Altered structural network architecture is predictive of the presence of psychotic symptoms in patients with 22q11.2 deletion syndrome

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

Hippocampal volume reduction in chromosome 22q11.2 deletion syndrome (22q11.2DS): a longitudinal study of morphometry and symptomatology

Autor: Astrid Flahault, Marie-Christine Ottet, Martin Debbané, Marie Schaer, Stephan Eliez

Publikováno v: Psychiatry Research, Vol. 203, No 1 (2012) pp. 1-5
Psychiatry research

Recent studies observed an association between the structural integrity of the hippocampal structure and the manifestations of clinically significant psychotic symptoms in participants at high risk for psychosis. The present study sought to investiga

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ee616f9112f0e2622c315633422cfcc
https://archive-ouverte.unige.ch/unige:29189

Eye gaze during face processing in children and adolescents with 22q11.2 deletion syndrome

Autor: Bronwyn Glaser, Stylianos E. Antonarakis, Martin Debbané, Marie-Christine Ottet, Pascal Eric Zesiger, Patrik Vuilleumier, Stephan Eliez

Publikováno v: Journal of the American Academy of Child and Adolescent Psychiatry
Journal of the American Academy of Child & Adolescent Psychiatry, Vol. 49, No 7 (2010) pp. 665-674

Objective The 22q11.2 deletion syndrome (22q11DS) is a neurogenetic syndrome with high risk for the development of psychiatric disorder. There is interest in identifying reliable markers for measuring and monitoring socio-emotional impairments in 22q

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0240b7c6301a1681242e6cf24b4408c0
https://pubmed.ncbi.nlm.nih.gov/20610136

Reduced fronto-temporal and limbic connectivity in the 22q11.2 deletion syndrome: vulnerability markers for developing schizophrenia?

Autor: Stephan Eliez, Marie-Christine Ottet, Leila Cammoun, Jean-Philippe Thiran, Marie Schaer, Maude Schneider, Martin Debbané

Publikováno v: PloS one
Plos One, vol. 8, no. 3, pp. e58429
PLoS ONE
PLoS ONE, Vol 8, Iss 3, p e58429 (2013)
PLOS ONE, Vol. 8, No 3 (2013) P. e58429

The 22q11.2 deletion syndrome (22q11DS) is a widely recognized genetic model allowing the study of neuroanatomical biomarkers that underlie the risk for developing schizophrenia. Recent advances in magnetic resonance image analyses enable the examina

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::383766a84ea030d75e0a23c184ec54db

Regional cortical volumes and congenital heart disease: a MRI study in 22q11.2 deletion syndrome

Autor: Maude Schneider, Bronwyn Glaser, Meritxell Bach Cuadra, Marie-Christine Ottet, Stephan Eliez, Jean-Philippe Thiran, Martin Debbané, Marie Schaer

Publikováno v: Journal of neurodevelopmental disorders
Journal of Neurodevelopmental Disorders, Vol. 2, No 4 (2010) pp. 224-234
Journal of Neurodevelopmental Disorders, vol. 2, no. 4, pp. 224-234

Children with congenital heart disease (CHD) who survive surgery often present impaired neurodevelopment and qualitative brain anomalies. However, the impact of CHD on total or regional brain volumes only received little attention. We address this qu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15d61f60645b51678175e708f5d0c16e