A Major Upgrade of the H.E.S.S. Cherenkov Cameras von Lypova, Iryna, Giavitto, Gianluca, Ashton, Terry, Balzer, Arnim, Berge, David, Brun, Francois, Chaminade, Thomas, Delagnes, Eric, Fontaine, Gerard, Füßling, Matthias, Giebels, Berrie, Glicenstein, Jean-Francois, Gräber, Tobias, Hinton, Jim, Jahnke, Albert, Klepser, Stefan, Kossatz, Marko, Kretzschmann, Axel, Lefranc, Valentin, Leich, Holger, Lüdecke, Hartmut, Manigot, Pascal, Marandon, Vincent, Moulin, Emmanuel, de Naurois, Mathieu, Nayman, Patrick, Ohm, Stefan, Penno, Marek, Ross, Duncan, Salek, David, Schade, Markus, Schwab, Thomas, Simoni, Rachel, Stegmann, Christian, Steppa, Constantin, Thornhill, Julian, Toussnel, Francois

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A NECTAr-based upgrade for the Cherenkov cameras of the H.E.S.S. 12-meter telescopes von Ashton, T., Backes, M., Balzer, A., Berge, D., Bolmont, J., Bonnefoy, S., Brun, F., Chaminade, T., Delagnes, E., Fontaine, G., Füßling, M., Giavitto, G., Giebels, B., Glicenstein, J.-F., Gräber, T., Hinton, J.A., Jahnke, A., Klepser, S., Kossatz, M., Kretzschmann, A., Lefranc, V., Leich, H., Lenain, J.-P., Lüdecke, H., Lypova, I., Manigot, P., Marandon, V., Moulin, E., Murach, T., de Naurois, M., Nayman, P., Ohm, S., Penno, M., Ross, D., Salek, D., Schade, M., Schwab, T., Shiningayamwe, K., Stegmann, C., Steppa, C., Tavernet, J.-P., Thornhill, J., Toussenel, F., Vincent, P.

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The upgrade of the H.E.S.S. cameras von Giavitto, Gianluca, Ashton, Terry, Balzer, Arnim, Berge, David, Brun, Francois, Chaminade, Thomas, Delagnes, Eric, Fontaine, Gerard, Füßling, Matthias, Giebels, Berrie, Glicenstein, Jean-Francois, Gräber, Tobias, Hinton, Jim, Jahnke, Albert, Klepser, Stefan, Kossatz, Marko, Kretzschmann, Axel, Lefranc, Valentin, Leich, Holger, Lüdecke, Hartmut, Lypova, Iryna, Manigot, Pascal, Marandon, Vincent, Moulin, Emmanuel, Naurois, Mathieu de, Nayman, Patrick, Ohm, Stefan, Penno, Marek, Ross, Duncan, Salek, David, Schade, Markus, Schwab, Thomas, Simoni, Rachel, Stegmann, Christian, Steppa, Constantin, Thornhill, Julian, Toussnel, Francois

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The upgrade of the H.E.S.S. cameras von Giavitto, Gianluca, Ashton, Terry, Balzer, Arnim, Berge, David, Brun, Francois, Chaminade, Thomas, Delagnes, Eric, Fontaine, Gerard, Füßling, Matthias, Giebels, Berrie, Glicenstein, Jean-Francois, Gräber, Tobias, Hinton, Jim, Jahnke, Albert, Klepser, Stefan, Kossatz, Marko, Kretzschmann, Axel, Lefranc, Valentin, Leich, Holger, Lüdecke, Hartmut, Lypova, Iryna, Manigot, Pascal, Marandon, Vincent, Moulin, Emmanuel, de Naurois, Mathieu, Nayman, Patrick, Ohm, Stefan, Penno, Marek, Ross, Duncan, Salek, David, Schade, Markus, Schwab, Thomas, Simoni, Rachel, Stegmann, Christian, Steppa, Constantin, Thornhill, Julian, Toussnel, Francois

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A NECTAr-based upgrade for the Cherenkov cameras of the H.E.S.S. 12-meter telescopes von Ashton, Terry, Backes, Michael, Balzer, Arnim, Berge, David, Bolmont, Julien, Bonnefoy, Simon, Brun, Francois, Chaminade, Thomas, Delagnes, Eric, Fontaine, Gerard, Füßling, Matthias, Giavitto, Gianluca, Giebels, Berrie, Jean-Francois Glicenstein, Gräber, Tobias, Hinton, Jim, Jahnke, Albert, Klepser, Stefan, Kossatz, Marko, Kretzschmann, Axel, Lefranc, Valentin, Leich, Holger, Lenain, Jean-Philippe, Lüdecke, Hartmut, Lypova, Iryna, Manigot, Pascal, Marandon, Vincent, Moulin, Emmanuel, Murach, Thomas, Mathieu de Naurois, Nayman, Patrick, Ohm, Stefan, Penno, Marek, Ross, Duncan, Salek, David, Schade, Markus, Schwab, Thomas, Shiningayamwe, Kleopas, Stegmann, Christian, Steppa, Constantin, Jean-Paul Tavernet, Thornhill, Julian, Toussnel, Francois, Vincent, Pascal

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A NECTAr-based upgrade for the Cherenkov cameras of the H.E.S.S. 12-meter telescopes von Ashton, Terry, Backes, Michael, Balzer, Arnim, Berge, David, Bolmont, Julien, Bonnefoy, Simon, Brun, Francois, Chaminade, Thomas, Delagnes, Eric, Fontaine, Gerard, Füssling, Matthias, Giavitto, Gianluca, Giebels, Berrie, Glicenstein, Jean-Francois, Gräber, Tobias, Hinton, Jim, Jahnke, Albert, Klepser, Stefan, Kossatz, Marko, Kretzschmann, Axel, Lefranc, Valentin, Leich, Holger, Lenain, Jean-Philippe, Lüdecke, Hartmut, Lypova, Iryna, Manigot, Pascal, Marandon, Vincent, Moulin, Emmanuel, Murach, Thomas, De Naurois, Mathieu, Nayman, Patrick, Ohm, Stefan, Penno, Marek, Ross, Duncan, Salek, David, Schade, Markus, Schwab, Thomas, Shiningayamwe, Kleopas, Stegmann, Christian, Steppa, Constantin, Tavernet, Jean-Paul, Thornhill, Julian, Toussnel, Francois, Vincent, Pascal

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Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome von Kuechler, Alma, Zink, Alexander M, Wieland, Thomas, Lüdecke, Hermann-Josef, Cremer, Kirsten, Salviati, Leonardo, Magini, Pamela, Najafi, Kimia, Zweier, Christiane, Czeschik, Johanna Christina, Aretz, Stefan, Endele, Sabine, Tamburrino, Federica, Pinato, Claudia, Clementi, Maurizio, Gundlach, Jasmin, Maylahn, Carina, Mazzanti, Laura, Wohlleber, Eva, Schwarzmayr, Thomas, Kariminejad, Roxana, Schlessinger, Avner, Wieczorek, Dagmar, Strom, Tim M, Novarino, Gaia, Engels, Hartmut

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Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability von Bramswig, Nuria C., Lüdecke, Hermann-Josef, Hamdan, Fadi F., Altmüller, Janine, Beleggia, Filippo, Elcioglu, Nursel H., Freyer, Catharine, Gerkes, Erica H., Demirkol, Yasemin Kendir, Knupp, Kelly G., Kuechler, Alma, Li, Yun, Lowenstein, Daniel H., Michaud, Jacques L., Park, Kristen, Stegmann, Alexander P.A., Veenstra-Knol, Hermine E., Wieland, Thomas, Wollnik, Bernd, Engels, Hartmut, Strom, Tim M., Kleefstra, Tjitske, Wieczorek, Dagmar

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De novo microdeletions and point mutations affecting SOX2 in three individuals with intellectual disability but without major eye malformations von Dennert, Nicola, Engels, Hartmut, Cremer, Kirsten, Becker, Jessica, Wohlleber, Eva, Albrecht, Beate, Ehret, Julia K., Lüdecke, Hermann‐Josef, Suri, Mohnish, Carignani, Giulia, Renieri, Alessandra, Kukuk, Guido M., Wieland, Thomas, Andrieux, Joris, Strom, Tim M., Wieczorek, Dagmar, Dieux‐Coëslier, Anne, Zink, Alexander M.

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Bainbridge-Ropers syndrome caused by loss-of-function variants in ASXL3: a recognizable condition von Kuechler, Alma, Czeschik, Johanna Christina, Graf, Elisabeth, Grasshoff, Ute, Hüffmeier, Ulrike, Busa, Tiffany, Beck-Woedl, Stefanie, Faivre, Laurence, Rivière, Jean-Baptiste, Bader, Ingrid, Koch, Johannes, Reis, André, Hehr, Ute, Rittinger, Olaf, Sperl, Wolfgang, Haack, Tobias B, Wieland, Thomas, Engels, Hartmut, Prokisch, Holger, Strom, Tim M, Lüdecke, Hermann-Josef, Wieczorek, Dagmar

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Variants in CPLX1 in two families with autosomal-recessive severe infantile myoclonic epilepsy and ID von Redler, Silke, Strom, Tim M, Wieland, Thomas, Cremer, Kirsten, Engels, Hartmut, Distelmaier, Felix, Schaper, Jörg, Küchler, Alma, Lemke, Johannes R, Jeschke, Stephanie, Schreyer, Nicole, Sticht, Heinrich, Koch, Margarete, Lüdecke, Hermann-Josef, Wieczorek, Dagmar

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De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder von Reijnders, Margot R.F., Miller, Kerry A., Alvi, Mohsan, Goos, Jacqueline A.C., Lees, Melissa M., de Burca, Anna, Henderson, Alex, Kraus, Alison, Mikat, Barbara, de Vries, Bert B.A., Isidor, Bertrand, Kerr, Bronwyn, Marcelis, Carlo, Schluth-Bolard, Caroline, Deshpande, Charu, Ruivenkamp, Claudia A.L., Wieczorek, Dagmar, Baralle, Diana, Blair, Edward M., Engels, Hartmut, Lüdecke, Hermann-Josef, Eason, Jacqueline, Santen, Gijs W.E., Clayton-Smith, Jill, Chandler, Kate, Tatton-Brown, Katrina, Payne, Katelyn, Helbig, Katherine, Radtke, Kelly, Nugent, Kimberly M., Cremer, Kirsten, Strom, Tim M., Bird, Lynne M., Sinnema, Margje, Bitner-Glindzicz, Maria, van Dooren, Marieke F., Alders, Marielle, Koopmans, Marije, Brick, Lauren, Kozenko, Mariya, Harline, Megan L., Klaassens, Merel, Steinraths, Michelle, Cooper, Nicola S., Edery, Patrick, Yap, Patrick, Terhal, Paulien A., van der Spek, Peter J., Lakeman, Phillis, Taylor, Rachel L., Littlejohn, Rebecca O., Pfundt, Rolph, Mercimek-Andrews, Saadet, Stegmann, Alexander P.A., Kant, Sarina G., McLean, Scott, Joss, Shelagh, Swagemakers, Sigrid M.A., Douzgou, Sofia, Wall, Steven A., Küry, Sébastien, Calpena, Eduardo, Koelling, Nils, McGowan, Simon J., Twigg, Stephen R.F., Mathijssen, Irene M.J., Nellaker, Christoffer, Brunner, Han G., Wilkie, Andrew O.M.

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A new face of Borjeson–Forssman–Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype von Zweier, Christiane, Kraus, Cornelia, Brueton, Louise, Cole, Trevor, Degenhardt, Franziska, Engels, Hartmut, Gillessen-Kaesbach, Gabriele, Graul-Neumann, Luitgard, Horn, Denise, Hoyer, Juliane, Just, Walter, Rauch, Anita, Reis, André, Wollnik, Bernd, Zeschnigk, Michael, Lüdecke, Hermann-Josef, Wieczorek, Dagmar

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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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Genetic variants in components of the NALCN–UNC80–UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies) von Bramswig, Nuria C., Bertoli-Avella, Aida M., Albrecht, Beate, Al Aqeel, Aida I., Alhashem, Amal, Al-Sannaa, Nouriya, Bah, Maissa, Bröhl, Katharina, Depienne, Christel, Dorison, Nathalie, Doummar, Diane, Ehmke, Nadja, Elbendary, Hasnaa M., Gorokhova, Svetlana, Héron, Delphine, Horn, Denise, James, Kiely, Keren, Boris, Kuechler, Alma, Ismail, Samira, Issa, Mahmoud Y., Marey, Isabelle, Mayer, Michèle, McEvoy-Venneri, Jennifer, Megarbane, Andre, Mignot, Cyril, Mohamed, Sarar, Nava, Caroline, Philip, Nicole, Ravix, Cecile, Rolfs, Arndt, Sadek, Abdelrahim Abdrabou, Segebrecht, Lara, Stanley, Valentina, Trautman, Camille, Valence, Stephanie, Villard, Laurent, Wieland, Thomas, Engels, Hartmut, Strom, Tim M., Zaki, Maha S., Gleeson, Joseph G., Lüdecke, Hermann-Josef, Bauer, Peter, Wieczorek, Dagmar

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Expanding the clinical spectrum of the 'HDAC8-phenotype' - implications for molecular diagnostics, counseling and risk prediction von Parenti, I., Gervasini, C., Pozojevic, J., Wendt, K.S., Watrin, E., Azzollini, J., Braunholz, D., Buiting, K., Cereda, A., Engels, H., Garavelli, L., Glazar, R., Graffmann, B., Larizza, L., Lüdecke, H.J., Mariani, M., Masciadri, M., Pié, J., Ramos, F.J., Russo, S., Selicorni, A., Stefanova, M., Strom, T.M., Werner, R., Wierzba, J., Zampino, G., Gillessen-Kaesbach, G., Wieczorek, D., Kaiser, F.J.

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De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder von Reijnders, Margot R.F, Miller, Kerry A, Alvi, Mohsan, Goos, Jacqueline A.C, Lees, Melissa M, de Burca, Anna, Henderson, Alex, Kraus, Alison, Mikat, Barbara, de Vries, Bert B.A, Isidor, Bertrand, Kerr, Bronwyn, Marcelis, Carlo, Schluth-Bolard, Caroline, Deshpande, Charu, Ruivenkamp, Claudia A.L, Wieczorek, Dagmar, Baralle, Diana, Blair, Edward M, Engels, Hartmut, Lüdecke, Hermann Josef, Eason, Jacqueline, Santen, Gijs W.E, Clayton-Smith, Jill, Chandler, Kate, Tatton-Brown, Katrina, Payne, Katelyn, Helbig, Katherine, Radtke, Kelly, Nugent, Kimberly M, Cremer, Kirsten, Strom, Tim M, Bird, Lynne M, Sinnema, Margje, Bitner-Glindzicz, Maria, van Dooren, Marieke F, Alders, Marielle, Koopmans, Marije, Brick, Lauren, Kozenko, Mariya, Harline, Megan L, Klaassens, Merel, Steinraths, Michelle, Cooper, Nicola S, Edery, Patrick, Yap, Patrick, Terhal, Paulien A, van der Spek, Peter J, Lakeman, Phillis, Taylor, Rachel L, The Deciphering Developmental Disorders Study

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A new face of Borjeson-Forssman-Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype von Zweier, Christiane, Kraus, Cornelia, Brueton, Louise, Cole, Trevor, Degenhardt, Franziska, Engels, Hartmut, Gillessen-Kaesbach, Gabriele, Graul-Neumann, Luitgard, Horn, Denise, Hoyer, Juliane, Just, Walter, Rauch, Anita, Reis, André, Wollnik, Bernd, Zeschnigk, Michael, Lüdecke, Hermann-Josef, Wieczorek, Dagmar

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Simulation results of the grid-serving multi-use of residential battery storage systems for prosumers von Wagner, Henrik, Lüdecke, Marcel, Scheunert, Alexandra, Wegkamp, Carsten, Engel, Bernd, Weyer, Hartmut

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A new face of Borjeson–Forssman–Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype von Zweier, Christiane

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