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  1. Article

    Open Access

    Genetic risk for schizophrenia is associated with altered visually-induced gamma band activity: evidence from a population sample stratified polygenic risk

    Gamma oscillations (30–90 Hz) have been proposed as a signature of cortical visual information processing, particularly the balance between excitation and inhibition, and as a biomarker of neuropsychiatric dis...

    S. I. Dimitriadis, G. Perry, S. F. Foley, K. E. Tansey in Translational Psychiatry (2021)

  2. Article

    Open Access

    Erratum: Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia

    Correction to: Molecular Psychiatry (2017) 22: 1502-1508; advance online publication, 12 July 2017; doi: 10.1038/mp.2016.97 In the first paragraph of the Results section and Figure 1, the authors incorrectly r...

    S E Legge, M L Hamshere, S Ripke, A F Pardinas, J I Goldstein in Molecular Psychiatry (2018)

  3. Article

    Open Access

    Erratum: Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia

    Correction to: Molecular Psychiatry advance online publication, 12 July 2016; doi:10.1038/mp.2016.97 The ninth author’s name was presented incorrectly. It should have been listed as LF Jarskog.

    S E Legge, M L Hamshere, S Ripke, A F Pardinas, J I Goldstein in Molecular Psychiatry (2017)

  4. Article

    Open Access

    Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia

    The antipsychotic clozapine is uniquely effective in the management of schizophrenia; however, its use is limited by its potential to induce agranulocytosis. The causes of this, and of its precursor neutropeni...

    S E Legge, M L Hamshere, S Ripke, A F Pardinas, J I Goldstein in Molecular Psychiatry (2017)

  5. Article

    Open Access

    Investigating the genetic underpinnings of early-life irritability

    Severe irritability is one of the commonest reasons prompting referral to mental health services. It is frequently seen in neurodevelopmental disorders that manifest early in development, especially attention-...

    L Riglin, O Eyre, M Cooper, S Collishaw, J Martin, K Langley in Translational Psychiatry (2017)

  6. Article

    Open Access

    Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia

    Borderline personality disorder (BOR) is determined by environmental and genetic factors, and characterized by affective instability and impulsivity, diagnostic symptoms also observed in manic phases of bipola...

    S H Witt, F Streit, M Jungkunz, J Frank, S Awasthi in Translational Psychiatry (2017)

  7. Article

    Open Access

    Schizophrenia copy number variants and associative learning

    Large-scale genomic studies have made major progress in identifying genetic risk variants for schizophrenia. A key finding from these studies is that there is an increased burden of genomic copy number variant...

    N E Clifton, A J Pocklington, B Scholz, E Rees, J T R Walters in Molecular Psychiatry (2017)

  8. 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)

  9. Article

    Open Access

    Erratum: Genome-wide analysis of over 106 000 individuals identifies 9 neuroticism-associated loci

    Correction to: Molecular Psychiatry 21, 749–757; doi:10.1038/mp.2016.49 The GWAS of neuroticism conducted within the Queensland Institute of Medical Research (QIMR) Berghofer Medical Research Institute cohort ...

    D J Smith, V Escott-Price, G Davies, M E S Bailey, L Colodro-Conde in Molecular Psychiatry (2016)

  10. Article

    Open Access

    Psychiatric gene discoveries shape evidence on ADHD’s biology

    A strong motivation for undertaking psychiatric gene discovery studies is to provide novel insights into unknown biology. Although attention-deficit hyperactivity disorder (ADHD) is highly heritable, and large...

    A Thapar, J Martin, E Mick, A Arias Vásquez, K Langley, S W Scherer in Molecular Psychiatry (2016)

  11. Article

    Erratum: Common alleles contribute to schizophrenia in CNV carriers

    Correction to: Molecular Psychiatry (2015); advance online publication 22 September 2015; doi:10.1038/mp.2015.143 The first author in Reference 33 was listed incorrectly in the reference list and in the last p...

    K E Tansey, E Rees, D E Linden, S Ripke, K D Chambert, J L Moran in Molecular Psychiatry (2016)

  12. Article

    Open Access

    Common alleles contribute to schizophrenia in CNV carriers

    The genetic architecture of schizophrenia is complex, involving risk alleles ranging from common alleles of weak effect to rare alleles of large effect, the best exemplar of the latter being large copy number ...

    K E Tansey, E Rees, D E Linden, S Ripke, K D Chambert, J L Moran in Molecular Psychiatry (2016)

  13. Article

    Open Access

    Genome-wide analysis of over 106 000 individuals identifies 9 neuroticism-associated loci

    Neuroticism is a personality trait of fundamental importance for psychological well-being and public health. It is strongly associated with major depressive disorder (MDD) and several other psychiatric conditi...

    D J Smith, V Escott-Price, G Davies, M E S Bailey, L Colodro-Conde in Molecular Psychiatry (2016)

  14. Article

    Open Access

    Copy number variation in bipolar disorder

    Large (>100 kb), rare (<1% in the population) copy number variants (CNVs) have been shown to confer risk for schizophrenia (SZ), but the findings for bipolar disorder (BD) are less clear. In a new BD sample fr...

    E K Green, E Rees, J T R Walters, K-G Smith, L Forty, D Grozeva in Molecular Psychiatry (2016)

  15. No Access

    Article

    A novel Alzheimer disease locus located near the gene encoding tau protein

    APOE ɛ4, the most significant genetic risk factor for Alzheimer disease (AD), may mask effects of other loci. We re-analyzed genome-wide association study (GWAS) data from the International Genomics of Alzheimer’...

    G Jun, C A Ibrahim-Verbaas, M Vronskaya, J-C Lambert, J Chung in Molecular Psychiatry (2016)

  16. No Access

    Article

    Genetic overlap between Alzheimer’s disease and Parkinson’s disease at the MAPT locus

    We investigated the genetic overlap between Alzheimer’s disease (AD) and Parkinson’s disease (PD). Using summary statistics (P-values) from large recent genome-wide association studies (GWAS) (total n=89 904 indi...

    R S Desikan, A J Schork, Y Wang, A Witoelar, M Sharma, L K McEvoy in Molecular Psychiatry (2015)

  17. Article

    Open Access

    Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia

    Antagonists of the N-methyl-D-aspartate (NMDA)-type glutamate receptor induce psychosis in healthy individuals and exacerbate schizophrenia symptoms in patients. In this study we have produced an animal model ...

    A Ingason, I Giegling, A M Hartmann, J Genius, B Konte in Translational Psychiatry (2015)

  18. Article

    Open Access

    Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia

    Genetic associations involving both rare and common alleles have been reported for schizophrenia but there have been no systematic scans for rare recessive genotypes using fully phased trio data. Here, we use ...

    E Rees, G Kirov, J T Walters, A L Richards, D Howrigan in Translational Psychiatry (2015)

  19. 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)

  20. No Access

    Article

    Schizophrenia genetics: emerging themes for a complex disorder

    After two decades of frustration, genetic studies of schizophrenia have entered an era of spectacular success. Advances in genoty** technologies and high throughput sequencing, increasing analytic rigour and...

    D H Kavanagh, K E Tansey, M C O'Donovan, M J Owen in Molecular Psychiatry (2015)

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