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
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
Mandibulofacial dysostosis with microcephaly: mutation and database update
- Creator: Huang, Lijia , Vanstone, Megan R. , Estrella, Jane , Faghfoury, Hanna , Favaro, Francine P. , Goel, Himanshu , Gregersen, Pernille A. , Gripp, Karen W. , Grix, Art , Guion-Almeida, Maria-Leine , Harr, Margaret H. , Hudson, Cindy , Hartley, Taila , Hunter, Alasdair G. W. , Johnson, John , Joss, Shelagh K. , Kimball, Amy , Kini, Usha , Kline, Antoine D. , Lauzon, Julie , Lildballe, Dorte L. , López-González, Vanesa , Martinezmoles, Johanna , Osmond, Matthew , Meldrum, Cliff , Mirzaa, Ghayda M. , Morel, Chantal F. , Morton, Jenny E. V. , Pyle, Louise C. , Quintero-Rivera, Fabiola , Richer, Julie , Scheuerle, Angela E. , Schönewolf-Greulich, Bitten , Shears, Deborah J. , Barrowman, Nick , Silver, Josh , Smith, Amanda C. , Temple, I. Karen , van de Kamp, Jiddeke M. , van Dijk, Fleur S. , Vandersteen, Anthony M. , White, Sue M. , Zackai, Elaine H. , Zou, Ruobing , Consortium, Care4Rare Canada , Allanson, Judith , Bulman, Dennis E. , Boycott, Kym M. , Lines, Matthew A. , Baker, Laura , Dabir, Tabib A. , Dipple, Katrina M. , Dobyns, William B.
- Resource Type: journal article
- Date: 2015
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