A comparative study of cognition and brain anatomy between two neurodevelopmental disorders: 22q11.2 deletion syndrome and Williams syndrome
- Creator: Campbell, Linda E. , Stevens, Angela , Daly, Eileen , Toal, Fiona , Azuma, Rayna , Karmiloff-Smith, Annette , Murphy, Declan G. M. , Murphy, Kieran C.
- Resource Type: journal article
- Date: 2009
Brain structural differences associated with the behavioural phenotype in children with Williams syndrome
- Creator: Campbell, Linda E. , Daly, Eileen , Toal, Fiona , Stevens, Angela , Azuma, Rayna , Karmiloff-Smith, Annette , Murphy, Declan G. M. , Murphy, Kieran C.
- Resource Type: journal article
- Date: 2009
Visuospatial working memory in children and adolescents with 22q11.2 deletion syndrome: an fMRI study
- Creator: Azuma, Rayna , Daly, Eileen M. , Williams, Steven C. R. , Owen, Michael J. , Murphy, Declan G. M. , Murphy, Kieran C. , Campbell, Linda E. , Stevens, Angela F. , Deeley, Quinton , Giampietro, Vincent , Brammer, Michael J. , Glaser, Beate , Ambery, Fiona Z. , Morris, Robin G.
- Resource Type: journal article
- Date: 2009
Executive functions and memory abilities in children with 22q11.2 deletion syndrome
- Creator: Campbell, Linda E. , Azuma, Rayna , Ambery, Fiona , Stevens, Angela , Smith, Anna , Morris, Robin G. , Murphy, Declan G. M. , Murphy, Kieran C.
- Resource Type: journal article
- Date: 2010
Is theory of mind related to social dysfunction and emotional problems in 22q11.2 deletion syndrome (velo-cardio-facial syndrome)?
- Creator: Campbell, Linda E. , Stevens, Angela F. , McCabe, Kathryn , Cruickshank, Lynne , Morris, Robin G. , Murphy, Declan G. M. , Murphy, Kieran C.
- Resource Type: journal article
- Date: 2011
Biological insights from 108 schizophrenia-associated genetic loci
- Creator: Ripke, Stephan , Neale, Benjamin M. , Pers, Tune H. , Julià, Antonio , Kahn, René S. , Kalaydjieva, Luba , Karachanak-Yankova, Sena , Karjalainen, Juha , Kavanagh, David , Keller, Matthew C. , Kennedy, James L. , Khrunin, Audrey , Kim, Yunjung , Agartz, Iingrid , Klovins, Janis , Knowles, James A. , Konte, Bettina , Kucinskas, Vaidutis , Ausrele Kucinskiene, Zita , Kuzelova-Ptackova, Hana , Kähler, Anna K. , Laurent, Claudine , Lee Chee Keong, Jimmy , Hong Lee, S. , Agerbo, Esben , Legge, Sophie E. , Lerer, Bernard , Li, Miaoxin , Li, Tao , Liang, Kung-Yee , Lieberman, Jeffrey , Limborska, Svetlana , Loughland, Carmel M. , Lubinski, Jan , Lönnqvist, Jouko , Albus, Margot , Macek Jr, Milan , Magnusson, Patrik K. E. , Maher, Brion S. , Maier, Wolfgang , Mallet, Jacques , Marsal, Sara , Mattheisen, Manuel , Mattingsdal, Morten , McCarley, Robert W. , McDonald, Colm , Alexander, Madeline , McIntosh, Andrew M. , Meier, Sandra , Meijer, Carin J. , Melegh, Bela , Melle, Iingrid , Mesholam-Gately, Raquelle I. , Metspalu, Andres , Michie, Patricia T. , Milani, Lili , Milanova, Virha , Amin, Farooq , Mokrab, Younes , Morris, Derek W. , Mors, Ole , Murphy, Kieran C. , Murray, Robin M. , Myin-Germeys, Inez , Müller-Myhsok, Bertram , Nelis, Mari , Nenadic, Igor , Nertney, Deborah A. , Bacanu, Silviu A. , Nestadt, Gerald , Nicodemus, Kristin K. , Nikitina-Zake, Liene , Nisenbaum, Laura , Nordin, Annelie , O'Callaghan, Eadbhard , O'Dushlaine, Colm , O'Neill, F. Anthony , Oh, Sang-Yun , Olincy, Ann , Begemann, Martin , Olsen, Line , Van Os, Jim , Psychosis Endophenotypes International Consortium , Pantelis, Christos , Papadimitriou, George N. , Papiol, Sergi , Parkhomenko, Elena , Pato, Michele T. , Paunio, Tiina , Pejovic-Milovancevic, Milica , Belliveau Jr, Richard A. , Perkins, Diana O. , Pietiläinen, Olli , Pimm, Jonathan , Pocklington, Andrew J. , Powell, John , Price, Alkes , Pulver, Ann E. , Purcell, Shaun M. , Quested, Digby , Rasmussen, Henrik B. , Bene, Judit , Reichenberg, Abraham , Reimers, Mark A. , Richards, Alexander L. , Roffman, Joshua L. , Roussos, Panos , Ruderfer, Douglas M. , Salomaa, Veikko , Sanders, Alan R. , Schall, Ulrich , Schubert, Christian R. , Corvin, Aiden , Bergen, Sarah E. , Schulze, Thomas G. , Schwab, Sibylle G. , Scolnick, Edward M. , Scott, Rodney J. , Seidman, Larry J. , Shi, Jianxin , Sigurdsson, Engilbert , Silagadze, Teimuraz , Silverman, Jeremy M. , Sim, Kang , Bevilacqua, Elizabeth , Slominsky, Petr , Smoller, Jordan W. , So, Hon-Cheong , Spencer, Chris C. A. , Stahl, Eli A. , Stefansson, Hreinn , Steinberg, Stacy , Stogmann, Elisabeth , Straub, Richard E. , Strengman, Eric , Bigdeli, Tim B. , Strohmaier, Jana , Scott Stroup, T. , Subramaniam, Mythily , Suvisaari, Jaana , Svrakic, Dragan M. , Szatkiewicz, Jin P. , Söderman, Erik , Thirumalai, Srinivas , Toncheva, Draga , Tosato, Sarah , Black, Donald W. , Veijola, Juha , Waddington, John , Walsh, Dermot , Wang, Dai , Wang, Qiang , Webb, Bradley T. , Weiser, Mark , Wildenauer, Dieter B. , Williams, Nigel M. , Williams, Stephanie , Bruggeman, Richard , Witt, Stephanie H. , Wolen, Aaron R. , Wong, Emily H. M. , Wormley, Brandon K. , Simon Xi, Hualin , Zai, Clement C. , Zheng, Xuebin , Zimprich, Fritz , Wray, Naomi R. , Stefansson, Kari , Buccola, Nancy G. , Visscher, Peter M. , Welcome Trust Case-Control Consortium, , Adolfsson, Rolf , Andreassen, Ole A. , Blackwood, Douglas H. R. , Bramon, Elvira , Buxbaum, Joseph D. , Børglum, Anders D. , Cichon, Sven , Darvasi, Ariel , Buckner, Randy L. , Domenici, Enrico , Ehrenreich, Hannelore , Esko, Tõnu , Gejman, Pablo V. , Gill, Michael , Gurling, Hugh , Hultman, Christina M. , Iwata, Nakao , Jablensky, Assen V. , Jönsson, Erik G. , Byerley, William , Kendler, Kenneth S. , Kirov, George , Knight, Jo , Lencz, Todd , Levinson, Douglas F. , Li, Qingqin S. , Liu, Jianjun , Malhotra, Anil K. , McCarroll, Steven A. , McQuillin, Andrew , Cahn, Wiepke , Moran, Jennifer L. , Mortensen, Preben B. , Mowry, Bryan J. , Nöthen, Markus M. , Ophoff, Roel A. , Owen, Michael J. , Palotie, Aarno , Pato, Carlos N. , Petryshen, Tracey L. , Posthuma, Danielle , Cai, Guiqing , Rietschel, Marcella , Riley, Brien P. , Rujescu, Dan , Sham, Pak C. , Sklar, Pamela , St Clair, David , Weinberger, David R. , Wendland, Jens R. , Werge, Thomas , Daly, Mark J. , Walters, James T. R. , Campion, Dominique , Sullivan, Patrick F. , O'Donovan, Michael C. , Cantor, Rita M. , Carr, Vaughan J. , Carrera, Noa , Catts, Stanley V. , Chambert, Kimberly D. , Chan, Raymond C. K. , Chen, Ronald Y. L. , Chen, Eric Y. H. , Cheng, Wei , Farh, Kai-How , Cheung, Eric F. C. , Ann Chong, Siow , Robert Cloninger, C. , Cohen, David , Cohen, Nadine , Cormican, Paul , Craddock, Nick , Crowley, James J. , Curtis, David , Davidson, Michael , Holmans, Peter A. , Davis, Kenneth L. , Degenhardt, Franziska , Del Favero, Jurgen , Demontis, Ditte , Dikeos, Dimitris , Dinan, Timothy , Djurovic, Srdjan , Donohoe, Gary , Drapeau, Elodie , Duan, Jubao , Lee, Phil , Dudbridge, Frank , Durmishi, Naser , Eichhammer, Peter , Eriksson, Johan , Escott-Price, Valentina , Essioux, Laurent , Fanous, Ayman H. , Farrell, Martilias S. , Frank, Josef , Franke, Lude , Bulik-Sullivan, Brendan , Freedman, Robert , Freimer, Nelson B. , Friedl, Marion , Friedman, Joseph I. , Fromer, Menachem , Genovese, Giulio , Georgieva, Lyudmila , Giegling, Ina , Giusti-Rodríguez, Paola , Godard, Stephanie , Collier, David A. , Goldstein, Jacqueline I. , Golimbet, Vera , Gopal, Srihari , Gratten, Jacob , de Haan, Lieuwe , Hammer, Christian , Hamshere, Marian L. , Hansen, Mark , Hansen, Thomas , Haroutunian, Vahram , Huang, Hailiang , Hartmann, Annette M. , Henskens, Frans A. , Herms, Stefan , Hirschhorn, Joel N. , Hoffmann, Per , Hofman, Andrea , Hollegaard, Mads V. , Hougaard, David M. , Ikeda, Masashi , Joa, Inge
- Resource Type: journal article
- Date: 2014
Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 deletion syndrome
- Creator: Schneider, Maude , Debbané, Martin , Antshel, Kevin M. , Fremont, Wanda , McDonald-McGinn, Donna M. , Gur, Raquel E. , Zackai, Elaine H. , Vorstman, Jacob , Duijff, Sasja N. , Klaassen, Petra W. J. , Swillen, Ann , Gothelf, Doron , Bassett, Anne S. , Green, Tamar , Weizman, Abraham , Van Amelsvoort, Therese , Evers, Laurens , Boot, Erik , Shashi, Vandana , Hooper, Stephen R. , Bearden, Carrie E. , Jalbrzikowski, Maria , Armando, Marco , Chow, Eva W. C. , Vicari, Stefano , Murphy, Declan G. , Ousley, Opal , Campbell, Linda E. , Simon, Tony J. , Eliez, Stephan , Fung, Wai Lun Alan , van den Bree, Marianne B. M. , Owen, Michael , Murphy, Kieran C. , Niarchou, Maria , Kates, Wendy R.
- Resource Type: journal article
- Date: 2014
An fMRI study of facial emotion processing in children and adolescents with 22q11.2 deletion syndrome
- Creator: Azuma, Rayna , Deeley, Quinton , Campbell, Linda E. , Daly, Eileen M. , Giampietro, Vincent , Brammer, Michael J. , Murphy, Kieran C. , Murphy, Declan G. M.
- Resource Type: journal article
- Date: 2015
Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome
- Creator: Vorstman, Jacob A. S. , Breetvelt, Elemi J. , Chow, Eva W. C. , Fung, Wai Lun Alan , Butcher, Nancy J. , Young, Donald A. , McDonald-McGinn, Donna M. , Vogels, Annick , van Amelsvoort, Therese , Gothelf, Doron , Weinberger, Ronnie , Weizman, Abraham , Duijff, Sasja N. , Klaassen, Petra W. J. , Koops, Sanne , Kates, Wendy R. , Antshel, Kevin M. , Simon, Tony J. , Ousley, Opal Y. , Swillen, Ann , Gur, Raquel E. , Bearden, Carrie E. , Kahn, René S. , Eliez, Stephan , Bassett, Anne S. , Emanuel, Beverly S. , Zackai, Elaine H. , Kushan, Leila , Fremont, Wanda , Schoch, Kelly , Stoddard, Joel , Cubells, Joseph , Fu, Fiona , Campbell, Linda E. , Schneider, Maude , Fritsch, Rosemarie , Vergaelen, Elfi , Neeleman, Marjolein , Boot, Erik , Debbané, Martin , Philip, Nicole , Green, Tamar , van den Bree, Marianne B. M. , Murphy, Declan , Canyelles, Jaume Morey , Jalbrzikowski, Maria , Arango, Celso , Murphy, Kieran C. , Pontillo, Maria , Armando, Marco , Vicari, Stefano , Shashi, Vandana , Hooper, Stephen R.
- Resource Type: journal article
- Date: 2015
Visual perception and processing in children with 22q11.2 deletion syndrome: associations with social cognition measures of face identity and emotion recognition
- Creator: McCabe, Kathryn L. , Marlin, Stuart , Cooper, Gavin , Morris, Robin , Schall, Ulrich , Murphy, Declan G. , Murphy, Kieran C. , Campbell, Linda E.
- Resource Type: journal article
- Date: 2016
Complete sequence of the 22q11.2 allele in 1,053 subjects with 22q11.2 deletion syndrome reveals modifiers of conotruncal heart defects
- Creator: Zhao, Yingjie , Diacou, Alexander , Johnston, H. Richard , Musfee, Fadi I. , McDonald-McGinn, Donna M. , McGinn, Daniel , Crowley, T. Blaine , Repetto, Gabriela M. , Swillen, Ann , Breckpot, Jeroen , Vermeesch, Joris R. , Kates, Wendy R. , Digilio, M. Cristina , Unolt, Marta , Marino, Bruno , Pontillo, Maria , Armando, Marco , Di Fabio, Fabio , Vicari, Stefano , van den Bree, Marianne , Campbell, Linda , Moss, Hayley , Owen, Michael J. , Murphy, Kieran C. , Murphy, Clodagh M. , Murphy, Declan , Schoch, Kelly , Shashi, Vandana , Tassone, Flora , Simon, Tony J. , Shprintzen, Robert J. , Philip, Nicole , Heine-Suñer, Damian , García-Miñaúr, Sixto , Fernández, Luis , Antonarakis, Stylianos E. , Biondi, Massimo , Boot, Erik , Breetvelt, Elemi , Busa, Tiffany , Butcher, Nancy , Buzzanca, Antonino , Carmel, Miri , Cleynen, Isabelle , Cutler, David , Dallapiccola, Bruno , de la Fuente Sanches, Maria Angeles , Epstein, Michael P. , Evers, Rens , Fernandez, L , Fritsch, Rosemarie , Algas, Fernando Garcia , Guo, Tingwei , Gur, Raquel , Hestand, Matthew S. , Heung, Tracy , Hooper, Stephen , Jin, Andrea , Kushan-Wells, Leila , Laorden-Nieto, Alejandra Terese , Lattanzi, Guido , Marshall, Christian , McCabe, Kathryn , Michaelovsky, Elena , Ornstein, Claudia , Silversides, Candice , Tran, Oanh , van Duin, Esther D. A. , Vergaelen, Elfi , Warren, Steve T. , Weinberger, Ronnie , Weizman, Abraham , Zhang, Zhengdong , Zwick, Michael , Bearden, Carrie E. , Vingerhoets, Claudia , van Amelsvoort, Therese , Eliez, Stephan , Schneider, Maude , Vorstman, Jacob A. S. , Gothelf, Doron , Zackai, Elaine , Agopian, A. J. , Gur, Raquel E. , Bassett, Anne S. , Emanuel, Beverly S. , Goldmuntz, Elizabeth , Mitchell, Laura E. , Wang, Tao , Morrow, Bernice E.
- Resource Type: journal article
- Date: 2020
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome
- Creator: Davies, Robert W. , Fiksinski, Ania M. , McDonald-McGinn, Donna M. , Swillen, Ann , Chow, Eva W. C. , van den Bree, Marianne , Emanuel, Beverly S. , Vermeesch, Joris R. , van Amelsvoort, Therese , Arango, Celso , Armando, Marco , Campbell, Linda E. , Breetvelt, Elemi J. , Cubells, Joseph F. , Eliez, Stephan , Garcia-Minaur, Sixto , Gothelf, Doron , Kates, Wendy R. , Murphy, Kieran C. , Murphy, Clodagh M. , Murphy, Declan G. , Philip, Nicole , Repetto, Gabriela M. , Williams, Nigel M. , Shashi, Vandana , Simon, Tony J. , Suñer, Damiàn Heine , Vicari, Stefano , Scherer, Stephen W. , Epstein, Michael P. , Warren, Stephen T. , Morrison, Sinead , Chawner, Samuel , Vingerhoets, Claudia , Hooper, Stephen R. , Breckpot, Jeroen , Vergaelen, Elfi , Vogels, Annick , Monks, Stephen , Prasad, Sarah E. , Sandini, Corrado , Schneider, Maude , Maeder, Johanna , Fraguas, David , Evers, Rens , Monfeuga, Thomas , Tassone, Flora , Morey-Canyelles, Jaume , Ousley, Opal Y. , Antshel, Kevin M. , Fremont, Wanda , Fritsch, Rosemarie , Ornstein, Claudia , Daly, Eileen M. , Costain, Gregory A. , Boot, Erik , Bassett, Anne S. , Heung, Tracy , Crowley, T. Blaine , Zackai, Elaine H. , Calkins, Monica E. , Gur, Ruben C. , McCabe, Kathryn L. , Busa, Tiffany , Schoch, Kelly , Pontillo, Maria , Duijff, Sasja N. , Owen, Michael J. , Kahn, René S. , Houben, Michiel , Kushan, Leila , Jalbrzikowski, Maria , Carmel, Miri , Mekori-Domachevsky, Ehud , Michaelovsky, Elena , Weinberger, Ronnie , Bearden, Carrie E. , Vorstman, Jacob A. S. , Gur, Raquel E. , Morrow, Bernice E.
- Resource Type: journal article
- Date: 2020