Zobrazeno 1 - 10
of 141
pro vyhledávání: '"Maude Schneider"'
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 16, Iss 1, Pp 1-16 (2024)
Abstract Backgrounds Social skills are frequently impaired in neurodevelopmental disorders and genetic conditions, including 22q11.2 deletion syndrome (22q11DS) and autism spectrum disorders (ASD). Although often assessed with questionnaires, direct
Externí odkaz:
https://doaj.org/article/8b7a92d3aa0f48ff9020bc620b8e0e51
Autor:
Yingjie Zhao, Yujue Wang, Lijie Shi, Donna M. McDonald-McGinn, T. Blaine Crowley, Daniel E. McGinn, Oanh T. Tran, Daniella Miller, Jhih-Rong Lin, Elaine Zackai, H. Richard Johnston, Eva W. C. Chow, Jacob A. S. Vorstman, Claudia Vingerhoets, Therese van Amelsvoort, Doron Gothelf, Ann Swillen, Jeroen Breckpot, Joris R. Vermeesch, Stephan Eliez, Maude Schneider, Marianne B. M. van den Bree, Michael J. Owen, Wendy R. Kates, Gabriela M. Repetto, Vandana Shashi, Kelly Schoch, Carrie E. Bearden, M. Cristina Digilio, Marta Unolt, Carolina Putotto, Bruno Marino, Maria Pontillo, Marco Armando, Stefano Vicari, Kathleen Angkustsiri, Linda Campbell, Tiffany Busa, Damian Heine-Suñer, Kieran C. Murphy, Declan Murphy, Sixto García-Miñaúr, Luis Fernández, International 22q11.2 Brain and Behavior Consortium (IBBC), Zhengdong D. Zhang, Elizabeth Goldmuntz, Raquel E. Gur, Beverly S. Emanuel, Deyou Zheng, Christian R. Marshall, Anne S. Bassett, Tao Wang, Bernice E. Morrow
Publikováno v:
npj Genomic Medicine, Vol 8, Iss 1, Pp 1-15 (2023)
Abstract Congenital heart disease (CHD) affecting the conotruncal region of the heart, occurs in 40–50% of patients with 22q11.2 deletion syndrome (22q11.2DS). This syndrome is a rare disorder with relative genetic homogeneity that can facilitate i
Externí odkaz:
https://doaj.org/article/8c4a618d8f784a9c9f58db40b2e0cf57
Publikováno v:
Frontiers in Psychiatry, Vol 13 (2022)
BackgroundCarriers of the 22q11.2 deletion syndrome (22q11DS) have an enhanced risk of developing psychotic disorders. Full-blown psychosis is typically diagnosed by late adolescence/adulthood. However, cognitive decline is already apparent as early
Externí odkaz:
https://doaj.org/article/c220cbcdca5c4ffea2c0789ede225403
Autor:
Valentina Mancini, Johanna Maeder, Karin Bortolin, Maude Schneider, Marie Schaer, Stephan Eliez
Publikováno v:
Translational Psychiatry, Vol 11, Iss 1, Pp 1-12 (2021)
Abstract Cognitive deficits in individuals at risk of psychosis represent a significant challenge for research, as current strategies for symptomatic treatment are often ineffective. Recent studies showed that atypical cognitive development predicts
Externí odkaz:
https://doaj.org/article/c0cdff24ebf34feda962ddee99d3f65b
Publikováno v:
BMC Psychiatry, Vol 21, Iss 1, Pp 1-18 (2021)
Abstract Background The 22q11.2 deletion syndrome (22q11DS) is a genetic syndrome that results in a highly variable profile of affected individuals of which impairments in the social domain and increased psychopathology are the most prominent. Notabl
Externí odkaz:
https://doaj.org/article/841489ab359e409f86192e945f737fc4
Autor:
Ilya M. Veer, Antje Riepenhausen, Matthias Zerban, Carolin Wackerhagen, Lara M. C. Puhlmann, Haakon Engen, Göran Köber, Sophie A. Bögemann, Jeroen Weermeijer, Aleksandra Uściłko, Netali Mor, Marta A. Marciniak, Adrian Dahl Askelund, Abbas Al-Kamel, Sarah Ayash, Giulia Barsuola, Vaida Bartkute-Norkuniene, Simone Battaglia, Yaryna Bobko, Sven Bölte, Paolo Cardone, Edita Chvojková, Kaja Damnjanović, Joana De Calheiros Velozo, Lena de Thurah, Yacila I. Deza-Araujo, Annika Dimitrov, Kinga Farkas, Clémence Feller, Mary Gazea, Donya Gilan, Vedrana Gnjidić, Michal Hajduk, Anu P. Hiekkaranta, Live S. Hofgaard, Laura Ilen, Zuzana Kasanova, Mohsen Khanpour, Bobo Hi Po Lau, Dionne B. Lenferink, Thomas B. Lindhardt, Dávid Á. Magas, Julian Mituniewicz, Laura Moreno-López, Sofiia Muzychka, Maria Ntafouli, Aet O’Leary, Ilenia Paparella, Nele Põldver, Aki Rintala, Natalia Robak, Anna M. Rosická, Espen Røysamb, Siavash Sadeghi, Maude Schneider, Roma Siugzdaite, Mirta Stantić, Ana Teixeira, Ana Todorovic, Wendy W. N. Wan, Rolf van Dick, Klaus Lieb, Birgit Kleim, Erno J. Hermans, Dorota Kobylińska, Talma Hendler, Harald Binder, Inez Myin-Germeys, Judith M. C. van Leeuwen, Oliver Tüscher, Kenneth S. L. Yuen, Henrik Walter, Raffael Kalisch
Publikováno v:
Translational Psychiatry, Vol 11, Iss 1, Pp 1-11 (2021)
Abstract The SARS-CoV-2 pandemic is not only a threat to physical health but is also having severe impacts on mental health. Although increases in stress-related symptomatology and other adverse psycho-social outcomes, as well as their most important
Externí odkaz:
https://doaj.org/article/4e12843f37be4cbc84aa71973320b0ee
Autor:
Joëlle Bagautdinova, Maria C. Padula, Daniela Zöller, Corrado Sandini, Maude Schneider, Marie Schaer, Stephan Eliez
Publikováno v:
Translational Psychiatry, Vol 10, Iss 1, Pp 1-15 (2020)
Abstract Disruptions of white matter microstructure have been widely reported in schizophrenia. However, the emergence of these alterations during preclinical stages remains poorly understood. 22q11.2 Deletion Syndrome (22q11.2DS) represents a unique
Externí odkaz:
https://doaj.org/article/3b197287a82046eaacd74998839eb366
Autor:
Maude Schneider, Thomas Vaessen, Esther D. A. van Duin, Zuzana Kasanova, Wolfgang Viechtbauer, Ulrich Reininghaus, Claudia Vingerhoets, Jan Booij, Ann Swillen, Jacob A. S. Vorstman, Thérèse van Amelsvoort, Inez Myin-Germeys
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 12, Iss 1, Pp 1-11 (2020)
Abstract Background 22q11.2 deletion syndrome (22q11DS) is a genetic disorder associated with an increased risk of psychiatric disorders. Vulnerability for psychopathology has been related to an increased reactivity to stress. Here, we examined affec
Externí odkaz:
https://doaj.org/article/e5c9717a88ca4f39bcb6f0b689677f25
Autor:
Laura Ilen, Clémence Feller, Stephan Eliez, Eva Micol, Farnaz Delavari, Carmen Sandi, Olivia Zanoletti, Maude Schneider
Publikováno v:
Comprehensive Psychoneuroendocrinology, Vol 9, Iss , Pp 100103- (2022)
Background: 22q11.2 deletion syndrome (22q11DS) is a neurogenetic condition associated to a high risk for psychiatric disorders, including psychosis. Individuals with 22q11DS are thought to experience increased levels of chronic stress, which could l
Externí odkaz:
https://doaj.org/article/73f4b40cf89d4d6b898e746fe61926cb
Autor:
Corrado Sandini, Daniela Zöller, Maude Schneider, Anjali Tarun, Marco Armando, Barnaby Nelson, Paul G Amminger, Hok Pan Yuen, Connie Markulev, Monica R Schäffer, Nilufar Mossaheb, Monika Schlögelhofer, Stefan Smesny, Ian B Hickie, Gregor Emanuel Berger, Eric YH Chen, Lieuwe de Haan, Dorien H Nieman, Merete Nordentoft, Anita Riecher-Rössler, Swapna Verma, Andrew Thompson, Alison Ruth Yung, Patrick D McGorry, Dimitri Van De Ville, Stephan Eliez
Publikováno v:
eLife, Vol 10 (2021)
Causal interactions between specific psychiatric symptoms could contribute to the heterogenous clinical trajectories observed in early psychopathology. Current diagnostic approaches merge clinical manifestations that co-occur across subjects and coul
Externí odkaz:
https://doaj.org/article/a5a6f78b8748495e9632964859498719