Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Ronnie Weinberger"'
Autor:
Tyler M. Moore, Deby Salzer, Carrie E. Bearden, Monica E. Calkins, Wendy R. Kates, Leila Kushan, Robert Sean Gallagher, Dafna Sofrin Frumer, Ronnie Weinberger, Donna M. McDonald-McGinn, Raquel E. Gur, Doron Gothelf
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 13, Iss 1, Pp 1-8 (2021)
Abstract Background Pathways leading to psychosis in 22q11.2 deletion syndrome (22q11.2DS) have been the focus of intensive research during the last two decades. One of the common clinical risk factors for the evolution of psychosis in 22q11.2DS is t
Externí odkaz:
https://doaj.org/article/91d96000cb084140a83be350981f884c
Autor:
Ruben C. Gur, Tyler M. Moore, Ronnie Weinberger, Ehud Mekori‐Domachevsky, Raz Gross, Beverly S. Emanuel, Elaine H. Zackai, Edward Moss, Robert Sean Gallagher, Daniel E. McGinn, Terrence Blaine Crowley, Donna McDonald‐McGinn, Doron Gothelf, Raquel E. Gur
Publikováno v:
Brain and Behavior, Vol 11, Iss 8, Pp n/a-n/a (2021)
Abstract Intelligence quotient (IQ) testing is standard for evaluating cognitive abilities in genomic studies but requires professional expertise in administration and interpretation, and IQ scores do not translate into insights on implicated brain s
Externí odkaz:
https://doaj.org/article/93a1926652d441a1b7d5166241c9b622
Autor:
Ran Barzilay, Ruben C. Gur, Lauren K. White, Doron Gothelf, Donna M. McDonald-McGinn, Raquel E. Gur, Shachar Shani, Tyler M. Moore, Elaine H. Zackai, Ronnie Weinberger, Noam Matalon, Beverly S. Emanuel
Publikováno v:
Journal of Psychiatric Research. 138:319-325
Background The presentation of neurogenetic disorders such as 22q11.2 Deletion Syndrome (22q11.2DS) includes broad neuropsychiatric phenotypes that impact functioning and require assessment and treatment. Like in non-syndromal neuropsychiatric disord
Autor:
Yaffa Serur, Efrat Sher-Censor, Dafna Sofrin-Frumer, Keren Daon, Dolly Sobol-Havia, Ronnie Weinberger, Cory Shulman, Doron Gothelf
Publikováno v:
Child Psychiatry & Human Development.
This study examined the associations of parents' expressed emotion (EE) and parenting stress, with behavioral problems of children with 22q11.2 deletion syndrome, idiopathic autism (iASD) and typically developing (TD) children. Parents of children ag
Autor:
Deby Salzer, Carrie E. Bearden, Leila Kushan, Robert Sean Gallagher, Dafna Sofrin Frumer, Doron Gothelf, Wendy R. Kates, Donna M. McDonald-McGinn, Raquel E. Gur, Monica E. Calkins, Tyler M. Moore, Ronnie Weinberger
Publikováno v:
Journal of neurodevelopmental disorders, vol 13, iss 1
Journal of Neurodevelopmental Disorders
Journal of Neurodevelopmental Disorders, Vol 13, Iss 1, Pp 1-8 (2021)
Journal of Neurodevelopmental Disorders
Journal of Neurodevelopmental Disorders, Vol 13, Iss 1, Pp 1-8 (2021)
Background Pathways leading to psychosis in 22q11.2 deletion syndrome (22q11.2DS) have been the focus of intensive research during the last two decades. One of the common clinical risk factors for the evolution of psychosis in 22q11.2DS is the presen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d2a7cc43ee2353eecdc5d4a15736e9a
https://escholarship.org/uc/item/6m66k192
https://escholarship.org/uc/item/6m66k192
Autor:
Daniel E. McGinn, Ruben C. Gur, Ehud Mekori-Domachevsky, Beverly S. Emanuel, Doron Gothelf, Donna M. McDonald-McGinn, Raquel E. Gur, Raz Gross, Edward Moss, Robert Sean Gallagher, Tyler M. Moore, Terrence B. Crowley, Ronnie Weinberger, Elaine H. Zackai
Publikováno v:
Brain and Behavior
Brain and Behavior, Vol 11, Iss 8, Pp n/a-n/a (2021)
Brain and Behavior, Vol 11, Iss 8, Pp n/a-n/a (2021)
Intelligence quotient (IQ) testing is standard for evaluating cognitive abilities in genomic studies but requires professional expertise in administration and interpretation, and IQ scores do not translate into insights on implicated brain systems th
Autor:
Ehud Mekori-Domachevsky, Doron Gothelf, Shachar Shani, Abraham Weizman, Idit Dekel, Michal Taler, Yael Guri, Shira Dar, Ronnie Weinberger
Publikováno v:
Schizophrenia research. 231
Background Individuals with 22q11.2 deletion syndrome (22q11.2DS) are at risk for having both psychotic and immune disorders, thus, implying a possible link between the two. The aim of the current study was to evaluate the usefulness of the neutrophi
Autor:
Doron Gothelf, Stephan Eliez, Shachar Shani, Mariela Mosheva, Johanna Maeder, Ronnie Weinberger, Maude Schneider, Dana Basel
Publikováno v:
European Child and Adolescent Psychiatry (2021)
This study aimed to retrospectively evaluate an association between stimulant treatment for attention-deficit/hyperactivity disorder (ADHD) in individuals with 22q11.2DS and the development of psychotic disorders, to evaluate long-term effectiveness
Autor:
Abraham Weizman, Ehud Mekori-Domachevsky, Amos Frisch, Elena Michaelovsky, Doron Gothelf, Ronnie Weinberger, Miri Carmel
Publikováno v:
The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry. 22(1)
22q11.2 deletion syndrome (DS) is the strongest known genetic risk for schizophrenia. Methylome screening was conducted to elucidate possible involvement of epigenetic alterations in the emergence of schizophrenia spectrum disorders (SZ-SD) in 22q11.
Autor:
Richard Duncan, Tao Wang, Carrie E. Bearden, David J. Cutler, Stephen T. Warren, Maria Pontillo, Robert Sean Gallagher, Elemi J. Breetvelt, Tingwei Guo, Nancy J. Butcher, Jennifer G. Mulle, Claudia Ornstein, Claudia Vingerhoets, Clodagh M. Murphy, Ehud Mekori-Domachevsky, Wendy R. Kates, Jacob A. S. Vorstman, Tracy Heung, Joris Vermeesch, Maria Gudbrandsen, Ann Swillen, H. Richard Johnston, Oanh Tran, Marco Armando, Joseph F. Cubells, Raoul Belzeaux, Jeroen Breckpot, Bruno Marino, Tony J. Simon, Harold I. Salmons, Maria Jalbrzikowski, Wanda Fremont, Anna J. Voss, Worrawat Engchuan, Opal Y. Ousley, Stefano Vicari, Jordi Rosell, Sixto García-Miñaur, Declan G. Murphy, Alexander Diacou, Ania Fiksinski, Abraham Weizman, Edward Moss, Stephan Eliez, Miri Carmel, Vandana Shashi, Anne S. Bassett, Ronnie Weinberger, Hayley Moss, Marianne Bernadette van den Bree, Kelly Schoch, Maude Schneider, Linda E. Campbell, Sasja N. Duijff, Eileen Daly, Annick Vogels, Stephen R. Hooper, David Fraguas, Sarah E. Prasad, Chelsea Lowther, Michael John Owen, Frédérique Béna, Gabriela M. Repetto, Eva W.C. Chow, Bernice E. Morrow, Robert J. Sharkus, Celso Arango, Christian R. Marshall, Jasna Raventos-Simic, Jaume Morey-Canyelles, Tiffany Busa, Andrea Jin, James T.R. Walters, Leila Kushan, Wolfram Demaerel, Monica E. Calkins, Jhih Rong Lin, Elaine H. Zackai, Esther D.A. van Duin, Antonio Buzzanca, Corrado Sandini, Kieran C. Murphy, Beverly S. Emanuel, Erik Boot, Maria Niarchou, Nigel Williams, Elfi Vergaelen, Maria Cristina Digilio, Daniele Merico, Karlene Coleman, Gregory A. Costain, Matthew S. Hestand, Peter Holmans, Michael E. Zwick, Michael P. Epstein, Damià H. Suñer, Yingjie Zhao, Marta Unolt, Kathryn McCabe, Aaron M. Holleman, Zhengdong Zhang, Rosemarie Fritsch, Alex V. Kotlar, Elena Michaelovsky, T. Blaine Crowley, Brenna Lilley, Sunny X. Tang, Rens Evers, Ruben C. Gur, Isabelle Cleynen, Flora Tassone, Nicole Philip, Kevin M. Antshel, Koen Devriendt, Antonio F. Pardiñas, Pankaj Chopra, Thomas Monfeuga, Fabio Di Fabio, Therese van Amelsvoort, Aaron Golden, Doron Gothelf, Donna M. McDonald-McGinn, Raquel E. Gur, Daniel E. McGinn
Publikováno v:
Molecular Psychiatry
Molecular Psychiatry, Nature Publishing Group, 2020, ⟨10.1038/s41380-020-0654-3⟩
Molecular Psychiatry, 2020, ⟨10.1038/s41380-020-0654-3⟩
Molecular Psychiatry (2020)
Molecular psychiatry
Molecular Psychiatry, 26(8), 4496-4510. Nature Publishing Group
Molecular Psychiatry, Nature Publishing Group, 2020, ⟨10.1038/s41380-020-0654-3⟩
Molecular Psychiatry, 2020, ⟨10.1038/s41380-020-0654-3⟩
Molecular Psychiatry (2020)
Molecular psychiatry
Molecular Psychiatry, 26(8), 4496-4510. Nature Publishing Group
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=doi_dedup___::a4c91788310dcf6c66ef3ac3973170b9
http://hdl.handle.net/20.500.12278/33344
http://hdl.handle.net/20.500.12278/33344