A Major Upgrade of the H.E.S.S. Cherenkov Cameras

by 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

A NECTAr-based upgrade for the Cherenkov cameras of the H.E.S.S. 12-meter telescopes

by 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.
Published in Astroparticle physics

The upgrade of the H.E.S.S. cameras

by 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
Published in Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment

The upgrade of the H.E.S.S. cameras

by 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

A NECTAr-based upgrade for the Cherenkov cameras of the H.E.S.S. 12-meter telescopes

by 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

Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome

by 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
Published in European journal of human genetics : EJHG

Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability

by 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
Published in Human genetics

Bainbridge-Ropers syndrome caused by loss-of-function variants in ASXL3: a recognizable condition

by 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
Published in European journal of human genetics : EJHG

Variants in CPLX1 in two families with autosomal-recessive severe infantile myoclonic epilepsy and ID

by 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
Published in European journal of human genetics : EJHG

De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder

by 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.
Published in American journal of human genetics

De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum

by 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
Published in Human genetics

Genetic variants in components of the NALCN–UNC80–UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies)

by 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
Published in Human genetics