Schaer, Marie

 
 
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2017

Scientific Articles

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Altered structural network architecture is predictive of the presence of psychotic symptoms in patients with 22q11.2 deletion syndromePadula, Maria; Scariati Jaussi, Elisa; Schaer, Marie; Sandini, Corrado; ... Eliez, Stéphan
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Disentangling resting-state BOLD variability and PCC functional connectivity in 22q11.2 deletion syndromeZoeller, Daniela; Schaer, Marie; Scariati Jaussi, Elisa; Padula, Maria; ... Van De Ville, Dimitri
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Implication of reward alterations in the expression of negative symptoms in 22q11.2 deletion syndrome: a behavioural and DTI studyDubourg, Lydia; Schneider, Maude; Padula, Maria; Chambaz, Léa; ... Eliez, Stéphan
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Morphological brain changes associated with negative symptoms in patients with 22q11.2 Deletion SyndromeMihailov, Angéline; Padula, Maria; Scariati Jaussi, Elisa; Schaer, Marie; ... Eliez, Stéphan
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Multimodal investigation of triple network connectivity in patients with 22q11DS and association with executive functionsPadula, Maria; Schaer, Marie; Scariati Jaussi, Elisa; Maeder, Johanna; ... Eliez, Stéphan
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Psychotic symptoms influence the development of anterior cingulate BOLD variability in 22q11.2 deletion syndromeZoeller, Daniela; Padula, Maria; Sandini, Corrado; Schneider, Maude; ... Eliez, Stéphan
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Social orienting and joint attention in preschoolers with autism spectrum disordersFranchini, Martina; Glaser, Bronwyn; Woodde Wilde, Hilary; Gentaz, Edouard; ... Schaer, Marie
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Subthreshold Psychosis in 22q11.2 Deletion Syndrome: Multisite Naturalistic StudyWeisman, Omri; Guri, Yael; Gur, Raquel E; McDonald-McGinn, Donna M; ... Gothelf, Doron

Professional Articles

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Adolescence is the starting point of sex-dichotomous COMT genetic effectsSannino, S; Padula, Maria; Managò, F; Schaer, Marie; ... Papaleo, F

Thesis supervisions

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Investigating candidate biomarkers of psychosis through multimodal neuroimaging in 22q11.2 deletion syndromePadula, Maria;
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Vers une meilleure compréhension de l’hétérogénéité du développement sociocommunicatif chez les jeunes enfants avec un Trouble du Spectre de l’AutismeFranchini, Martina;

2016

Scientific Articles

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Aberrant Development of Speech Processing in Young Children with Autism: New Insights from Neuroimaging BiomarkersSperdin, Holger Franz; Schaer, Marie;
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Abnormal spindle-like microcephaly-associated (ASPM) mutations strongly disrupt neocortical structure but spare the hippocampus and long-term memoryPassemard, Sandrine; Verloes, Alain; Billette de Villemeur, Thierry; Boespflug-Tanguy, Odile; ... Schaer, Marie
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An affected core drives network integration deficits of the structural connectome in 22q11.2 deletion syndromeVáša, František; Griffa, Alessandra; Scariati Jaussi, Elisa; Schaer, Marie; ... Hagmann, Patric
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Brief Report: A Preference for Biological Motion Predicts a Reduction in Symptom Severity 1 Year Later in Preschoolers with Autism Spectrum DisordersFranchini, Martina; Wood de Wilde, Hilary; Glaser, Bronwyn; Gentaz, Edouard; ... Schaer, Marie
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Developmental trajectories of executive functions in 22q11.2 deletion syndromeMaeder, Johanna; Schneider, Maude; Bostelmann, Mathilde; Debbané, Martin; ... Eliez, Stéphan
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Large-scale functional network reorganization in 22q11.2 deletion syndrome revealed by modularity analysisScariati Jaussi, Elisa; Schaer, Marie; Karahanoglu, Fikret Isik; Schneider, Maude; ... Eliez, Stéphan
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Long-range dysconnectivity in frontal and midline structures is associated to psychosis in 22q11.2 deletion syndromeScariati Jaussi, Elisa; Padula, Maria; Schaer, Marie; Eliez, Stéphan;
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Visual memory profile in 22q11.2 microdeletion syndrome: are there differences in performance and neurobiological substrates between tasks linked to ventral and dorsal visual brain structures? A cross-sectional and longitudinal studyBostelmann, Mathilde; Schneider, Maude; Padula, Maria; Maeder, Johanna; ... Eliez, Stéphan
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Visual processing of emotional dynamic faces in 22q11.2 deletion syndromeFranchini, Martina; Schaer, Marie; Glaser, Bronwyn; Kott-Radecka, Monika; ... Eliez, Stéphan
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