| P50 | author | Jessica A. Turner | Q30514179 |
| P2093 | author name string | Wenhao Jiang | |
| | Tricia Z King | |
| P2860 | cites work | Why most published research findings are false | Q21092395 |
| | The impact of environmental factors in severe psychiatric disorders | Q21129355 |
| | A review of structural neuroimaging in schizophrenia: from connectivity to connectomics | Q21558428 |
| | Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium | Q23747506 |
| | Subcortical brain alterations in major depressive disorder: findings from the ENIGMA Major Depressive Disorder working group | Q23747515 |
| | Voxel-based morphometry for separation of schizophrenia from other types of psychosis in first episode psychosis | Q24187709 |
| | The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data | Q24289484 |
| | Biological insights from 108 schizophrenia-associated genetic loci | Q24561833 |
| | Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis | Q24597718 |
| | A review of MRI findings in schizophrenia | Q24657354 |
| | Magnetic resonance imaging and the prediction of outcome in first-episode schizophrenia: a review of current evidence and directions for future research | Q28082090 |
| | Genetic and genomic analyses as a basis for new diagnostic nosologies | Q28083879 |
| | Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies | Q28190066 |
| | Uncovering the hidden risk architecture of the schizophrenias: confirmation in three independent genome-wide association studies | Q28247877 |
| | Genome-wide association study identifies five new schizophrenia loci | Q28248384 |
| | Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs | Q28296286 |
| | Association of the NRG1 gene and schizophrenia: a meta-analysis | Q28300667 |
| | Evidence for the contribution of NOS1 gene polymorphism (rs3782206) to prefrontal function in schizophrenia patients and healthy controls | Q28649673 |
| | A polygenic theory of schizophrenia | Q28972276 |
| | Identification of loci associated with schizophrenia by genome-wide association and follow-up | Q29417130 |
| | Identification of Distinct Psychosis Biotypes Using Brain-Based Biomarkers | Q30363008 |
| | Structural brain imaging in schizophrenia: a selective review | Q30581145 |
| | Decreased left middle temporal gyrus volume in antipsychotic drug-naive, first-episode schizophrenia patients and their healthy unaffected siblings | Q30586690 |
| | Human brain imaging studies of DISC1 in schizophrenia, bipolar disorder and depression: a systematic review | Q30619216 |
| | Neuroimaging and plasticity in schizophrenia | Q30658428 |
| | Structural and Functional Brain Abnormalities in Schizophrenia | Q30870932 |
| | Neuroimaging findings from childhood onset schizophrenia patients and their non-psychotic siblings | Q30918698 |
| | What is the impact of genome-wide supported risk variants for schizophrenia and bipolar disorder on brain structure and function? A systematic review | Q30928632 |
| | Multimodal neuroimaging as a window into the pathological physiology of schizophrenia: Current trends and issues | Q30984559 |
| | Factorial invariance across gender for the primary symptom dimensions of the SCL-90 | Q44657669 |
| | ZNF804A risk allele is associated with relatively intact gray matter volume in patients with schizophrenia. | Q45145657 |
| | Catechol-O-methyl transferase Val158Met gene polymorphism in schizophrenia: working memory, frontal lobe MRI morphology and frontal cerebral blood flow. | Q45236947 |
| | A genome-wide supported variant in CACNA1C influences hippocampal activation during episodic memory encoding and retrieval | Q45885056 |
| | Childhood adversity impacts on brain subcortical structures relevant to depression. | Q45930817 |
| | BDNF val66met modulates the association between childhood trauma, cognitive and brain abnormalities in psychoses. | Q45963847 |
| | Hippocampal and frontolimbic function as intermediate phenotype for psychosis: evidence from healthy relatives and a common risk variant in CACNA1C. | Q46014279 |
| | Genetic vulnerability to affective psychopathology in childhood: a combined voxel-based morphometry and functional magnetic resonance imaging study | Q46092008 |
| | The effect of the neurogranin schizophrenia risk variant rs12807809 on brain structure and function. | Q46280471 |
| | Brain-derived neurotrophic factor Val66Met polymorphism and early life adversity affect hippocampal volume | Q46547554 |
| | Effects of MIR137 on fronto-amygdala functional connectivity | Q46690026 |
| | Impact of catechol-O-methyltransferase Val(108/158) Met genotype on hippocampal and prefrontal gray matter volume | Q46743546 |
| | The association between the Val158Met polymorphism of the catechol-O-methyl transferase gene and morphological abnormalities of the brain in chronic schizophrenia. | Q46837612 |
| | The Val66Met polymorphism of the brain-derived neurotrophic factor gene affects age-related brain morphology | Q46876182 |
| | BDNF Val66Met allele is associated with reduced hippocampal volume in healthy subjects | Q46915507 |
| | Brain Structure Biomarkers in the Psychosis Biotypes: Findings From the Bipolar-Schizophrenia Network for Intermediate Phenotypes | Q47386048 |
| | Brain function in carriers of a genome-wide supported bipolar disorder variant | Q48102784 |
| | Association of rs1006737 in CACNA1C with alterations in prefrontal activation and fronto-hippocampal connectivity | Q48165250 |
| | Effects of a genome-wide supported psychosis risk variant on neural activation during a theory-of-mind task | Q48271431 |
| | Allelic variation in RGS4 impacts functional and structural connectivity in the human brain. | Q48272520 |
| | Cortical Surface Area Differentiates Familial High Risk Individuals Who Go on to Develop Schizophrenia. | Q48287618 |
| | Catechol O-methyltransferase val158met genotype and neural mechanisms related to affective arousal and regulation | Q48347908 |
| | Neuregulin 1 (8p12) and childhood-onset schizophrenia: susceptibility haplotypes for diagnosis and brain developmental trajectories. | Q48399002 |
| | Relationship of catechol-O-methyltransferase variants to brain structure and function in a population at high risk of psychosis. | Q48407361 |
| | Boundaries of schizoaffective disorder: revisiting Kraepelin | Q48419260 |
| | Possible effect of the APOE epsilon 4 allele on the hippocampal volume and asymmetry in schizophrenia | Q48494424 |
| | Is neuregulin 1 involved in determining cerebral volumes in schizophrenia? Preliminary results showing a decrease in superior temporal gyrus volume. | Q48635266 |
| | Genetic risk variants of schizophrenia associated with left superior temporal gyrus volume. | Q48701657 |
| | BDNF Val66Met genotype modulates the effect of childhood adversity on subgenual anterior cingulate cortex volume in healthy subjects | Q48870134 |
| | Molecular and genetic evidence for abnormalities in the nodes of Ranvier in schizophrenia. | Q48916208 |
| | Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap. | Q50034912 |
| | Genes and structural brain imaging in schizophrenia | Q31149261 |
| | Functional variation of the dopamine D2 receptor gene is associated with emotional control as well as brain activity and connectivity during emotion processing in humans | Q33711011 |
| | Hippocampal volume reduction in first-episode and chronic schizophrenia: a review and meta-analysis | Q33885557 |
| | Genetic architectures of psychiatric disorders: the emerging picture and its implications | Q33949729 |
| | Altered cortical network dynamics: a potential intermediate phenotype for schizophrenia and association with ZNF804A. | Q33979177 |
| | A schizophrenia risk gene, ZNF804A, influences neuroanatomical and neurocognitive phenotypes | Q34128269 |
| | Diagnostic Criteria for Use in Psychiatric Research | Q34226390 |
| | Heterogeneity of brain structural variation and the structural imaging endophenotypes in schizophrenia | Q34337988 |
| | Improved detection of common variants associated with schizophrenia and bipolar disorder using pleiotropy-informed conditional false discovery rate | Q34342469 |
| | A systematic review and meta-analysis on the association between BDNF val(66)met and hippocampal volume--a genuine effect or a winners curse? | Q34344423 |
| | Common genetic variants influence human subcortical brain structures | Q34458961 |
| | Assessing brain structural associations with working-memory related brain patterns in schizophrenia and healthy controls using linked independent component analysis | Q34499669 |
| | Association between brain-derived neurotrophic factor Val66Met gene polymorphism and progressive brain volume changes in schizophrenia | Q34706991 |
| | Cognitive and magnetic resonance imaging brain morphometric correlates of brain-derived neurotrophic factor Val66Met gene polymorphism in patients with schizophrenia and healthy volunteers | Q34726039 |
| | Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study | Q34923924 |
| | Neural mechanisms of a genome-wide supported psychosis variant | Q34978645 |
| | Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder | Q35059381 |
| | The association of genetic variation in CACNA1C with structure and function of a frontotemporal system | Q35599625 |
| | Imaging genetics and psychiatric disorders | Q35698177 |
| | Genetic Variation in CACNA1C Affects Brain Circuitries Related to Mental Illness | Q35764284 |
| | Epistasis between catechol-O-methyltransferase and type II metabotropic glutamate receptor 3 genes on working memory brain function | Q35894585 |
| | Effective connectivity of AKT1-mediated dopaminergic working memory networks and pharmacogenetics of anti-dopaminergic treatment | Q35918802 |
| | The COMT Val158Met polymorphism and temporal lobe morphometry in healthy adults. | Q35944710 |
| | Frequency-Specific Neural Signatures of Spontaneous Low-Frequency Resting State Fluctuations in Psychosis: Evidence From Bipolar-Schizophrenia Network on Intermediate Phenotypes (B-SNIP) Consortium | Q36148517 |
| | Identification of shared risk loci and pathways for bipolar disorder and schizophrenia | Q36271840 |
| | Imaging Genetics and Genomics in Psychiatry: A Critical Review of Progress and Potential | Q36304801 |
| | Structural brain changes in schizophrenia at different stages of the illness: A selective review of longitudinal magnetic resonance imaging studies | Q36348922 |
| | Imaging phenotypes and genotypes in schizophrenia | Q36440915 |
| | The effect of neurogranin on neural correlates of episodic memory encoding and retrieval | Q36471529 |
| | Genetic schizophrenia risk variants jointly modulate total brain and white matter volume | Q36612177 |
| | Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept | Q36856776 |
| | Does Biology Transcend the Symptom-based Boundaries of Psychosis? | Q37114217 |
| | Brain volumes in schizophrenia: a meta-analysis in over 18 000 subjects | Q37131066 |
| | Guided exploration of genomic risk for gray matter abnormalities in schizophrenia using parallel independent component analysis with reference | Q37231051 |
| | Cognitive state and connectivity effects of the genome-wide significant psychosis variant in ZNF804A. | Q50663179 |
| | The brain-derived neurotrophic factor val66met polymorphism and variation in human cortical morphology. | Q51935722 |
| | The Symptom Check-List-90-R (SCL-90-R): a German validation study. | Q51974070 |
| | Beyond heritability: Improving discoverability in imaging genetics. | Q52316260 |
| | Neuregulin-1 haplotype HAPICE is associated with lower hippocampal volumes in schizophrenic patients and in non-affected family members | Q56992227 |
| | Association of schizophrenia polygenic risk score with manic and depressive psychosis in bipolar disorder | Q58756313 |
| | Genome-wide analysis reveals extensive genetic overlap between schizophrenia, bipolar disorder, and intelligence | Q60460217 |
| | Association of Polygenic Liabilities for Major Depression, Bipolar Disorder, and Schizophrenia With Risk for Depression in the Danish Population. | Q61849573 |
| | Commonality in dysregulated expression of gene sets in cortical brains of individuals with autism, schizophrenia, and bipolar disorder | Q64283871 |
| | Schizophrenia-associated genomic copy number variants and subcortical brain volumes in the UK Biobank | Q91211817 |
| | Impact of interacting functional variants in COMT on regional gray matter volume in human brain | Q37243074 |
| | Influence of ZNF804a on brain structure volumes and symptom severity in individuals with schizophrenia. | Q37367250 |
| | Association of a risk allele of ANK3 with cognitive performance and cortical thickness in patients with first-episode psychosis | Q37404810 |
| | Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder | Q37571848 |
| | ZNF804A genotype modulates neural activity during working memory for faces. | Q37592871 |
| | Further evidence for the impact of a genome-wide-supported psychosis risk variant in ZNF804A on the Theory of Mind Network | Q37642441 |
| | Effects of ZNF804A on neurophysiologic measures of cognitive control | Q37655180 |
| | Imaging genetics--days of future past | Q37676588 |
| | Genetic relationships between schizophrenia, bipolar disorder, and schizoaffective disorder | Q37699386 |
| | GeneAnalytics Pathway Analysis and Genetic Overlap among Autism Spectrum Disorder, Bipolar Disorder and Schizophrenia. | Q37729086 |
| | ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties | Q37739910 |
| | Genome wide association studies (GWAS) and copy number variation (CNV) studies of the major psychoses: what have we learnt? | Q37938511 |
| | Brain connectivity in psychiatric imaging genetics | Q37958477 |
| | Modifiable factors that alter the size of the hippocampus with ageing | Q37992811 |
| | Defining psychosis: the evolution of DSM-5 schizophrenia spectrum disorders | Q38140665 |
| | Genetics of psychiatric disorders in the GWAS era: an update on schizophrenia | Q38144755 |
| | Functional connectivity measures as schizophrenia intermediate phenotypes: advances, limitations, and future directions | Q38567253 |
| | Working memory genetics in schizophrenia and related disorders: An RDoC perspective | Q38586015 |
| | Domains of physical activity and brain volumes: A population-based study | Q38684079 |
| | Improving classification of psychoses | Q38803931 |
| | Towards diagnostic markers for the psychoses | Q38803934 |
| | Largest GWAS of PTSD (N=20 070) yields genetic overlap with schizophrenia and sex differences in heritability. | Q38821961 |
| | Subcortical brain volume differences in participants with attention deficit hyperactivity disorder in children and adults: a cross-sectional mega-analysis. | Q38951375 |
| | Enhancing the Informativeness and Replicability of Imaging Genomics Studies | Q38993924 |
| | Distinct Subcortical Volume Alterations in Pediatric and Adult OCD: A Worldwide Meta- and Mega-Analysis | Q39409083 |
| | Citation bias and selective focus on positive findings in the literature on the serotonin transporter gene (5-HTTLPR), life stress and depression. | Q39497742 |
| | Schizophrenia: a disconnection syndrome? | Q40428268 |
| | G-protein genomic association with normal variation in gray matter density | Q40653111 |
| | Impact of polygenic schizophrenia-related risk and hippocampal volumes on the onset of psychosis | Q41084707 |
| | Interactions between BDNF Val66Met polymorphism and early life stress predict brain and arousal pathways to syndromal depression and anxiety. | Q43920402 |
| | Partial support for ZNF804A genotype-dependent alterations in prefrontal connectivity | Q43962534 |
| | Effects of a CACNA1C genotype on attention networks in healthy individuals | Q44490894 |
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P921 | main subject | schizophrenia | Q41112 |
| P304 | page(s) | 494 | |
| P577 | publication date | 2019-07-12 | |
| P1433 | published in | Frontiers in Psychiatry | Q27723495 |
| P1476 | title | Imaging Genetics Towards a Refined Diagnosis of Schizophrenia | |
| P478 | volume | 10 | |