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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
Perez-Palma, Eduardo ORCID: 0000-0003-0546-5141, Helbig, Ingo ORCID: 0000-0001-8486-0558, Klein, Karl Martin ORCID: 0000-0002-6654-1665, Anttila, Verneri, Horn, Heiko, Reinthaler, Eva Maria, Gormley, Padhraig ORCID: 0000-0002-8908-6968, Ganna, Andrea ORCID: 0000-0002-8147-240X, Byrnes, Andrea, Pernhorst, Katharina, Toliat, Mohammad R., Saarentaus, Elmo ORCID: 0000-0002-8475-7187, Howrigan, Daniel P., Hoffman, Per, Miquel, Juan Francisco, De Ferrari, Giancarlo V., Nuernberg, Peter, Lerche, Holger, Zimprich, Fritz ORCID: 0000-0002-6998-5480, Neubauer, Bern A., Becker, Albert J., Rosenow, Felix, Perucca, Emilio, Zara, Federico ORCID: 0000-0001-9744-5222, Weber, Yvonne G. and Lal, Dennis
(2017).
Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies.
J. Med. Genet., 54 (9).
S. 598 - 607.
LONDON:
BMJ PUBLISHING GROUP.
ISSN 1468-6244
Lal, Dennis, Reinthaler, Eva M., Dejanovici, Borislav, May, Patrick ORCID: 0000-0001-8698-3770, Thiele, Holger, Lehesjoki, Anna-Elina, Schwarz, Gunter, Riesch, Erik, Ikram, M. Arfan, van Duijn, Cornelia M., Uitterlinden, Andre G., Hofman, Albert, Steinboeck, Hannelore, Gruber-Sedlmayr, Ursula, Neophytou, Birgit, Zara, Federico ORCID: 0000-0001-9744-5222, Hahn, Andreas, Gormley, Padhraig ORCID: 0000-0002-8908-6968, Becker, Felicitas, Weber, Yvonne G., Cilio, Maria Roberta, Kunz, Wolfram S. ORCID: 0000-0003-1113-3493, Krause, Roland ORCID: 0000-0001-9938-7126, Zimprich, Fritz ORCID: 0000-0002-6998-5480, Lemke, Johannes R., Nuernberg, Peter, Sander, Thomas, Lerche, Holger and Neubauer, Bernd A.
(2016).
Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy Syndromes.
PLoS One, 11 (3).
SAN FRANCISCO:
PUBLIC LIBRARY SCIENCE.
ISSN 1932-6203
Dejanovic, Borislav, Djemie, Tania, Gruenewald, Nora, Suls, Arvid ORCID: 0000-0003-0328-198X, Kress, Vanessa, Hetsch, Florian, Craiu, Dana, Zemel, Matthew, Gormley, Padhraig ORCID: 0000-0002-8908-6968, Lal, Dennis, Myers, Candace T., Mefford, Heather C., Palotie, Aarno, Helbig, Ingo ORCID: 0000-0001-8486-0558, Meier, Jochen C., De Jonghe, Peter, Weckhuysen, Sarah ORCID: 0000-0003-2878-1147 and Schwarz, Guenter ORCID: 0000-0002-2118-9338
(2015).
Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathy.
EMBO Mol. Med., 7 (12).
S. 1580 - 1595.
HOBOKEN:
WILEY.
ISSN 1757-4684