The efficacy of the Friendly Attac serious digital game to promote prosocial bystander behavior in cyberbullying among young adolescents: A cluster-randomized controlled trial von DeSmet, A., Bastiaensens, S., Van Cleemput, K., Poels, K., Vandebosch, H., Deboutte, G., Herrewijn, L., Malliet, S., Pabian, S., Van Broeckhoven, F., De Troyer, O., Deglorie, G., Van Hoecke, S., Samyn, K., De Bourdeaudhuij, I.

Volltext

Psychometric data of a questionnaire to measure cyberbullying bystander behavior and its behavioral determinants among adolescents von DeSmet, A., Bastiaensens, S., Van Cleemput, K., Poels, K., Vandebosch, H., Deboutte, G., Herrewijn, L., Malliet, S., Pabian, S., Van Broeckhoven, F., De Troyer, O., Deglorie, G., Van Hoecke, S., Samyn, K., De Bourdeaudhuij, I.

Volltext

Psychometric data of a questionnaire to measure cyberbullying bystander behavior and its behavioral determinants among adolescents von DeSmet, A, Bastiaensens, S, Van Cleemput, K, Poels, K, Vandebosch, H, Deboutte, G, Herrewijn, L, Malliet, S, Pabian, S, Van Broeckhoven, F, De Troyer, O, Deglorie, G, Van Hoecke, S, Samyn, K, De Bourdeaudhuij, I

Volltext

Mutations in DNAJC5, Encoding Cysteine-String Protein Alpha, Cause Autosomal-Dominant Adult-Onset Neuronal Ceroid Lipofuscinosis von Nosková, Lenka, Stránecký, Viktor, Hartmannová, Hana, Přistoupilová, Anna, Barešová, Veronika, Ivánek, Robert, Hůlková, Helena, Jahnová, Helena, van der Zee, Julie, Staropoli, John F., Sims, Katherine B., Tyynelä, Jaana, Van Broeckhoven, Christine, Nijssen, Peter C.G., Mole, Sara E., Elleder, Milan, Kmoch, Stanislav

Volltext

Stearoyl-CoA desaturase-1 impairs the reparative properties of macrophages and microglia in the brain von Bogie, Jeroen F J, Grajchen, Elien, Wouters, Elien, Corrales, Aida Garcia, Dierckx, Tess, Vanherle, Sam, Mailleux, Jo, Gervois, Pascal, Wolfs, Esther, Dehairs, Jonas, Van Broeckhoven, Jana, Bowman, Andrew P, Lambrichts, Ivo, Gustafsson, Jan-Åke, Remaley, Alan T, Mulder, Monique, Swinnen, Johannes V, Haidar, Mansour, Ellis, Shane R, Ntambi, James M, Zelcer, Noam, Hendriks, Jerome J A

Volltext

CD36-mediated uptake of myelin debris by macrophages and microglia reduces neuroinflammation von Grajchen, Elien, Wouters, Elien, van de Haterd, Britt, Haidar, Mansour, Hardonnière, Kévin, Dierckx, Tess, Van Broeckhoven, Jana, Erens, Celine, Hendrix, Sven, Kerdine-Römer, Saadia, Hendriks, Jerome J. A, Bogie, Jeroen F. J

Volltext

Progranulin genetic variability contributes to amyotrophic lateral sclerosis von SLEEGERS, K, BROUWERS, N, CRUTS, M, SCHYMKOWITZ, J, DE JONGHE, P, ROUSSEAU, F, VAN DEN BERG, L. H, ROBBERECHT, W, VAN BROECKHOVEN, C, MAURER-STROH, S, VAN ES, M. A, VAN DAMME, P, VAN VUGHT, P. W. J, VAN DER ZEE, J, SERNEELS, S, DE POORER, T, VAN DEN BROECK, M

Volltext

Rare variants in IFFO1, DTNB, NLRC3 and SLC22A10 associate with Alzheimer’s disease CSF profile of neuronal injury and inflammation von Neumann, Alexander, Küçükali, Fahri, Bos, Isabelle, Vos, Stephanie J. B., Engelborghs, Sebastiaan, De Pooter, Tim, Joris, Geert, De Rijk, Peter, De Roeck, Ellen, Tsolaki, Magda, Verhey, Frans, Martinez-Lage, Pablo, Tainta, Mikel, Frisoni, Giovanni, Blin, Oliver, Richardson, Jill, Bordet, Régis, Scheltens, Philip, Popp, Julius, Peyratout, Gwendoline, Johannsen, Peter, Frölich, Lutz, Vandenberghe, Rik, Freund-Levi, Yvonne, Streffer, Johannes, Lovestone, Simon, Legido-Quigley, Cristina, ten Kate, Mara, Barkhof, Frederik, Strazisar, Mojca, Zetterberg, Henrik, Bertram, Lars, Visser, Pieter Jelle, van Broeckhoven, Christine, Sleegers, Kristel

Volltext

Loss of ALS-associated TDP-43 in zebrafish causes muscle degeneration, vascular dysfunction, and reduced motor neuron axon outgrowth von Schmid, Bettina, Hruscha, Alexander, Hogl, Sebastian, Banzhaf-Strathmann, Julia, Strecker, Katrin, van der Zee, Julie, Teucke, Mathias, Eimer, Stefan, Hegermann, Jan, Kittelmann, Maike, Kremmer, Elisabeth, Cruts, Marc, Solchenberger, Barbara, Hasenkamp, Laura, van Bebber, Frauke, Van Broeckhoven, Christine, Edbauer, Dieter, Lichtenthaler, Stefan F., Haass, Christian

Volltext

Highly efficient gene delivery by mRNA electroporation in human hematopoietic cells: superiority to lipofection and passive pulsing of mRNA and to electroporation of plasmid cDNA f... von Van Tendeloo, Viggo F.I., Ponsaerts, Peter, Lardon, Filip, Nijs, Griet, Lenjou, Marc, Van Broeckhoven, Christine, Van Bockstaele, Dirk R., Berneman, Zwi N.

Volltext

Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b C4b binding sites von Brouwers, N, Van Cauwenberghe, C, Engelborghs, S, Lambert, J-C, Bettens, K, Le Bastard, N, Pasquier, F, Montoya, A Gil, Peeters, K, Mattheijssens, M, Vandenberghe, R, De Deyn, P P, Cruts, M, Amouyel, P, Sleegers, K, Van Broeckhoven, C

Volltext

Glucocorticoid Receptor Gene-Based SNP Analysis in Patients with Recurrent Major Depression von VAN WEST, Dirk, VAN DEN EEDE, Filip, VAN BROECKHOVEN, Christine, CLAES, Stephan, DEL-FAVERO, Jurgen, SOUERY, Daniel, NORRBACK, Karl-Fredrik, VAN DUIJN, Cornelia, SLUIJS, Sam, ADOLFSSON, Rolf, MENDLEWICZ, Julien, DEBOUTTE, Dirk

Volltext

A Genomewide Screen for Late-Onset Alzheimer Disease in a Genetically Isolated Dutch Population von Liu, Fan, Arias-Vásquez, Alejandro, Sleegers, Kristel, Aulchenko, Yurii S., Kayser, Manfred, Sanchez-Juan, Pascual, Feng, Bing-Jian, Bertoli-Avella, Aida M., van Swieten, John, Axenovich, Tatiana I., Heutink, Peter, van Broeckhoven, Christine, Oostra, Ben A., van Duijn, Cornelia M.

Volltext

Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology von Chapuis, J, Hansmannel, F, Gistelinck, M, Mounier, A, Van Cauwenberghe, C, Kolen, K V, Geller, F, Sottejeau, Y, Harold, D, Dourlen, P, Grenier-Boley, B, Kamatani, Y, Delepine, B, Demiautte, F, Zelenika, D, Zommer, N, Hamdane, M, Bellenguez, C, Dartigues, J-F, Hauw, J-J, Letronne, F, Ayral, A-M, Sleegers, K, Schellens, A, Broeck, L V, Engelborghs, S, De Deyn, P P, Vandenberghe, R, O'Donovan, M, Owen, M, Epelbaum, J, Mercken, M, Karran, E, Bantscheff, M, Drewes, G, Joberty, G, Campion, D, Octave, J-N, Berr, C, Lathrop, M, Callaerts, P, Mann, D, Williams, J, Buée, L, Dewachter, I, Van Broeckhoven, C, Amouyel, P, Moechars, D, Dermaut, B, Lambert, J-C

Volltext

Mutations in SEPT9 cause hereditary neuralgic amyotrophy von Jonghe, Peter De, Goossens, Dirk, Kurlemann, Gert, Mononen, Tarja, Nelis, Eva, Ringelstein, E Bernd, Schirmacher, Anja, Prats, José M, Bird, Thomas D, Kuhlenbäumer, Gregor, Stögbauer, Florian, Meuleman, Jan, Young, Peter, Del-Favero, Jurgen, Broeckhoven, Christine Van, Irobi, Joy, Betz, Benjamin G, Hannibal, Mark C, Watts, Giles D J, Timmerman, Vincent, Serradell, Adolfo Pou, Vriendt, Els De, Airaksinen, Eila, Hor, Hyun, Halfter, Hartmut, Chance, Phillip F, Verpoorten, Nathalie

Volltext

Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease von BROUWERS, N, SLEEGERS, K, SCHYMKOWITZ, J, ROUSSEAU, F, MARTIN, J.-J, CRUTS, M, DE DEYN, P. P, VAN BROECKHOVEN, C, ENGELBORGHS, S, MAURER-STROH, S, GIJSELINCK, I, VAN DER ZEE, J, PICKUT, B. A, VAN DEN BROECK, M, MATTHEIJSSENS, M, PEETERS, K

Volltext

ATXN2 Trinucleotide Repeat Length Correlates with Risk of ALS von Sproviero, William, Shatunov, Aleksey, Stahl, Daniel, Shoai, Maryam, van Rheenen, Wouter, Jones, Ashley R, Al-Sarraj, Safa, Andersen, Peter M, Bonini, Nancy M, Conforti, Francesca L, Van Damme, Philip, Daoud, Hussein, Del Mar Amador, Maria, Fogh, Isabella, Forzan, Monica, Gaastra, Ben, Gellera, Cinzia, Gitler, Aaron D, Hardy, John, Fratta, Pietro, La Bella, Vincenzo, Le Ber, Isabelle, Van Langenhove, Tim, Lattante, Serena, Lee, Yi-Chung, Malaspina, Andrea, Meininger, Vincent, Millecamps, Stèphanie, Orrell, Richard, Rademakers, Rosa, Robberecht, Wim, Rouleau, Guy, Ross, Owen A, Salachas, Francois, Sidle, Katie, Smith, Bradley N, Soong, Bing-Wen, Sorarù, Gianni, Stevanin, Giovanni, Kabashi, Edor, Troakes, Claire, van Broeckhoven, Christine, Veldink, Jan H, van den Berg, Leonard H, Shaw, Christopher E, Powell, John F, Al-Chalabi, Ammar

Volltext

The dopamine D4 receptor gene 48-base-pair-repeat polymorphism and mood disorders: A meta-analysis von López León, Sandra, Croes, Esther A., Sayed-Tabatabaei, Fakhredin A., Claes, Stephan, Broeckhoven, Christine Van, van Duijn, Cornelia M.

Volltext

APOE and Alzheimer disease: a major gene with semi-dominant inheritance von Genin, E, Hannequin, D, Wallon, D, Sleegers, K, Hiltunen, M, Combarros, O, Bullido, M J, Engelborghs, S, De Deyn, P, Berr, C, Pasquier, F, Dubois, B, Tognoni, G, Fiévet, N, Brouwers, N, Bettens, K, Arosio, B, Coto, E, Del Zompo, M, Mateo, I, Epelbaum, J, Frank-Garcia, A, Helisalmi, S, Porcellini, E, Pilotto, A, Forti, P, Ferri, R, Scarpini, E, Siciliano, G, Solfrizzi, V, Sorbi, S, Spalletta, G, Valdivieso, F, Vepsäläinen, S, Alvarez, V, Bosco, P, Mancuso, M, Panza, F, Nacmias, B, Bossù, P, Hanon, O, Piccardi, P, Annoni, G, Seripa, D, Galimberti, D, Licastro, F, Soininen, H, Dartigues, J-F, Kamboh, M I, Van Broeckhoven, C, Lambert, J C, Amouyel, P, Campion, D

Volltext

Exome‐wide rare variant analysis of Alzheimer’s disease biomarkers: The EMIF‐AD multimodal biomarker discovery study von Neumann, Alexander, Vangoidsenhoven, Michelle, Küçükali, Fahri, Vos, Stephanie J. B., ten Kate, Mara, Barkhof, Frederik, Zetterberg, Henrik, Bertram, Lars, Visser, Pieter Jelle, Van Broeckhoven, Christine, Sleegers, Kristel

Volltext