res Team, IHGC, Gormley, P., Kurki, M. I., Hiekkala, M. E., Häppölä, P., Palta, P., Surakka, I., Kaunisto, M. A., Hämäläinen, E., Vepsäläinen, S., Havanka, H., Harno, H., Ilmavirta, M., Nissilä, M., Säkö, E., Sumelahti, M-L., Liukkonen, J., Sillanpaa, M., Metsähonkala, L. & 15 othersKoskinen, S., Lehtimaki, T., Raitakari, O., Männikko, M., Jousilahti, P., Anttila, V., Salomaa, V., Artto, V., Färkkilä, M., Daly, M. J., Neale, B. M., Ripatti, S., Kallela, M., Wessman, M. & Palotie, A., 16 May 2018, In : Neuron. 98, 4, p. 743–753 11 p.

Research output: Contribution to journalArticleScientificpeer-review

Molecular genetic overlap between migraine and major depressive disorder

Int Headache Genetics Consortium, Yang, Y., Zhao, H., Boomsma, D. I., Kallela, M., Wessman, M., Anttila, V., Palta, P., Muona, M., Sarin, A-P., Wedenoja, J., Färkkilä, M., Artto, V., Kaunisto, M., Vepsäläinen, S., Hämäläinen, E., Eriksson, J. G., Heikkilä, K., Kaprio, J., Wessman, M. & 4 othersPalotie, A., Kurki, M. I., Pärn, K. & Neale, B. M., Aug 2018, In : European Journal of Human Genetics. 26, 8, p. 1202-1216 15 p.

Research output: Contribution to journalArticleScientificpeer-review

Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum

GoT2D T2D-GENES Consortium, SIGMA Consortium Helmsley IBD Exom, FinMetSeq Consortium, iPSYCH-Broad Consortium, Ganna, A., Kurki, M., Havulinna, A. S., Saarentaus, E., Ripatti, S., Hämäläinen, E., Moilanen, J. S., Kuismin, O., Palotie, A. & Neale, B. M., 7 Jun 2018, In : American Journal of Human Genetics. 102, 6, p. 1204-1211 8 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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