A binational study assessing risk and resilience factors in 22q11.2 deletion syndrome

Autor: Gur, Raquel E., White, Lauren K., Shani, Shachar, Barzilay, Ran, Moore, Tyler M., Emanuel, Beverly S., Zackai, Elaine H., McDonald-McGinn, Donna M., Matalon, Noam, Weinberger, Ronnie, Gur, Ruben C., Gothelf, Doron

Publikováno v: In Journal of Psychiatric Research June 2021 138:319-325

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Performance on a computerized neurocognitive battery in 22q11.2 deletion syndrome: A comparison between US and Israeli cohorts

Autor: Yi, James J., Weinberger, Ronnie, Moore, Tyler M., Calkins, Monica E., Guri, Yael, McDonald-McGinn, Donna M., Zackai, Elaine H., Emanuel, Beverly S., Gur, Raquel E., Gothelf, Doron, Gur, Ruben C.

Publikováno v: In Brain and Cognition July 2016 106:33-41

Schizophrenia-like neurophysiological abnormalities in 22q11.2 deletion syndrome and their association to COMT and PRODH genotypes

Autor: Zarchi, Omer, Carmel, Miri, Avni, Chen, Attias, Josef, Frisch, Amos, Michaelovsky, Elena, Patya, Miriam, Green, Tamar, Weinberger, Ronnie, Weizman, Abraham, Gothelf, Doron

Publikováno v: In Journal of Psychiatric Research November 2013 47(11):1623-1629

Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

Autor: Cleynen, Isabelle, Engchuan, Worrawat, Hestand, Matthew S, Heung, Tracy, Holleman, Aaron M, Johnston, H Richard, Monfeuga, Thomas, McDonald-McGinn, Donna M, Gur, Raquel E, Morrow, Bernice E, Swillen, Ann, Vorstman, Jacob AS, Bearden, Carrie E, Chow, Eva WC, 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, Tran, Oanh, Holmans, Peter, Pardinas, Antonio, Walters, James TR, Demaerel, Wolfram, Boot, Erik, Butcher, Nancy J, Costain, Gregory A, Lowther, Chelsea, Evers, Rens, van Amelsvoort, Therese AMJ, 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, Monica E, Gallagher, Robert S, Gur, Ruben C, Tang, Sunny X, Fritsch, Rosemarie, Ornstein, 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, Maria, Murphy, Clodagh M, Murphy, Declan G, Buzzanca, Antonio, Fabio, Fabio Di, Digilio, Maria C, Pontillo, Maria, Marino, Bruno, Vicari, Stefano, Coleman, Karlene, Cubells, Joseph F, Ousley, Opal Y, Carmel, Miri, Gothelf, Doron, Mekori-Domachevsky, Ehud, Michaelovsky, Elena, Weinberger, Ronnie, Weizman, Abraham, Kushan, Leila, Jalbrzikowski, Maria, Armando, Marco, Eliez, Stéphan, Sandini, Corrado, Schneider, Maude

Publikováno v: Molecular psychiatry, vol 26, iss 8

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 contribute to schizophrenia, in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::32f66e4eba32686804f3949cd756407d
https://escholarship.org/uc/item/1wx189cs