Browsing by Author "a2100934-384b-4041-9bd3-84dd3295f194"

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    • Copy number variation analysis in adults with catatonia confirms haploinsufficiency of SHANK3 as a predisposing ... 
      Jeroen, Breckpot; Vercruyssen, Marieke; Weyts, Eddy; Vandevoort, Sean; D'Haenens, Greet; Van Buggenhout, Griet; Leempoels, Lore; Brischoux-Boucher, Elise; Van Maldergem, Lionel; Renieri, Alessandra; Mencarelli, Maria Antonietta; D'Angelo, Carla; Mericq, Verónica; Hoffer, Mariette J.; Tauber, Maithé; Molinas, Catherine; Castiglioni, Claudia; Brison, Nathalie; Vermeesch, Joris R.; Danckaerts, Marina; Sienaert, Pascal; Devriendt, Koenraad; Vogels, Annick (Elsevier, 2016)
      Background: Catatonia is a motor dysregulation syndrome co-occurring with a variety of psychiatric and medical disorders. Response to treatment with benzodiazepines and electroconvulsive therapy suggests a neurobiological ...
    • Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion 
      Cleynen, Isabelle; Engchuan, Worrawat; Hestand, Matthew S.; Heung, Tracy; Holleman, Aarón M.; Johnston, H. Richard; Monfeuga, Thomas; McDonald McGinn, Donna M.; Gur, Raquel E.; Morrow, Bernice E.; Swillen, Ann; Vorstman, Jacob A. S.; Bearden, Carrie E.; Chow, Eva W. C.; van den Bree, Marianne; Emanuel, Beverly S.; Vermeesch, Joris R.; Warren, Stephen T.; Owen, Michael J.; Chopra, Pankaj; Cutler, David J.; Duncan, Richard; Kotlar, Alex V.; Mulle, Jennifer G.; Voss, Anna J.; Zwick, Michael E.; Diacou, Alexander; Golden, Aaron; Guo, Tingwei; Lin, Jhih Rong; Wang, Tao; Zhang, Zhengdong; Zhao, Yingjie; Marshall, Christian; Merico, Daniele; Jin, Andrea; Lilley, Brenna; Salmons, Harold I.; Oanh, Tran; Pardinas, Antonio; Walters, James T. R.; Demaerel, Wolfram; Boot, Erik; Butcher, Nancy J.; Costain, Gregory A.; Lowther, Chelsea; Evers, Rens; van Amelsvoort, Therese A. M. J.; van Duin, Esther; Vingerhoets, Claudia; Breckpot, Jeroen; Devriendt, Koen; Vergaelen, Elfi; Vogels, Annick; Crowley, T. Blaine; McGinn, Daniel E.; Moss, Edward M.; Sharkus, Robert J.; Unolt, Marta; Zackai, Elaine H.; Calkins, Mónica E.; Gallagher, Robert S.; Gur, Rubén C.; Tang, Sunny X.; Fritsch Montero, Rosemarie; Ornstein Letelier, Claudia; Repetto, Gabriela M.; Breetvelt, Elemi; Duijff, Sasja N.; Fiksinski, Ania; Moss, Hayley; Niarchou, Maria; Murphy, Kieran C.; Prasad, Sarah E.; Daly, Eileen M.; Gudbrandsen, María; Murphy, Clodagh M.; Murphy, Declan G.; Buzzanca, Antonio; Di Fabio, Fabio; Digilio, María C.; Pontillo, María; Marino, Bruno; Vicari, Stefano; Coleman, Karlene; Cubells, Joseph F.; Ousley, Opal Y.; Carmel, Miri; Gothelf, Doron; Mekori Domachevsky, Ehud; Michaelovsky, Elena; Weinberger, Ronnie; Eliez, Stephan; Sandini, Corrado; Schneider, Maude; Bena, Frederique Sloan; Antshel, Kevin M.; Fremont, Wanda; Kates, Wendy R.; Belzeaux, Raoul; Busa, Tiffany; Schoch, Kelly; Shashi, Vandana; Simon, Tony J.; Tassone, Flora; Arango, Celso; Suner, Damia H.; Raventos Simic, Jasna; Epstein, Michael P.; Williams, Nigel M.; Bassett, Anne S. (Nature, 2020)
      Schizophrenia occurs in about one in four individuals with 22q11.2 deletion syndrome (22q11.2DS). The aim of this International Brain and Behavior 22q11.2DS Consortium (IBBC) study was to identify genetic factors that ...