Jasmonate-Induced Defense Mechanisms in the Belowground Antagonistic Interaction Between Pythium arrhenomanes and Meloidogyne graminicola in Rice by Verbeek, Ruben E M, Van Buyten, Evelien, Alam, Md Zahangir, De Vleesschauwer, David, Van Bockhaven, Jonas, Asano, Takayuki, Kikuchi, Shoshi, Haeck, Ashley, Demeestere, Kristof, Gheysen, Godelieve, Höfte, Monica, Kyndt, Tina

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Superior triacylglycerol (TAG) accumulation in starchless mutants of Scenedesmus obliquus: (I) mutant generation and characterization by de Jaeger, Lenny, Verbeek, Ruben EM, Draaisma, René B, Martens, Dirk E, Springer, Jan, Eggink, Gerrit, Wijffels, René H

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Superior triacylglycerol mutant generation and characterization by de Jaeger, Lenny, Verbeek, Ruben EM, Draaisma, Renñ B, Martens, Dirk E, Springer, Jan, Eggink, Gerrit, Wijffels, Renñ H

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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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A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder by van der Zwaag, Bert, Staal, Wouter G., Hochstenbach, Ron, Poot, Martin, Spierenburg, Henk A., de Jonge, Maretha V., Verbeek, Nienke E., van 't Slot, Ruben, van Es, Michael A., Staal, Frank J., Freitag, Christine M., Buizer-Voskamp, Jacobine E., Nelen, Marcel R., van den Berg, Leonard H., van Amstel, Hans K. Ploos, van Engeland, Herman, Burbach, J. Peter H.

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Gene-network analysis identifies susceptibility genes related to glycobiology in autism by van der Zwaag, Bert, Franke, Lude, Poot, Martin, Hochstenbach, Ron, Spierenburg, Henk A, Vorstman, Jacob A S, van Daalen, Emma, de Jonge, Maretha V, Verbeek, Nienke E, Brilstra, Eva H, van 't Slot, Ruben, Ophoff, Roel A, van Es, Michael A, Blauw, Hylke M, Veldink, Jan H, Buizer-Voskamp, Jacobine E, Beemer, Frits A, van den Berg, Leonard H, Wijmenga, Cisca, van Amstel, Hans Kristian Ploos, van Engeland, Herman, Burbach, J Peter H, Staal, Wouter G

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Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patients by Kovel, Carolien G.F., Brilstra, Eva H., Kempen, Marjan J.A., Slot, Ruben, Nijman, Isaac J., Afawi, Zaid, De Jonghe, Peter, Djémié, Tania, Guerrini, Renzo, Hardies, Katia, Helbig, Ingo, Hendrickx, Rik, Kanaan, Moine, Kramer, Uri, Lehesjoki, Anna‐Elina E., Lemke, Johannes R., Marini, Carla, Mei, Davide, Møller, Rikke S., Pendziwiat, Manuela, Stamberger, Hannah, Suls, Arvid, Weckhuysen, Sarah, Koeleman, Bobby P.C., R, Balling, N, Barisic, S, Baulac, HS, Caglayan, DC, Craiu, C, Depienne, P, Gormley, H, Hjalgrim, D, Hoffman‐Zacharska, J, Jähn, KM, Klein, V, Komarek, E, LeGuern, H, Lerche, P, May, H, Muhle, D, Pal, A, Palotie, F, Rosenow, K, Selmer, JM, Serratosa, SM, Sisodiya, U, Stephani, K, Sterbova, P, Striano, T, Talvik, M, van Haelst, N, Verbeek, S, von Spiczak, YG, Weber

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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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A Co-segregatin Microduplication of Chromosome 15q11.2 Pinpoints Two Risk Genes for Autism Spectrum Disorder by ZWAAG, Bert Van Der, STAAL, Wouter G, FREITAG, Christine M, BUIZER-VOSKAMP, Jacobine E, NELEN, Marcel R, VAN DEN BERG, Leonard H, VAN AMSTEL, Hans K. Ploos, VAN ENGELAND, Herman, BURBACH, J. Peter H, HOCHSTENBACH, Ron, POOT, Martin, SPIERENBURG, Henk A, DE JONGE, Maretha V, VERBEEK, Nienke E, VAN 'T SLOT, Ruben, VAN ES, Michael A, STAAL, Frank J

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