Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia by Sintas, Cèlia, Carreño, Oriel, Fernàndez-Castillo, Noèlia, Corominas, Roser, Vila-Pueyo, Marta, Toma, Claudio, Cuenca-León, Ester, Barroeta, Isabel, Roig, Carles, Volpini, Víctor, Macaya, Alfons, Cormand, Bru

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Chiari malformation type I: a case-control association study of 58 developmental genes by Urbizu, Aintzane, Toma, Claudio, Poca, Maria A, Sahuquillo, Juan, Cuenca-León, Ester, Cormand, Bru, Macaya, Alfons

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GNAO1 encephalopathy: further delineation of a severe neurodevelopmental syndrome affecting females by Marcé-Grau, Anna, Dalton, James, López-Pisón, Javier, García-Jiménez, María Concepción, Monge-Galindo, Lorena, Cuenca-León, Ester, Giraldo, Jesús, Macaya, Alfons

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Genome-wide DNA methylation analysis in an antimigraine-treated preclinical model of cortical spreading depolarization by Vila-Pueyo, Marta, Cuenca-León, Ester, Queirós, Ana C., Kulis, Marta, Sintas, Cèlia, Cormand, Bru, Martín-Subero, José Ignacio, Pozo-Rosich, Patricia, Fernàndez-Castillo, Noèlia, Macaya, Alfons

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mutation in the first intracellular loop of CACNA1A prevents P/Q channel modulation by SNARE proteins and lowers exocytosis by Serra, Selma A, Cuenca-León, Ester, Llobet, Artur, Rubio-Moscardo, Francisca, Plata, Cristina, Carreño, Oriel, Fernàndez-Castillo, Noèlia, Corominas, Roser, Valverde, Miguel A, Macaya, Alfons, Cormand, Bru, Fernández-Fernández, José M

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The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families by Hiekkala, Marjo Eveliina, Vuola, Pietari, Artto, Ville, Häppölä, Paavo, Häppölä, Elisa, Vepsäläinen, Salli, Cuenca-León, Ester, Lal, Dennis, Gormley, Padhraig, Hämäläinen, Eija, Ilmavirta, Matti, Nissilä, Markku, Säkö, Erkki, Sumelahti, Marja-Liisa, Harno, Hanna, Havanka, Hannele, Keski-Säntti, Petra, Färkkilä, Markus, Palotie, Aarno, Wessman, Maija, Kaunisto, Mari Anneli, Kallela, Mikko

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Two-stage case-control association study of dopamine-related genes and migraine by Corominas, Roser, Ribases, Marta, Camiña, Montserrat, Cuenca-León, Ester, Pardo, Julio, Boronat, Susana, Sobrido, María-Jesús, Cormand, Bru, Macaya, Alfons

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Paroxysmal exercise-induced dyskinesia, writer's cramp, migraine with aura and absence epilepsy in twin brothers with a novel SLC2A1 missense mutation by Urbizu, Aintzane, Cuenca-León, Ester, Raspall-Chaure, Miquel, Gratacòs, Margarida, Conill, Joan, Redecillas, Susana, Roig-Quilis, Manuel, Macaya, Alfons

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Habitual sleep disturbances and migraine: a Mendelian randomization study by Guo, Yanjun, Chasman, Daniel I., Saxena, Richa, Gormley, Padhraig, Anttila, Verneri, Winsvold, Bendik S., Palta, Priit, Pers, Tune H., Farh, Kai‐How, Cuenca‐Leon, Ester, Muona, Mikko, Furlotte, Nicholas A., Kurth, Tobias, Ingason, Andres, McMahon, George, Terwindt, Gisela M., Kallela, Mikko, Freilinger, Tobias M., Ran, Caroline, Gordon, Scott G., Stam, Anine H., Steinberg, Stacy, Borck, Guntram, Koiranen, Markku, Quaye, Lydia, Adams, Hieab H. H., Lehtimäki, Terho, Sarin, Antti‐Pekka, Wedenoja, Juho, Buring, Julie E., Ridker, Paul M., Hrafnsdottir, Maria Gudlaug, Stefansson, Hreinn, Ring, Susan M., Hottenga, Jouke‐Jan, Penninx, Brenda W. J. H., Färkkilä, Markus, Artto, Ville, Kaunisto, Mari, Vepsäläinen, Salli, Malik, Rainer, Heath, Andrew C., Madden, Pamela A. F., Kals, Mart, Pärn, Kalle, Hämäläinen, Eija, Huang, Hailiang, Byrnes, Andrea E., Franke, Lude, Huang, Jie, Stergiakouli, Evie, Lee, Phil H., Sandor, Cynthia, Webber, Caleb, Cader, Zameel, Muller‐Myhsok, Bertram, Schreiber, Stefan, Meitinger, Thomas, Eriksson, Johan G., Salomaa, Veikko, Heikkilä, Kauko, Loehrer, Elizabeth, Uitterlinden, Andre G., Hofman, Albert, van Duijn, Cornelia M., Cherkas, Lynn, Pedersen, Linda M., Stubhaug, Audun, Nielsen, Christopher S., Männikkö, Minna, Mihailov, Evelin, Milani, Lili, Göbel, Hartmut, Esserlind, Ann‐Louise, Christensen, Anne Francke, Hansen, Thomas Folkmann, Kaprio, Jaakko, Aromaa, Arpo J., Raitakari, Olli, Ikram, M. Arfan, Spector, Tim, Järvelin, Marjo‐Riitta, Metspalu, Andres, Kubisch, Christian, Strachan, David P., Ferrari, Michel D., Belin, Andrea C., Wessman, Maija, van den Maagdenberg, Arn M. J. M., Zwart, John‐Anker, Boomsma, Dorret I., Smith, George Davey, Stefansson, Kari, Eriksson, Nicholas, Daly, Mark J., Neale, Benjamin M., Olesen, Jes, Chasman, Daniel I., Nyholt, Dale R., Palotie, Aarno

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Paroxysmal non-kinesigenic dyskinesia due to a PNKD recurrent mutation: Report of two Southern European families by Pons, Roser, Cuenca-León, Ester, Miravet, Elena, Pons, Montse, Xaidara, Athina, Youroukos, Sotiris, Macaya, Alfons

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The role of specialist nurses in detecting spasticity and related symptoms in multiple sclerosis by Artola, Montse, Hernando, Ana, Vidal, Oscar, Vidal, Núria, Cuenca, Ester, Horno, Rosalía, Robles, Miguel Ángel, Oriol, Clara, Peralta, Silvia, Solana, M. A. José, Rubio, Matilde, Montero, Cristina, Lleixà, Mercè, Zabay, Cinta, Martin, Montse, Leon, Isabel, Molinos, Consuelo, Matamoros, Mandi, Mercadé, Laura, Fornali, Olga, Montero, Laura, Saiz, Albert, Solà‐Valls, Núria

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Late-onset episodic ataxia type 2 associated with a novel loss-of-function mutation in the CACNA1A gene by Cuenca-León, Ester, Banchs, Isabel, Serra, Selma A, Latorre, Pilar, Fernàndez-Castillo, Noèlia, Corominas, Roser, Valverde, Miguel A, Volpini, Víctor, Fernández-Fernández, José M, Macaya, Alfons, Cormand, Bru

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Genetic causal relationship between immune diseases and migraine: a Mendelian randomization study by Li, Guanglu, Duan, Shaojie, Zheng, Tao, Zhu, Tiantian, Qu, Baoquan, Liu, Lei, Liu, Zunjing

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Cerebral small vessel disease genomics and its implications across the lifespan by Sargurupremraj, Muralidharan, Suzuki, Hideaki, Jian, Xueqiu, Sarnowski, Chloé, Evans, Tavia E., Eiriksdottir, Gudny, Sakaue, Saori, Terzikhan, Natalie, Zhao, Wei, Armstrong, Nicola J., Yanek, Lisa R., Kumar, Rajan B., van den Akker, Erik B., McWhirter, Rebekah E., Trompet, Stella, Mishra, Aniket, Saba, Yasaman, Satizabal, Claudia L., Beaudet, Gregory, Petit, Laurent, Tsuchida, Ami, Schilling, Sabrina, Sigurdsson, Sigurdur, Lewis, Cora E., Lopez, Oscar L., Smith, Jennifer A., Valdés Hernández, Maria C., van der Grond, Jeroen, Wright, Margaret J., Knol, Maria J., Thomson, Russell J., Le Grand, Quentin, Duperron, Marie-Gabrielle, Smith, Albert V., Schreiner, Pamela J., Evans, Denis A., Rotter, Jerome I., Beiser, Alexa S., Maniega, Susana Muñoz, Beekman, Marian, Trollor, Julian, Stott, David J., Vernooij, Meike W., Wittfeld, Katharina, Niessen, Wiro J., Soumaré, Aicha, Sidney, Stephen, Turner, Stephen T., Davies, Gail, Thalamuthu, Anbupalam, Völker, Uwe, van Buchem, Mark A., Dupuis, Josée, Bastin, Mark E., Teumer, Alexander, Amouyel, Philippe, Kwok, John B., Bülow, Robin, Deary, Ian J., Schofield, Peter R., Brodaty, Henry, Jiang, Jiyang, Tabara, Yasuharu, Setoh, Kazuya, Miyamoto, Susumu, Yoshida, Kazumichi, Nagata, Manabu, Matsuda, Fumihiko, Psaty, Bruce M., Bennett, David A., De Jager, Philip L., Mosley, Thomas H., Sachdev, Perminder S., Schmidt, Reinhold, Evangelou, Evangelos, Trégouët, David-Alexandre, Ikram, Mohammad A., DeCarli, Charles, Srikanth, Velandai K., Jukema, J. Wouter, Slagboom, Eline P., Kardia, Sharon L. R., Okada, Yukinori, Mazoyer, Bernard, Wardlaw, Joanna M., Nyquist, Paul A., Mather, Karen A., Grabe, Hans J., Schmidt, Helena, Van Duijn, Cornelia M., Gudnason, Vilmundur, Longstreth, William T., Launer, Lenore J., Lathrop, Mark, Seshadri, Sudha, Tzourio, Christophe, Adams, Hieab H., Matthews, Paul M., Fornage, Myriam, Debette, Stéphanie

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Contribution of syntaxin 1A to the genetic susceptibility to migraine: A case–control association study in the Spanish population by Corominas, Roser, Ribasés, Marta, Cuenca-León, Ester, Narberhaus, Bernat, Serra, Selma A., del Toro, Mireia, Roig, Manuel, Fernández-Fernández, José M., Macaya, Alfons, Cormand, Bru

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Familial hemiplegic migraine: linkage to chromosome 14q32 in a Spanish kindred by Cuenca-León, Ester, Corominas, Roser, Montfort, Magda, Artigas, Josep, Roig, Manuel, Bayés, Mònica, Cormand, Bru, Macaya, Alfons

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A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine by Guo, Yanjun, Rist, Pamela M., Daghlas, Iyas, Giulianini, Franco, Kurth, Tobias, Chasman, Daniel I.

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Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families by Gormley, Padhraig, Kurki, Mitja I., Hiekkala, Marjo Eveliina, Häppölä, Paavo, Mitchell, Adele A., Lal, Dennis, Palta, Priit, Surakka, Ida, Kaunisto, Mari Anneli, Hämäläinen, Eija, Vepsäläinen, Salli, Havanka, Hannele, Harno, Hanna, Ilmavirta, Matti, Sumelahti, Marja-Liisa, Sillanpää, Matti, Metsähonkala, Liisa, Koskinen, Seppo, Raitakari, Olli, Jousilahti, Pekka, Anttila, Verneri, Salomaa, Veikko, Artto, Ville, Agee, Michelle, Alipanahi, Babak, Auton, Adam, Bell, Robert K., Elson, Sarah L., Furlotte, Nicholas A., Huber, Karen E., Kleinman, Aaron, Litterman, Nadia K., McCreight, Jennifer C., McIntyre, Matthew H., Mountain, Joanna L., Pitts, Steven J., Sathirapongsasuti, J. Fah, Shelton, Janie F., Shringarpure, Suyash, Tian, Chao, Vacic, Vladimir, Wilson, Catherine H., Anttila, Verneri, Artto, Ville, Belin, Andrea Carmine, Børte, Sigrid, Cherkas, Lynn, Christensen, Anne Francke, Cuenca-Leon, Ester, Dichgans, Martin, van Duijn, Cornelia, Esko, Tonu, Esserlind, Ann-Louise, Frants, Rune R., Freilinger, Tobias, Furlotte, Nick, Gormley, Padhraig, Hansen, Thomas Folkmann, Hiekkala, Marjo, Ikram, M Arfan, Ingason, Andres, Kajanne, Risto, Kallela, Mikko, Kaprio, Jaakko, Kaunisto, Mari, Kubisch, Christian, Kurth, Tobias, Launer, Lenore, Lehtimaki, Terho, Lessel, Davor, Ligthart, Lannie, Litterman, Nadia, van den Maagdenberg, Arn, Macaya, Alfons, Malik, Rainer, Muller-Myhsok, Bertram, Neale, Benjamin M., Northover, Carrie, Palta, Priit, Pedersen, Nancy, Posthuma, Danielle, Pressman, Alice, Quaye, Lydia, Raitakari, Olli, Schürks, Markus, Sintas, Celia, Stefansson, Kari, Stefansson, Hreinn, Steinberg, Stacy, Strachan, David, Terwindt, Gisela, Vila-Pueyo, Marta, Winsvold, Bendik S., Wrenthal, William, Daly, Mark J., Neale, Benjamin M., Ripatti, Samuli, Kallela, Mikko, Wessman, Maija, Palotie, Aarno

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Elucidating the relationship between migraine risk and brain structure using genetic data by Mitchell, Brittany L, Diaz-Torres, Santiago, Bivol, Svetlana, Cuellar-Partida, Gabriel, Gormley, Padhraig, Anttila, Verneri, Winsvold, Bendik S, Palta, Priit, Esko, Tonu, Pers, Tune H, Farh, Kai-How, Cuenca-Leon, Ester, Muona, Mikko, Furlotte, Nicholas A, Kurth, Tobias, Ingason, Andres, McMahon, George, Ligthart, Lannie, Terwindt, Gisela M, Kallela, Mikko, Freilinger, Tobias M, Ran, Caroline, Gordon, Scott G, Stam, Anine H, Steinberg, Stacy, Borck, Guntram, Koiranen, Markku, Quaye, Lydia, Adams, Hieab H H, Lehtimäki, Terho, Sarin, Antti-Pekka, Wedenoja, Juho, Hinds, David A, Buring, Julie E, Schürks, Markus, Ridker, Paul M, Hrafnsdottir, Maria Gudlaug, Stefansson, Hreinn, Ring, Susan M, Hottenga, Jouke-Jan, Penninx, Brenda W J H, Färkkilä, Markus, Artto, Ville, Kaunisto, Mari, Vepsäläinen, Salli, Malik, Rainer, Heath, Andrew C, Madden, Pamela A F, Martin, Nicholas G, Montgomery, Grant W, Kurki, Mitja, Kals, Mart, Mägi, Reedik, Pärn, Kalle, Hämäläinen, Eija, Huang, Hailiang, Byrnes, Andrea E, Franke, Lude, Huang, Jie, Stergiakouli, Evie, Lee, Phil H, Sandor, Cynthia, Webber, Caleb, Cader, Zameel, Muller-Myhsok, Bertram, Schreiber, Stefan, Meitinger, Thomas, Eriksson, Johan G, Salomaa, Veikko, Heikkilä, Kauko, Loehrer, Elizabeth, Uitterlinden, Andre G, Hofman, Albert, van Duijn, Cornelia M, Cherkas, Lynn, Pedersen, Linda M, Stubhaug, Audun, Nielsen, Christopher S, Männikkö, Minna, Mihailov, Evelin, Milani, Lili, Göbel, Hartmut, Esserlind, Ann-Louise, Christensen, Anne Francke, Hansen, Thomas Folkmann, Werge, Thomas, Børte, Sigrid, Cormand, Bru, Eising, Else, Griffiths, Lyn, Hamalainen, Eija, Hiekkala, Marjo, Kajanne, Risto, Launer, Lenore, Lehtimaki, Terho, Leslsel, Davor, Macaya, Alfons, Mangino, Massimo, Pedersen, Nancy, Posthuma, Danielle

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Migraine, inflammatory bowel disease and celiac disease: A Mendelian randomization study by Welander, Nike Zoe, Rask‐Andersen, Mathias, Harder, Aster V. E., Gormley, Padhraig, Anttila, Verneri, Palta, Priit, Esko, Tonu, Pers, Tune H., Cuenca‐Leon, Ester, Furlotte, Nicholas A., Kurth, Tobias, Ligthart, Lannie, Kallela, Mikko, Freilinger, Tobias M., Ran, Caroline, Gordon, Scott G., Stam, Anine H., Steinberg, Stacy, Borck, Guntram, Koiranen, Markku, Quaye, Lydia, Adams, Hieab H. H., Lehtimäki, Terho, Sarin, Antti‐Pekka, Hinds, David A., Buring, Julie E., Schürks, Markus, Hrafnsdottir, Maria Gudlaug, Hottenga, Jouke‐Jan, Penninx, Brenda W. J. H., Färkkilä, Markus, Artto, Ville, Kaunisto, Mari, Malik, Rainer, Heath, Andrew C., Martin, Nicholas G., Montgomery, Grant W., Kurki, Mitja, Kals, Mart, Mägi, Reedik, Pärn, Kalle, Hämäläinen, Eija, Huang, Hailiang, Byrnes, Andrea E., Franke, Lude, Huang, Jie, Lee, Phil H., Sandor, Cynthia, Webber, Caleb, Schreiber, Stefan, Eriksson, Johan G., Salomaa, Veikko, Heikkilä, Kauko, Loehrer, Elizabeth, Uitterlinden, Andre G., Hofman, Albert, Duijn, Cornelia M., Cherkas, Lynn, Stubhaug, Audun, Nielsen, Christopher S., Männikö, Minna, Mihailov, Evelin, Milani, Lili, Esserlind, Ann‐Louise, Werge, Thomas, Børte, Sigrid, Cormand, Bru, Eising, Else, Griffiths, Lyn, Hamalainen, Eija, Kajanne, Risto, Launer, Lenore, Lehtimaki, Terho, Lessel, Davor, Macaya, Alfons, Posthuma, Danielle, Pozo‐Rosich, Patricia, Pressman, Alice, Sintas, Celia, Zhao, Huiying, Kaprio, Jaakko, Aromaa, Arpo J., Ikram, M. Arfan, Spector, Tim, Järvelin, Marjo‐Riitta, Metspalu, Andres, Kubisch, Christian, Ferrari, Michel D., Dichgans, Martin, Wessman, Maija, Maagdenberg, Arn M. J. M., Boomsma, Dorret I., Smith, George Davey, Neale, Benjamin M., Olesen, Jes, Chasman, Daniel I., Nyholt, Dale R., Palotie, Aarno, Maagdenberg, Arn M. J. M., Schiöth, Helgi Birgir

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