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Number of items: 3.

2018

Gormley, Padhraig ORCID: 0000-0002-8908-6968, Kurki, Mitja I., Hiekkala, Marjo Eveliina, Veerapen, Kumar, Happola, Paavo, Mitchell, Adele A., Lal, Dennis, Palta, Priit ORCID: 0000-0001-9320-7008, Surakka, Ida, Kaunisto, Mari Anneli, Hamalainen, Eija, Vepsalainen, Salli, Havanka, Hannele, Harno, Hanna ORCID: 0000-0002-6526-9436, Ilmavirta, Matti, Nissila, Markku, Sako, Erkki, Sumelahti, Marja-Liisa, Liukkonen, Jarmo, Sillanpaa, Matti, Metsahonkala, Liisa, Koskinen, Seppo, Lehtimaki, Terho, Raitakari, Olli, Mannikko, Minna, Ran, Caroline ORCID: 0000-0003-0239-9871, Belin, Andrea Carmine ORCID: 0000-0001-6668-3172, Jousilahti, Pekka, Anttila, Verneri, Salomaa, Veikko, Artto, Ville, Farkkila, Markus, Runz, Heiko, Daly, Mark J., Neale, Benjamin M., Ripatti, Samuli, Kallela, Mikko, Wessman, Maija and Palotie, Aarno (2018). Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families. Neuron, 98 (4). S. 743 - 758. CAMBRIDGE: CELL PRESS. ISSN 1097-4199

Hiekkala, Marjo Eveliina, Vuola, Pietari, Artto, Ville, Happola, Paavo, Happola, Elisa, Vepsalainen, Salli, Cuenca-Leon, Ester, Lal, Dennis, Gormley, Padhraig ORCID: 0000-0002-8908-6968, Hamalainen, Eija, Ilmavirta, Matti, Nissila, Markku, Sako, Erkki, Sumelahti, Marja-Liisa, Harno, Hanna ORCID: 0000-0002-6526-9436, Havanka, Hannele, Keski-Santti, Petra, Farkkila, Markus, Palotie, Aarno, Wessman, Maija, Kaunisto, Mari Anneli and Kallela, Mikko (2018). The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families. Cephalalgia, 38 (12). S. 1849 - 1864. LONDON: SAGE PUBLICATIONS LTD. ISSN 1468-2982

2010

Anttila, Verneri ORCID: 0000-0002-0073-4675, Stefansson, Hreinn ORCID: 0000-0002-9331-6666, Kallela, Mikko, Todt, Unda, Terwindt, Gisela M., Calafato, M. Stella, Nyholt, Dale R., Dimas, Antigone S., Freilinger, Tobias, Mueller-Myhsok, Bertram, Artto, Ville, Inouye, Michael ORCID: 0000-0001-9413-6520, Alakurtti, Kirsi, Kaunisto, Mari A., Haemaelaeinen, Eija, de Vries, Boukje, Stam, Anine H., Weller, Claudia M., Heinze, Axel, Heinze-Kuhn, Katja, Goebel, Ingrid, Borck, Guntram, Goebel, Hartmut, Steinberg, Stacy, Wolf, Christiane, Bjoernsson, Asgeir, Gudmundsson, Gretar, Kirchmann, Malene, Hauge, Anne, Werge, Thomas, Schoenen, Jean, Eriksson, Johan G., Hagen, Knut, Stovner, Lars, Wichmann, Erich, Meitinger, Thomas ORCID: 0000-0002-8838-8403, Alexander, Michael, Moebus, Susanne, Schreiber, Stefan, Aulchenko, Yurii S., Breteler, Monique M. B., Uitterlinden, Andre G., Hofman, Albert, van Duijn, Cornelia M., Tikka-Kleemola, Paevi, Vepsaelaeinen, Salli, Lucae, Susanne, Tozzi, Federica ORCID: 0000-0002-3536-2920, Muglia, Pierandrea ORCID: 0000-0002-3973-8606, Barrett, Jeffrey, Kaprio, Jaakko ORCID: 0000-0002-3716-2455, Faerkkilae, Markus, Peltonen, Leena, Stefansson, Kari, Zwart, John-Anker, Ferrari, Michel D., Olesen, Jes ORCID: 0000-0002-6712-2702, Daly, Mark, Wessman, Maija, van den Maagdenberg, Arn M. J. M., Dichgans, Martin, Kubisch, Christian ORCID: 0000-0003-4220-0978, Dermitzakis, Emmanouil T., Frants, Rune R. and Palotie, Aarno (2010). Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1. Nature Genet., 42 (10). S. 869 - 875. NEW YORK: NATURE PUBLISHING GROUP. ISSN 1546-1718

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