Velo-Cardio-Facial Syndrome

Por Gothelf, Doron, Frisch, Amos, Michaelovsky, Elena, Weizman, Abraham, Shprintzen, Robert J.
Publicado em 2009

Risk gene-set and pathways in 22q11.2 deletion-related schizophrenia: a genealogical molecular approach

Por Michaelovsky, Elena, Carmel, Miri, Frisch, Amos, Salmon-Divon, Mali, Pasmanik-Chor, Metsada, Weizman, Abraham, Gothelf, Doron
Publicado no Transl Psychiatry (2019)

Genotype-phenotype correlation in 22q11.2 deletion syndrome

Por Michaelovsky, Elena, Frisch, Amos, Carmel, Miri, Patya, Miriam, Zarchi, Omer, Green, Tamar, Basel-Vanagaite, Lina, Weizman, Abraham, Gothelf, Doron
Publicado em 2012

Biological Effects of COMT Haplotypes and Psychosis Risk in 22q11.2 Deletion Syndrome

Por Gothelf, Doron, Law, Amanda J., Frisch, Amos, Chen, Jingshan, Zarchi, Omer, Michaelovsky, Elena, Ren-Patterson, Renee, Lipska, Barbara K., Carmel, Miri, Kolachana, Bhaskar, Weizman, Abraham, Weinberger, Daniel R.
Publicado em 2013

Runs of Homozygosity, Copy Number Variation, and Risk for Depression and Suicidal Behavior in an Arab Bedouin Kindred

Por Melhem, Nadine M., Hamdan, Sami, Klei, Lambertus, Wood, Shawn, Zelazny, Jamie, Frisch, Amos, Weizman, Abraham, Carmel, Miri, Michaelovsky, Elena, Farbstein, Ilana, Wasserman, Danuta, el Heib, Muhammad, Ferrell, Robert, Apter, Alan, Devlin, Bernie, Brent, David
Publicado no Psychiatr Genet (2017)

Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3

Por Guo, Tingwei, Repetto, Gabriela M., McDonald McGinn, Donna M., Chung, Jonathan H., Nomaru, Hiroko, Campbell, Christopher L., Blonska, Anna, Bassett, Anne S., Chow, Eva W.C., Mlynarski, Elisabeth E., Swillen, Ann, Vermeesch, Joris, Devriendt, Koen, Gothelf, Doron, Carmel, Miri, Michaelovsky, Elena, Schneider, Maude, Eliez, Stephan, Antonarakis, Stylianos E., Coleman, Karlene, Tomita-Mitchell, Aoy, Mitchell, Michael E., Digilio, M. Cristina, Dallapiccola, Bruno, Marino, Bruno, Philip, Nicole, Busa, Tiffany, Kushan-Wells, Leila, Bearden, Carrie E., Piotrowicz, Małgorzata, Hawuła, Wanda, Roberts, Amy E., Tassone, Flora, Simon, Tony J., van Duin, Esther D.A., van Amelsvoort, Thérèse A., Kates, Wendy R., Zackai, Elaine, Johnston, H. Richard, Cutler, David J., Agopian, A.J., Goldmuntz, Elizabeth, Mitchell, Laura E., Wang, Tao, Emanuel, Beverly S., Morrow, Bernice E.
Publicado no Circ Cardiovasc Genet (2017)

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

Por 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 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., Tran, Oanh, Holmans, Peter, 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, 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, Di Fabio, Fabio, 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, Béna, Frédérique Sloan, Antshel, Kevin M., Fremont, Wanda, Kates, Wendy R., Belzeaux, Raoul, Busa, Tiffany, Philip, Nicole, Campbell, Linda E., McCabe, Kathryn L., Hooper, Stephen R., Schoch, Kelly, Shashi, Vandana, Simon, Tony J., Tassone, Flora, Arango, Celso, Fraguas, David, García-Miñaúr, Sixto, Morey-Canyelles, Jaume, Rosell, Jordi, Suñer, Damià H., Raventos-Simic, Jasna, Epstein, Michael P., Williams, Nigel M., Bassett, Anne S.
Publicado no Mol Psychiatry (2020)