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D Rujescu

Showing results (81-90 of 104) with videos related to

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Translational Psychiatry|July 8, 2015
Duplications in RB1CC1 are associated with schizophrenia; identification in large European sample setsF Degenhardt, L Priebe, S Meier, et al.
Psychological Medicine|November 3, 2017
Associations between psychosis endophenotypes across brain functional, structural, and cognitive domainsR Blakey, S Ranlund, E Zartaloudi, et al.
Molecular Psychiatry|August 10, 2016
Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropeniaS E Legge, M L Hamshere, S Ripke, et al.
Molecular Psychiatry|July 13, 2016
Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropeniaS E Legge, M L Hamshere, S Ripke, et al.
Molecular Psychiatry|January 4, 2018
Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropeniaS E Legge, M L Hamshere, S Ripke, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 30, 2024
Contribution of Rare and Potentially Functionally Relevant Sequence Variants in Schizophrenia Risk-Locus Xq28,distalI Claus, S Sivalingam, A C Koller, et al.
Molecular Psychiatry|April 7, 2010
Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorderH J Williams, N Norton, S Dwyer, et al.
Translational Psychiatry|July 27, 2012
Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seekingA Terracciano, T Esko, A R Sutin, et al.
Molecular Psychiatry|December 18, 2013
Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT)T Lencz, E Knowles, G Davies, et al.
Molecular Psychiatry|August 2, 2007
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophreniaC Francks, S Maegawa, J Laurén, et al.
Pageof 11

Showing results (81-90 of 104) with videos related to

Sort By:
Pageof 11
Translational Psychiatry|July 8, 2015
Duplications in RB1CC1 are associated with schizophrenia; identification in large European sample setsF Degenhardt, L Priebe, S Meier, et al.
Psychological Medicine|November 3, 2017
Associations between psychosis endophenotypes across brain functional, structural, and cognitive domainsR Blakey, S Ranlund, E Zartaloudi, et al.
Molecular Psychiatry|August 10, 2016
Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropeniaS E Legge, M L Hamshere, S Ripke, et al.
Molecular Psychiatry|July 13, 2016
Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropeniaS E Legge, M L Hamshere, S Ripke, et al.
Molecular Psychiatry|January 4, 2018
Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropeniaS E Legge, M L Hamshere, S Ripke, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 30, 2024
Contribution of Rare and Potentially Functionally Relevant Sequence Variants in Schizophrenia Risk-Locus Xq28,distalI Claus, S Sivalingam, A C Koller, et al.
Molecular Psychiatry|April 7, 2010
Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorderH J Williams, N Norton, S Dwyer, et al.
Translational Psychiatry|July 27, 2012
Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seekingA Terracciano, T Esko, A R Sutin, et al.
Molecular Psychiatry|December 18, 2013
Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT)T Lencz, E Knowles, G Davies, et al.
Molecular Psychiatry|August 2, 2007
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophreniaC Francks, S Maegawa, J Laurén, et al.
Pageof 11