Preexisting Poliovirus-Specific IgA in the Circulation Correlates with Protection against Virus Excretion in the Elderly by Buisman, Anne-Marie, Abbink, Frithjofna, Schepp, Rutger M., Sonsma, Jan A. J., Herremans, Tineke, Kimman, Tjeerd G.

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Pathogenesis of poliovirus infection in PVRTg mice: poliovirus replicates in peritoneal macrophages by Buisman, A. M, Sonsma, J. A. J, van Wijk, M. G. S, Vermeulen, J. P, Roholl, P. J, Kimman, T. G

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Mucosal and Systemic Immunity against Poliovirus in Mice Transgenic for the Poliovirus Receptor: The Poliovirus Receptor Is Necessary for a Virus-Specific Mucosal IgA Response by Buisman, A. M., Sonsma, J. A. J., Kimman, T. G., Koopmans, M. P. G.

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Mucosal and systemic immunity against poliovirus in mice transgenic for the poliovirus receptor: The poliovirus receptor is necessary for a virus-specific mucosal by Buisman, A M, Sonsma, J A J, Kimman, T G, Koopmans, M P G

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Mosaicism of de novo pathogenic SCN1A variants in epilepsy is a frequent phenomenon that correlates with variable phenotypes by de Lange, Iris M., Koudijs, Marco J., Slot, Ruben, Gunning, Boudewijn, Sonsma, Anja C. M., van Gemert, Lisette J. J. M., Mulder, Flip, Carbo, Ellen C., van Kempen, Marjan J. A., Verbeek, Nienke E., Nijman, Isaac J., Ernst, Robert F., Savelberg, Sanne M. C., Knoers, Nine V. A. M., Brilstra, Eva H., Koeleman, Bobby P. C.

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Genetic Diversity in the Major Capsid L1 Protein of HPV-16 and HPV-18 in the Netherlands by King, Audrey J, Sonsma, Jan A, Vriend, Henrike J, van der Sande, Marianne A B, Feltkamp, Mariet C, Boot, Hein J, Koopmans, Marion P G

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Modifier genes in SCN1A‐related epilepsy syndromes by de Lange, Iris M., Mulder, Flip, Slot, Ruben, Sonsma, Anja C. M., Kempen, Marjan J. A., Nijman, Isaac J., Ernst, Robert F., Knoers, Nine V. A. M., Brilstra, Eva H., Koeleman, Bobby P. C.

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Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies by Lal, Dennis, Ruppert, Ann-Kathrin, Trucks, Holger, Schulz, Herbert, de Kovel, Carolien G, Kasteleijn-Nolst Trenité, Dorothée, Sonsma, Anja C M, Koeleman, Bobby P, Lindhout, Dick, Weber, Yvonne G, Lerche, Holger, Kapser, Claudia, Schankin, Christoph J, Kunz, Wolfram S, Surges, Rainer, Elger, Christian E, Gaus, Verena, Schmitz, Bettina, Helbig, Ingo, Muhle, Hiltrud, Stephani, Ulrich, Klein, Karl M, Rosenow, Felix, Neubauer, Bernd A, Reinthaler, Eva M, Zimprich, Fritz, Feucht, Martha, Møller, Rikke S, Hjalgrim, Helle, De Jonghe, Peter, Suls, Arvid, Lieb, Wolfgang, Franke, Andre, Strauch, Konstantin, Gieger, Christian, Schurmann, Claudia, Schminke, Ulf, Nürnberg, Peter, Sander, Thomas

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Correction: Genetic Diversity in the Major Capsid L1 Protein of HPV-16 and HPV-18 in the Netherlands by King, Audrey J, Sonsma, Jan A, Vriend, Henrike J, van der Sande, Marianne A B, Feltkamp, Mariet C, Boot, Hein J, Koopmans, Marion P G

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Influence of common SCN1A promoter variants on the severity of SCN1A‐related phenotypes by Lange, Iris M., Weuring, Wout, ‘t Slot, Ruben, Gunning, Boudewijn, Sonsma, Anja C. M., McCormack, Mark, Kovel, Carolien, Gemert, Lisette J. J. M., Mulder, Flip, Kempen, Marjan J. A., Knoers, Nine V. A. M., Brilstra, Eva H., Koeleman, Bobby P. C.

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Clinical and genetic analysis of a family with two rare reflex epilepsies by Kasteleijn-Nolst Trenité, Dorothée G.A, Volkers, Linda, Strengman, Eric, Schippers, Herman M, Perquin, Willem, de Haan, Gerrit-Jan, Gkountidi, Anastasia O, Slot, Ruben van’t, van de Graaf, Stan F, Jocic-Jakubi, Bosanka, Capovilla, Giuseppe, Covanis, Athanasios, Parisi, Pasquale, Veggiotti, Pierangelo, Brinciotti, Mario, Incorpora, Gemma, Piccioli, Marta, Cantonetti, Laura, Berkovic, Samuel F, Scheffer, Ingrid E, Brilstra, Eva H, Sonsma, Anja C.M, Bader, Adri J, de Kovel, Carolien G.F, Koeleman, Bobby P.C

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Carbamazepine‐ and oxcarbazepine‐induced hyponatremia in people with epilepsy by Berghuis, Bianca, Palen, Job, Haan, Gerrit‐Jan, Lindhout, Dick, Koeleman, Bobby P. C., Sander, Josemir W., Møller, Rikke S., Nikanorova, Marina, Ingason, Andrés, Depondt, Chantal, Johnson, Michael R, Langley, Sarah R., Klein, Karl Martin, McCormack, Mark, Delanty, Norman, Cavalleri, Gianpiero L., Zijl, Janic, Muhle, Hiltrud, Borghei, Mojgansadat, Donatello, Simona, Willis, Joseph, Leu, Costin, Heggeli, Kristin, Avbersek, Andreja, Sisodiya, Sanjay M., Gamberdella, Antonio, Weckhuysen, Sarah, Kunz, Wolfram S., Striano, Pasquale, Zara, Federico, Brodie, Martin J., Stefánsson, Kári, Marson, Anthony G, Jorgensen, Andrea, Auce, Pauls, Francis, Ben, Srivastava, Prashant, Sills, Graeme J., Primec, Zvonka Rener, Krause, Roland, Wolking, Stefan, Weber, Yvonne, Rau, Sarah, Hengsbach, Christian, Lerche, Holger, Sonsma, Anja, Krenn, Martin, Zimprich, Fritz, Pataraia, Ekaterina

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A genome‐wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine by Berghuis, Bianca, Stapleton, Caragh, Sonsma, Anja C. M., Hulst, Janic, Haan, Gerrit‐Jan, Lindhout, Dick, Demurtas, Rita, Krause, Roland, Depondt, Chantal, Kunz, Wolfram S., Zara, Federico, Striano, Pasquale, Craig, John, Auce, Pauls, Marson, Anthony G., Stefansson, Hreinn, O'Brien, Terence J., Johnson, Michael R., Sills, Graeme J., Wolking, Stefan, Lerche, Holger, Sisodiya, Sanjay M., Sander, Josemir W., Cavalleri, Gianpiero L., Koeleman, Bobby P. C., McCormack, Mark, Avbersek, Andreja, Leu, Costin, Heggeli, Kristin, Willis, Joseph, Speed, Douglas, Sargsyan, Narek, Chinthapalli, Krishna, Borghei, Mojgansadat, Coppola, Antonietta, Gambardella, Antonio, Becker, Felicitas, Rau, Sarah, Hengsbach, Christian, Weber, Yvonne G., Delanty, Norman, Campbell, Ellen, Gudmundsson, Lárus J., Ingason, Andres, Stefánsson, Kári, Schneider, Reinhard, Balling, Rudi, Francis, Ben, Jorgensen, Andrea, Morris, Andrew, Langley, Sarah, Srivastava, Prashant, Brodie, Martin, Todaro, Marian, Petrovski, Slave, Hutton, Jane, Zimprich, Fritz, Krenn, Martin, Muhle, Hiltrud, Martin Klein, Karl, Moller, Rikke, Nikanorova, Marina, Weckhuysen, Sarah, Rener‐Primec, Zvonka

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Association of ultra‐rare coding variants with genetic generalized epilepsy: A case–control whole exome sequencing study by Stanley, Kate E., Bobbili, Dheeraj R., Dhindsa, Ryan S., May, Patrick, Alldredge, Brian K., Allen, Andrew S., Altmüller, Janine, Amrom, Dina, Andermann, Eva, Auce, Pauls, Avbersek, Andreja, Bautista, Jocelyn F., Becker, Felicitas, Bellows, Susannah T., Berghuis, Bianca, Bluvstein, Judith, Boro, Alex, Burgess, Rosemary, Caglayan, Hande, Cascino, Gregory D., Chung, Seo‐Kyung, Cieuta‐Walti, Cécile, Consalvo, Damian, Cossette, Patrick, Crumrine, Patricia, Delanty, Norman, Depondt, Chantal, Desbiens, Richard, Dlugos, Dennis, Epstein, Michael P., Everett, Kate, Fountain, Nathan B., Francis, Ben, French, Jacqueline, Friedman, Daniel, Geller, Eric B., Girard, Simon, Glauser, Tracy, Glynn, Simon, Gravel, Micheline, Haas, Kevin, Haut, Sheryl R., Heinzen, Erin L., Helbig, Ingo, Hildebrand, Michael S., Jorgensen, Andrea, Joshi, Sucheta, Kirsch, Heidi E., Knowlton, Robert C., Koeleman, Bobby P. C., Kossoff, Eric H., Krause, Roland, Kunz, Wolfram S., Langley, Sarah R., LeGuern, Eric, Lerche, Holger, Leu, Costin, Lortie, Anne, Marson, Anthony G., Mebane, Caroline, Mefford, Heather C., Meloche, Caroline, Motika, Paul V., Muhle, Hiltrud, Nabbout, Rima, Nguyen, Dang K., Nikanorova, Marina, Novotny, Edward J., Ottman, Ruth, O’Brien, Terence J., Paolicchi, Juliann M., Parent, Jack M., Peter, Sarah, Petrou, Steven, Pickrell, William O., Poduri, Annapurna, Radtke, Rodney A., Rees, Mark I., Regan, Brigid M., Sadleir, Lynette G., Sander, Josemir W., Sander, Thomas, Scheffer, Ingrid E., Singh, Rani K., Sirven, Joseph, Sisodiya, Sanjay M., Smith, Michael C., Sonsma, Anja C. M., Sullivan, Joseph, Thio, Liu Lin, Thomas, Rhys H., Venkat, Anu, Von Allmen, Gretchen K., Wang, Quanli, Weber, Yvonne G., Weckhuysen, Sarah, Widdess‐Walsh, Peter, Winawer, Melodie R., Wolking, Stefan, Zimprich, Fritz

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Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillations by Smith, Alexander W., Carpay, Johannes A., Devinsky, Orrin, Braun, Kees P. J., Smit, Dirk J. A., Avbersek, Andreja, Becker, Albert J., Berkovic, Samuel F., Boysen, Katja E., Campbell, Ellen, Cascino, Gregory D., Catarino, Claudia B., Chinthapalli, Krishna, Coffey, Alison J., Coppola, Antonietta, Cossette, Patrick, De Jonghe, Peter, Dlugos, Dennis J., Feucht, Martha, Freytag, Saskia, Geller, Eric B., Guo, Youling, Hakonarson, Hakon, Haut, Sheryl, Heinzen, Erin L., Hengsbach, Christian, Johnson, Michael R., Kälviäinen, Reetta, Kirsch, Heidi E., Lau, Yu‐Lung, Lehesjoki, Anna‐Elina, Lerche, Holger, Lieb, Wolfgang, Malovini, Alberto, McCormack, Mark, Molloy, Anne M., Rau, Sarah, Schachter, Steven C., Vari, Maria S., Weber, Yvonne G., Weisenberg, Judith, Wolff, Markus, Yang, Wanling, Zara, Federico, Howrigan, Daniel P., Cerrato, Felecia, Gabriel, Stacey B., Daly, Mark J., Neale, Benjamin M., Lowenstein, Daniel H., Cossette, Patrick, Cotsapas, Chris, Petrovski, Slavé, Sisodiya, Sanjay M., Freyer, Catharine, McKenna, Kevin, Bennett, Caitlin A., Burgess, Rosemary, O'Brien, Terence J., Stamberger, Hannah, Krestel, Heinz, Gallati, Sabina, Papacostas, Savvas S., Tanteles, George A., Klein, Karl Martin, Rademacher, Michael, Afawi, Zaid, Korczyn, Amos D., Kanaan, Moien, Lemke, Johannes R., Wolking, Stefan, Schulze‐Bonhage, Andreas, Schubert‐Bast, Susanne, Korinthenberg, Rudolf, Dennig, Dieter, Madeleyn, Rene, Kälviäinen, Reetta, Linnankivi, Tarja, Rees, Mark I., Schneider, Natascha, Sills, Graeme J., Shukralla, Arif, McCormack, Mark, Canafoglia, Laura, Franceschetti, Silvana, Iacomino, Michele, Stella Vari, Maria, Salpietro, Vincenzo, Labate, Angelo, Manna, Lorella, Parrini, Elena, Inoue, Yushi, Topaloglu, Pınar, Yücesan, Emrah, Poduri, Annapurna, Buono, Russell J., Sperling, Michael R., Lo, Warren, Hegde, Manu, Helbig, Katherine L.

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Corrigendum to “Clinical and genetic analysis of a family with two rare reflex epilepsies” [Seizure – Eur. J. Epilepsy 29 (2015) 90–96] by Trenité, Dorothée G.A. Kasteleijn-Nolst, Volkers, Linda, Strengman, Eric, Schippers, Herman M, Perquin, Willem, de Haan, Gerrit-Jan, Gkountidi, Anastasia O, van’t Slot, Ruben, van de Graaf, Stan F, Jocic-Jakubi, Bosanka, Capovilla, Giuseppe, Covanis, Athanasios, Parisi, Pasquale, Veggiotti, Pierangelo, Brinciotti, Mario, Incorpora, Gemma, Piccioli, Marta, Cantonetti, Laura, Berkovic, Samuel F, Scheffer, Ingrid E, Brilstra, Eva H, Sonsma, Anja C.M, Bader, Adri J, de Kovel, Carolien G.F, Koeleman, Bobby P.C

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Mosaicism of de novo pathogenic SCN 1A variants in epilepsy is a frequent phenomenon that correlates with variable phenotypes by de Lange, Iris M., Koudijs, Marco J., van 't Slot, Ruben, Gunning, Boudewijn, Sonsma, Anja C. M., van Gemert, Lisette J. J. M., Mulder, Flip, Carbo, Ellen C., van Kempen, Marjan J. A., Verbeek, Nienke E., Nijman, Isaac J., Ernst, Robert F., Savelberg, Sanne M. C., Knoers, Nine V. A. M., Brilstra, Eva H., Koeleman, Bobby P. C.

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P.046 Serological micro-array for simultaneous detection of antibodies to measles, mumps and rubella viruses by Reimerink, J, Godeke, G.J, van Binnendijk, R.S, Sonsma, J, Koopmans, M.P.G

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Burden Analysis of Rare Microdeletions Suggests a Strong Impact of Neurodevelopmental Genes in Genetic Generalised Epilepsies: e1005226 by Lal, Dennis, Ruppert, Ann-Kathrin, Trucks, Holger, Schulz, Herbert, Kovel, Carolien Gde, Trenité, Dorothée Kasteleijn-Nolst, Sonsma, Anja CM, Koeleman, Bobby P, Lindhout, Dick, Weber, Yvonne G, Lerche, Holger, Kapser, Claudia, Schankin, Christoph J, Kunz, Wolfram S, Surges, Rainer, Elger, Christian E, Gaus, Verena, Schmitz, Bettina, Helbig, Ingo, Muhle, Hiltrud, Stephani, Ulrich, Klein, Karl M, Rosenow, Felix, Neubauer, Bernd A, Reinthaler, Eva M, Zimprich, Fritz, Feucht, Martha, Møller, Rikke S, Hjalgrim, Helle, Jonghe, Peter De, Suls, Arvid, Lieb, Wolfgang, Franke, Andre, Strauch, Konstantin, Gieger, Christian, Schurmann, Claudia, Schminke, Ulf, Nürnberg, Peter, Sander, Thomas, Consortium, EPICURE

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Serological micro-array for simultaneous detection of antibodies to measles, mumps and rubella viruses by Reimerink, J, Godeke, G J, van Binnendijk, RS, Sonsma, J, Koopmans, MPG

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