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Bruce I Turetsky

Showing results (101-110 of 131) with videos related to

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Schizophrenia Research|September 25, 2014
Verbal working memory in schizophrenia from the Consortium on the Genetics of Schizophrenia (COGS) study: the moderating role of smoking status and antipsychotic medicationsJunghee Lee, Michael F Green, Monica E Calkins, et al.
Schizophrenia Research|November 25, 2015
Genetic assessment of additional endophenotypes from the Consortium on the Genetics of Schizophrenia Family StudyTiffany A Greenwood, Laura C Lazzeroni, Monica E Calkins, et al.
Schizophrenia Research|January 11, 2014
Deficient prepulse inhibition in schizophrenia detected by the multi-site COGSNeal R Swerdlow, Gregory A Light, Joyce Sprock, et al.
Schizophrenia Research|October 13, 2014
The utility of P300 as a schizophrenia endophenotype and predictive biomarker: clinical and socio-demographic modulators in COGS-2Bruce I Turetsky, Erich M Dress, David L Braff, et al.
JAMA Psychiatry|October 10, 2019
Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) StudyTiffany A Greenwood, Laura C Lazzeroni, Adam X Maihofer, et al.
Schizophrenia Research|May 28, 2017
Deficient prepulse inhibition in schizophrenia in a multi-site cohort: Internal replication and extensionNeal R Swerdlow, Gregory A Light, Michael L Thomas, et al.
Schizophrenia Bulletin|June 7, 2014
Comparison of the heritability of schizophrenia and endophenotypes in the COGS-1 family studyGregory Light, Tiffany A Greenwood, Neal R Swerdlow, et al.
Biological Psychiatry. Cognitive Neuroscience and Neuroimaging|April 27, 2025
Presence, severity, and functional associations of incomplete hippocampal inversion in 22q11.2 deletion syndromeDavid Roalf, Ally Atkins, Adam Czernuszenko, et al.
Journal of Neurodevelopmental Disorders|June 25, 2024
Computer-vision analysis of craniofacial dysmorphology in 22q11.2 deletion syndrome and psychosis spectrum disordersDavid R Roalf, Donna M McDonald-McGinn, Joelle Jee, et al.
Schizophrenia Research|March 10, 2007
Multi-site studies of acoustic startle and prepulse inhibition in humans: initial experience and methodological considerations based on studies by the Consortium on the Genetics of SchizophreniaNeal R Swerdlow, Joyce Sprock, Gregory A Light, et al.
Pageof 14

Showing results (101-110 of 131) with videos related to

Sort By:
Pageof 14
Schizophrenia Research|September 25, 2014
Verbal working memory in schizophrenia from the Consortium on the Genetics of Schizophrenia (COGS) study: the moderating role of smoking status and antipsychotic medicationsJunghee Lee, Michael F Green, Monica E Calkins, et al.
Schizophrenia Research|November 25, 2015
Genetic assessment of additional endophenotypes from the Consortium on the Genetics of Schizophrenia Family StudyTiffany A Greenwood, Laura C Lazzeroni, Monica E Calkins, et al.
Schizophrenia Research|January 11, 2014
Deficient prepulse inhibition in schizophrenia detected by the multi-site COGSNeal R Swerdlow, Gregory A Light, Joyce Sprock, et al.
Schizophrenia Research|October 13, 2014
The utility of P300 as a schizophrenia endophenotype and predictive biomarker: clinical and socio-demographic modulators in COGS-2Bruce I Turetsky, Erich M Dress, David L Braff, et al.
JAMA Psychiatry|October 10, 2019
Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) StudyTiffany A Greenwood, Laura C Lazzeroni, Adam X Maihofer, et al.
Schizophrenia Research|May 28, 2017
Deficient prepulse inhibition in schizophrenia in a multi-site cohort: Internal replication and extensionNeal R Swerdlow, Gregory A Light, Michael L Thomas, et al.
Schizophrenia Bulletin|June 7, 2014
Comparison of the heritability of schizophrenia and endophenotypes in the COGS-1 family studyGregory Light, Tiffany A Greenwood, Neal R Swerdlow, et al.
Biological Psychiatry. Cognitive Neuroscience and Neuroimaging|April 27, 2025
Presence, severity, and functional associations of incomplete hippocampal inversion in 22q11.2 deletion syndromeDavid Roalf, Ally Atkins, Adam Czernuszenko, et al.
Journal of Neurodevelopmental Disorders|June 25, 2024
Computer-vision analysis of craniofacial dysmorphology in 22q11.2 deletion syndrome and psychosis spectrum disordersDavid R Roalf, Donna M McDonald-McGinn, Joelle Jee, et al.
Schizophrenia Research|March 10, 2007
Multi-site studies of acoustic startle and prepulse inhibition in humans: initial experience and methodological considerations based on studies by the Consortium on the Genetics of SchizophreniaNeal R Swerdlow, Joyce Sprock, Gregory A Light, et al.
Pageof 14