Measurement of optical to electrical and electrical to optical delays with ps-level uncertainty by Peek, H Z, Pinkert, T J, Jansweijer, P P M, Koelemeij, J C J

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White Rabbit: Sub-nanosecond timing over Ethernet by Jansweijer, P.P.M., Peek, H.Z., de Wolf, E.

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ATLAS Muon Drift Tube Electronics by Arai, Y, Ball, B, Beretta, M, Boterenbrood, H, Brandenburg, G W, Ceradini, F, Chapman, J W, Dai, T, Ferretti, C, Fries, T, Gregory, J, Costa, J Guimarães da, Harder, S, Hazen, E, Huth, J, Jansweijer, P P M, Kirsch, L E, König, A C, Lanza, A, Mikenberg, G, Oliver, J, Posch, C, Richter, R, Riegler, W, Spiriti, E, Taylor, F E, Vermeulen, J C, Wadsworth, B, Wijnen, T A M

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Measuring propagation delay over a coded serial communication channel using FPGAs by Jansweijer, P.P.M., Peek, H.Z.

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Using VDSL2 over copper in the vertical string by Heine, E., Hogenbirk, J., Jansweijer, P.P.M., Peek, H.Z.

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Measurement of optical to electrical and electrical to optical delays with ps-level uncertainty by Peek, H Z, Pinkert, T J, Jansweijer, P P M, Koelemeij, J C J

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First electrical White Rabbit absolute calibration inter-comparison by Jansweijer, P P M, Boukadida, N A D, Hanhijärvi, K, Wallin, A, Eglin, B, E Laier English

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Letter of intent for KM3NeT 2.0 by Adrián-Martínez, S, Aharonian, F, Aiello, S, Albert, A, Ameli, F, Anassontzis, E, Andre, M, Anton, G, Ardid, M, Avgitas, T, Barbarino, G, Barbarito, E, Belhorma, B, Belias, A, Bertin, V, Beurthey, S, Biagi, S, Biagioni, A, Bormuth, R, Bouhadef, B, Boutonnet, C, Bozza, C, Bruijn, R, Cecchini, S, Celli, S, Champion, C, Classen, L, Cocimano, R, Coelho, J A B, Colonges, S, Creusot, A, Cuttone, G, De Bonis, G, De Rosa, G, Di Palma, I, Dornic, D, Drakopoulou, E, Drury, L, Eberl, T, Eichie, S, Khayati, N El, Elsaesser, D, Fassi, F, Fermani, P, Filippidis, C, Frascadore, G, Gebyehu, M, Gracia, R, Graf, K, Grella, G, Habel, R, Hallmann, S, Haren, H van, Harissopulos, S, Heijboer, A, Heine, E, Henry, S, Hugon, C M F, Jansweijer, P, Jongen, M, Jong, M de, Kappes, A, Katz, U F, Alvarez, C D Llorens, Presti, D Lo, Lotze, M, Maccioni, E, Martínez-Mora, J A, Morganti, M, Moussa, A, Musumeci, M, Nicolau, C A, Olcina, I, Papaikonomou, A, P v la, G E, Perrina, C, Piattelli, P, Popa, V, Pratolongo, F, Quinn, L, Racca, C, Razis, P, Resvanis, L, Santangelo, A, Santonocito, D, Sciacca, V, Sedita, M, Sgura, I, Siotis, I, Spisso, B, Stavropoulos, G, Steijger, J, Tézier, D, Theraube, S, Timmer, P, Tzamariudaki, E, Elewyck, V Van, Vivolo, D, Volkert, M, Wiggers, L

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Truncating titin mutations are associated with a mild and treatable form of dilated cardiomyopathy by Jansweijer, Joeri A., Nieuwhof, Karin, Russo, Francesco, Hoorntje, Edgar T., Jongbloed, Jan D.H., Lekanne Deprez, Ronald H., Postma, Alex V., Bronk, Marieke, van Rijsingen, Ingrid A.W., de Haij, Simone, Biagini, Elena, van Haelst, Paul L., van Wijngaarden, Jan, van den Berg, Maarten P., Wilde, Arthur A.M., Mannens, Marcel M.A.M., de Boer, Rudolf A., van Spaendonck‐Zwarts, Karin Y., van Tintelen, J. Peter, Pinto, Yigal M.

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Meier-Gorlin syndrome genotype-phenotype studies: 35 individuals with pre-replication complex gene mutations and 10 without molecular diagnosis by DE MUNNIK, Sonja A, BICKNELL, Louise S, HAGEN, Johanna M.van, HENNEKAM, Raoul C, JANSWEIJER, Maaike Ce, JOHNSON, Diana, KANT, Sarina G, OPITZ, John M, RADHA RAMADEVI, A, REARDON, Willie, ROSS, Alison, SARDA, Pierre, AFTIMOS, Salim, SCHRANDER-STUMPEL, Constance Trm, SCHOOTS, Jeroen, KAREN TEMPLE, I, TERHAL, Paulien A, TOUTAIN, Annick, WISE, Carol A, WRIGHT, Michael, SKIDMORE, David L, ESAMUELS, Mark, HHOEFSLOOT, Lies, AL-AAMA, Jumana Y, VAMKNOERS, Nine, BRUNNER, Han G, JACKSON, Andrew P, BONGERS, Ernie Mhf, BEVER, Yolande Van, BOBER, Michael B, CLAYTON-SMITH, Jill, EDREES, Alaa Y, FEINGOLD, Murray, FRYER, Alan

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Contribution of CYLN2 and GTF2IRD1 to neurological and cognitive symptoms in Williams Syndrome by van Hagen, J.M, van der Geest, J.N, van der Giessen, R.S, Lagers-van Haselen, G.C, Eussen, H.J.F.M.M, Gille, J.J.P, Govaerts, L.C.P, Wouters, C.H, de Coo, I.F.M, Hoogenraad, C.C, Koekkoek, S.K.E, Frens, M.A, van Camp, N, van der Linden, A, Jansweijer, M.C.E, Thorgeirsson, S.S, De Zeeuw, C.I

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Implications of LHCb measurements and future prospects by Buras, A. J., Girrbach, J., Kagan, A., Nir, Y., Paradisi, P., Silvestrini, L., Virto, J., Abellan Beteta, C., Amhis, Y., Anelli, M., Artamonov, A., Beigbeder-Beau, C., Bencivenni, G., Bifani, S., Bocci, V., Boer Rookhuizen, H., Borgia, A., Brook, N. H., Cachemiche, J.-P., Chanal, H., Ciba, K., Cogan, J., De Miranda, J. M., Di Canto, A., Domke, M., Drancourt, C., Dupertuis, F., van Eijk, D., Eklund, L., Färber, C., Fuchs, H., Gandelman, M., Gotti, C., Grabalosa Gándara, M., Graciani Diaz, R., Greening, E., Harnew, N., Harrison, P. F., Hussain, N., Johnson, D., Karavichev, O., Kravchuk, L., Kristic, R., Krocker, G., Laptev, S., Maciuc, F., Mancinelli, G., Marconi, U., Mathe, Z., McNulty, R., Minard, M.-N., Morawski, P., Nguyen, T. D., Oblakowska-Mucha, A., Okhrimenko, O., van Overbeek, M., Patrick, G. N., Petridis, K., Pietrzyk, B., Polycarpo, E., Popov, D., Potterat, C., Pugatch, V., Puig Navarro, A., Reid, M. M., Richards, A., Rives Molina, V., Sabatino, G., Sanmartin Sedes, B., Schaack, P., Schiller, M., Schindler, H., Schlupp, M., Schmelling, M., Schmidt, B., Schopper, A., Schune, M.-H., Shcheglov, Y., Storaci, B., Szumlak, T., Teodorescu, E., van Tilburg, J., Tournefier, E., Tuning, N., Ubeda Garcia, M., Velthuis, J. J., Veltri, M., Vink, W., Vorobyev, A., Voss, H., Wandernoth, S., Wang, J., Watson, N. K., Wenerke, P., Witek, M., Wright, S., Xue, T., Yuan, X., Zhang, F., Zverev, E.

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Meier–Gorlin syndrome: Growth and secondary sexual development of a microcephalic primordial dwarfism disorder by de Munnik, Sonja A., Otten, Barto J., Schoots, Jeroen, Bicknell, Louise S., Aftimos, Salim, Al‐Aama, Jumana Y., van Bever, Yolande, Bober, Michael B., Borm, George F., Clayton‐Smith, Jill, Deal, Cheri L., Edrees, Alaa Y., Feingold, Murray, Fryer, Alan, van Hagen, Johanna M., Hennekam, Raoul C., Jansweijer, Maaike C.E., Johnson, Diana, Kant, Sarina G., Opitz, John M., Ramadevi, A. Radha, Reardon, Willie, Ross, Alison, Sarda, Pierre, Schrander‐Stumpel, Constance T.R.M., Sluiter, A. Erik, Temple, I. Karen, Terhal, Paulien A., Toutain, Annick, Wise, Carol A., Wright, Michael, Skidmore, David L., Samuels, Mark E., Hoefsloot, Lies H., Knoers, Nine V.A.M., Brunner, Han G., Jackson, Andrew P., Bongers, Ernie M.H.F.

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ETpathfinder: a cryogenic testbed for interferometric gravitational-wave detectors by Utina, A, Amato, A, Arends, J, Arina, C, de Baar, M, Baars, M, Baer, P, Beaumont, W, Bertolini, A, van Beuzekom, M, Biersteker, S, Binetti, A, ter Brake, H J M, Bruno, G, Bryant, J, Bulten, H J, Busch, L, Cebeci, P, Collette, C, Cooper, S, Cornelissen, R, Cuijpers, P, van Dael, M, Danilishin, S, Diksha, D, van Doesburg, S, Doets, M, Elsinga, R, Erends, V, van Erps, J, Freise, A, Frenaij, H, Garcia, R, Grohmann, S, Van Haevermaet, H, Heijnen, S, van Heijningen, J V, Hennes, E, Hennig, J-S, Hennig, M, Hertog, T, Hild, S, Hoft, G, Hopman, M, Iandolo, G A, Ietswaard, C, Jamshidi, R, Jansweijer, P, Jones, A, Jones, P, Knust, N, Koekoek, G, Koroveshi, X, Kraan, M, van de Kraats, M, Kranzhoff, S L, Kuijer, P, Lam, K, Letendre, N, Li, P, Limburg, R, Linde, F, Locquet, J-P, Lueck, H, Martínez, M, Masserot, A, Meylahn, F, Molenaar, M, Mow-Lowry, C, Mundet, J, Munneke, B, van Nieuwland, L, Pacaud, E, Petit, S, Van Ranst, Z, Raskin, G, Recaman, P M, Rolland, L, de Roo, L, Roose, E, Rosier, J C, Ryckbosch, D, Schouteden, K, Sevrin, A, Sider, A, Singha, A, Spagnuolo, V, Steinlechner, J, Steinlechner, S, Swinkels, B, Szilasi, N, Tacca, M, Vecchio, A, Verkooijen, H, Vermeer, C H, Vervaeke, M, Visser, G, Werneke, P, Westhofen, C, Xhahi, A

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Variable phenotypes associated with 10q23 microdeletions involving the PTEN and BMPR1A genes by Menko, FH, Kneepkens, CMF, De Leeuw, N, Peeters, EAJ, Van Maldergem, L, Kamsteeg, EJ, Davidson, R, Rozendaal, L, Lasham, CA, Peeters-Scholte, CMP, Jansweijer, MC, Hilhorst-Hofstee, Y, Gille, JJP, Heins, YM, Nieuwint, AWM, Sistermans, EA

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The prototype detection unit of the KM3NeT detector: KM3NeT Collaboration by Adrián-Martínez, S., Ageron, M., Anghinolfi, M., Anvar, S., Baret, B., Belias, A., Berbee, E., Billault, M., Bouché, V., Bozza, C., Calamai, M., Capone, A., Caramete, L., Cecchini, S., Cereseto, R., Château, F., Chiarusi, T., Christopoulou, B., Cocimano, R., Colonges, S., Cosquer, A., Costa, M., Creusot, A., Cuttone, G., D’Amato, C., D’Amico, A., De Rosa, G., Deniskina, N., Distefano, C., Di Capua, F., Drouhin, D., Eberl, T., Elsaesser, D., Fusco, L. A., Gal, T., Galatà, S., Giordano, V., Gracia Ruiz, R., Grella, G., Grmek, A., van Haren, H., Heine, E., Henry, S., Herold, B., Hevinga, M. A., Hofestädt, J., Hößl, J., Jansweijer, P., de Jong, M., Kadler, M., Kappos, E., Kouchner, A., Kulikovskiy, V., Lahmann, R., Le Provost, H., Lenis, D., Löhner, H., Loucatos, S., Mariş, O., Martini, A., Morganti, M., Musico, P., Nicolau, C. A., Orlando, A., Papaleo, R., Peek, H., Pellegrino, C., Pellegriti, M. G., Piattelli, P., Pikounis, K., Popa, V., Pühlhofer, G., Raffaelli, F., Rapidis, P. A., Real, D., Resvanis, L., Saldaña, M., Sapienza, P., Sedita, M., Seitz, T., Simeone, F., Spurio, M., Steijger, J., Stolarczyk, T., Stransky, D., Taiuti, M., Thompson, L. F., Trovato, A., Tselengidou, M., Tsirigotis, A., Tzamarias, S., Tzamariudaki, E., Van Elewyck, V., Vermeulen, J., Vernin, P., Vicini, P., Viola, S., Vivolo, D., Zonca, E., Zornoza, J. D.

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European Cardiomyopathy Pilot Registry: EURObservational Research Programme of the European Society of Cardiology by Elliott, Perry, Charron, Philippe, Blanes, Juan Ramon Gimeno, Tavazzi, Luigi, Tendera, Michal, Konté, Marème, Laroche, Cécile, Maggioni, Aldo P

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Heritability in genetic heart disease: the role of genetic background by Jansweijer, Joeri A, van Spaendonck-Zwarts, Karin Y, Tanck, Michael W T, van Tintelen, J Peter, Christiaans, Imke, van der Smagt, Jasper J, Vermeer, Alexa M C, Bos, J Martijn, Moss, Arthur J, Swan, Heikki, Priori, Sylvia G, Rydberg, Annika, Tfelt-Hansen, Jacob, Ackerman, Michael J, Olivotto, Iacopo, Charron, Philippe, Gimeno, Juan R, van den Berg, Maarten P, Wilde, Arthur AM, Pinto, Yigal M

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An interface board for the control and data acquisition of the Medipix2 chip by San Segundo Bello, David, van Beuzekom, Martin, Jansweijer, Peter, Verkooijen, Hans, Visschers, Jan

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A method to stabilise the performance of negatively fed KM3NeT photomultipliers by Adrián-Martínez, S., Ageron, M., Aiello, S., Albert, A., Ameli, F., Anassontzis, E. G., Andre, M., Androulakis, G., Anghinolfi, M., Anton, G., Ardid, M., Avgitas, T., Barbarino, G., Barbarito, E., Baret, B., Barrios-Martí, J., Belias, A., Berbee, E., Berg, A. van den, Bertin, V., Beurthey, S., Beveren, V. van, Beverini, N., Biagi, S., Biagioni, A., Billault, M., Bondì, M., Bormuth, R., Bouhadef, B., Bourlis, G., Bourret, S., Boutonnet, C., Bouwhuis, M., Bozza, C., Bruijn, R., Brunner, J., Buis, E., Buompane, R., Busto, J., Cacopardo, G., Caillat, L., Calamai, M., Calvo, D., Capone, A., Caramete, L., Cecchini, S., Celli, S., Champion, C., Cherubini, S., Chiarella, V., Chiarelli, L., Chiarusi, T., Circella, M., Classen, L., Cobas, D., Cocimano, R., Coelho, J.A.B., Coleiro, A., Colonges, S., Coniglione, R., Cordelli, M., Cosquer, A., Coyle, P., Creusot, A., Cuttone, G., D'Amato, C., D'Amico, A., D'Onofrio, A., Bonis, G. De, Sio, C. De, Capua, F. Di, Palma, I. Di, Distefano, C., Donzaud, C., Dornic, D., Dorosti-Hasankiadeh, Q., Drakopoulou, E., Drouhin, D., Durocher, M., Eberl, T., Eichie, S., Eijk, D. van, Bojaddaini, I. El, Elsaesser, D., Enzenhöfer, A., Favaro, M., Fermani, P., Ferrara, G., Frascadore, G., Furini, M., Fusco, L.A., Gal, T., Galatà, S., Garufi, F., Gay, P., Gebyehu, M., Giacomini, F., Gialanella, L., Giordano, V., Gizani, N.

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