Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Elisa Scariati"'
Autor:
Maria C. Padula, Elisa Scariati, Marie Schaer, Corrado Sandini, Marie Christine Ottet, Maude Schneider, Dimitri Van De Ville, Stephan Eliez
Publikováno v:
NeuroImage: Clinical, Vol 16, Iss , Pp 142-150 (2017)
22q11.2 deletion syndrome (22q11DS) represents a homogeneous model of schizophrenia particularly suitable for the search of neural biomarkers of psychosis. Impairments in structural connectivity related to the presence of psychotic symptoms have been
Externí odkaz:
https://doaj.org/article/cd64c08000c94ef78f68fcd1b0bd7ad1
Publikováno v:
Frontiers in Psychiatry, Vol 9 (2018)
22q11.2 deletion syndrome (22q11DS) is a neurogenetic disorder that causes a high risk of developing schizophrenia, thus representing a unique model for the investigation of biomarkers of psychosis. Cognitive and clinical risk factors have been ident
Externí odkaz:
https://doaj.org/article/c970e42249834d868075c867c49ccf71
Autor:
Corrado Sandini, Daniela Zöller, Elisa Scariati, Maria C. Padula, Maude Schneider, Marie Schaer, Dimitri Van De Ville, Stephan Eliez
Publikováno v:
Frontiers in Neuroscience, Vol 12 (2018)
Background: Schizophrenia is currently considered a neurodevelopmental disorder of connectivity. Still few studies have investigated how brain networks develop in children and adolescents who are at risk for developing psychosis. 22q11.2 Deletion Syn
Externí odkaz:
https://doaj.org/article/965c40dfd7e84cbe92a6390ee1442d89
Autor:
František Váša, Alessandra Griffa, Elisa Scariati, Marie Schaer, Sébastien Urben, Stephan Eliez, Patric Hagmann
Publikováno v:
NeuroImage: Clinical, Vol 10, Iss C, Pp 239-249 (2016)
Chromosome 22q11.2 deletion syndrome (22q11DS) is a genetic disease known to lead to cerebral structural alterations, which we study using the framework of the macroscopic white-matter connectome. We create weighted connectomes of 44 patients with 22
Externí odkaz:
https://doaj.org/article/3c148161ae344fa6b2a73fc578f057ad
Autor:
Maria Carmela Padula, Marie Schaer, Elisa Scariati, A Kadir Mutlu, Daniela Zöller, Maude Schneider, Stephan Eliez
Publikováno v:
PLoS ONE, Vol 12, Iss 11, p e0187493 (2017)
Several neurodevelopmental diseases are characterized by impairments in cortical morphology along with altered white matter connectivity. However, the relationship between these two measures is not yet clear. In this study, we propose a novel methodo
Externí odkaz:
https://doaj.org/article/413f693da1ff4910b8f70efd95ca9d3d
Autor:
Stephan Eliez, Johanna Maeder, Maria Carmela Padula, Marie Schaer, Maude Schneider, Elisa Scariati
Publikováno v:
Human Brain Mapping. 38:2177-2189
Large-scale brain networks play a prominent role in cognitive abilities and their activity is impaired in psychiatric disorders, such as schizophrenia. Patients with 22q11.2 deletion syndrome (22q11DS) are at high risk of developing schizophrenia and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10cb107e2647f9d0fdf17f4035453655
https://doi.org/10.1002/hbm.23512
https://doi.org/10.1002/hbm.23512
Publikováno v:
Journal of Neural Transmission. 123:823-839
Patients affected by 22q11.2 deletion syndrome (22q11DS) present a characteristic cognitive and psychiatric profile and have a genetic predisposition to develop schizophrenia. Although brain morphological alterations have been shown in the syndrome,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2057fa4f9a8eb3905fb644ba3a3da2d0
https://doi.org/10.1007/s00702-016-1548-z
https://doi.org/10.1007/s00702-016-1548-z
Autor:
Daniela Zöller, Maria Carmela Padula, Marie Schaer, Maude Schneider, Corrado Sandini, Stephan Eliez, Marco Armando, Elisa Scariati
Publikováno v:
Psychological Medicine, Vol. 48, No 14 (2018) pp. 2375-2383
Background. Patients with 22q11.2 deletion syndrome (22q11DS) present a high risk of developing psychosis. While clinical and cognitive predictors for the conversion towards a full-blown psychotic disorder are well defined and largely used in practic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38aa8623c55e4034f96bc11d7e654d5f
https://pubmed.ncbi.nlm.nih.gov/29338796
https://pubmed.ncbi.nlm.nih.gov/29338796
Autor:
Marie Schaer, Corrado Sandini, Dimitri Van De Ville, Maude Schneider, Elisa Scariati, Stephan Eliez, Maria Carmela Padula
Publikováno v:
Biological Psychiatry: Cognitive Neuroscience and Neuroimaging, Vol. 3, No 5 (2018) pp. 433-442
Background 22q11.2 deletion syndrome (22q11DS) is the third-largest known genetic risk factor for the development of psychosis. Dysconnectivity has consistently been implicated in the physiopathology of psychosis. Structural covariance of cortical mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e650800c2cced9c1a4d4f59f0b0ed78c
https://archive-ouverte.unige.ch/unige:104870
https://archive-ouverte.unige.ch/unige:104870
Autor:
Marie Schaer, Corrado Sandini, Stephan Eliez, Elisa Scariati, Maria Carmela Padula, Dimitri Van De Ville, Maude Schneider, Daniela Zöller
Publikováno v:
Schizophrenia Research, Vol. 193 (2018) pp. 319-328
Chromosome 22q11.2 deletion syndrome (22q11DS) is a neurodevelopmental disorder associated with a broad phenotype of clinical, cognitive and psychiatric features. Due to the very high prevalence of schizophrenia (30-40%), the investigation of psychot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::811beeeb80503451b31ac5c697b9355d
https://pubmed.ncbi.nlm.nih.gov/28803847
https://pubmed.ncbi.nlm.nih.gov/28803847