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  1. Article

    Open Access

    Evidence supporting the use of a brief cognitive assessment in routine clinical assessment for psychosis

    Cognitive impairment is a core feature of psychosis. Full cognitive assessments are not often conducted in routine clinical practice as administration is time-consuming. Here, we investigated whether brief tes...

    M. Cowman, E. Lonergan, T. Burke, C. R. Bowie, A. Corvin, D. W. Morris in Schizophrenia (2022)

  2. Article

    Open Access

    Publisher Correction: Brain charts for the human lifespan

    R. A. I. Bethlehem, J. Seidlitz, S. R. White, J. W. Vogel, K. M. Anderson in Nature (2022)

  3. Article

    Open Access

    Brain charts for the human lifespan

    Over the past few decades, neuroimaging has become a ubiquitous tool in basic research and clinical studies of the human brain. However, no reference standards currently exist to quantify individual difference...

    R. A. I. Bethlehem, J. Seidlitz, S. R. White, J. W. Vogel, K. M. Anderson in Nature (2022)

  4. Article

    Open Access

    Erratum: GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium

    Correction to: Molecular Psychiatry (2017) 22, 336–345; doi:10.1038/mp.2016.244;published online 17 January 2017 Data access for several cohorts used in this study was provided by the National Center for Biote...

    J W Trampush, M L Z Yang, J Yu, E Knowles, G Davies, D C Liewald in Molecular Psychiatry (2017)

  5. Article

    Open Access

    GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium

    The complex nature of human cognition has resulted in cognitive genomics lagging behind many other fields in terms of gene discovery using genome-wide association study (GWAS) methods. In an attempt to overcom...

    J W Trampush, M L Z Yang, J Yu, E Knowles, G Davies, D C Liewald in Molecular Psychiatry (2017)

  6. Article

    Open Access

    MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls

    Variants at microRNA-137 (MIR137), one of the most strongly associated schizophrenia risk loci identified to date, have been associated with poorer cognitive performance. As microRNA-137 is known to regulate the ...

    D Cosgrove, D Harold, O Mothersill, R Anney, M J Hill, N J Bray in Translational Psychiatry (2017)

  7. Article

    Erratum: Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium

    Correction to: Molecular Psychiatry (2015); advance online publication 2 June 2015; doi:10.1038/mp.2015.63 Following publication of the above article, the authors noticed that the forty-third author’s last nam...

    T G M van Erp, D P Hibar, J M Rasmussen, D C Glahn, G D Pearlson in Molecular Psychiatry (2016)

  8. Article

    Open Access

    Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium

    The profile of brain structural abnormalities in schizophrenia is still not fully understood, despite decades of research using brain scans. To validate a prospective meta-analysis approach to analyzing multic...

    T G M van Erp, D P Hibar, J M Rasmussen, D C Glahn, G D Pearlson in Molecular Psychiatry (2016)

  9. No Access

    Article

    Evaluating historical candidate genes for schizophrenia

    Prior to the genome-wide association era, candidate gene studies were a major approach in schizophrenia genetics. In this invited review, we consider the current status of 25 historical candidate genes for sch...

    M S Farrell, T Werge, P Sklar, M J Owen, R A Ophoff, M C O'Donovan in Molecular Psychiatry (2015)

  10. No Access

    Article

    Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia

    Bipolar disorder and schizophrenia are two often severe disorders with high heritabilities. Recent studies have demonstrated a large overlap of genetic risk loci between these disorders but diagnostic and mole...

    D M Ruderfer, A H Fanous, S Ripke, A McQuillin, R L Amdur in Molecular Psychiatry (2014)

  11. No Access

    Article

    Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene

    Genes that are differentially expressed between schizophrenia patients and healthy controls may have key roles in the pathogenesis of schizophrenia. We analyzed two large-scale genome-wide expression studies, ...

    X-j Luo, M Li, L Huang, S Steinberg, M Mattheisen, G Liang in Molecular Psychiatry (2014)

  12. No Access

    Article

    De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability

    Schizophrenia is a serious psychiatric disorder with a broadly undiscovered genetic etiology. Recent studies of de novo mutations (DNMs) in schizophrenia and autism have reinforced the hypothesis that rare geneti...

    S E McCarthy, J Gillis, M Kramer, J Lihm, S Yoon, Y Berstein in Molecular Psychiatry (2014)

  13. Article

    Erratum: Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility

    Correction to: Molecular Psychiatry advance online publication, 9 April 2013; doi:10.1038/mp.2013.37 After the above article was published, the authors noted that L Gan was linked to the wrong affiliation. Add...

    M Li, X-j Luo, M Rietschel, C M Lewis, M Mattheisen in Molecular Psychiatry (2014)

  14. No Access

    Article

    Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility

    Bipolar disorder (BD) is a polygenic disorder that shares substantial genetic risk factors with major depressive disorder (MDD). Genetic analyses have reported numerous BD susceptibility genes, while some vari...

    M Li, X-j Luo, M Rietschel, C M Lewis, M Mattheisen in Molecular Psychiatry (2014)

  15. No Access

    Article

    Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT)

    It has long been recognized that generalized deficits in cognitive ability represent a core component of schizophrenia (SCZ), evident before full illness onset and independent of medication. The possibility of...

    T Lencz, E Knowles, G Davies, S Guha, D C Liewald, J M Starr in Molecular Psychiatry (2014)

  16. Article

    Open Access

    Effects of ZNF804A on auditory P300 response in schizophrenia

    The common variant rs1344706 within the zinc-finger protein gene ZNF804A has been strongly implicated in schizophrenia (SZ) susceptibility by a series of recent genetic association studies. Although associated wi...

    T O'Donoghue, D W Morris, C Fahey, A Da Costa, S Moore in Translational Psychiatry (2014)

  17. Article

    Open Access

    Evidence that duplications of 22q11.2 protect against schizophrenia

    A number of large, rare copy number variants (CNVs) are deleterious for neurodevelopmental disorders, but large, rare, protective CNVs have not been reported for such phenotypes. Here we show in a CNV analysis...

    E Rees, G Kirov, A Sanders, J T R Walters, K D Chambert, J Shi in Molecular Psychiatry (2014)

  18. No Access

    Article

    Common variant at 16p11.2 conferring risk of psychosis

    Epidemiological and genetic data support the notion that schizophrenia and bipolar disorder share genetic risk factors. In our previous genome-wide association study, meta-analysis and follow-up (totaling as m...

    S Steinberg, S de Jong, M Mattheisen, J Costas, D Demontis in Molecular Psychiatry (2014)

  19. Article

    Open Access

    Duplications in RB1CC1 are associated with schizophrenia; identification in large European sample sets

    Schizophrenia (SCZ) is a severe and debilitating neuropsychiatric disorder with an estimated heritability of ~80%. Recently, de novo mutations, identified by next-generation sequencing (NGS) technology, have been...

    F Degenhardt, L Priebe, S Meier, L Lennertz, F Streit, S H Witt in Translational Psychiatry (2013)

  20. Article

    Erratum: Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC

    Correction to: Molecular Psychiatry advance online publication, 22 May 2012; doi: 10.1038/mp.2012.67 Following the online publication of this article, the authors noted an error in Dr O’Neill's name. The compl...

    M L Hamshere, J T R Walters, R Smith, A L Richards, E Green in Molecular Psychiatry (2013)

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