The AMC13XG: a new generation clock/timing/DAQ module for CMS MicroTCA by Hazen, E, Heister, A, Hill, C, Rohlf, J, Wu, S X, Zou, D

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Adenine is an anti-inflammatory metabolite found to be more abundant in M-CSF over GM-CSF-differentiated human macrophages by Harber, Karl J, Nguyen, Thuc-Anh, Schomakers, Bauke V, Heister, Daan A F, de Vries, Helga E., van Weeghel, Michel, Van den Bossche, Jan, de Winther, Menno P J

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COVID19 Impairs Cardiac Function via Endothelial H19 and IL6 Signaling by Juni, Rio P., Phelp, Philippa G., Bink, Diewertje I., Kremer, Veerle, van Bergen, Anke S., Espinosa Gonzalez, Pedro, Rombouts, Karlijn B., Harber, Karl J., Heister, Daan A.F., Yeung, Kak K., Van den Bossche, Jan, Kuster, Diederik W.D., Krijnen, Paul A.J., Niessen, Hans W.M., Boon, Reinier A.

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A novel D458V mutation in the SANS PDZ binding motif causes atypical Usher syndrome by KALAY, E, DE BROUWER, A. P. M, BRUNNER, H. G, KREMER, H, CAYLAN, R, NABUURS, S. B, WOLLNIK, B, KARAGUZEL, A, HEISTER, J. G. A. M, ERDOL, H, CREMERS, F. P. M, CREMERS, C. W. R. J

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Four novel TMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss by Kalay, E., Karaguzel, A., Caylan, R., Heister, A., Cremers, F.P.M., Cremers, C.W.R.J., Brunner, H.G., de Brouwer, A.P.M., Kremer, H.

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A novel locus for autosomal recessive nonsyndromic hearing impairment, DFNB63, maps to chromosome 11q13.2-q13.4 by KALAY, E, CAYLAN, R, KREMER, H, KIROGLU, A. F, YASAR, T, COLLIN, R. W. J, HEISTER, J. G. A. M, OOSTRIK, J, CREMERS, C. W. R. J, BRUNNER, H. G, KARAGUZEL, A

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An exploratory study of the relationship between four candidate genes and neurocognitive performance in adult ADHD by Boonstra, A. Marije, Kooij, J.J. Sandra, Buitelaar, Jan K., Oosterlaan, Jaap, Sergeant, Joseph A., Heister, J.G.A.M. Angelien, Franke, Barbara

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Coherent large beamwidth processing of radio-echo sounding data by Heister, Anton, Scheiber, Rolf

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ROSC after cardiac arrest-the RACA score to predict outcome after out-of-hospital cardiac arrest by Gräsner, Jan-Thorsten, Meybohm, Patrick, Lefering, Rolf, Wnent, Jan, Bahr, Jan, Messelken, Martin, Jantzen, Tanja, Franz, Rüdiger, Scholz, Jens, Schleppers, Alexander, Böttiger, Bernd W., Bein, Berthold, Fischer, Matthias

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First look at the physics case of TLEP by Bicer, M., Duran Yildiz, H., Coignet, G., Delmastro, M., Grojean, C, Antusch, S., Sen, T., He, H.-J., Potamianos, K., Haug, S., Moreno, A., Heister, A., Sanz, V., Wang, L.-T., Dam, M., Boehm, C., Glover, N., Krauss, F., Lenz, A., Syphers, M., Leonidopoulos, C., Ciulli, V., Lenzi, P., Sguazzoni, G., Boscolo, M., Dosselli, U., Frasciello, O., Milardi, C., Zobov, M., van der Bij, J., de Gruttola, M., Bachtis, M., Butterworth, A., Bernet, C., Botta, C., Deniau, L., d’Enterria, D., Ganis, G., Goddard, B., Jowett, J. M., Lourenço, C., Malgeri, L., Meschi, E., Moortgat, F., Musella, P., Osborne, J. A., Perrozzi, L., Pierini, M., Rinolfi, L., de Roeck, A., Rojo, J., Sciabà, A., Valassi, A., Waaijer, C. S., Wenninger, J., Woehri, H., Koratzinos, M., Mermod, P., Onel, Y., Talman, R., Castaneda Miranda, E., Bulyak, E., Porsuk, D., Kovalskyi, D., Padhi, S., Faccioli, P., Appleby, R. B., Cuna, H. Maury, Gracios, C., Munoz-Hernandez, G. A., Trentadue, L., Torrente-Lujan, E., Bertsche, D., Gramolin, A., Telnov, V., Petroff, P., Azzi, P., Nicrosini, O., Montagna, G., Laplace, S., Gizani, N., Craig, N., Luci, C., Mele, B., Silvestrini, L., Ciuchini, M., Aleksan, R., Ganjour, S., Lançon, E., Locci, E., Schwemling, P., Tanguy, C., Zinn-Justin, J., Moretti, S., Kikuchi, M., Koiso, H., Ohmi, K., Oide, K., Pauletta, G., Chattopadhyay, S.

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A novel skeletal disorder characterized by progressive spondyloarthropathy is caused by a recessive ANKH mutation by Kühnisch, J, Morava, E, Drijvers, J.M, Robben, J.H, Cremers, C, van Setten, P, Branten, A, Stumpp, S, de Jong, A, Voesenek, K, Vermeer, S, Heister, A, der Grinten, H.L. Claahsen-van, O'Neill, C.W, Willemsen, M.A, Lefeber, D, Deen, P.M, Kremer, H, Wevers, R.A, Kornak, U

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Targeting the ACOD1-itaconate axis stabilizes atherosclerotic plaques by Harber, Karl J., Neele, Annette E., van Roomen, Cindy PAA, Gijbels, Marion JJ, Beckers, Linda, Toom, Myrthe den, Schomakers, Bauke V., Heister, Daan AF, Willemsen, Lisa, Griffith, Guillermo R., de Goede, Kyra E., van Dierendonck, Xanthe AMH, Reiche, Myrthe E., Poli, Aurélie, L-H Mogensen, Frida, Michelucci, Alessandro, Verberk, Sanne GS, de Vries, Helga, van Weeghel, Michel, Van den Bossche, Jan, de Winther, Menno PJ

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Search for gauge mediated SUSY breaking topologies in ee collisions at centre-of-mass energies up to 209 GeV by Heister et al, A.

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Near-threshold $$ \mathrm{D}\overline{\mathrm{D}} $$ spectroscopy and observation of a new charmonium state by Aaij, R., Abellán Beteta, C., Adeva, B., Adinolfi, M., Aidala, C. A., Ajaltouni, Z., Akar, S., Albicocco, P., Albrecht, J., Alessio, F., Alexander, M., Alfonso Albero, A., Alkhazov, G., Alvarez Cartelle, P., Alves, A. A., Amato, S., Amhis, Y., An, L., Anderlini, L., Andreassi, G., Andreotti, M., Andrews, J. E., Archilli, F., Arnau Romeu, J., Artamonov, A., Artuso, M., Arzymatov, K., Aslanides, E., Atzeni, M., Audurier, B., Bachmann, S., Back, J. J., Baker, S., Balagura, V., Baldini, W., Baranov, A., Barlow, R. J., Barsuk, S., Barter, W., Bartolini, M., Baryshnikov, F., Batozskaya, V., Batsukh, B., Battig, A., Battista, V., Bay, A., Bedeschi, F., Bediaga, I., Beiter, A., Bel, L. J., Belin, S., Beliy, N., Bellee, V., Belloli, N., Belous, K., Belyaev, I., Bencivenni, G., Ben-Haim, E., Benson, S., Beranek, S., Berezhnoy, A., Bernet, R., Berninghoff, D., Bertholet, E., Bertolin, A., Betancourt, C., Betti, F., Bettler, M. O., Bezshyiko, Ia, Bhasin, S., Bhom, J., Bieker, M. S., Bifani, S., Billoir, P., Birnkraut, A., Bizzeti, A., Bjørn, M., Blago, M. P., Blake, T., Blanc, F., Blusk, S., Bobulska, D., Bocci, V., Boente Garcia, O., Boettcher, T., Bondar, A., Bondar, N., Borghi, S., Borisyak, M., Borsato, M., Boubdir, M., Bowcock, T. J. V., Bozzi, C., Braun, S., Brodski, M., Brodzicka, J., Brossa Gonzalo, A., Brundu, D., Buchanan, E., Buonaura, A.

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Comparing emergency medical service systems—A project of the European Emergency Data (EED) Project by Fischer, Matthias, Kamp, Johannes, Garcia-Castrillo Riesgo, Luis, Robertson-Steel, Iain, Overton, Jerry, Ziemann, Alexandra, Krafft, Thomas

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Association of the dopamine transporter (SLC6A3/DAT1) gene 9-6 haplotype with adult ADHD by Franke, B., Hoogman, M., Arias Vasquez, A., Heister, J.G.A.M., Savelkoul, P.J., Naber, M., Scheffer, H., Kiemeney, L.A., Kan, C.C., Kooij, J.J.S., Buitelaar, J.K.

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Multicenter Analysis of the SLC6A3/DAT1 VNTR Haplotype in Persistent ADHD Suggests Differential Involvement of the Gene in Childhood and Persistent ADHD by Franke, Barbara, Vasquez, Alejandro Arias, Johansson, Stefan, Hoogman, Martine, Romanos, Jasmin, Boreatti-Hümmer, Andrea, Heine, Monika, Jacob, Christian P, Lesch, Klaus-Peter, Casas, Miguel, Ribasés, Marta, Bosch, Rosa, Sánchez-Mora, Cristina, Gómez-Barros, Núria, Fernàndez-Castillo, Noèlia, Bayés, Mònica, Halmøy, Anne, Halleland, Helene, Landaas, Elisabeth T, Fasmer, Ole B, Knappskog, Per M, Heister, Angelien J G A M, Kiemeney, Lambertus A, Kooij, J J Sandra, Boonstra, A Marije, Kan, Cees C, Asherson, Philip, Faraone, Stephen V, Buitelaar, Jan K, Haavik, Jan, Cormand, Bru, Ramos-Quiroga, Josep Antoni, Reif, Andreas

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Advances in Proof-Theoretic Semantics

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Characterization of functional domains in the human coronavirus HCV 229E receptor by Kolb, Andreas F, Maile, Julia, Heister, Angelien, Siddell, Stuart G

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Observation of the decay Ξ−b→pK−K by Aaij, R., Beaucourt, L., Chefdeville, M., Decamp, D., Déléage, N., Ghez, P., Marchand, J.-F., Minard, M.-N., Pietrzyk, B., t'Jampens, S., Tisserand, V., Tournefier, E., Ajaltouni, Z.J., Baalouch, M., Cogneras, E., Deschamps, O., Gazzoni, G., Gándara, M. Grabalosa, Hadjivasiliou, C., Henrard, P., Kozeiha, M., Lefèvre, R., Monteil, S., Perret, P., Vernet, M., Arnau Romeu, J., Aslanides, E., Cogan, J., Bruyn, K. De, Legac, R., Leroy, O., Mancinelli, G., Martin, M., Mordà, A., Serrano, J., Tayduganov, A., Tsaregorodtsev, A.

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