A matrix approach to detect temporal behavioral patterns at electric vehicle charging stations von Straka, Milan, Piatriková, Lucia, Peter van Bokhoven, Buzna, Ľuboš

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Network peak load reduction by home charge management of electric vehicles von Berende, Maarten, Refa, Nazir, van Bokhoven, Peter, Gardien, Lotte

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A matrix approach to detect temporal behavioral patterns at electric vehicle charging stations von Straka, Milan, Piatriková, Lucia, Bokhoven, Peter van, Buzna, Ľuboš

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Charge migration and charge transfer in molecular systems von Wörner, Hans Jakob, Arrell, Christopher A., Banerji, Natalie, Cannizzo, Andrea, Chergui, Majed, Das, Akshaya K., Hamm, Peter, Keller, Ursula, Kraus, Peter M., Liberatore, Elisa, Lopez-Tarifa, Pablo, Lucchini, Matteo, Meuwly, Markus, Milne, Chris, Moser, Jacques-E., Rothlisberger, Ursula, Smolentsev, Grigory, Teuscher, Joël, van Bokhoven, Jeroen A., Wenger, Oliver

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Restructuring of Palladium Nanoparticles during Oxidation by Molecular Oxygen von Usoltsev, Oleg, Stoian, Dragos, Skorynina, Alina, Kozyr, Elizaveta, Njoroge, Peter N., Pellegrini, Riccardo, Groppo, Elena, van Bokhoven, Jeroen A., Bugaev, Aram

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Cadherin-13 is a critical regulator of GABAergic modulation in human stem-cell-derived neuronal networks von Mossink, Britt, van Rhijn, Jon-Ruben, Wang, Shan, Linda, Katrin, Vitale, Maria R., Zöller, Johanna E. M., van Hugte, Eline J. H., Bak, Jitske, Verboven, Anouk H. A., Selten, Martijn, Negwer, Moritz, Latour, Brooke L., van der Werf, Ilse, Keller, Jason M., Klein Gunnewiek, Teun M., Schoenmaker, Chantal, Oudakker, Astrid, Anania, Alessia, Jansen, Sophie, Lesch, Klaus-Peter, Frega, Monica, van Bokhoven, Hans, Schubert, Dirk, Nadif Kasri, Nael

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Deciphering the Glycosylome of Dystroglycanopathies Using Haploid Screens for Lassa Virus Entry von Jae, Lucas T., Raaben, Matthijs, Riemersma, Moniek, van Beusekom, Ellen, Blomen, Vincent A., Velds, Arno, Kerkhoven, Ron. M., Carette, Jan E., Topaloglu, Haluk, Meinecke, Peter, Wessels, Marja W., Lefeber, Dirk J., Whelan, Sean P., van Bokhoven, Hans, Brummelkamp, Thijn R.

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MicroRNA-137 Controls AMPA-Receptor-Mediated Transmission and mGluR-Dependent LTD von Olde Loohuis, Nikkie F.M., Ba, Wei, Stoerchel, Peter H., Kos, Aron, Jager, Amanda, Schratt, Gerhard, Martens, Gerard J.M., van Bokhoven, Hans, Nadif Kasri, Nael, Aschrafi, Armaz

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Mutations in PIGU Impair the Function of the GPI Transamidase Complex, Causing Severe Intellectual Disability, Epilepsy, and Brain Anomalies von Knaus, Alexej, Kortüm, Fanny, Kleefstra, Tjitske, Stray-Pedersen, Asbjørg, Đukić, Dejan, Murakami, Yoshiko, Gerstner, Thorsten, van Bokhoven, Hans, Iqbal, Zafar, Horn, Denise, Kinoshita, Taroh, Hempel, Maja, Krawitz, Peter M.

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Perspective: Opportunities for ultrafast science at SwissFEL von Abela, Rafael, Beaud, Paul, van Bokhoven, Jeroen A., Chergui, Majed, Feurer, Thomas, Haase, Johannes, Ingold, Gerhard, Johnson, Steven L., Knopp, Gregor, Lemke, Henrik, Milne, Chris J., Pedrini, Bill, Radi, Peter, Schertler, Gebhard, Standfuss, Jörg, Staub, Urs, Patthey, Luc

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Size-Selective Reactivity of Subnanometer Ag4 and Ag16 Clusters on a TiO2 Surface von Chen, Po-Tuan, Tyo, Eric C, Hayashi, Michitoshi, Pellin, Michael J, Safonova, Olga, Nachtegaal, Maarten, van Bokhoven, Jeroen A, Vajda, Stefan, Zapol, Peter

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Patients’ readiness to receive psychosocial care during nurse-led routine diabetes consultations in primary care: A mixed methods study von van Dijk-de Vries, Anneke, van Bokhoven, Marloes A., de Jong, Sabine, Metsemakers, Job F.M., Verhaak, Peter F.M., van der Weijden, Trudy, van Eijk, Jacques Th. M.

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Experimental and theoretical investigation of the vibrational band structure of the 1 Πu5−1 Πg5 high-spin system of C2 von Bornhauser, P., Visser, B., Beck, M., Knopp, G., van Bokhoven, J. A., Marquardt, R., Radi, P. P.

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Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice von Vissers, Lisenka E L M, Cox, Timothy C, Maga, A Murat, Short, Kieran M, Wiradjaja, Fenny, Janssen, Irene M, Jehee, Fernanda, Bertola, Debora, Liu, Jia, Yagnik, Garima, Sekiguchi, Kiyotoshi, Kiyozumi, Daiji, van Bokhoven, Hans, Marcelis, Carlo, Cunningham, Michael L, Anderson, Peter J, Boyadjiev, Simeon A, Passos-Bueno, Maria Rita, Veltman, Joris A, Smyth, Ian, Buckley, Michael F, Roscioli, Tony

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Asymmetry within and around the human planum temporale is sexually dimorphic and influenced by genes involved in steroid hormone receptor activity von Guadalupe, Tulio, Zwiers, Marcel P., Wittfeld, Katharina, Teumer, Alexander, Vasquez, Alejandro Arias, Hoogman, Martine, Hagoort, Peter, Fernandez, Guillen, Buitelaar, Jan, van Bokhoven, Hans, Hegenscheid, Katrin, Völzke, Henry, Franke, Barbara, Fisher, Simon E., Grabe, Hans J., Francks, Clyde

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Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2 von Kornak, Uwe, Reynders, Ellen, Dimopoulou, Aikaterini, van Reeuwijk, Jeroen, Fischer, Bjoern, Rajab, Anna, Budde, Birgit, Nürnberg, Peter, Foulquier, Francois, Lefeber, Dirk, Urban, Zsolt, Gruenewald, Stephanie, Annaert, Wim, Brunner, Han G, van Bokhoven, Hans, Wevers, Ron, Morava, Eva, Matthijs, Gert, Van Maldergem, Lionel, Mundlos, Stefan

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De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum von Kuechler, Alma, Willemsen, Marjolein H., Albrecht, Beate, Bacino, Carlos A., Bartholomew, Dennis W., van Bokhoven, Hans, van den Boogaard, Marie Jose H., Bramswig, Nuria, Büttner, Christian, Cremer, Kirsten, Czeschik, Johanna Christina, Engels, Hartmut, van Gassen, Koen, Graf, Elisabeth, van Haelst, Mieke, He, Weimin, Hogue, Jacob S., Kempers, Marlies, Koolen, David, Monroe, Glen, de Munnik, Sonja, Pastore, Matthew, Reis, André, Reuter, Miriam S., Tegay, David H., Veltman, Joris, Visser, Gepke, van Hasselt, Peter, Smeets, Eric E. J., Vissers, Lisenka, Wieland, Thomas, Wissink, Willemijn, Yntema, Helger, Zink, Alexander Michael, Strom, Tim M., Lüdecke, Hermann-Josef, Kleefstra, Tjitske, Wieczorek, Dagmar

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Population Impact of Girls-Only Human Papillomavirus 16/18 Vaccination in The Netherlands: Cross-Protective and Second-Order Herd Effects von Hoes, Joske, Woestenberg, Petra J, Bogaards, Johannes A, King, Audrey J, de Melker, Hester E, Berkhof, Johannes, Hoebe, Christian J P A, van der Sande, Marianne A B, van Benthem, Birgit H B

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Reduced Euchromatin histone methyltransferase 1 causes developmental delay, hypotonia, and cranial abnormalities associated with increased bone gene expression in Kleefstra syndrom... von Balemans, Monique C.M., Ansar, Muhammad, Oudakker, Astrid R., van Caam, Arjan P.M., Bakker, Brenda, Vitters, Elly L., van der Kraan, Peter M., de Bruijn, Diederik R.H., Janssen, Sanne M., Kuipers, Arthur J., Huibers, Manon M.H., Maliepaard, Eliza M., Walboomers, X. Frank, Benevento, Marco, Nadif Kasri, Nael, Kleefstra, Tjitske, Zhou, Huiqing, Van der Zee, Catharina E.E.M., van Bokhoven, Hans

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Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus von Crow, Yanick J, Hayward, Bruce E, Parmar, Rekha, Robins, Peter, Leitch, Andrea, Ali, Manir, Black, Deborah N, van Bokhoven, Hans, Brunner, Han G, Hamel, Ben C, Corry, Peter C, Cowan, Frances M, Frints, Suzanne G, Klepper, Joerg, Livingston, John H, Lynch, Sally Ann, Massey, Roger F, Meritet, Jean François, Michaud, Jacques L, Ponsot, Gerard, Voit, Thomas, Lebon, Pierre, Bonthron, David T, Jackson, Andrew P, Barnes, Deborah E, Lindahl, Tomas

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