Improved conversion efficiencies of thin-film silicon tandem (MICROMORPH™) photovoltaic modules von Cashmore, J.S., Apolloni, M., Braga, A., Caglar, O., Cervetto, V., Fenner, Y., Goldbach-Aschemann, S., Goury, C., Hötzel, J.E., Iwahashi, T., Kalas, J., Kitamura, M., Klindworth, M., Kupich, M., Leu, G.-F., Lin, J., Lindic, M.-H., Losio, P.A., Mates, T., Matsunaga, D., Mereu, B., Nguyen, X.-V., Psimoulis, I., Ristau, S., Roschek, T., Salabas, A., Salabas, E.L., Sinicco, I.

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Diagnostics of a hexamethyldisiloxane/oxygen deposition plasma von Leu, G.F., Brockhaus, A., Engemann, J.

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MgO thin film deposition using TVA (thermoionic vacuum arc) von Ehrich, H., Musa, G., Popescu, A., Mustata, I., Salabas, A., Cretu, M., Leu, G.F.

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CHD2 variants are a risk factor for photosensitivity in epilepsy von Galizia, Elizabeth C, Myers, Candace T, Leu, Costin, de Kovel, Carolien G F, Afrikanova, Tatiana, Cordero-Maldonado, Maria Lorena, Martins, Teresa G, Jacmin, Maxime, Drury, Suzanne, Krishna Chinthapalli, V, Muhle, Hiltrud, Pendziwiat, Manuela, Sander, Thomas, Ruppert, Ann-Kathrin, Møller, Rikke S, Thiele, Holger, Krause, Roland, Schubert, Julian, Lehesjoki, Anna-Elina, Nürnberg, Peter, Lerche, Holger, Palotie, Aarno, Coppola, Antonietta, Striano, Salvatore, Gaudio, Luigi Del, Boustred, Christopher, Schneider, Amy L, Lench, Nicholas, Jocic-Jakubi, Bosanka, Covanis, Athanasios, Capovilla, Giuseppe, Veggiotti, Pierangelo, Piccioli, Marta, Parisi, Pasquale, Cantonetti, Laura, Sadleir, Lynette G, Mullen, Saul A, Berkovic, Samuel F, Stephani, Ulrich, Helbig, Ingo, Crawford, Alexander D, Esguerra, Camila V, Kasteleijn-Nolst Trenité, Dorothee G A, Koeleman, Bobby P C, Mefford, Heather C, Scheffer, Ingrid E, Sisodiya, Sanjay M

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Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance von Dibbens, Leanne M., Mullen, Saul, Helbig, Ingo, Mefford, Heather C., Bayly, Marta A., Bellows, Susannah, Leu, Costin, Trucks, Holger, Obermeier, Tanja, Wittig, Michael, Franke, Andre, Caglayan, Hande, Yapici, Zuhal, Sander, Thomas, Eichler, Evan E., Scheffer, Ingrid E., Mulley, John C., Berkovic, Samuel F.

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Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy von Lal, Dennis, Trucks, Holger, Møller, Rikke S., Hjalgrim, Helle, Koeleman, Bobby P. C., Kovel, Carolien G. F., Visscher, Frank, Weber, Yvonne G., Lerche, Holger, Becker, Felicitas, Schankin, Christoph J., Neubauer, Bernd A., Surges, Rainer, Kunz, Wolfram S., Zimprich, Fritz, Franke, Andre, Illig, Thomas, Ried, Janina S., Leu, Costin, Nürnberg, Peter, Sander, Thomas

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Whole-genome linkage scan for epilepsy-related photosensitivity: A mega-analysis von de Kovel, C.G.F, Pinto, D, Tauer, U, Lorenz, S, Muhle, H, Leu, C, Neubauer, B.A, Hempelmann, A, Callenbach, P.M.C, Scheffer, I.E, Berkovic, S.F, Rudolf, G, Striano, P, Siren, A, Baykan, B, Sander, T, Lindhout, D, Trenité, D.G. Kasteleijn-Nolst, Stephani, U, Koeleman, B.P.C

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