20162018
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International and National Collaboration Publications and projects within past five years.

Publications 2016 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

Copy number loss in SFMBT1 is common among Finnish and Norwegian patients with iNPH

Korhonen, V. E., Helisalmi, S., Jokinen, A., Jokinen, I., Lehtola, J-M., Oinas, M., Lönnrot, K., Avellan, C., Kotkansalo, A., Frantzen, J., Rinne, J., Ronkainen, A., Kauppinen, M., Junkkari, A., Hiltunen, M., Soininen, H., Kurki, M., Jääskeläinen, J. E., Koivisto, A. M., Sato, H. & 4 othersKato, T., Remes, A. M., Eide, P. K. & Leinonen, V., Dec 2018, In : Neurology Genetics. 4, 6, 8 p., 291.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland

Martin, A. R., Karczewski, K. J., Kerminen, S., Kurki, M. I., Sarin, A-P., Artomov, M., Eriksson, J. G., Esko, T., Genovese, G., Havulinna, A. S., Kaprio, J., Konradi, A., Korányi, L., Kostareva, A., Männikkö, M., Metspalu, A., Perola, M., Prasad, R. B., Raitakari, O., Rotar, O. & 7 othersSalomaa, V., Groop, L., Palotie, A., Neale, B. M., Ripatti, S., Pirinen, M. & Daly, M. J., 3 May 2018, In : American Journal of Human Genetics. 102, 5, p. 760-775 16 p.

Research output: Contribution to journalArticleScientificpeer-review

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

Int IBD Genetics Consortium, NIDDK IBD Genetics Consortium, T2D-Genes Consortium, Rivas, M. A., Koskela, J., Pirinen, M., Kurki, M., Saavalainen, P., Farkkila, M., Kontula, K., Palotie, A. & Daly, M. J., May 2018, In : PLoS Genetics. 14, 5, 25 p., 1007329.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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Projects 2017 2017