Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Stephan Eliez

Showing results (131-140 of 222) with videos related to

Pageof 23
Sort By:
Schizophrenia Bulletin|August 5, 2020
Abnormal Auditory Processing and Underlying Structural Changes in 22q11.2 Deletion SyndromeLucia-Manuela Cantonas, Valentina Mancini, Tonia A Rihs, et al.
Biological Psychiatry. Cognitive Neuroscience and Neuroimaging|May 9, 2018
Cortical Dysconnectivity Measured by Structural Covariance Is Associated With the Presence of Psychotic Symptoms in 22q11.2 Deletion SyndromeCorrado Sandini, Elisa Scariati, Maria Carmela Padula, et al.
The American Journal of Psychiatry|March 4, 2006
No evidence for an effect of COMT Val158Met genotype on executive function in patients with 22q11 deletion syndromeBronwyn Glaser, Martin Debbane, Christine Hinard, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 11, 2003
White matter tract alterations in fragile X syndrome: preliminary evidence from diffusion tensor imagingNaama Barnea-Goraly, Stephan Eliez, Maj Hedeus, et al.
American Journal of Medical Genetics|February 13, 2002
Reduced size of the amygdala in individuals with 47,XXY and 47,XXX karyotypesAnil J Patwardhan, Wendy E Brown, Bruce G Bender, et al.
Journal of Neurodevelopmental Disorders|August 4, 2015
Structural and functional connectivity in the default mode network in 22q11.2 deletion syndromeMaria Carmela Padula, Marie Schaer, Elisa Scariati, et al.
Psychological Medicine|January 18, 2018
Cortical morphology development in patients with 22q11.2 deletion syndrome at ultra-high risk of psychosisMaria Carmela Padula, Marie Schaer, Marco Armando, et al.
Biological Psychiatry. Cognitive Neuroscience and Neuroimaging|June 7, 2024
Longitudinal Analysis of Brain Function-Structure Dependencies in 22q11.2 Deletion Syndrome and Psychotic SymptomsSilas Forrer, Farnaz Delavari, Corrado Sandini, et al.
Schizophrenia Bulletin|December 22, 2021
Agency Deficits in a Human Genetic Model of Schizophrenia: Insights From 22q11DS PatientsRoy Salomon, Oliver Alan Kannape, Henrique Galvan Debarba, et al.
IEEE Transactions on Medical Imaging|September 7, 2018
Robust Recovery of Temporal Overlap Between Network Activity Using Transient-Informed Spatio-Temporal RegressionDaniela M Zoller, Thomas A W Bolton, Fikret Isik Karahanoglu, et al.
Pageof 23

Showing results (131-140 of 222) with videos related to

Sort By:
Pageof 23
Schizophrenia Bulletin|August 5, 2020
Abnormal Auditory Processing and Underlying Structural Changes in 22q11.2 Deletion SyndromeLucia-Manuela Cantonas, Valentina Mancini, Tonia A Rihs, et al.
Biological Psychiatry. Cognitive Neuroscience and Neuroimaging|May 9, 2018
Cortical Dysconnectivity Measured by Structural Covariance Is Associated With the Presence of Psychotic Symptoms in 22q11.2 Deletion SyndromeCorrado Sandini, Elisa Scariati, Maria Carmela Padula, et al.
The American Journal of Psychiatry|March 4, 2006
No evidence for an effect of COMT Val158Met genotype on executive function in patients with 22q11 deletion syndromeBronwyn Glaser, Martin Debbane, Christine Hinard, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 11, 2003
White matter tract alterations in fragile X syndrome: preliminary evidence from diffusion tensor imagingNaama Barnea-Goraly, Stephan Eliez, Maj Hedeus, et al.
American Journal of Medical Genetics|February 13, 2002
Reduced size of the amygdala in individuals with 47,XXY and 47,XXX karyotypesAnil J Patwardhan, Wendy E Brown, Bruce G Bender, et al.
Journal of Neurodevelopmental Disorders|August 4, 2015
Structural and functional connectivity in the default mode network in 22q11.2 deletion syndromeMaria Carmela Padula, Marie Schaer, Elisa Scariati, et al.
Psychological Medicine|January 18, 2018
Cortical morphology development in patients with 22q11.2 deletion syndrome at ultra-high risk of psychosisMaria Carmela Padula, Marie Schaer, Marco Armando, et al.
Biological Psychiatry. Cognitive Neuroscience and Neuroimaging|June 7, 2024
Longitudinal Analysis of Brain Function-Structure Dependencies in 22q11.2 Deletion Syndrome and Psychotic SymptomsSilas Forrer, Farnaz Delavari, Corrado Sandini, et al.
Schizophrenia Bulletin|December 22, 2021
Agency Deficits in a Human Genetic Model of Schizophrenia: Insights From 22q11DS PatientsRoy Salomon, Oliver Alan Kannape, Henrique Galvan Debarba, et al.
IEEE Transactions on Medical Imaging|September 7, 2018
Robust Recovery of Temporal Overlap Between Network Activity Using Transient-Informed Spatio-Temporal RegressionDaniela M Zoller, Thomas A W Bolton, Fikret Isik Karahanoglu, et al.
Pageof 23