Genome-wide association analysis identifies 13 new risk loci for schizophrenia.

paper Cited Public

Authors: Ripke, Stephan; O'Dushlaine, Colm; Chambert, Kimberly; Moran, Jennifer L; Kähler, Anna K; Akterin, Susanne; Bergen, Sarah E; Collins, Ann L; Crowley, James J; Fromer, Menachem; Kim, Yunjung; Lee, Sang Hong; Magnusson, Patrik K E; Sanchez, Nick; Stahl, Eli A; Williams, Stephanie; Wray, Naomi R; Xia, Kai; Bettella, Francesco; Borglum, Anders D; Bulik-Sullivan, Brendan K; Cormican, Paul; Craddock, Nick; de Leeuw, Christiaan; Durmishi, Naser; Gill, Michael; Golimbet, Vera; Hamshere, Marian L; Holmans, Peter; Hougaard, David M; Kendler, Kenneth S; Lin, Kuang; Morris, Derek W; Mors, Ole; Mortensen, Preben B; Neale, Benjamin M; O'Neill, Francis A; Owen, Michael J; Milovancevic, Milica Pejovic; Posthuma, Danielle; Powell, John; Richards, Alexander L; Riley, Brien P; Ruderfer, Douglas; Rujescu, Dan; Sigurdsson, Engilbert; Silagadze, Teimuraz; Smit, August B; Stefansson, Hreinn; Steinberg, Stacy; Suvisaari, Jaana; Tosato, Sarah; Verhage, Matthijs; Walters, James T; Multicenter Genetic Studies of Schizophrenia Consortium; Levinson, Douglas F; Gejman, Pablo V; Kendler, Kenneth S; Laurent, Claudine; Mowry, Bryan J; O'Donovan, Michael C; Owen, Michael J; Pulver, Ann E; Riley, Brien P; Schwab, Sibylle G; Wildenauer, Dieter B; Dudbridge, Frank; Holmans, Peter; Shi, Jianxin; Albus, Margot; Alexander, Madeline; Campion, Dominique; Cohen, David; Dikeos, Dimitris; Duan, Jubao; Eichhammer, Peter; Godard, Stephanie; Hansen, Mark; Lerer, F Bernard; Liang, Kung-Yee; Maier, Wolfgang; Mallet, Jacques; Nertney, Deborah A; Nestadt, Gerald; Norton, Nadine; O'Neill, Francis A; Papadimitriou, George N; Ribble, Robert; Sanders, Alan R; Silverman, Jeremy M; Walsh, Dermot; Williams, Nigel M; Wormley, Brandon; Psychosis Endophenotypes International Consortium; Arranz, Maria J; Bakker, Steven; Bender, Stephan; Bramon, Elvira; Collier, David; Crespo-Facorro, Benedicto; Hall, Jeremy; Iyegbe, Conrad; Jablensky, Assen; Kahn, Rene S; Kalaydjieva, Luba; Lawrie, Stephen; Lewis, Cathryn M; Lin, Kuang; Linszen, Don H; Mata, Ignacio; McIntosh, Andrew; Murray, Robin M; Ophoff, Roel A; Powell, John; Rujescu, Dan; Van Os, Jim; Walshe, Muriel; Weisbrod, Matthias; Wiersma, Durk; Wellcome Trust Case Control Consortium 2; Donnelly, Peter; Barroso, Ines; Blackwell, Jenefer M; Bramon, Elvira; Brown, Matthew A; Casas, Juan P; Corvin, Aiden P; Deloukas, Panos; Duncanson, Audrey; Jankowski, Janusz; Markus, Hugh S; Mathew, Christopher G; Palmer, Colin N A; Plomin, Robert; Rautanen, Anna; Sawcer, Stephen J; Trembath, Richard C; Viswanathan, Ananth C; Wood, Nicholas W; Spencer, Chris C A; Band, Gavin; Bellenguez, Céline; Freeman, Colin; Hellenthal, Garrett; Giannoulatou, Eleni; Pirinen, Matti; Pearson, Richard D; Strange, Amy; Su, Zhan; Vukcevic, Damjan; Donnelly, Peter; Langford, Cordelia; Hunt, Sarah E; Edkins, Sarah; Gwilliam, Rhian; Blackburn, Hannah; Bumpstead, Suzannah J; Dronov, Serge; Gillman, Matthew; Gray, Emma; Hammond, Naomi; Jayakumar, Alagurevathi; McCann, Owen T; Liddle, Jennifer; Potter, Simon C; Ravindrarajah, Radhi; Ricketts, Michelle; Tashakkori-Ghanbaria, Avazeh; Waller, Matthew J; Weston, Paul; Widaa, Sara; Whittaker, Pamela; Barroso, Ines; Deloukas, Panos; Mathew, Christopher G; Blackwell, Jenefer M; Brown, Matthew A; Corvin, Aiden P; McCarthy, Mark I; Spencer, Chris C A; Bramon, Elvira; Corvin, Aiden P; O'Donovan, Michael C; Stefansson, Kari; Scolnick, Edward; Purcell, Shaun; McCarroll, Steven A; Sklar, Pamela; Hultman, Christina M; Sullivan, Patrick F
Year: 2013
Journal: Nature genetics
PMID: 23974872
DOI: 10.1038/ng.2742
PMCID: PMC3827979

Figure 1

Manhattan plot of the Swedish and PGC schizophrenia meta-analysis results. The x-axis is chromosomal position and the y-axis is –log10(P). The red line is the genome-wide significance level (5×10−8). Gene locations are indicated.

LLM interpretation

This is a Manhattan plot showing the results of a schizophrenia meta-analysis, with the x-axis representing chromosomal position (1–22) and the y-axis representing $-\log_{10}(P)$. Multiple genomic loci across several chromosomes exceed the red genome-wide significance threshold ($5 \times 10^{-8}$), with the most prominent peaks located on chromosomes 6 and 12. Specific significant genes and intergenic regions are labeled above their respective peaks.

Figure 2

Risk score profiling results using the PGC schizophrenia results as the discovery set and the Sweden data as the testing set. The x-axis shows ten P value thresholds (PT = 10−4, 10−3, …, 1). The y-axis is the Nagelkerke pseudo R2, the proportion of variance in case-control status explained by the risk score profile. The number atop each vertical bar is the P value for the capacity of the risk score profile to predict case-control status for that PT.

LLM interpretation

This bar chart shows the Nagelkerke pseudo $R^2$ (proportion of variance in case-control status explained) across ten P-value thresholds (PT) ranging from 0.0001 to 1. The $R^2$ value increases as the PT increases, plateauing at approximately 0.06 for PT values of 0.1 and above. Each bar is annotated with a P-value indicating the predictive capacity of the risk score profile, with all values showing high statistical significance (ranging from $1\text{e-}26$ to $9\text{e-}115$).

Figure 3

The main figure shows the results of ABPA modeling based on the Sweden + PGC results (population risk 0.01). The x-axis is the estimated number of SNPs on a log10 scale, and the y-axis estimates the total variance in liability explained. The results for five conditions are shown: schizophrenia (this analysis, red) and, for comparison, results from a published analysis of myocardial infarction (MI, purple), type 2 diabetes mellitus (T2D, blue), celiac disease (green), and rheumatoid arthritis (RA, teal). 71 The schizophrenia results are based on 1000 Genomes imputation, and the others on HapMap3 imputation. Color intensity reflects the probability density with darker colors indicating higher density. Contour lines show 50% and 95% credible regions for SCZ, and 95% credible regions for the other diseases. The insets depict estimated SNP distributions for the five disorders: (a) distribution of SNPs in terms of the variance in liability explained per SNP and (b) the estimated distribution of SNP genotypic relative risks (GRR). We again stress that multiple qualifiers are essential in interpreting these estimates.

LLM interpretation

This figure is a density plot with contour lines showing the results of ABPA modeling for five conditions: schizophrenia (SCZ, red), myocardial infarction (MI, purple), type 2 diabetes (T2D, blue), celiac disease (green), and rheumatoid arthritis (RA, teal). The x-axis represents the number of disease-associated GWAS SNPs on a $\log_{10}$ scale, and the y-axis represents the total liability-scale variance explained. Two insets show the density distributions for per-SNP liability-scale variance explained (a) and genotypic relative risk (b).

#	Section	Preview
20	Genetic architecture	To complement the GCTA analyses, we also applied ABPA (approximate Bayesian polygenic analysis) 66…
21	Genetic architecture	The Bayesian framework used by ABPA also allows simultaneous estimation of the number of independent…
22	Genetic architecture	input data. Additional analyses (not shown) indicate that most of the signal was derived from SNPs…
23	Genetic architecture	We previously estimated the heritability of schizophrenia in Sweden to be 0.64 (95% CI 0.617-0.675)…
24	Conclusions	These results provide deeper insight into the genetic architecture of schizophrenia than ever…
25	Conclusions	Common variation is an important (and perhaps predominant) genetic contributor to risk for…
26	Conclusions	Moreover, these thousands of independent loci appear to account for a considerable fraction of the…
27	Conclusions	Power calculations are a fundamental component of the design of genetic studies. However, relatively…
28	Conclusions	Thus, for the first time, we now have a clear path to increased knowledge about the etiology of…
29	Online Methods — Overview	We present here the pre-planned principal analyses for this project. In order to advance knowledge…
30	Online Methods — Subjects	All procedures were approved by ethical committees at the Karolinska Institutet and University of…
31	Online Methods — Subjects	Cases with schizophrenia were identified via the Swedish Hospital Discharge Register 76,77 which…
32	Online Methods — Subjects	The validity of this case definition of schizophrenia is described at length in the Supplement, and…
33	Online Methods — Subjects	Controls were selected at random from Swedish population registers with the goal of obtaining an…
34	Online Methods — Subjects	Of the potential cases and controls who were alive and contactable, refusal rates were higher for…
35	Online Methods — Genotyping, quality control, and imputation	DNA was extracted from peripheral blood samples at the Karolinska Institutet Biobank. Samples were…
36	Online Methods — Genotyping, quality control, and imputation	After basic quality control, 77,986 autosomal SNPs directly genotyped on all four GWAS platforms…
37	Online Methods — Genotyping, quality control, and imputation	Genotype imputation was performed using the pre-phasing/imputation stepwise approach implemented in…
38	Online Methods — Statistical analysis	We first analyzed Swedish cases and controls (N=11,244), and then conducted a meta-analysis with the…
39	Online Methods — Summarizing regional data using “clumping”	Many GWAS findings implicate an extended region containing multiple significant SNPs. These are not…

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External

Title	Authors	Journal	Year	Link
Assessment of Social Functioning in Patients With Schizophrenia and Their First-Degree Relatives.	Shimada T et al.	—	2026	→
Evaluating genetic-based disease prediction approaches through simulation.	Shpak M et al.	—	2026	→
Functional implications of polygenic risk for schizophrenia in human neurons.	Michael Deans PJ et al.	—	2026	→
Grin2a knockout in adolescent dopamine neurons disrupts prediction error signaling and produces a phenotype relevant to schizophrenia.	Kielhold ML et al.	—	2026	→
Immunogenetic Variants in Major Mental and Neurodevelopmental Disorders.	Le Clerc S et al.	—	2026	→
Large-scale dependent multiple testing via higher-order hidden Markov models.	Li C et al.	—	2026	→
Mendelian randomization facilitates identification of schizophrenia risk enhancer RNAs.	Ye L et al.	—	2026	→
Pathway-Informed Machine Learning Identifies Genetic Predictors of High-Dose Methotrexate-Induced Mucositis in Pediatric Acute Lymphoblastic Leukemia.	Zhang XYC et al.	—	2026	→
Polygenic risk for schizophrenia predicting test-measured and self-reported cognitive performance in individuals without psychosis.	Rosenqvist E et al.	—	2026	→
Probiotics, psychobiotics, and postbiotics: a therapeutic modality for the management of schizophrenia.	Ashique S et al.	—	2026	→
Schizophrenia: Genetics, neurological mechanisms, and therapeutic approaches.	Lim DXE et al.	—	2026	→
The Eph-ephrin system in neuropsychiatric and neurodevelopmental disorders.	Bordignon A et al.	—	2026	→
The GluA1 cytoplasmic tail regulates intracellular AMPA receptor trafficking and synaptic transmission onto dentate gyrus GABAergic interneurons, gating response to novelty.	Leana-Sandoval G et al.	—	2026	→
Whole-genome sequence-based association analysis of African American individuals with bipolar disorder and schizophrenia.	Li R et al.	—	2026	→
Aggregating dependent signals with heavy-tailed combination tests.	Gui L et al.	—	2025	→
Analysis of biased allelic enhancer activity of schizophrenia-linked common variants.	Gao C et al.	—	2025	→
A non-coding RNA risk pathway in schizophrenia: miR-137 enhances the lncRNA GOMAFU through a pathological transcription network.	Teng P et al.	—	2025	→
A phenotypic journey into NT5DC proteins in cancer and other diseases.	Cros-Perrial E et al.	—	2025	→
A review of post-GWAS studies in schizophrenia.	Maserrat S et al.	—	2025	→
A self-supervised learning framework for discovering cortical folding patterns under genetic influence: Application to the Anterior Cingulate Cortex.	Dufournet A et al.	—	2025	→
Biology, function and structure of the calcium homeostasis modulator family.	Polfer R et al.	—	2025	→
Coconut: covariate-assisted composite null hypothesis testing with applications to replicability analysis of high-throughput experimental data.	Li Y et al.	—	2025	→
Comparing Alzheimer's genes in African, European, and Amerindian induced pluripotent stem cell-derived microglia.	Moura S et al.	—	2025	→
Control of striatal circuit development by the chromatin regulator <i>Zswim6</i>.	Choi K et al.	—	2025	→
Decoding the Molecular Mechanisms of miRNAs: Protein Interactions in Schizophrenia Pathogenesis.	Ashique S et al.	—	2025	→
Dissecting Schizophrenia Biology Using Pleiotropy With Cognitive Genomics.	Bhattacharyya U et al.	—	2025	→
Effects of Risperidone and Aripiprazole Antipsychotic Drugs on Behavioral Changes and the Expression Levels of DRD2, HTR2A, AKT1, and CACNA1C Genes in the Hippocampus of a Ketamine-induced Schizophrenia-like Rat Model.	Naderi M et al.	—	2025	→
Epigenetic Control in Schizophrenia.	D'Addario C et al.	—	2025	→
Increased plasma TRANK1 levels in first-episode drug-naïve schizophrenia: Association with delayed memory decline.	Yin XY et al.	—	2025	→
Influence of antipsychotic drugs on microglia-mediated neuroinflammation in schizophrenia: perspectives in an astrocyte-microglia co-culture model.	Faustmann TJ et al.	—	2025	→
Integrating AI and genomics: predictive CNN models for schizophrenia phenotypes.	Henriques G et al.	—	2025	→
Limitations of Correlation Coefficients in Research on Functional Connectomes and Psychological Processes.	Fu H et al.	—	2025	→
Loss of negative regulation by HDAC1 and REST contributes to MAD1 overexpression in breast cancer.	Copeland SE et al.	—	2025	→
Multitrait Analysis to Decipher the Intertwined Genetic Architecture of Neuroanatomical Phenotypes and Psychiatric Disorders.	Auvergne A et al.	—	2025	→
Neuronal Synaptic Communication and Mitochondrial Energetics in Human Health and Disease.	Glausier JR	—	2025	→
NT5DC2 downregulation suppresses monoamine oxidase activity and promotes catecholamine synthesis in PC12D cells.	Yamaguchi H et al.	—	2025	→
Perturbed cell fate decision by schizophrenia-associated AS3MT<sup>d2d3</sup> isoform during corticogenesis.	Kim S et al.	—	2025	→
Preclinical Models for Schizophrenia and Sleep Oscillations: From Biomarkers to Mechanisms.	Vyazovskiy VV et al.	—	2025	→
Schizophrenia risk gene ZNF536 modulates retinoic acid response and neuronal gene networks in SH-SY5Y cells.	Kurishev AO et al.	—	2025	→
The GRIA1 AMPA receptor subunit and selective learning.	Strickland JA et al.	—	2025	→
The schizophrenia-associated gene CSMD1 encodes a complement classical pathway inhibitor predominantly expressed by astrocytes and at synapses in mice and humans.	Byrne RAJ et al.	—	2025	→
Aberrant neuronal connectivity and network activity of neurons derived from patients with idiopathic schizophrenia.	Heider J et al.	—	2024	→
A genome-wide methylation analysis of Chinese Han patients with chronic insomnia disorder.	Li X et al.	—	2024	→
Association of Occupational Dysfunction and Hospital Admissions With Different Polygenic Profiles in Bipolar Disorder.	Jonsson L et al.	—	2024	→
Causal Relationship Between Ferritin and Neuropsychiatric Disorders: A Two-Sample Mendelian Randomization Study.	Sun W et al.	—	2024	→
Cell-type specific methylation changes in the newborn child associated to obstetric pain relief.	Tran CJ et al.	—	2024	→
Current progress in understanding schizophrenia using genomics and pluripotent stem cells: A meta-analytical overview.	Choudhary A et al.	—	2024	→
Cytokine gene polymorphisms and suicide risk in an Indian ancestral population: A case-control study.	Kaushik R et al.	—	2024	→
Detecting outliers in case-control cohorts for improving deep learning networks on Schizophrenia prediction.	Martins D et al.	—	2024	→
Developmental psychopathology as a meta-paradigm: From zero-sum science to epistemological pluralism in theory and research.	Beauchaine TP	—	2024	→
Enhancing schizophrenia phenotype prediction from genotype data through knowledge-driven deep neural network models.	Martins D et al.	—	2024	→
Epigenome-wide mediation analysis of the relationship between psychosocial stress and cardiometabolic risk factors in the Health and Retirement Study (HRS).	Opsasnick LA et al.	—	2024	→
FMR1 genetically interacts with DISC1 to regulate glutamatergic synaptogenesis.	Honda T et al.	—	2024	→
Functional gradient dysfunction in drug-naïve first-episode schizophrenia and its correlation with specific transcriptional patterns and treatment predictions.	Yao G et al.	—	2024	→
Generation and transcriptomic characterization of MIR137 knockout miniature pig model for neurodevelopmental disorders.	Xu S et al.	—	2024	→
Identifying diseases associated with Post-COVID syndrome through an integrated network biology approach.	Krishna N et al.	—	2024	→
<i>miR-137</i> regulates PTP61F, affecting insulin signaling, metabolic homeostasis, and starvation resistance in <i>Drosophila</i>.	Saedi H et al.	—	2024	→
Impacts of CACNB4 overexpression on dendritic spine density in both sexes and relevance to schizophrenia.	Parker EM et al.	—	2024	→
Interaction between RNF4 and SART3 is associated with the risk of schizophrenia.	Cheng Y et al.	—	2024	→
Linking Polygenic Risk of Schizophrenia to Variation in Magnetic Resonance Imaging Brain Measures: A Comprehensive Systematic Review.	Jameei H et al.	—	2024	→
Monozygotic twins discordant for schizophrenia differ in maturation and synaptic transmission.	Stern S et al.	—	2024	→
Ngfr<sup>+</sup> cholinergic projection from SI/nBM to mPFC selectively regulates temporal order recognition memory.	Mei F et al.	—	2024	→
Novel genetic loci of inhibitory control in ADHD and healthy children and genetic correlations with ADHD.	Pang T et al.	—	2024	→
Nuclear microRNA-mediated transcriptional control determines adult microglial homeostasis and brain function.	Li Z et al.	—	2024	→
Oscillatory-Quality of sleep spindles links brain state with sleep regulation and function.	Blanco-Duque C et al.	—	2024	→
Polygenic effects on brain functional endophenotype for deficit and non-deficit schizophrenia.	Fang J et al.	—	2024	→
Polygenic Risk Scores and Twin Concordance for Schizophrenia and Bipolar Disorder.	Song J et al.	—	2024	→
Role of NT5DC2 in tyrosine hydroxylase phosphorylation based on the analysis of NT5DC2-binding proteins.	Yamaguchi H et al.	—	2024	→
rvTWAS: identifying gene-trait association using sequences by utilizing transcriptome-directed feature selection.	He J et al.	—	2024	→
Scaled and efficient derivation of loss-of-function alleles in risk genes for neurodevelopmental and psychiatric disorders in human iPSCs.	Zhang H et al.	—	2024	→
Schizophrenia and Bone Marrow Disorders: An Emerging Clinical Association.	Jayakumar J et al.	—	2024	→
Temporal changes in brain morphology related to inflammation and schizophrenia: an omnigenic Mendelian randomization study.	Liu Y et al.	—	2024	→
The Role of 3' Regulatory Region Flanking Kinectin 1 Gene in Schizophrenia.	Guo X et al.	—	2024	→
Transcriptional control of CCAAT/enhancer binding protein zeta gene in chicken adipose tissue.	Gao L et al.	—	2024	→
Understanding copy number variations through their genes: a molecular view on 16p11.2 deletion and duplication syndromes.	Leone R et al.	—	2024	→
Unravelling the genetic basis of Schizophrenia.	Casey C et al.	—	2024	→
Whole-exome sequencing of individuals from an isolated population under extreme conditions implicates rare risk variants of schizophrenia.	Chen L et al.	—	2024	→
A Comprehensive Analysis of Cerebellar Volumes in the 22q11.2 Deletion Syndrome.	Schmitt JE et al.	—	2023	→
A gene based combination test using GWAS summary data.	Zhang J et al.	—	2023	→
A higher dysregulation burden of brain DNA methylation in female patients implicated in the sex bias of Schizophrenia.	Zhou J et al.	—	2023	→
A novel risk variant block across introns 36-45 of CACNA1C for schizophrenia: a cohort-wise replication and cerebral region-wide validation study.	Guo X et al.	—	2023	→
A pangenome reference of 36 Chinese populations.	Gao Y et al.	—	2023	→
Brain transcriptome-wide association study implicates novel risk genes underlying schizophrenia risk.	Zhang C et al.	—	2023	→
Common genetic variants contribute to heritability of age at onset of schizophrenia.	Sada-Fuente E et al.	—	2023	→
Depression trajectories and cytokines in schizophrenia spectrum disorders - A longitudinal observational study.	Hoprekstad GE et al.	—	2023	→
Dysfunction of cAMP-Protein Kinase A-Calcium Signaling Axis in Striatal Medium Spiny Neurons: A Role in Schizophrenia and Huntington's Disease Neuropathology.	Fjodorova M et al.	—	2023	→
Effect of rs1108580 of DBH and rs1006737 of CACNA1C on Cognition and Tardive Dyskinesia in a North Indian Schizophrenia Cohort.	Punchaichira TJ et al.	—	2023	→
Evaluating 17 methods incorporating biological function with GWAS summary statistics to accelerate discovery demonstrates a tradeoff between high sensitivity and high positive predictive value.	Moore A et al.	—	2023	→
Excitatory Dysfunction Drives Network and Calcium Handling Deficits in 16p11.2 Duplication Schizophrenia Induced Pluripotent Stem Cell-Derived Neurons.	Parnell E et al.	—	2023	→
Exploring the Hypothesis of a Schizophrenia and Bipolar Disorder Continuum: Biological, Genetic and Pharmacologic Data.	de Sousa TR et al.	—	2023	→
Gene and schizophrenia in the pregenome and postgenome-wide association studies era: a bibliometric analysis and network visualization.	Zakaria WNA et al.	—	2023	→
Genes implicated by a methylome-wide schizophrenia study in neonatal blood show differential expression in adult brain samples.	van den Oord EJCG et al.	—	2023	→
Genetic Influences on Cognitive Dysfunction in Schizophrenia.	Greenwood TA	—	2023	→
Genetic Influences on Outcomes of Psychotherapy in Borderline Personality Disorder: A Narrative Review of Implications for Personalized Treatment.	Ansari D et al.	—	2023	→
Genetics of bipolar disorder: insights into its complex architecture and biology from common and rare variants.	Hara T et al.	—	2023	→
Genetic variations in DOCK4 contribute to schizophrenia susceptibility in a Chinese cohort: A genetic neuroimaging study.	Xu X et al.	—	2023	→
Genomic analysis of firework fear and noise reactivity in standard poodles.	Handegård KW et al.	—	2023	→
Genomic insights into schizophrenia.	Owen MJ	—	2023	→
Glutamatergic dysfunction leads to a hyper-dopaminergic phenotype through deficits in short-term habituation: a mechanism for aberrant salience.	Panayi MC et al.	—	2023	→
Impact of traumatic life events and polygenic risk scores for major depression and posttraumatic stress disorder on Iraq/Afghanistan Veterans.	Lipsky RK et al.	—	2023	→
Independent Associated SNPs at SORCS3 and Its Protein Interactors for Multiple Brain-Related Disorders and Traits.	Kamran M et al.	—	2023	→
Inflammation and cognition in severe mental illness: patterns of covariation and subgroups.	Sæther LS et al.	—	2023	→
Mendelian Randomization Study Using Dopaminergic Neuron-Specific eQTL Identifies Novel Risk Genes for Schizophrenia.	Dang X et al.	—	2023	→
Methylation in MAD1L1 is associated with the severity of suicide attempt and phenotypes of depression.	Sokolov AV et al.	—	2023	→
MicroRNA137-loaded lipid nanoparticles regulate synaptic proteins in the prefrontal cortex.	Palumbo MC et al.	—	2023	→
miRNA cargo in circulating vesicles from neurons is altered in individuals with schizophrenia and associated with severe disease.	Barnett MM et al.	—	2023	→
New insights into the structure and function of CNNM proteins.	Chen YS et al.	—	2023	→
One versus two biological parents with mental disorders: Relationship to educational attainment in the next generation.	Sidorchuk A et al.	—	2023	→
Overlap of Neuroanatomical Involvement in Frontotemporal Dementia and Primary Psychiatric Disorders: A Meta-analysis.	Ulugut H et al.	—	2023	→
Pleiotropic CACNA1C Variants and Neuronal Function in Psychosis.	Docherty AR	—	2023	→
Polygenic liabilities underlying job stress and exhaustion over a 10-year follow-up: A general population study.	Saarinen A et al.	—	2023	→
Predicting eating disorder and anxiety symptoms using disorder-specific and transdiagnostic polygenic scores for anorexia nervosa and obsessive-compulsive disorder.	Yilmaz Z et al.	—	2023	→
Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia.	Wen J et al.	—	2023	→
Role of cryptic rearrangements of human chromosomes in the aetiology of schizophrenia.	Jurisova L et al.	—	2023	→
Schizophrenia-associated Mitotic Arrest Deficient-1 (MAD1) regulates the polarity of migrating neurons in the developing neocortex.	Goo BS et al.	—	2023	→
The contribution of copy number variants to psychiatric symptoms and cognitive ability.	Mollon J et al.	—	2023	→
The prediction of Alzheimer's disease through multi-trait genetic modeling.	Clark K et al.	—	2023	→
Therapeutic potential for KCC2-targeted neurological diseases.	Tomita K et al.	—	2023	→
The thalamus in psychosis spectrum disorder.	Anticevic A et al.	—	2023	→
A functional neuroimaging association study on the interplay between two schizophrenia genome-wide associated genes (CACNA1C and ZNF804A).	Guardiola-Ripoll M et al.	—	2022	→
A Genome-Wide Association Study Reveals a <i>BDNF</i>-Centered Molecular Network Associated with Alcohol Dependence and Related Clinical Measures.	Levchenko A et al.	—	2022	→
AMPA receptors in schizophrenia: A systematic review of postmortem studies on receptor subunit expression and binding.	Yonezawa K et al.	—	2022	→
Analysis of <i>CACNA1C</i> and <i>KCNH2</i> Risk Variants on Cardiac Autonomic Function in Patients with Schizophrenia.	Refisch A et al.	—	2022	→
Applying a Fast-Scan Cyclic Voltammetry to Explore Dopamine Dynamics in Animal Models of Neuropsychiatric Disorders.	Grinevich VP et al.	—	2022	→
Association between C-reactive protein levels and antipsychotic treatment during 12 months follow-up period after acute psychosis.	Fathian F et al.	—	2022	→
Association between schizophrenia and prostate cancer risk: Results from a pool of cohort studies and Mendelian randomization analysis.	Ge F et al.	—	2022	→
Associations between polygenic risk, negative symptoms, and functional connectome topology during a working memory task in early-onset schizophrenia.	Deng M et al.	—	2022	→
C/EBPZ modulates the differentiation and proliferation of preadipocytes.	Chen Y et al.	—	2022	→
Characterizing the polygenic overlaps of bipolar disorder subtypes with schizophrenia and major depressive disorder.	Li Z et al.	—	2022	→
Cognitive and perceptual impairments in schizophrenia extend to other psychotic disorders but not schizotypy.	Frattaroli N et al.	—	2022	→
Collagen VI deficiency causes behavioral abnormalities and cortical dopaminergic dysfunction.	Gregorio I et al.	—	2022	→
Comprehensive and integrative analyses identify TYW5 as a schizophrenia risk gene.	Zhang C et al.	—	2022	→
Consensus on potential biomarkers developed for use in clinical tests for schizophrenia.	Lin P et al.	—	2022	→
Contribution from MHC-Mediated Risk in Schizophrenia Can Reflect a More Ethnic-Specific Genetic and Comorbid Background.	Srinivas L et al.	—	2022	→
Cross-Disorder Analysis of De Novo Mutations in Neuropsychiatric Disorders.	Li K et al.	—	2022	→
Cross Talk proposal: The kids will be fine: parental stress rodent models are good for assessing influences on human neurobiology.	Moon N et al.	—	2022	→
Current advancements of modelling schizophrenia using patient-derived induced pluripotent stem cells.	Dubonyte U et al.	—	2022	→
DeepNull models non-linear covariate effects to improve phenotypic prediction and association power.	McCaw ZR et al.	—	2022	→
Dissecting the association between psychiatric disorders and neurological proteins: a genetic correlation and two-sample bidirectional Mendelian randomization study.	Huang H et al.	—	2022	→
Distinct contributions of GluA1-containing AMPA receptors of different hippocampal subfields to salience processing, memory and impulse control.	Kilonzo K et al.	—	2022	→
DNA Methylation Pattern of Gene Promoters of MB-COMT, DRD2, and NR3C1 in Turkish Patients Diagnosed with Schizophrenia.	Aytac HM et al.	—	2022	→
Emerging evidence for astrocyte dysfunction in schizophrenia.	de Oliveira Figueiredo EC et al.	—	2022	→
Estimating SNP heritability in presence of population substructure in biobank-scale datasets.	Lin Z et al.	—	2022	→
Evaluating brain structure traits as endophenotypes using polygenicity and discoverability.	Matoba N et al.	—	2022	→
Examining pathways between genetic liability for schizophrenia and patterns of tobacco and cannabis use in adolescence.	Jones HJ et al.	—	2022	→
Feature and decision-level fusion for schizophrenia detection based on resting-state fMRI data.	Algumaei AH et al.	—	2022	→
Five Major Psychiatric Disorders and Alzheimer's Disease: A Bidirectional Mendelian Randomization Study.	Wei T et al.	—	2022	→
Functional characterization of the schizophrenia associated gene AS3MT identifies a role in neuronal development.	Washer SJ et al.	—	2022	→
Gene-based association tests using GWAS summary statistics and incorporating eQTL.	Cao X et al.	—	2022	→
Genes of the Glutamatergic System and Tardive Dyskinesia in Patients with Schizophrenia.	Fedorenko OY et al.	—	2022	→
Genetics of social anxiety disorder: a systematic review.	Baba A et al.	—	2022	→
Genome-wide analysis reveals genetic overlap between alcohol use behaviours, schizophrenia and bipolar disorder and identifies novel shared risk loci.	Wiström ED et al.	—	2022	→
Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci.	Yin X et al.	—	2022	→
High DAPK1 Expression Promotes Tumor Metastasis of Gastric Cancer.	Wang Q et al.	—	2022	→
How Variation in Risk Allele Output and Gene Interactions Shape the Genetic Architecture of Schizophrenia.	Kasap M et al.	—	2022	→
Identification of genetic variants influencing methylation in brain with pleiotropic effects on psychiatric disorders.	Pineda-Cirera L et al.	—	2022	→
Impaired migration of autologous induced neural stem cells from patients with schizophrenia and implications for genetic risk for psychosis.	Lee J et al.	—	2022	→
Infection Polygenic Factors Account for a Small Proportion of the Relationship Between Infections and Mental Disorders.	Shorter JR et al.	—	2022	→
Inflammation in first-episode psychosis: The contribution of inflammatory biomarkers to the emergence of negative symptoms, a systematic review and meta-analysis.	Dunleavy C et al.	—	2022	→
Integration of multidimensional splicing data and GWAS summary statistics for risk gene discovery.	Ji Y et al.	—	2022	→
Integrative Analyses of Transcriptomes to Explore Common Molecular Effects of Antipsychotic Drugs.	Truong TTT et al.	—	2022	→
Lack of Support for the Genes by Early Environment Interaction Hypothesis in the Pathogenesis of Schizophrenia.	Vassos E et al.	—	2022	→
Larval Zebrafish as a Model for Mechanistic Discovery in Mental Health.	Tan JXM et al.	—	2022	→
Lifestyle Modifies the Diabetes-Related Metabolic Risk, Conditional on Individual Genetic Differences.	Shin J et al.	—	2022	→
Magical thinking in individuals with high polygenic risk for schizophrenia but no non-affective psychoses-a general population study.	Saarinen A et al.	—	2022	→
Mapping genomic loci implicates genes and synaptic biology in schizophrenia.	Trubetskoy V et al.	—	2022	→
Mapping miRNA Research in Schizophrenia: A Scientometric Review.	Lim M et al.	—	2022	→
MicroRNAs and Synaptic Plasticity: From Their Molecular Roles to Response to Therapy.	Mohammadi AH et al.	—	2022	→
Morphometric Integrated Classification Index: A Multisite Model-Based, Interpretable, Shareable and Evolvable Biomarker for Schizophrenia.	Xie Y et al.	—	2022	→
Neuroimaging Findings in Neurodevelopmental Copy Number Variants: Identifying Molecular Pathways to Convergent Phenotypes.	Silva AI et al.	—	2022	→
Phenotyping Young GluA1 Deficient Mice - A Behavioral Characterization in a Genetic Loss-of-Function Model.	Reiber M et al.	—	2022	→
Polygenic risk scores for schizophrenia and major depression are associated with socio-economic indicators of adversity in two British community samples.	Machlitt-Northen S et al.	—	2022	→
Prospects for improved prevention and treatment of neuropsychiatric disorders: <i>Neuroscience Applied</i>.	Meyer-Lindenberg A et al.	—	2022	→
Regulatory variants at 2q33.1 confer schizophrenia risk by modulating distal gene TYW5 expression.	Li S et al.	—	2022	→
Revisiting tandem repeats in psychiatric disorders from perspectives of genetics, physiology, and brain evolution.	Xiao X et al.	—	2022	→
Short-chain fatty acids in patients with schizophrenia and ultra-high risk population.	Peng H et al.	—	2022	→
Single nucleus multi-omics identifies human cortical cell regulatory genome diversity.	Luo C et al.	—	2022	→
SYNCRIP controls miR-137 and striatal learning in animal models of methamphetamine abstinence.	Kim B et al.	—	2022	→
The Current Progress of Psychiatric Genomics.	Nishioka M	—	2022	→
The impact of educational attainment, intelligence and intellectual disability on schizophrenia: a Swedish population-based register and genetic study.	Song J et al.	—	2022	→
The role of microRNAs in diseases and related signaling pathways.	Vaghf A et al.	—	2022	→
Total Brain Volumetric Measures and Schizophrenia Risk: A Two-Sample Mendelian Randomization Study.	Zhu D et al.	—	2022	→
Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants.	Sanders B et al.	—	2022	→
TwinEQTL: ultrafast and powerful association analysis for eQTL and GWAS in twin studies.	Xia K et al.	—	2022	→
Unusual Molecular Regulation of Dorsolateral Prefrontal Cortex Layer III Synapses Increases Vulnerability to Genetic and Environmental Insults in Schizophrenia.	Arnsten AFT et al.	—	2022	→
Visual masking deficits in schizophrenia: a view into the genetics of the disease through an endophenotype.	Shaqiri A et al.	—	2022	→
A Case for Thalamic Mechanisms of Schizophrenia: Perspective From Modeling 22q11.2 Deletion Syndrome.	Jiang Y et al.	—	2021	→
A genetic risk score using human chromosomal-scale length variation can predict schizophrenia.	Toh C et al.	—	2021	→
A Human-Specific Schizophrenia Risk Tandem Repeat Affects Alternative Splicing of a Human-Unique Isoform AS3MTd2d3 and Mushroom Dendritic Spine Density.	Cai X et al.	—	2021	→
Akt-mTOR hypoactivity in bipolar disorder gives rise to cognitive impairments associated with altered neuronal structure and function.	Vanderplow AM et al.	—	2021	→
Alteration of NMDA receptor trafficking as a cellular hallmark of psychosis.	Espana A et al.	—	2021	→
Altered Peripheral Immune Profiles in First-Episode, Drug-Free Patients With Schizophrenia: Response to Antipsychotic Medications.	Chen L et al.	—	2021	→
Alternative Diagnostic Models of the Psychotic Disorders: Evidence-Based Choices.	Cohen BM et al.	—	2021	→
Analysis of whole exome sequencing in severe mental illness hints at selection of brain development and immune related genes.	Mahadevan J et al.	—	2021	→
An integrative analysis of genomic and exposomic data for complex traits and phenotypic prediction.	Zhou X et al.	—	2021	→
A polygenic resilience score moderates the genetic risk for schizophrenia.	Hess JL et al.	—	2021	→
Assessing olfactory, memory, social and circadian phenotypes associated with schizophrenia in a genetic model based on Rim.	Hidalgo S et al.	—	2021	→
Calcium Channel Splice Variants and Their Effects in Brain and Cardiovascular Function.	Yeow SQZ et al.	—	2021	→
Causal inference for heritable phenotypic risk factors using heterogeneous genetic instruments.	Wang J et al.	—	2021	→
Causal influences of neuroticism on mental health and cardiovascular disease.	Zhang F et al.	—	2021	→
Clinical evidence that a dysregulated master neural network modulator may aid in diagnosing schizophrenia.	Nomoto M et al.	—	2021	→
Combining Structural-Equation Modeling with Genomic-Relatedness-Matrix Restricted Maximum Likelihood in OpenMx.	Kirkpatrick RM et al.	—	2021	→
Conformational heterogeneity coupled with β-fibril formation of a scaffold protein involved in chronic mental illnesses.	Cukkemane A et al.	—	2021	→
Developmental Characterization of Schizophrenia-Associated Gene Zswim6 in Mouse Forebrain.	Chang CC et al.	—	2021	→
Dissecting Molecular Genetic Mechanisms of 1q21.1 CNV in Neuropsychiatric Disorders.	Yoon J et al.	—	2021	→
Duration Mismatch Negativity Predicts Remission in First-Episode Schizophrenia Patients.	Nakajima S et al.	—	2021	→
Effect of selection bias on two sample summary data based Mendelian randomization.	Wang K et al.	—	2021	→
Effects of Importin α1/KPNA1 deletion and adolescent social isolation stress on psychiatric disorder-associated behaviors in mice.	Sakurai K et al.	—	2021	→
Environmental Risk Factors for Schizophrenia and Bipolar Disorder and Their Relationship to Genetic Risk: Current Knowledge and Future Directions.	Robinson N et al.	—	2021	→
Estimating the Prevalence and Genetic Risk Mechanisms of ARFID in a Large Autism Cohort.	Koomar T et al.	—	2021	→
Evaluation of the relationship between VRK2, rs4380187 polymorphisms, and genetic susceptibility to schizophrenia in the Chinese Han population.	Liu X et al.	—	2021	→
Evidence for the Association between the Intronic Haplotypes of Ionotropic Glutamate Receptors and First-Episode Schizophrenia.	Hirschfeldova K et al.	—	2021	→
Exosome Transplantation From Patients With Schizophrenia Causes Schizophrenia-Relevant Behaviors in Mice: An Integrative Multi-omics Data Analysis.	Du Y et al.	—	2021	→
Exploring the biological role of postzygotic and germinal de novo mutations in ASD.	Alonso-Gonzalez A et al.	—	2021	→
Fine structure analysis of perineuronal nets in the ketamine model of schizophrenia.	Kaushik R et al.	—	2021	→
Gene expression in the dorsolateral and ventromedial prefrontal cortices implicates immune-related gene networks in PTSD.	Logue MW et al.	—	2021	→
Genetic architecture of schizophrenia: a review of major advancements.	Legge SE et al.	—	2021	→
Genetic influences on externalizing psychopathology overlap with cognitive functioning and show developmental variation.	Mollon J et al.	—	2021	→
Genetic testing for suicide risk assessment: Theoretical premises, research challenges and ethical concerns.	Mishara BL et al.	—	2021	→
Genetic variants in miRNAs differentially expressed during brain development and their relevance to psychiatric disorders susceptibility.	Brum CB et al.	—	2021	→
Genome-wide analyses of smoking behaviors in schizophrenia: Findings from the Psychiatric Genomics Consortium.	Peterson RE et al.	—	2021	→
Genome-Wide Association Studies of Schizophrenia and Bipolar Disorder in a Diverse Cohort of US Veterans.	Bigdeli TB et al.	—	2021	→
Genome-wide association study accounting for anticholinergic burden to examine cognitive dysfunction in psychotic disorders.	Eum S et al.	—	2021	→
Genome wide association study identifies four loci for early onset schizophrenia.	Guo S et al.	—	2021	→
Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression.	Forstner AJ et al.	—	2021	→
Genome-wide association study of problematic opioid prescription use in 132,113 23andMe research participants of European ancestry.	Sanchez-Roige S et al.	—	2021	→
Global Brain Flexibility During Working Memory Is Reduced in a High-Genetic-Risk Group for Schizophrenia.	Dimitriadis SI et al.	—	2021	→
GW-SEM 2.0: Efficient, Flexible, and Accessible Multivariate GWAS.	Pritikin JN et al.	—	2021	→
IgGs-Abzymes from the Sera of Patients with Multiple Sclerosis Recognize and Hydrolyze miRNAs.	Ermakov EA et al.	—	2021	→
Increased schizophrenia family history burden and reduced premorbid IQ in treatment-resistant schizophrenia: a Swedish National Register and Genomic Study.	Kowalec K et al.	—	2021	→
Increasing the resolution and precision of psychiatric genome-wide association studies by re-imputing summary statistics using a large, diverse reference panel.	Chatzinakos C et al.	—	2021	→
Integrating genomics and transcriptomics: Towards deciphering ADHD.	Pujol-Gualdo N et al.	—	2021	→
Involvement of the nuclear factor-κB transcriptional complex in prefrontal cortex immune activation in bipolar disorder.	Roman KM et al.	—	2021	→
<i>VTRNA2-1</i>: Genetic Variation, Heritable Methylation and Disease Association.	Dugué PA et al.	—	2021	→
KALRN: A central regulator of synaptic function and synaptopathies.	Parnell E et al.	—	2021	→
Kleine-Levin syndrome is associated with birth difficulties and genetic variants in the <i>TRANK1</i> gene loci.	Ambati A et al.	—	2021	→
Knock-Down of Hippocampal DISC1 in Immune-Challenged Mice Impairs the Prefrontal-Hippocampal Coupling and the Cognitive Performance Throughout Development.	Xu X et al.	—	2021	→
MicroRNA-195 predicts olanzapine response in drug-free patients with schizophrenia: A prospective cohort study.	Huang X et al.	—	2021	→
MicroRNAs in the Onset of Schizophrenia.	Thomas KT et al.	—	2021	→
Mood Stabilizers in Psychiatric Disorders and Mechanisms Learnt from In Vitro Model Systems.	Nayak R et al.	—	2021	→
Multivariate alterations in insula - Medial prefrontal cortex linked to genetics in 12q24 in schizophrenia.	Jiang W et al.	—	2021	→
Mutations in DISC1 alter IP<sub>3</sub>R and voltage-gated Ca<sup>2+</sup> channel functioning, implications for major mental illness.	Rittenhouse AR et al.	—	2021	→
Neurexins in autism and schizophrenia-a review of patient mutations, mouse models and potential future directions.	Tromp A et al.	—	2021	→
Neurogranin, Encoded by the Schizophrenia Risk Gene NRGN, Bidirectionally Modulates Synaptic Plasticity via Calmodulin-Dependent Regulation of the Neuronal Phosphoproteome.	Hwang H et al.	—	2021	→
Neuroinflammation in schizophrenia: the role of nuclear factor kappa B.	Murphy CE et al.	—	2021	→
Neurological Phenotype of Mowat-Wilson Syndrome.	Cordelli DM et al.	—	2021	→
nMAGMA: a network-enhanced method for inferring risk genes from GWAS summary statistics and its application to schizophrenia.	Yang A et al.	—	2021	→
Oxidative Stress-Related Mechanisms in Schizophrenia Pathogenesis and New Treatment Perspectives.	Ermakov EA et al.	—	2021	→
Rare germline variants in individuals diagnosed with schizophrenia within multiplex families.	Li S et al.	—	2021	→
Rare variants in the endocytic pathway are associated with Alzheimer's disease, its related phenotypes, and functional consequences.	Zhan L et al.	—	2021	→
Resolving cell state in iPSC-derived human neural samples with multiplexed fluorescence imaging.	Tomov ML et al.	—	2021	→
Resting state alpha oscillatory activity is a valid and reliable marker of schizotypy.	Trajkovic J et al.	—	2021	→
Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations.	Rees E et al.	—	2021	→
Schizophrenia risk alleles often affect the expression of many genes and each gene may have a different effect on the risk: A mediation analysis.	Peng X et al.	—	2021	→
Semi-parametric empirical Bayes factor for genome-wide association studies.	Morisawa J et al.	—	2021	→
Sex-Specific Associations of <i>MIR137</i> Polymorphisms With Schizophrenia in a Han Chinese Cohort.	Yin J et al.	—	2021	→
Sex-specific sensitivity to methamphetamine-induced schizophrenia-relevant behaviours in <i>neuregulin 1 type III</i> overexpressing mice.	Chesworth R et al.	—	2021	→
Shared Genetic Liability and Causal Associations Between Major Depressive Disorder and Cardiovascular Diseases.	Zhang F et al.	—	2021	→
Socioeconomic Deprivation Index Is Associated With Psychiatric Disorders: An Observational and Genome-wide Gene-by-Environment Interaction Analysis in the UK Biobank Cohort.	Ye J et al.	—	2021	→
Structural neuroimaging phenotypes of a novel multi-gene risk score in youth bipolar disorder.	Cazes J et al.	—	2021	→
Swedish large-scale schizophrenia study: Why do patients and healthy controls participate?	Dufva YE et al.	—	2021	→
Systematic discovery of signaling pathways linking immune activation to schizophrenia.	Gao Y et al.	—	2021	→
The association between family history and genomic burden with schizophrenia mortality: a Swedish population-based register and genetic sample study.	Kowalec K et al.	—	2021	→
The Causal Effects of Insomnia on Bipolar Disorder, Depression, and Schizophrenia: A Two-Sample Mendelian Randomization Study.	Huang P et al.	—	2021	→
The dihydropyrimidine dehydrogenase gene contributes to heritable differences in sleep in mice.	Keenan BT et al.	—	2021	→
The Drosophila ortholog of the schizophrenia-associated CACNA1A and CACNA1B voltage-gated calcium channels regulate memory, sleep and circadian rhythms.	Hidalgo S et al.	—	2021	→
The GluA1 AMPAR subunit is necessary for hedonic responding but not hedonic value in female mice.	Strickland JA et al.	—	2021	→
The state of the science in psychiatric genomics.	Sullivan PF et al.	—	2021	→
The VNTR of the <i>AS3MT</i> gene is associated with brain activations during a memory span task and their training-induced plasticity.	Zhao W et al.	—	2021	→
Traumatic Events, Social Adversity and Discrimination as Risk Factors for Psychosis - An Umbrella Review.	Varchmin L et al.	—	2021	→
Understanding the role of gut microbiota in the pathogenesis of schizophrenia.	Ghorbani M et al.	—	2021	→
What Have We Learned About the Genetics of Obsessive-Compulsive and Related Disorders in Recent Years?	Mattheisen M et al.	—	2021	→
Zinc Finger Proteins in Neuro-Related Diseases Progression.	Bu S et al.	—	2021	→
A genome-wide multiphenotypic association analysis identified candidate genes and gene ontology shared by four common risky behaviors.	Ye J et al.	—	2020	→
A <i>Caenorhabditis elegans</i> Model for Integrating the Functions of Neuropsychiatric Risk Genes Identifies Components Required for Normal Dendritic Morphology.	Aguirre-Chen C et al.	—	2020	→
Alteration of the gut microbiome in first-episode drug-naïve and chronic medicated schizophrenia correlate with regional brain volumes.	Ma X et al.	—	2020	→
A major role for common genetic variation in anxiety disorders.	Purves KL et al.	—	2020	→
[A new look at the genetics of neurocognitive deficits in schizophrenia].	Fedorenko OY et al.	—	2020	→
Arsenic Metabolism in Mice Carrying a <i>BORCS7/AS3MT</i> Locus Humanized by Syntenic Replacement.	Koller BH et al.	—	2020	→
Association between a <i>TCF4</i> Polymorphism and Susceptibility to Schizophrenia.	Gao JY et al.	—	2020	→
Associations between gut microbiota and Alzheimer's disease, major depressive disorder, and schizophrenia.	Zhuang Z et al.	—	2020	→
Associations between schizophrenia polygenic risk and apathy in schizophrenia spectrum disorders and healthy controls.	Lyngstad SH et al.	—	2020	→
Association test using Copy Number Profile Curves (CONCUR) enhances power in rare copy number variant analysis.	Brucker A et al.	—	2020	→
A truncating Aspm allele leads to a complex cognitive phenotype and region-specific reductions in parvalbuminergic neurons.	Garrett L et al.	—	2020	→
A Unifying Framework for Imputing Summary Statistics in Genome-Wide Association Studies.	Wu Y et al.	—	2020	→
Biological stress response in women at risk of postpartum psychosis: The role of life events and inflammation.	Aas M et al.	—	2020	→
Biomarkers in Psychiatry: Concept, Definition, Types and Relevance to the Clinical Reality.	García-Gutiérrez MS et al.	—	2020	→
Cav1.2 channelopathies causing autism: new hallmarks on Timothy syndrome.	Marcantoni A et al.	—	2020	→
Characterization of Single Gene Copy Number Variants in Schizophrenia.	Szatkiewicz JP et al.	—	2020	→
Chronicity and Sex Affect Genetic Risk Prediction in Schizophrenia.	Meier SM et al.	—	2020	→
Common variants in FAN1, located in 15q13.3, confer risk for schizophrenia and bipolar disorder in Han Chinese.	Jian X et al.	—	2020	→
Consistent gene signature of schizophrenia identified by a novel feature selection strategy from comprehensive sets of transcriptomic data.	Yang Q et al.	—	2020	→
Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry.	Bigdeli TB et al.	—	2020	→
CORE GREML for estimating covariance between random effects in linear mixed models for complex trait analyses.	Zhou X et al.	—	2020	→
De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia.	Rees E et al.	—	2020	→
DNA Methylation Analysis of the NR3C1 Gene in Patients with Schizophrenia.	Liu L et al.	—	2020	→
Do Current Measures of Polygenic Risk for Mental Disorders Contribute to Population Variance in Mental Health?	Marsman A et al.	—	2020	→
Emerging phenotyping strategies will advance our understanding of psychiatric genetics.	Sanchez-Roige S et al.	—	2020	→
Establishment of Best Practices for Evidence for Prediction: A Review.	Poldrack RA et al.	—	2020	→
Evaluating the Impact of Nonrandom Mating: Psychiatric Outcomes Among the Offspring of Pairs Diagnosed With Schizophrenia and Bipolar Disorder.	Nordsletten AE et al.	—	2020	→
Evaluation of the relationships of the WBP1L gene with schizophrenia and the general psychopathology scale based on a case-control study.	Guan F et al.	—	2020	→
Fine-mapping of ZDHHC2 identifies risk variants for schizophrenia in the Han Chinese population.	Zhang H et al.	—	2020	→
Focus on Causality in ESC/iPSC-Based Modeling of Psychiatric Disorders.	Hoffmann A et al.	—	2020	→
Genetic Intersections of Language and Neuropsychiatric Conditions.	Koomar T et al.	—	2020	→
Genetic polymorphisms of PIP5K2A and course of schizophrenia.	Poltavskaya EG et al.	—	2020	→
Genetic predictors of hippocampal subfield volume in PTSD cases and trauma-exposed controls.	Morey RA et al.	—	2020	→
Genetics of schizophrenia (Review).	Trifu SC et al.	—	2020	→
Glutamate in schizophrenia: Neurodevelopmental perspectives and drug development.	Egerton A et al.	—	2020	→
Identification of 34 genes conferring genetic and pharmacological risk for the comorbidity of schizophrenia and smoking behaviors.	Ma Y et al.	—	2020	→
IGREX for quantifying the impact of genetically regulated expression on phenotypes.	Cai M et al.	—	2020	→
<i>MIR137</i> polygenic risk is associated with schizophrenia and affects functional connectivity of the dorsolateral prefrontal cortex.	Liu S et al.	—	2020	→
Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia.	Halvorsen M et al.	—	2020	→
Increased expression of schizophrenia-associated gene C4 leads to hypoconnectivity of prefrontal cortex and reduced social interaction.	Comer AL et al.	—	2020	→
Integrative analysis of Mendelian randomization and Bayesian colocalization highlights four genes with putative BMI-mediated causal pathways to diabetes.	Liu Q et al.	—	2020	→
Investigation of Schizophrenia with Human Induced Pluripotent Stem Cells.	Powell SK et al.	—	2020	→
Irritability as a Transdiagnostic Vulnerability Trait:Current Issues and Future Directions.	Beauchaine TP et al.	—	2020	→
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.	Satterstrom FK et al.	—	2020	→
Longitudinal epigenome-wide association studies of three male military cohorts reveal multiple CpG sites associated with post-traumatic stress disorder.	Snijders C et al.	—	2020	→
Loss of MicroRNA-137 Impairs the Homeostasis of Potassium in Neurons via KCC2.	Mi TW et al.	—	2020	→
LPM: a latent probit model to characterize the relationship among complex traits using summary statistics from multiple GWASs and functional annotations.	Ming J et al.	—	2020	→
Machine learning analysis of exome trios to contrast the genomic architecture of autism and schizophrenia.	Sardaar S et al.	—	2020	→
Minimal phenotyping yields genome-wide association signals of low specificity for major depression.	Cai N et al.	—	2020	→
miRNA regulation of social and anxiety-related behaviour.	Narayanan R et al.	—	2020	→
Neurodevelopmental concepts of schizophrenia in the genome-wide association era: AKT/mTOR signaling as a pathological mediator of genetic and environmental programming during development.	Howell KR et al.	—	2020	→
Neuronal Plasticity: Neuronal Organization is Associated with Neurological Disorders.	Dhuriya YK et al.	—	2020	→
Novel genetic susceptibility loci identified by family based whole exome sequencing in Han Chinese schizophrenia patients.	Li M et al.	—	2020	→
NT5DC2 affects the phosphorylation of tyrosine hydroxylase regulating its catalytic activity.	Nakashima A et al.	—	2020	→
Obsessive-compulsive disorder and attention-deficit/hyperactivity disorder: distinct associations with DNA methylation and genetic variation.	Goodman SJ et al.	—	2020	→
Overdispersed gene expression in schizophrenia.	Huang G et al.	—	2020	→
Pathogenesis and management of Brugada syndrome in schizophrenia: A scoping review.	Rastogi A et al.	—	2020	→
Penalized regression and model selection methods for polygenic scores on summary statistics.	Pattee J et al.	—	2020	→
Peripheral complement proteins in schizophrenia: A systematic review and meta-analysis of serological studies.	Mongan D et al.	—	2020	→
Polygenic effects of schizophrenia on hippocampal grey matter volume and hippocampus-medial prefrontal cortex functional connectivity.	Liu S et al.	—	2020	→
Polygenic risk for autism spectrum disorder affects left amygdala activity and negative emotion in schizophrenia.	Qin Y et al.	—	2020	→
Polygenic Risk Scores for Subtyping of Schizophrenia.	Chen J et al.	—	2020	→
Postzygotic Somatic Mutations in the Human Brain Expand the Threshold-Liability Model of Schizophrenia.	Singh SM et al.	—	2020	→
Proof-of-concept study of a multi-gene risk score in adolescent bipolar disorder.	Dimick MK et al.	—	2020	→
Prospective study of polygenic risk, protective factors, and incident depression following combat deployment in US Army soldiers.	Choi KW et al.	—	2020	→
Rare variants and biological pathways identified in treatment-refractory depression.	McClain LL et al.	—	2020	→
RDoC and Psychopathology among Youth: Misplaced Assumptions and an Agenda for Future Research.	Beauchaine TP et al.	—	2020	→
Reconsideration of the Semaphorin-3A Binding Motif Found in Chondroitin Sulfate Using <i>Galnac4s-6st</i>-Knockout Mice.	Nadanaka S et al.	—	2020	→
Schizophrenia in a genomic era: a review from the pathogenesis, genetic and environmental etiology to diagnosis and treatment insights.	Zamanpoor M	—	2020	→
Specificity and Continuity of Schizophrenia and Bipolar Disorder: Relation to Biomarkers.	Yamada Y et al.	—	2020	→
Synaptic and brain-expressed gene sets relate to the shared genetic risk across five psychiatric disorders.	Hammerschlag AR et al.	—	2020	→
SZDB2.0: an updated comprehensive resource for schizophrenia research.	Wu Y et al.	—	2020	→
The complement system in schizophrenia: where are we now and what's next?	Woo JJ et al.	—	2020	→
The effect of LRRK2 loss-of-function variants in humans.	Whiffin N et al.	—	2020	→
The Gene Polymorphism of VMAT2 Is Associated with Risk of Schizophrenia in Male Han Chinese.	Han H et al.	—	2020	→
The Inflamed Brain in Schizophrenia: The Convergence of Genetic and Environmental Risk Factors That Lead to Uncontrolled Neuroinflammation.	Comer AL et al.	—	2020	→
The influence of dopaminergic polymorphisms on selective stopping.	Rincón-Pérez I et al.	—	2020	→
The polygenic architecture of schizophrenia - rethinking pathogenesis and nosology.	Smeland OB et al.	—	2020	→
Two Thalamic Regions Screened Using Laser Capture Microdissection with Whole Human Genome Microarray in Schizophrenia Postmortem Samples.	Bakshi K et al.	—	2020	→
Understanding the genetics of neuropsychiatric disorders: the potential role of genomic regulatory blocks.	Barešić A et al.	—	2020	→
Whole-Genome Approach Discovers Novel Genetic and Nongenetic Variance Components Modulated by Lifestyle for Cardiovascular Health.	Zhou X et al.	—	2020	→
Wnt receptor gene <i>FZD1</i> was associated with schizophrenia in genome-wide SNP analysis of the Australian Schizophrenia Research Bank cohort.	Liu X et al.	—	2020	→
Aberrant calcium channel splicing drives defects in cortical differentiation in Timothy syndrome.	Panagiotakos G et al.	—	2019	→
Association of Childhood Exposure to Nitrogen Dioxide and Polygenic Risk Score for Schizophrenia With the Risk of Developing Schizophrenia.	Horsdal HT et al.	—	2019	→
Association of Hydroxylmethyl Glutaryl Coenzyme A Reductase Inhibitors, L-Type Calcium Channel Antagonists, and Biguanides With Rates of Psychiatric Hospitalization and Self-Harm in Individuals With Serious Mental Illness.	Hayes JF et al.	—	2019	→
Attenuation of Novelty-Induced Hyperactivity of <i>Gria1-/-</i> Mice by Cannabidiol and Hippocampal Inhibitory Chemogenetics.	Aitta-Aho T et al.	—	2019	→
A VNTR Regulates miR-137 Expression Through Novel Alternative Splicing and Contributes to Risk for Schizophrenia.	Pacheco A et al.	—	2019	→
Biological and practical implications of genome-wide association study of schizophrenia using Bayesian variable selection.	Rowe B et al.	—	2019	→
CACNA1C risk variant affects microstructural connectivity of the amygdala.	Koch K et al.	—	2019	→
Case Report of Childhood-Onset Psychosis in a Patient with a Known WNT10A Mutation.	Kobza AO et al.	—	2019	→
Childhood Trauma in Schizophrenia: Current Findings and Research Perspectives.	Popovic D et al.	—	2019	→
Commonality in dysregulated expression of gene sets in cortical brains of individuals with autism, schizophrenia, and bipolar disorder.	Guan J et al.	—	2019	→
Common-variant associations with fragile X syndrome.	Crowley JJ et al.	—	2019	→
Computational Modeling of Genetic Contributions to Excitability and Neural Coding in Layer V Pyramidal Cells: Applications to Schizophrenia Pathology.	Mäki-Marttunen T et al.	—	2019	→
Detection of Putative Functional Single Nucleotide Polymorphisms in Blood Pressure Loci and Validation of Association Between Single Nucleotide Polymorphism in WBP1L and Hypertension in the Chinese Han Population.	Zhang H et al.	—	2019	→
Effects of Common and Rare Chromosome 4 GABAergic Gene Variation on Alcohol Use and Antisocial Behavior.	Deak JD et al.	—	2019	→
Endophenotypes in Schizophrenia: Digging Deeper to Identify Genetic Mechanisms.	Greenwood TA et al.	—	2019	→
Essential genetic findings in neurodevelopmental disorders.	Cardoso AR et al.	—	2019	→
Exploring genetic variation that influences brain methylation in attention-deficit/hyperactivity disorder.	Pineda-Cirera L et al.	—	2019	→
Functional genomics reveal gene regulatory mechanisms underlying schizophrenia risk.	Huo Y et al.	—	2019	→
Genetic Control of Expression and Splicing in Developing Human Brain Informs Disease Mechanisms.	Walker RL et al.	—	2019	→
Genetics of obsessive-compulsive disorder.	Purty A et al.	—	2019	→
Genetic Studies of Tic Disorders and Tourette Syndrome.	Qi Y et al.	—	2019	→
Genetic Variants in the 9p21.3 Locus Associated with Glioma Risk in Children, Adolescents, and Young Adults: A Case-Control Study.	Dahlin AM et al.	—	2019	→
Genetic Variation in the Psychiatric Risk Gene CACNA1C Modulates Reversal Learning Across Species.	Sykes L et al.	—	2019	→
Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect.	Ikeda M et al.	—	2019	→
Genome-wide association study identifies 30 loci associated with bipolar disorder.	Stahl EA et al.	—	2019	→
Genome-wide association study in two populations to determine genetic variants associated with Toxoplasma gondii infection and relationship to schizophrenia risk.	Wang AW et al.	—	2019	→
Genotype-covariate correlation and interaction disentangled by a whole-genome multivariate reaction norm model.	Ni G et al.	—	2019	→
GWAS of Behavioral Traits.	Mehta D et al.	—	2019	→
Hippocampal-prefrontal coherence mediates working memory and selective attention at distinct frequency bands and provides a causal link between schizophrenia and its risk gene GRIA1.	Bygrave AM et al.	—	2019	→
Identification by nano-LC-MS/MS of NT5DC2 as a protein binding to tyrosine hydroxylase: Down-regulation of NT5DC2 by siRNA increases catecholamine synthesis in PC12D cells.	Nakashima A et al.	—	2019	→
Identification of Specific Nuclear Genetic Loci and Genes That Interact With the Mitochondrial Genome and Contribute to Fecundity in <i>Caenorhabditis elegans</i>.	Zhu Z et al.	—	2019	→
Identification of the primate-specific gene BTN3A2 as an additional schizophrenia risk gene in the MHC loci.	Wu Y et al.	—	2019	→
Impact of Polygenic Risk for Schizophrenia on Cortical Structure in UK Biobank.	Neilson E et al.	—	2019	→
Improving Imputation Accuracy by Inferring Causal Variants in Genetic Studies.	Wu Y et al.	—	2019	→
Integration of methylation QTL and enhancer-target gene maps with schizophrenia GWAS summary results identifies novel genes.	Wu C et al.	—	2019	→
Interaction between childhood adversity and functional polymorphisms in the dopamine pathway on first-episode psychosis.	Trotta A et al.	—	2019	→
Machine learning in schizophrenia genomics, a case-control study using 5,090 exomes.	Trakadis YJ et al.	—	2019	→
Methylation age acceleration does not predict mortality in schizophrenia.	Kowalec K et al.	—	2019	→
MiR-137 Deficiency Causes Anxiety-Like Behaviors in Mice.	Yan HL et al.	—	2019	→
Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson's disease heritability.	Reynolds RH et al.	—	2019	→
Multiplexed and high-throughput neuronal fluorescence imaging with diffusible probes.	Guo SM et al.	—	2019	→
Multi-scale analysis of schizophrenia risk genes, brain structure, and clinical symptoms reveals integrative clues for subtyping schizophrenia patients.	Ma L et al.	—	2019	→
Next-generation sequencing refines the genetic architecture of Greek GnRH-deficient patients.	Stamou MI et al.	—	2019	→
Non-coding RNAs: the gatekeepers of neural network activity.	Zampa F et al.	—	2019	→
Polygenic risk for schizophrenia and season of birth within the UK Biobank cohort.	Escott-Price V et al.	—	2019	→
Polygenic risk score increases schizophrenia liability through cognition-relevant pathways.	Toulopoulou T et al.	—	2019	→
Postmortem brain tissue as an underutilized resource to study the molecular pathology of neuropsychiatric disorders across different ethnic populations.	Vornholt E et al.	—	2019	→
Preventing discrimination based on psychiatric risk biomarkers.	Brannan C et al.	—	2019	→
Protein-Protein Interaction Network Analysis Reveals Several Diseases Highly Associated with Polycystic Ovarian Syndrome.	Ramly B et al.	—	2019	→
Reduced cortical thickness related to single nucleotide polymorphisms in the major histocompatibility complex region in antipsychotic-naive schizophrenia.	Tao B et al.	—	2019	→
Risperidone administered during adolescence induced metabolic, anatomical and inflammatory/oxidative changes in adult brain: A PET and MRI study in the maternal immune stimulation animal model.	Casquero-Veiga M et al.	—	2019	→
Schizophrenia and Hereditary Polyneuropathy: <i>PMP22</i> Deletion as a Common Pathophysiological Link?	Endres D et al.	—	2019	→
Schizophrenia Identification Using Multi-View Graph Measures of Functional Brain Networks.	Xiang Y et al.	—	2019	→
Social and non-social autism symptoms and trait domains are genetically dissociable.	Warrier V et al.	—	2019	→
Statistical Association Mapping of Population-Structured Genetic Data.	Najafi A et al.	—	2019	→
Targeted Sequencing of 10,198 Samples Confirms Abnormalities in Neuronal Activity and Implicates Voltage-Gated Sodium Channels in Schizophrenia Pathogenesis.	Rees E et al.	—	2019	→
Temporal dynamics of miRNAs in human DLPFC and its association with miRNA dysregulation in schizophrenia.	Hu Z et al.	—	2019	→
The effect of a genetic variant at the schizophrenia associated AS3MT/BORCS7 locus on striatal dopamine function: A PET imaging study.	D'Ambrosio E et al.	—	2019	→
The role of polygenic risk score gene-set analysis in the context of the omnigenic model of schizophrenia.	Rammos A et al.	—	2019	→
Toward an animal model of borderline personality disorder.	Corniquel MB et al.	—	2019	→
Towards a Unifying Cognitive, Neurophysiological, and Computational Neuroscience Account of Schizophrenia.	Heinz A et al.	—	2019	→
Transient Knock-Down of Prefrontal DISC1 in Immune-Challenged Mice Causes Abnormal Long-Range Coupling and Cognitive Dysfunction throughout Development.	Xu X et al.	—	2019	→
Unraveling the genetic architecture of major depressive disorder: merits and pitfalls of the approaches used in genome-wide association studies.	Schwabe I et al.	—	2019	→
Unravelling the genetic basis of schizophrenia and bipolar disorder with GWAS: A systematic review.	Prata DP et al.	—	2019	→
Vitamin D in Synaptic Plasticity, Cognitive Function, and Neuropsychiatric Illness.	Mayne PE et al.	—	2019	→
Zinc finger proteins in psychiatric disorders and response to psychotropic medications.	Squassina A et al.	—	2019	→
A comprehensive review of the genetic and biological evidence supports a role for MicroRNA-137 in the etiology of schizophrenia.	Sakamoto K et al.	—	2018	→
A copy number variation generated by complicated organization of PCDHA gene cluster is associated with egg performance traits in Xinhua E-strain.	Huang T et al.	—	2018	→
A direct regulatory link between microRNA-137 and SHANK2: implications for neuropsychiatric disorders.	de Sena Cortabitarte A et al.	—	2018	→
Age at first birth in women is genetically associated with increased risk of schizophrenia.	Ni G et al.	—	2018	→
A genome-wide association study identifies two novel susceptibility loci and trans population polygenicity associated with bipolar disorder.	Ikeda M et al.	—	2018	→
Altered Expression Profile of IgLON Family of Neural Cell Adhesion Molecules in the Dorsolateral Prefrontal Cortex of Schizophrenic Patients.	Karis K et al.	—	2018	→
A molecule-based genetic association approach implicates a range of voltage-gated calcium channels associated with schizophrenia.	Li W et al.	—	2018	→
An approximate Bayesian significance test for genomic evaluations.	Wittenburg D et al.	—	2018	→
A Neuroscience-Oriented Research Approach to Borderline Personality Disorder.	Stanley B et al.	—	2018	→
A novel homozygous mutation in GAD1 gene described in a schizophrenic patient impairs activity and dimerization of GAD67 enzyme.	Magri C et al.	—	2018	→
A polygenic risk score analysis of psychosis endophenotypes across brain functional, structural, and cognitive domains.	Ranlund S et al.	—	2018	→
Association between cerebral dopamine neurotrophic factor (CDNF) 2 polymorphisms and schizophrenia susceptibility and symptoms in the Han Chinese population.	Yang Y et al.	—	2018	→
Association between genetic variability of neuronal nitric oxide synthase and sensorimotor gating in humans.	Rovný R et al.	—	2018	→
Association between PLA2G12A polymorphism and patients with schizophrenia in a southern Chinese Han population.	Hui L et al.	—	2018	→
Associations between psychosis endophenotypes across brain functional, structural, and cognitive domains.	Blakey R et al.	—	2018	→
Axo-myelinic neurotransmission: a novel mode of cell signalling in the central nervous system.	Micu I et al.	—	2018	→
Axon guidance pathway genes are associated with schizophrenia risk.	Wang Z et al.	—	2018	→
Beyond heritability: improving discoverability in imaging genetics.	Fan CC et al.	—	2018	→
Blood-Derived RNA- and microRNA-Hydrolyzing IgG Antibodies in Schizophrenia Patients.	Ermakov EA et al.	—	2018	→
Ca2+ Channels in Anterior Pituitary Somatotrophs: A Therapeutic Perspective.	Nussinovitch I	—	2018	→
Calcium Channels, Synaptic Plasticity, and Neuropsychiatric Disease.	Nanou E et al.	—	2018	→
Characterization of a Human-Specific Tandem Repeat Associated with Bipolar Disorder and Schizophrenia.	Song JHT et al.	—	2018	→
Childhood-Onset Schizophrenia: Insights from Induced Pluripotent Stem Cells.	Hoffmann A et al.	—	2018	→
Combining multi-modality data for searching biomarkers in schizophrenia.	Guo S et al.	—	2018	→
Common and Rare Genetic Risk Factors Converge in Protein Interaction Networks Underlying Schizophrenia.	Chang X et al.	—	2018	→
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.	Pardiñas AF et al.	—	2018	→
Comprehensive integrative analyses identify GLT8D1 and CSNK2B as schizophrenia risk genes.	Yang CP et al.	—	2018	→
Control of CNS functions by RNA-binding proteins in neurological diseases.	Zhou Y et al.	—	2018	→
Double hits in schizophrenia.	Vorstman JAS et al.	—	2018	→
Early Senescence and Leukocyte Telomere Shortening in SCHIZOPHRENIA: A Role for Cytomegalovirus Infection?	Solana C et al.	—	2018	→
Effects of common GRM5 genetic variants on cognition, hippocampal volume and mGluR5 protein levels in schizophrenia.	Matosin N et al.	—	2018	→
Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls.	Cosgrove D et al.	—	2018	→
eHealth provides a novel opportunity to exploit the advantages of the Nordic countries in psychiatric genetic research, building on the public health care system, biobanks, and registries.	Andreassen OA	—	2018	→
Embracing Psychosis: A Cognitive Insight Intervention Improves Personal Narratives and Meaning-Making in Patients With Schizophrenia.	Moritz S et al.	—	2018	→
Empirical Bayes Estimation of Semi-parametric Hierarchical Mixture Models for Unbiased Characterization of Polygenic Disease Architectures.	Nishino J et al.	—	2018	→
Evidence for genetic contribution to the increased risk of type 2 diabetes in schizophrenia.	Hackinger S et al.	—	2018	→
Examining the role of common and rare mitochondrial variants in schizophrenia.	Gonçalves VF et al.	—	2018	→
Exploring Genetic Variation that Influences Brain Methylation in Attention-Deficit/Hyperactivity Disorder	Pineda-Cirera L et al.	—	2018	—
Fetal Origins of Mental Disorders? An Answer Based on Mendelian Randomization.	Arafat S et al.	—	2018	→
From Maps to Multi-dimensional Network Mechanisms of Mental Disorders.	Braun U et al.	—	2018	→
Functional analysis of schizophrenia genes using GeneAnalytics program and integrated databases.	Sundararajan T et al.	—	2018	→
Further evidence for the genetic association between <i>CACNA1I</i> and schizophrenia.	Xie Y et al.	—	2018	→
Gene-environment interaction and psychiatric disorders: Review and future directions.	Assary E et al.	—	2018	→
Genetically predicted complement component 4A expression: effects on memory function and middle temporal lobe activation.	Donohoe G et al.	—	2018	→
Genetic association and meta-analysis of a schizophrenia GWAS variant rs10489202 in East Asian populations.	Yang Y et al.	—	2018	→
Genetic risk mechanisms of posttraumatic stress disorder in the human brain.	Bharadwaj RA et al.	—	2018	→
Genetic risk scores and family history as predictors of schizophrenia in Nordic registers.	Lu Y et al.	—	2018	→
Genetic variation in 117 myelination-related genes in schizophrenia: Replication of association to lipid biosynthesis genes.	Stokowy T et al.	—	2018	→
Genetic vulnerability to schizophrenia is associated with cannabis use patterns during adolescence.	Hiemstra M et al.	—	2018	→
Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity.	Smit DJA et al.	—	2018	→
Greater extracellular free-water in first-episode psychosis predicts better neurocognitive functioning.	Lyall AE et al.	—	2018	→
HAHap: a read-based haplotyping method using hierarchical assembly.	Lin YY et al.	—	2018	→
Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland.	Martin AR et al.	—	2018	→
Heritability of Schizophrenia and Schizophrenia Spectrum Based on the Nationwide Danish Twin Register.	Hilker R et al.	—	2018	→
How can genetics help understand the relationship between cognitive dysfunction and schizophrenia?	Smeland OB et al.	—	2018	→
Hydrolysis by catalytic IgGs of microRNA specific for patients with schizophrenia.	Ermakov EA et al.	—	2018	→
Identification of expression quantitative trait loci associated with schizophrenia and affective disorders in normal brain tissue.	Bhalala OG et al.	—	2018	→
Identification of miR-22-3p, miR-92a-3p, and miR-137 in peripheral blood as biomarker for schizophrenia.	Ma J et al.	—	2018	→
Imaging genetics of schizophrenia in the post-GWAS era.	Arslan A	—	2018	→
Improving genetic prediction by leveraging genetic correlations among human diseases and traits.	Maier RM et al.	—	2018	→
Integrating eQTL data with GWAS summary statistics in pathway-based analysis with application to schizophrenia.	Wu C et al.	—	2018	→
Integration of Enhancer-Promoter Interactions with GWAS Summary Results Identifies Novel Schizophrenia-Associated Genes and Pathways.	Wu C et al.	—	2018	→
Interactome analysis reveals ZNF804A, a schizophrenia risk gene, as a novel component of protein translational machinery critical for embryonic neurodevelopment.	Zhou Y et al.	—	2018	→
Investigating the genetic architecture of general and specific psychopathology in adolescence.	Jones HJ et al.	—	2018	→
<i>VRK2</i>, a Candidate Gene for Psychiatric and Neurological Disorders.	Li M et al.	—	2018	→
JEPEGMIX2: improved gene-level joint analysis of eQTLs in cosmopolitan cohorts.	Chatzinakos C et al.	—	2018	→
Jointly determining significance levels of primary and replication studies by controlling the false discovery rate in two-stage genome-wide association studies.	Jiang W et al.	—	2018	→
LSMM: a statistical approach to integrating functional annotations with genome-wide association studies.	Ming J et al.	—	2018	→
Male increase in brain gene expression variability is linked to genetic risk for schizophrenia.	Chen J et al.	—	2018	→
Mapping the Schizophrenia Genes by Neuroimaging: The Opportunities and the Challenges.	Arslan A	—	2018	→
Meta-analysis of GABRB2 polymorphisms and the risk of schizophrenia combined with GWAS data of the Han Chinese population and psychiatric genomics consortium.	Zhang T et al.	—	2018	→
Meta-analysis on the association between genetic polymorphisms and prepulse inhibition of the acoustic startle response.	Quednow BB et al.	—	2018	→
Method to estimate the approximate samples size that yield a certain number of significant GWAS signals in polygenic traits.	Bacanu SA et al.	—	2018	→
microRNAs Sculpt Neuronal Communication in a Tight Balance That Is Lost in Neurological Disease.	Thomas KT et al.	—	2018	→
Models of Schizotypy: The Importance of Conceptual Clarity.	Grant P et al.	—	2018	→
Multilocus genetic profile in dopaminergic pathway modulates the striatum and working memory.	Wang C et al.	—	2018	→
National-scale precision medicine for psychiatric disorders in Sweden.	Bergen SE et al.	—	2018	→
Next-generation sequencing analysis of multiplex families with atypical psychosis.	Okayama T et al.	—	2018	→
Non-coding RNA dysregulation in the amygdala region of schizophrenia patients contributes to the pathogenesis of the disease.	Liu Y et al.	—	2018	→
Nutrient Sensing, Signaling and Ageing: The Role of IGF-1 and mTOR in Ageing and Age-Related Disease.	Johnson SC	—	2018	→
Outgroup emotion processing in the vACC is modulated by childhood trauma and CACNA1C risk variant.	Krautheim JT et al.	—	2018	→
Partial loss of psychiatric risk gene Mir137 in mice causes repetitive behavior and impairs sociability and learning via increased Pde10a.	Cheng Y et al.	—	2018	→
Perspectives of psychiatric investigators and IRB chairs regarding benefits of psychiatric genetics research.	Roberts LW et al.	—	2018	→
Polygenic Risk Scores in Clinical Psychology: Bridging Genomic Risk to Individual Differences.	Bogdan R et al.	—	2018	→
Polygenic Risk Scores, School Achievement, and Risk for Schizophrenia: A Danish Population-Based Study.	Sørensen HJ et al.	—	2018	→
Predicting Violent Behavior: What Can Neuroscience Add?	Poldrack RA et al.	—	2018	→
Prenatal one-carbon metabolism dysregulation programs schizophrenia-like deficits.	Alachkar A et al.	—	2018	→
Psychiatric Genomics: An Update and an Agenda.	Sullivan PF et al.	—	2018	→
Psychiatry and developmental psychopathology: Unifying themes and future directions.	Beauchaine TP et al.	—	2018	→
Rare disruptive variants in the DISC1 Interactome and Regulome: association with cognitive ability and schizophrenia.	Teng S et al.	—	2018	→
Re-assessment of multiple testing strategies for more efficient genome-wide association studies.	Otani T et al.	—	2018	→
Recently evolved human-specific methylated regions are enriched in schizophrenia signals.	Banerjee N et al.	—	2018	→
Regulation of the Expression of the Psychiatric Risk Gene <i>Cacna1c</i> during Associative Learning.	Sykes L et al.	—	2018	→
Replicated associations of FADS1, MAD1L1, and a rare variant at 10q26.13 with bipolar disorder in Chinese population.	Zhao L et al.	—	2018	→
Replication of GWAS identified miR-137 and its target gene polymorphisms in Schizophrenia of South Indian population and meta-analysis with Psychiatric Genomics Consortium.	Sudesh R et al.	—	2018	→
Sample Size for Successful Genome-Wide Association Study of Major Depressive Disorder.	Nishino J et al.	—	2018	→
Sequence and Haplotypes Variation of the Ovine Uncoupling Protein-1 Gene (UCP1) and Their Association with Growth and Carcass Traits in New Zealand Romney Lambs.	An Q et al.	—	2018	→
The cAMP responsive element-binding (CREB)-1 gene increases risk of major psychiatric disorders.	Xiao X et al.	—	2018	→
The Complex Interaction of Mitochondrial Genetics and Mitochondrial Pathways in Psychiatric Disease.	Cuperfain AB et al.	—	2018	→
The contribution of alternative splicing to genetic risk for psychiatric disorders.	Reble E et al.	—	2018	→
The effect of weight on mental health: New evidence using genetic IVs.	Willage B	—	2018	→
The Emerging Immunogenetic Architecture of Schizophrenia.	Pouget JG	—	2018	→
The Genetics of Endophenotypes of Neurofunction to Understand Schizophrenia (GENUS) consortium: A collaborative cognitive and neuroimaging genetics project.	Blokland GAM et al.	—	2018	→
The impact of epigenomic next-generation sequencing approaches on our understanding of neuropsychiatric disorders.	Schang AL et al.	—	2018	→
The influence of MIR137 on white matter fractional anisotropy and cortical surface area in individuals with familial risk for psychosis.	Vogel BO et al.	—	2018	→
The schizophrenia- and autism-associated gene, transcription factor 4 regulates the columnar distribution of layer 2/3 prefrontal pyramidal neurons in an activity-dependent manner.	Page SC et al.	—	2018	→
Tracing Early Neurodevelopment in Schizophrenia with Induced Pluripotent Stem Cells.	Ahmad R et al.	—	2018	→
Transcriptome analysis in whole blood reveals increased microbial diversity in schizophrenia.	Olde Loohuis LM et al.	—	2018	→
Transcriptomic signatures of schizophrenia revealed by dopamine perturbation in an ex vivo model.	Duan J et al.	—	2018	→
Unbiased lipidomic profiling reveals metabolomic changes during the onset and antipsychotics treatment of schizophrenia disease.	Yan L et al.	—	2018	→
Use of schizophrenia and bipolar disorder polygenic risk scores to identify psychotic disorders.	Calafato MS et al.	—	2018	→
Using Full Genomic Information to Predict Disease: Breaking Down the Barriers Between Complex and Mendelian Diseases.	Jordan DM et al.	—	2018	→
Using mouse transgenic and human stem cell technologies to model genetic mutations associated with schizophrenia and autism.	St Clair D et al.	—	2018	→
Voltage-gated calcium channel activity and complex related genes and schizophrenia: A systematic investigation based on Han Chinese population.	Zhang T et al.	—	2018	→
Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection.	Vuckovic D et al.	—	2018	→
10 Years of GWAS Discovery: Biology, Function, and Translation.	Visscher PM et al.	—	2017	→
Adaptive combination of Bayes factors as a powerful method for the joint analysis of rare and common variants.	Lin WY et al.	—	2017	→
A Gene-Based Analysis of Acoustic Startle Latency.	Smith AK et al.	—	2017	→
Altered balance of excitatory and inhibitory learning in a genetically modified mouse model of glutamatergic dysfunction relevant to schizophrenia.	Sanderson DJ et al.	—	2017	→
Analysis of Shared Haplotypes amongst Palauans Maps Loci for Psychotic Disorders to 4q28 and 5q23-q31.	Bodea CA et al.	—	2017	→
An update on stem cell biology and engineering for brain development.	Parr CJC et al.	—	2017	→
Application of CRISPR/Cas9 to the study of brain development and neuropsychiatric disease.	Powell SK et al.	—	2017	→
A Quarter Century of Progress in Psychiatric Genetics.	Smoller JW	—	2017	→
A Recurrent De Novo Nonsense Variant in ZSWIM6 Results in Severe Intellectual Disability without Frontonasal or Limb Malformations.	Palmer EE et al.	—	2017	→
A review of molecular genetic studies of neurocognitive deficits in schizophrenia.	Zai G et al.	—	2017	→
Association between the variability of the ABCA13 gene and the risk of major depressive disorder and schizophrenia in the Han Chinese population.	Chen J et al.	—	2017	→
Association of ARHGAP18 polymorphisms with schizophrenia in the Chinese-Han population.	Guo W et al.	—	2017	→
Association of Common Variants in TGFA with Increased Risk of Knee Osteoarthritis Susceptibility.	Cui G et al.	—	2017	→
Attempts to replicate genetic associations with schizophrenia in a cohort from north India.	Prasad S et al.	—	2017	→
Can lncRNAs be indicators for the diagnosis of early onset or acute schizophrenia and distinguish major depressive disorder and generalized anxiety disorder?-A cross validation analysis.	Cui X et al.	—	2017	→
Challenges and opportunities for the development of new antipsychotic drugs.	Forray C et al.	—	2017	→
Clinically proven drug targets differentially expressed in the prefrontal cortex of schizophrenia patients.	Voisey J et al.	—	2017	→
Common variants of T-cells contribute differently to phenotypic variation in sarcoidosis.	Rivera NV et al.	—	2017	→
Common variants on 2p16.1, 6p22.1 and 10q24.32 are associated with schizophrenia in Han Chinese population.	Yu H et al.	—	2017	→
Consensus paper of the WFSBP Task Force on Biological Markers: Criteria for biomarkers and endophenotypes of schizophrenia, part III: Molecular mechanisms.	Schmitt A et al.	—	2017	→
Controlling the joint local false discovery rate is more powerful than meta-analysis methods in joint analysis of summary statistics from multiple genome-wide association studies.	Jiang W et al.	—	2017	→
Correcting for cell-type effects in DNA methylation studies: reference-based method outperforms latent variable approaches in empirical studies.	Hattab MW et al.	—	2017	→
Danger: High Voltage-The Role of Voltage-Gated Calcium Channels in Central Nervous System Pathology.	Schampel A et al.	—	2017	→
D-cycloserine in Schizophrenia: New Strategies for Improving Clinical Outcomes by Enhancing Plasticity.	Goff DC	—	2017	→
Diagnostic and therapeutic potential of microRNAs in neuropsychiatric disorders: Past, present, and future.	Alural B et al.	—	2017	→
Direct evidence for a polygenic etiology in familial multiple myeloma.	Halvarsson BM et al.	—	2017	→
DNA Methylation Analysis of BRD1 Promoter Regions and the Schizophrenia rs138880 Risk Allele.	Dyrvig M et al.	—	2017	→
DRD2 co-expression network and a related polygenic index predict imaging, behavioral and clinical phenotypes linked to schizophrenia.	Pergola G et al.	—	2017	→
Drosophila and genome-wide association studies: a review and resource for the functional dissection of human complex traits.	Wangler MF et al.	—	2017	→
Drug Abuse and Psychosis: New Insights into Drug-induced Psychosis.	Ham S et al.	—	2017	→
Drug enrichment and discovery from schizophrenia genome-wide association results: an analysis and visualisation approach.	Gaspar HA et al.	—	2017	→
Editorial: Minding Glial Cells in the Novel Understandings of Mental Illness.	Kato TA et al.	—	2017	→
Effects of environmental risks and polygenic loading for schizophrenia on cortical thickness.	Neilson E et al.	—	2017	→
Epigenomics of Major Depressive Disorders and Schizophrenia: Early Life Decides.	Hoffmann A et al.	—	2017	→
Epistatic and Independent Effects on Schizophrenia-Related Phenotypes Following Co-disruption of the Risk Factors Neuregulin-1 × DISC1.	O'Tuathaigh CM et al.	—	2017	→
Ethical Application of Precision Medicine to Schizophrenia Management.	Daws S	—	2017	→
Evaluation of European Schizophrenia GWAS Loci in Asian Populations via Comprehensive Meta-Analyses.	Xiao X et al.	—	2017	→
Evaluation of shared genetic susceptibility loci between autoimmune diseases and schizophrenia based on genome-wide association studies.	Hoeffding LK et al.	—	2017	→
Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder.	Charney AW et al.	—	2017	→
Evidence of AS3MT<sup>d2d3</sup>-Associated Variants within 10q24.32-33 in the Genetic Risk of Major Affective Disorders.	Li L et al.	—	2017	→
Extracellular matrix alterations in the ketamine model of schizophrenia.	Matuszko G et al.	—	2017	→
Fast admixture analysis and population tree estimation for SNP and NGS data.	Cheng JY et al.	—	2017	→
Gene2Function: An Integrated Online Resource for Gene Function Discovery.	Hu Y et al.	—	2017	→
Generating testable hypotheses for schizophrenia and rheumatoid arthritis pathogenesis by integrating epidemiological, genomic, and protein interaction data.	Malavia TA et al.	—	2017	→
Genetic and epigenetic regulation on the transcription of GABRB2: Genotype-dependent hydroxymethylation and methylation alterations in schizophrenia.	Zong L et al.	—	2017	→
Genetic association analysis of microRNA137 and its target complex 1 with schizophrenia in Han Chinese.	Lu W et al.	—	2017	→
Genetic evidence for role of integration of fast and slow neurotransmission in schizophrenia.	Devor A et al.	—	2017	→
Genetic interaction of DISC1 and Neurexin in the development of fruit fly glutamatergic synapses.	Pandey H et al.	—	2017	→
Genetics implicate common mechanisms in autism and schizophrenia: synaptic activity and immunity.	Liu X et al.	—	2017	→
Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics.	Giegling I et al.	—	2017	→
Genetics of Schizophrenia: Overview of Methods, Findings and Limitations.	Henriksen MG et al.	—	2017	→
Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia.	Li Z et al.	—	2017	→
Genome-Wide Association Studies of a Broad Spectrum of Antisocial Behavior.	Tielbeek JJ et al.	—	2017	→
Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia.	Witt SH et al.	—	2017	→
Genome-Wide Association Study of Psychosis Proneness in the Finnish Population.	Ortega-Alonso A et al.	—	2017	→
Genome-wide association study of subcortical brain volume in PTSD cases and trauma-exposed controls.	Morey RA et al.	—	2017	→
Genomic Analysis of Genotype-by-Social Environment Interaction for <i>Drosophila melanogaster</i> Aggressive Behavior.	Rohde PD et al.	—	2017	→
Genomic approaches to the assessment of human spina bifida risk.	Ross ME et al.	—	2017	→
Genotype-environment interaction on human cognitive function conditioned on the status of breastfeeding and maternal smoking around birth.	Lee SH et al.	—	2017	→
GluA1 AMPAR subunit deletion reduces the hedonic response to sucrose but leaves satiety and conditioned responses intact.	Austen JM et al.	—	2017	→
Haplotype phasing of whole human genomes using bead-based barcode partitioning in a single tube.	Zhang F et al.	—	2017	→
Heritability of Neuropsychological Measures in Schizophrenia and Nonpsychiatric Populations: A Systematic Review and Meta-analysis.	Blokland GAM et al.	—	2017	→
HLAscan: genotyping of the HLA region using next-generation sequencing data.	Ka S et al.	—	2017	→
Human induced pluripotent stem cells for modelling neurodevelopmental disorders.	Ardhanareeswaran K et al.	—	2017	→
Identification of Genetic Loci Jointly Influencing Schizophrenia Risk and the Cognitive Traits of Verbal-Numerical Reasoning, Reaction Time, and General Cognitive Function.	Smeland OB et al.	—	2017	→
Identification of genetic loci shared between schizophrenia and the Big Five personality traits.	Smeland OB et al.	—	2017	→
Identification of shared risk loci and pathways for bipolar disorder and schizophrenia.	Forstner AJ et al.	—	2017	→
Immune involvement in the pathogenesis of schizophrenia: a meta-analysis on postmortem brain studies.	van Kesteren CF et al.	—	2017	→
Inhibition of the Schizophrenia-Associated MicroRNA miR-137 Disrupts Nrg1α Neurodevelopmental Signal Transduction.	Thomas KT et al.	—	2017	→
Loss of the neurodevelopmental gene Zswim6 alters striatal morphology and motor regulation.	Tischfield DJ et al.	—	2017	→
Microarray gene-expression study in fibroblast and lymphoblastoid cell lines from antipsychotic-naïve first-episode schizophrenia patients.	Gassó P et al.	—	2017	→
Migrainomics - identifying brain and genetic markers of migraine.	Nyholt DR et al.	—	2017	→
Mild traumatic brain injury is associated with reduced cortical thickness in those at risk for Alzheimer's disease.	Hayes JP et al.	—	2017	→
Mining the topography and dynamics of the 4D Nucleome to identify novel CNS drug pathways.	Higgins GA et al.	—	2017	→
MiR-137: an important player in neural development and neoplastic transformation.	Mahmoudi E et al.	—	2017	→
MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls.	Cosgrove D et al.	—	2017	→
Mitochondria in complex psychiatric disorders: Lessons from mouse models of 22q11.2 deletion syndrome: Hemizygous deletion of several mitochondrial genes in the 22q11.2 genomic region can lead to symptoms associated with neuropsychiatric disease.	Devaraju P et al.	—	2017	→
Molecular Mechanisms of Transcription Factor 4 in Pitt Hopkins Syndrome.	Rannals MD et al.	—	2017	→
Multimodal Neuroimaging in Schizophrenia: Description and Dissemination.	Aine CJ et al.	—	2017	→
Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia.	Leonenko G et al.	—	2017	→
Novel brain expressed RNA identified at the MIR137 schizophrenia-associated locus.	Gianfrancesco O et al.	—	2017	→
Perinatal Asphyxia in Rat Alters Expression of Novel Schizophrenia Risk Genes.	Paparelli A et al.	—	2017	→
Pharmacogenetics of antidepressant response: A polygenic approach.	García-González J et al.	—	2017	→
PKBγ/AKT3 loss-of-function causes learning and memory deficits and deregulation of AKT/mTORC2 signaling: Relevance for schizophrenia.	Howell KR et al.	—	2017	→
Pleiotropic effects of schizophrenia-associated genetic variants in neuron firing and cardiac pacemaking revealed by computational modeling.	Mäki-Marttunen T et al.	—	2017	→
Polygenic risk for five psychiatric disorders and cross-disorder and disorder-specific neural connectivity in two independent populations.	Wang T et al.	—	2017	→
Polygenic Risk for Schizophrenia Influences Cortical Gyrification in 2 Independent General Populations.	Liu B et al.	—	2017	→
Polygenic Risk Score associated with specific symptom dimensions in first-episode psychosis.	Sengupta SM et al.	—	2017	→
Polygenic scores via penalized regression on summary statistics.	Mak TSH et al.	—	2017	→
Possible role of rare variants in Trace amine associated receptor 1 in schizophrenia.	John J et al.	—	2017	→
Postsynaptic Density-95 Isoform Abnormalities in Schizophrenia.	Funk AJ et al.	—	2017	→
Potential Value of Genomic Copy Number Variations in Schizophrenia.	Zhuo C et al.	—	2017	→
Prevalences of autoimmune diseases in schizophrenia, bipolar I and II disorder, and controls.	Cremaschi L et al.	—	2017	→
Progress in Genetic Studies of Tourette's Syndrome.	Qi Y et al.	—	2017	→
Progress in genome-wide association studies of schizophrenia in Han Chinese populations.	Yue W et al.	—	2017	→
Psychosis risk research versus daily prognosis uncertainties: A qualitative study of French youth psychiatrists' attitudes toward predictive practices.	Benoit L et al.	—	2017	→
Recent Advances in Experimental Whole Genome Haplotyping Methods.	Huang M et al.	—	2017	→
Reduced levels of Cacna1c attenuate mesolimbic dopamine system function.	Terrillion CE et al.	—	2017	→
Relationship between serum calcium and neuropsychological performance might indicate etiological heterogeneity underlying cognitive deficits in schizophrenia and depression.	Sharma A et al.	—	2017	→
Role of 108 schizophrenia-associated loci in modulating psychopathological dimensions in schizophrenia and bipolar disorder.	Fabbri C et al.	—	2017	→
Schizophrenia and the neurodevelopmental continuum:evidence from genomics.	Owen MJ et al.	—	2017	→
Sequencing and de novo assembly of 150 genomes from Denmark as a population reference.	Maretty L et al.	—	2017	→
Short communication: Genetic association between schizophrenia and cannabis use.	Verweij KJ et al.	—	2017	→
Simultaneous inference of phenotype-associated genes and relevant tissues from GWAS data via Bayesian integration of multiple tissue-specific gene networks.	Wu M et al.	—	2017	→
Spatial and temporal expression patterns of genes around nine neuroticism-associated loci.	Ohi K et al.	—	2017	→
Synaptic activity: An emerging player in schizophrenia.	Sarkar A et al.	—	2017	→
SZDB: A Database for Schizophrenia Genetic Research.	Wu Y et al.	—	2017	→
SZGR 2.0: a one-stop shop of schizophrenia candidate genes.	Jia P et al.	—	2017	→
The 16p11.2 homologs fam57ba and doc2a generate certain brain and body phenotypes.	McCammon JM et al.	—	2017	→
The association between gene variants and longitudinal structural brain changes in psychosis: a systematic review of longitudinal neuroimaging genetics studies.	Harari JH et al.	—	2017	→
The Clinical Challenge of Autoimmune Psychosis: Learning from Anti-NMDA Receptor Autoantibodies.	Ellul P et al.	—	2017	→
The group II metabotropic glutamate receptor agonist LY354740 and the D2 receptor antagonist haloperidol reduce locomotor hyperactivity but fail to rescue spatial working memory in GluA1 knockout mice.	Boerner T et al.	—	2017	→
The neural diathesis-stress model of schizophrenia revisited: An update on recent findings considering illness stage and neurobiological and methodological complexities.	Pruessner M et al.	—	2017	→
The Schizophrenia-Associated BRD1 Gene Regulates Behavior, Neurotransmission, and Expression of Schizophrenia Risk Enriched Gene Sets in Mice.	Qvist P et al.	—	2017	→
The schizophrenia risk gene MIR137 acts as a hippocampal gene network node orchestrating the expression of genes relevant to nervous system development and function.	Olde Loohuis NF et al.	—	2017	→
The schizophrenia risk gene ZNF804A: clinical associations, biological mechanisms and neuronal functions.	Chang H et al.	—	2017	→
The schizophrenia susceptibility gene ZNF804A confers risk of major mood disorders.	Ou J et al.	—	2017	→
The sorting receptor SorCS3 is a stronger regulator of glutamate receptor functions compared to GABAergic mechanisms in the hippocampus.	Christiansen GB et al.	—	2017	→
The Weighting is the Hardest Part: On the Behavior of the Likelihood Ratio Test and the Score Test Under a Data-Driven Weighting Scheme in Sequenced Samples.	Minică CC et al.	—	2017	→
Thought Disorder in Schizophrenia and Bipolar Disorder Probands, Their Relatives, and Nonpsychiatric Controls.	Morgan CJ et al.	—	2017	→
Transcriptional signatures of schizophrenia in hiPSC-derived NPCs and neurons are concordant with post-mortem adult brains.	Hoffman GE et al.	—	2017	→
Unraveling the genetic architecture of copy number variants associated with schizophrenia and other neuropsychiatric disorders.	Rutkowski TP et al.	—	2017	→
Variation in global DNA hydroxymethylation with age associated with schizophrenia.	Jiang T et al.	—	2017	→
What has GWAS done for HLA and disease associations?	Kennedy AE et al.	—	2017	→
Whole-genome sequencing of monozygotic twins discordant for schizophrenia indicates multiple genetic risk factors for schizophrenia.	Tang J et al.	—	2017	→
A Case for Returning to Multiplex Families for Further Understanding the Heritability of Schizophrenia: A Psychiatrist's Perspective.	DeLisi LE	—	2016	→
A cis-eQTL in AHI1 confers risk to schizophrenia in European populations.	Ren Z et al.	—	2016	→
Across-cohort QC analyses of GWAS summary statistics from complex traits.	Chen GB et al.	—	2016	→
A genetic variant in CAMKK2 gene is possibly associated with increased risk of bipolar disorder.	Atakhorrami M et al.	—	2016	→
A Genome-Wide Association Study Provides New Evidence That CACNA1C Gene is Associated With Diabetic Cataract.	Chang C et al.	—	2016	→
A GWAS SNP for Schizophrenia Is Linked to the Internal MIR137 Promoter and Supports Differential Allele-Specific Expression.	Warburton A et al.	—	2016	→
A human-specific AS3MT isoform and BORCS7 are molecular risk factors in the 10q24.32 schizophrenia-associated locus.	Li M et al.	—	2016	→
A Loss-of-Function Variant in a Minor Isoform of ANK3 Protects Against Bipolar Disorder and Schizophrenia.	Hughes T et al.	—	2016	→
Altered neural signaling and immune pathways in peripheral blood mononuclear cells of schizophrenia patients with cognitive impairment: A transcriptome analysis.	Wu JQ et al.	—	2016	→
AMIGO-Kv2.1 Potassium Channel Complex Is Associated With Schizophrenia-Related Phenotypes.	Peltola MA et al.	—	2016	→
A Mutation in NPAS3 That Segregates with Schizophrenia in a Small Family Leads to Protein Aggregation.	Nucifora LG et al.	—	2016	→
Analysis of association between common variants in the SLCO6A1 gene with schizophrenia, bipolar disorder and major depressive disorder in the Han Chinese population.	Khan RA et al.	—	2016	→
Analysis of induced pluripotent stem cells carrying 22q11.2 deletion.	Toyoshima M et al.	—	2016	→
Analysis of the association of VIPR2 polymorphisms with susceptibility to schizophrenia.	Jin C et al.	—	2016	→
Analyzing the Role of MicroRNAs in Schizophrenia in the Context of Common Genetic Risk Variants.	Hauberg ME et al.	—	2016	→
A network of synaptic genes associated with schizophrenia and bipolar disorder.	Forero DA et al.	—	2016	→
An integrated genetic-epigenetic analysis of schizophrenia: evidence for co-localization of genetic associations and differential DNA methylation.	Hannon E et al.	—	2016	→
A novel 3q29 deletion associated with autism, intellectual disability, psychiatric disorders, and obesity.	Biamino E et al.	—	2016	→
A simple yet accurate correction for winner's curse can predict signals discovered in much larger genome scans.	Bigdeli TB et al.	—	2016	→
Association of CACNA1C and SYNE1 in offspring of patients with psychiatric disorders.	Gassó P et al.	—	2016	→
Association of DNA Methylation Differences With Schizophrenia in an Epigenome-Wide Association Study.	Montano C et al.	—	2016	→
Autophagy and Schizophrenia: A Closer Look at How Dysregulation of Neuronal Cell Homeostasis Influences the Pathogenesis of Schizophrenia.	Schneider JL et al.	—	2016	→
A Whole Methylome CpG-SNP Association Study of Psychosis in Blood and Brain Tissue.	van den Oord EJ et al.	—	2016	→
Balanced translocation linked to psychiatric disorder, glutamate, and cortical structure/function.	Thomson PA et al.	—	2016	→
Biomarkers for drug development in early psychosis: Current issues and promising directions.	Goff DC et al.	—	2016	→
Brain-Derived Neurotrophic Factor Gene Val66Met Polymorphism and Risk of Schizophrenia: A Meta-analysis of Case-Control Studies.	Kheirollahi M et al.	—	2016	→
Childhood body mass index and risk of schizophrenia in relation to childhood age, sex and age of first contact with schizophrenia.	Sørensen HJ et al.	—	2016	→
Clinical studies of neuroinflammatory mechanisms in schizophrenia.	Watkins CC et al.	—	2016	→
Cognitive endophenotypes inform genome-wide expression profiling in schizophrenia.	Zheutlin AB et al.	—	2016	→
Colocalization of GWAS and eQTL Signals Detects Target Genes.	Hormozdiari F et al.	—	2016	→
Combining Multiple Hypothesis Testing with Machine Learning Increases the Statistical Power of Genome-wide Association Studies.	Mieth B et al.	—	2016	→
Common alleles contribute to schizophrenia in CNV carriers.	Tansey KE et al.	—	2016	→
Common Polymorphisms Within QPCT Gene Are Associated with the Susceptibility of Schizophrenia in a Han Chinese Population.	Zhang QQ et al.	—	2016	→
Common susceptibility variants are shared between schizophrenia and psoriasis in the Han Chinese population.	Yin X et al.	—	2016	→
Common variants in CACNA1C and MDD susceptibility: A comprehensive meta-analysis.	Rao S et al.	—	2016	→
Common variants in QPCT gene confer risk of schizophrenia in the Han Chinese population.	Khan RA et al.	—	2016	→
Common variants on 17q25 and gene-gene interactions conferring risk of schizophrenia in Han Chinese population and regulating gene expressions in human brain.	Guan L et al.	—	2016	→
Comprehensive analysis of schizophrenia-associated loci highlights ion channel pathways and biologically plausible candidate causal genes.	Pers TH et al.	—	2016	→
Consensus paper of the WFSBP Task Force on Biological Markers: Criteria for biomarkers and endophenotypes of schizophrenia part II: Cognition, neuroimaging and genetics.	Schmitt A et al.	—	2016	→
Covariance Association Test (CVAT) Identifies Genetic Markers Associated with Schizophrenia in Functionally Associated Biological Processes.	Rohde PD et al.	—	2016	→
Currently recognized genes for schizophrenia: High-resolution chromosome ideogram representation.	Butler MG et al.	—	2016	→
Depression, Cytokine, and Cytokine by Treatment Interactions Modulate Gene Expression in Antipsychotic Naïve First Episode Psychosis.	Noto C et al.	—	2016	→
Developmental vitamin D deficiency and schizophrenia: the role of animal models.	Schoenrock SA et al.	—	2016	→
DNA methylation in a Scottish family multiply affected by bipolar disorder and major depressive disorder.	Walker RM et al.	—	2016	→
DNA methylation in peripheral tissue of schizophrenia and bipolar disorder: a systematic review.	Teroganova N et al.	—	2016	→
DNA variants in CACNA1C modify Parkinson disease risk only when vitamin D level is deficient.	Wang L et al.	—	2016	→
Down-Regulation of Hippocampal Genes Regulating Dopaminergic, GABAergic, and Glutamatergic Function Following Combined Neonatal Phencyclidine and Post-Weaning Social Isolation of Rats as a Neurodevelopmental Model for Schizophrenia.	Gaskin PL et al.	—	2016	→
Dysregulation of miRNA-9 in a Subset of Schizophrenia Patient-Derived Neural Progenitor Cells.	Topol A et al.	—	2016	→
Enrichment of SNPs in Functional Categories Reveals Genes Affecting Complex Traits.	Zhao H et al.	—	2016	→
Estimating Effect Sizes and Expected Replication Probabilities from GWAS Summary Statistics.	Holland D et al.	—	2016	→
Evaluation of voltage-dependent calcium channel γ gene families identified several novel potential susceptible genes to schizophrenia.	Guan F et al.	—	2016	→
Evidence of activation of the Toll-like receptor-4 proinflammatory pathway in patients with schizophrenia.	García-Bueno B et al.	—	2016	→
Exome arrays capture polygenic rare variant contributions to schizophrenia.	Richards AL et al.	—	2016	→
Exome Sequence Data From Multigenerational Families Implicate AMPA Receptor Trafficking in Neurocognitive Impairment and Schizophrenia Risk.	Kos MZ et al.	—	2016	→
FHSA-SED: Two-Locus Model Detection for Genome-Wide Association Study with Harmony Search Algorithm.	Tuo S et al.	—	2016	→
From Linkage Studies to Epigenetics: What We Know and What We Need to Know in the Neurobiology of Schizophrenia.	Cariaga-Martinez A et al.	—	2016	→
Functional Effects of Schizophrenia-Linked Genetic Variants on Intrinsic Single-Neuron Excitability: A Modeling Study.	Mäki-Marttunen T et al.	—	2016	→
Further evidence of VRK2 rs2312147 associated with schizophrenia.	Chang H et al.	—	2016	→
Gene expression elucidates functional impact of polygenic risk for schizophrenia.	Fromer M et al.	—	2016	→
Genetic Correlation Analysis Suggests Association between Increased Self-Reported Sleep Duration in Adults and Schizophrenia and Type 2 Diabetes.	Byrne EM et al.	—	2016	→
Genetic Evaluation of Schizophrenia Using the Illumina HumanExome Chip.	Moons T et al.	—	2016	→
Genetic Factors Affecting Late-Onset Alzheimer's Disease Susceptibility.	Rezazadeh M et al.	—	2016	→
Genetic Markers of Human Evolution Are Enriched in Schizophrenia.	Srinivasan S et al.	—	2016	→
Genetic polymorphisms and their association with the prevalence and severity of chronic postsurgical pain: a systematic review.	Hoofwijk DM et al.	—	2016	→
Genetic Relationship between Schizophrenia and Nicotine Dependence.	Chen J et al.	—	2016	→
Genetics of Schizophrenia: Historical Insights and Prevailing Evidence.	van de Leemput J et al.	—	2016	→
Genome-Wide Association and Exome Sequencing Study of Language Disorder in an Isolated Population.	Kornilov SA et al.	—	2016	→
Genome-Wide Association of Heroin Dependence in Han Chinese.	Kalsi G et al.	—	2016	→
Genome-Wide Association Studies Suggest Limited Immune Gene Enrichment in Schizophrenia Compared to 5 Autoimmune Diseases.	Pouget JG et al.	—	2016	→
Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder.	Song J et al.	—	2016	→
Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder.	Hou L et al.	—	2016	→
Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness.	Bigdeli TB et al.	—	2016	→
Genome-wide investigation of schizophrenia associated plasma Ndel1 enzyme activity.	Gadelha A et al.	—	2016	→
Genome-wide linkage on chromosome 10q26 for a dimensional scale of major depression.	Knowles EE et al.	—	2016	→
Genome-wide significant schizophrenia risk variation on chromosome 10q24 is associated with altered cis-regulation of BORCS7, AS3MT, and NT5C2 in the human brain.	Duarte RRR et al.	—	2016	→
High loading of polygenic risk in cases with chronic schizophrenia.	Meier SM et al.	—	2016	→
Identification and Potential Regulatory Properties of Evolutionary Conserved Regions (ECRs) at the Schizophrenia-Associated MIR137 Locus.	Gianfrancesco O et al.	—	2016	→
Identification of the BRD1 interaction network and its impact on mental disorder risk.	Fryland T et al.	—	2016	→
Identification of two clusters within schizophrenia with different structural, functional and clinical characteristics.	Lubeiro A et al.	—	2016	→
Immuno-psychiatry: an agenda for clinical practice and innovative research.	Leboyer M et al.	—	2016	→
Impact of polygenic schizophrenia-related risk and hippocampal volumes on the onset of psychosis.	Harrisberger F et al.	—	2016	→
Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia.	Genovese G et al.	—	2016	→
In Sickness and in Health: Perineuronal Nets and Synaptic Plasticity in Psychiatric Disorders.	Pantazopoulos H et al.	—	2016	→
Integrated Post-GWAS Analysis Sheds New Light on the Disease Mechanisms of Schizophrenia.	Lin JR et al.	—	2016	→
Integration of genome-wide association and extant brain expression QTL identifies candidate genes influencing prepulse inhibition in inbred F1 mice.	Sittig LJ et al.	—	2016	→
Leveraging Genomic Annotations and Pleiotropic Enrichment for Improved Replication Rates in Schizophrenia GWAS.	Wang Y et al.	—	2016	→
L-type calcium channels as drug targets in CNS disorders.	Ortner NJ et al.	—	2016	→
MicroRNA-137 Inhibits EFNB2 Expression Affected by a Genetic Variant and Is Expressed Aberrantly in Peripheral Blood of Schizophrenia Patients.	Wu S et al.	—	2016	→
miRNAs in NMDA receptor-dependent synaptic plasticity and psychiatric disorders.	Shen H et al.	—	2016	→
Modeling psychiatric disorders: from genomic findings to cellular phenotypes.	Falk A et al.	—	2016	→
Molecular substrates of schizophrenia: homeostatic signaling to connectivity.	Landek-Salgado MA et al.	—	2016	→
Multiple testing correction in linear mixed models.	Joo JW et al.	—	2016	→
Mutation screening of SCN2A in schizophrenia and identification of a novel loss-of-function mutation.	Carroll LS et al.	—	2016	→
Myelination-related genes are associated with decreased white matter integrity in schizophrenia.	Chavarria-Siles I et al.	—	2016	→
Nationwide Genomic Study in Denmark Reveals Remarkable Population Homogeneity.	Athanasiadis G et al.	—	2016	→
Neurodevelopmental Genomic Strategies in the Study of the Psychosis Spectrum.	Gur RE	—	2016	→
Neuroinflammation - using big data to inform clinical practice.	Dendrou CA et al.	—	2016	→
Neuropsychiatric genomics in precision medicine: diagnostics, gene discovery, and translation.	Need AC et al.	—	2016	→
New statistical approaches exploit the polygenic architecture of schizophrenia--implications for the underlying neurobiology.	Schork AJ et al.	—	2016	→
Patterns of genic intolerance of rare copy number variation in 59,898 human exomes.	Ruderfer DM et al.	—	2016	→
Phenotypic Manifestation of Genetic Risk for Schizophrenia During Adolescence in the General Population.	Jones HJ et al.	—	2016	→
Polygenetic components for schizophrenia, bipolar disorder and rheumatoid arthritis predict risk of schizophrenia.	Ohi K et al.	—	2016	→
Polygenic overlap between schizophrenia risk and antipsychotic response: a genomic medicine approach.	Ruderfer DM et al.	—	2016	→
Polymorphisms in MIR137HG and microRNA-137-regulated genes influence gray matter structure in schizophrenia.	Wright C et al.	—	2016	→
Protein Interaction Networks Link Schizophrenia Risk Loci to Synaptic Function.	Schwarz E et al.	—	2016	→
Psychiatric genetics in China: achievements and challenges.	Liu C et al.	—	2016	→
Rapporteur summaries of plenary, symposia, and oral sessions from the XXIIIrd World Congress of Psychiatric Genetics Meeting in Toronto, Canada, 16-20 October 2015.	Zai G et al.	—	2016	→
Rare variants are common in schizophrenia.	Gratten J	—	2016	→
Reciprocal Alterations in Regulator of G Protein Signaling 4 and microRNA16 in Schizophrenia.	Kimoto S et al.	—	2016	→
Regional brain dysregulation of Ca(2+)-handling systems in ketamine-induced rat model of experimental psychosis.	Lisek M et al.	—	2016	→
Replication of genome-wide association study (GWAS) susceptibility loci in a Latino bipolar disorder cohort.	Gonzalez S et al.	—	2016	→
Schizophrenia and subsequent neighborhood deprivation: revisiting the social drift hypothesis using population, twin and molecular genetic data.	Sariaslan A et al.	—	2016	→
Schizophrenia risk variants affecting microRNA function and site-specific regulation of NT5C2 by miR-206.	Hauberg ME et al.	—	2016	→
Serum IL-18 level, clinical symptoms and IL-18-607A/C polymorphism among chronic patients with schizophrenia in a Chinese Han population.	Zhang XY et al.	—	2016	→
Stimulation of Synaptic Vesicle Exocytosis by the Mental Disease Gene DISC1 is Mediated by N-Type Voltage-Gated Calcium Channels.	Tang W et al.	—	2016	→
Structural Brain Abnormalities in Youth With Psychosis Spectrum Symptoms.	Satterthwaite TD et al.	—	2016	→
Studying the Genetics of Complex Disease With Ancestry-Specific Human Phenotype Networks: The Case of Type 2 Diabetes in East Asian Populations.	Qiu J et al.	—	2016	→
Study of the tetraspanin 18 association with schizophrenia in a Han Chinese population.	Wu L et al.	—	2016	→
Summaries of plenary, symposia, and oral sessions at the XXII World Congress of Psychiatric Genetics, Copenhagen, Denmark, 12-16 October 2014.	Aas M et al.	—	2016	→
Systems psychopharmacology: A network approach to developing novel therapies.	Gebicke-Haerter PJ	—	2016	→
Targeted resequencing of regulatory regions at schizophrenia risk loci: Role of rare functional variants at chromatin repressive states.	González-Peñas J et al.	—	2016	→
Tcf4 transgenic female mice display delayed adaptation in an auditory latent inhibition paradigm.	Brzózka MM et al.	—	2016	→
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The Future is The Past: Methylation QTLs in Schizophrenia.	Hoffmann A et al.	—	2016	→
The Genetics of Addiction: Where Do We Go From Here?	Dick DM	—	2016	→
The impact of CACNA1C allelic variation on regional gray matter volume in Chinese population.	Huang L et al.	—	2016	→
The Major Histocompatibility Complex (MHC) in Schizophrenia: A Review.	Mokhtari R et al.	—	2016	→
The Multifarious Hippocampal Functions of MicroRNA-137.	Kos A et al.	—	2016	→
The Neuropsychiatric Disease-Associated Gene cacna1c Mediates Survival of Young Hippocampal Neurons.	Lee AS et al.	—	2016	→
The Relationship of Common Risk Variants and Polygenic Risk for Schizophrenia to Sensorimotor Gating.	Roussos P et al.	—	2016	→
The road to precision psychiatry: translating genetics into disease mechanisms.	Gandal MJ et al.	—	2016	→
The serum level of C-reactive protein (CRP) is associated with cognitive performance in acute phase psychosis.	Johnsen E et al.	—	2016	→
The statistical properties of gene-set analysis.	de Leeuw CA et al.	—	2016	→
Thinking About Data, Research Methods, and Statistical Analyses: Commentary on Sijtsma's (2014) "Playing with Data".	Waldman ID et al.	—	2016	→
Tissue-specific regulatory circuits reveal variable modular perturbations across complex diseases.	Marbach D et al.	—	2016	→
Top 10 Replicated Findings From Behavioral Genetics.	Plomin R et al.	—	2016	→
Towards a science of eating disorders: Replacing myths with realities: The fourth Birgit Olsson lecture.	Bulik CM	—	2016	→
Toward the integration of Omics data in epidemiological studies: still a "long and winding road".	López de Maturana E et al.	—	2016	→
Transcription factor 4 gene rs9960767 polymorphism in bipolar disorder.	Ozel MD et al.	—	2016	→
Transcriptomics analysis of iPSC-derived neurons and modeling of neuropsychiatric disorders.	Lin M et al.	—	2016	→
Translating Genetic Risk Loci Into Molecular Risk Mechanisms for Schizophrenia.	Bray NJ et al.	—	2016	→
Translating genome-wide association findings into new therapeutics for psychiatry.	Breen G et al.	—	2016	→
Translational research on cognitive and behavioural disorders in neurological and psychiatric diseases.	Corvol JC et al.	—	2016	→
Two-stage additional evidence support association of common variants in the HDAC3 with the increasing risk of schizophrenia susceptibility.	Jia X et al.	—	2016	→
Two-stage replication of previous genome-wide association studies of AS3MT-CNNM2-NT5C2 gene cluster region in a large schizophrenia case-control sample from Han Chinese population.	Guan F et al.	—	2016	→
Ultra-rare disruptive and damaging mutations influence educational attainment in the general population.	Ganna A et al.	—	2016	→
Upstream Pathways Controlling Mitochondrial Function in Major Psychosis: A Focus on Bipolar Disorder.	Machado AK et al.	—	2016	→
Utility and validity of DISC1 mouse models in biological psychiatry.	Tomoda T et al.	—	2016	→
Variations in Disrupted-in-Schizophrenia 1 gene modulate long-term longitudinal differences in cortical thickness in patients with a first-episode of psychosis.	Vázquez-Bourgon J et al.	—	2016	→
Voxel-Based Morphometry in Individuals at Genetic High Risk for Schizophrenia and Patients with Schizophrenia during Their First Episode of Psychosis.	Chang M et al.	—	2016	→
Weaving a Net of Neurobiological Mechanisms in Schizophrenia and Unraveling the Underlying Pathophysiology.	Bitanihirwe BK et al.	—	2016	→
A critical role of RBM8a in proliferation and differentiation of embryonic neural progenitors.	Zou D et al.	—	2015	→
Additive genetic risk from five serotonin system polymorphisms interacts with interpersonal stress to predict depression.	Vrshek-Schallhorn S et al.	—	2015	→
A Fast Method that Uses Polygenic Scores to Estimate the Variance Explained by Genome-wide Marker Panels and the Proportion of Variants Affecting a Trait.	Palla L et al.	—	2015	→
Altered CSMD1 Expression Alters Cocaine-Conditioned Place Preference: Mutual Support for a Complex Locus from Human and Mouse Models.	Drgonova J et al.	—	2015	→
Altered gene expression in schizophrenia: findings from transcriptional signatures in fibroblasts and blood.	Cattane N et al.	—	2015	→
Analysis of risk factors for schizophrenia with two different case definitions: a nationwide register-based external validation study.	Sørensen HJ et al.	—	2015	→
A New Method for Detecting Associations with Rare Copy-Number Variants.	Tzeng JY et al.	—	2015	→
Angiotensin converting enzyme activity is positively associated with IL-17a levels in patients with schizophrenia.	Gadelha A et al.	—	2015	→
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Associating schizophrenia, long non-coding RNAs and neurostructural dynamics.	Merelo V et al.	—	2015	→
Association of new deletion/duplication region at chromosome 1p21 with intellectual disability, severe speech deficit and autism spectrum disorder-like behavior: an all-in approach to solving the <i>DPYD</i> enigma.	Brečević L et al.	—	2015	→
Associations between DNA methylation and schizophrenia-related intermediate phenotypes - a gene set enrichment analysis.	Hass J et al.	—	2015	→
Association study of sepiapterin reductase gene promoter polymorphisms with schizophrenia in a Han Chinese population.	Fu J et al.	—	2015	→
Bioinformatic analyses and conceptual synthesis of evidence linking ZNF804A to risk for schizophrenia and bipolar disorder.	Hess JL et al.	—	2015	→
Borderline personality disorder and childhood maltreatment: a genome-wide methylation analysis.	Prados J et al.	—	2015	→
Brain structural and clinical changes after first episode psychosis: Focus on cannabinoid receptor 1 polymorphisms.	Suárez-Pinilla P et al.	—	2015	→
CACNA1C risk variant affects facial emotion recognition in healthy individuals.	Nieratschker V et al.	—	2015	→
Candidate gene-environment interaction research: reflections and recommendations.	Dick DM et al.	—	2015	→
Cerebralcare Granule® attenuates cognitive impairment in rats continuously overexpressing microRNA-30e.	Xu Y et al.	—	2015	→
Challenges in understanding psychiatric disorders and developing therapeutics: a role for zebrafish.	McCammon JM et al.	—	2015	→
Characterization of bipolar disorder patient-specific induced pluripotent stem cells from a family reveals neurodevelopmental and mRNA expression abnormalities.	Madison JM et al.	—	2015	→
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Copy number variations play important roles in heredity of common diseases: a novel method to calculate heritability of a polymorphism.	Nagao Y	—	2015	→
CX3CR1 is dysregulated in blood and brain from schizophrenia patients.	Bergon A et al.	—	2015	→
Delay in blood sampling for routine newborn screening is associated with increased risk of schizophrenia.	Nordentoft M et al.	—	2015	→
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Genetic analysis of schizophrenia and bipolar disorder reveals polygenicity but also suggests new directions for molecular interrogation.	Neale BM et al.	—	2015	→
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Integration of gene expression and GWAS results supports involvement of calcium signaling in Schizophrenia.	Hertzberg L et al.	—	2015	→
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Meta-analysis of data from the Psychiatric Genomics Consortium and additional samples supports association of CACNA1C with risk for schizophrenia.	Takahashi S et al.	—	2015	→
Meta gene set enrichment analyses link miR-137-regulated pathways with schizophrenia risk.	Wright C et al.	—	2015	→
MicroRNA-137 Controls AMPA-Receptor-Mediated Transmission and mGluR-Dependent LTD.	Olde Loohuis NF et al.	—	2015	→
MicroRNA-derived network analysis of differentially methylated genes in schizophrenia, implicating GABA receptor B1 [GABBR1] and protein kinase B [AKT1].	Gumerov V et al.	—	2015	→
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores.	Vilhjálmsson BJ et al.	—	2015	→
Multiple SNP Set Analysis for Genome-Wide Association Studies Through Bayesian Latent Variable Selection.	Lu ZH et al.	—	2015	→
Network-Based Analysis of Schizophrenia Genome-Wide Association Data to Detect the Joint Functional Association Signals.	Chang S et al.	—	2015	→
[Neurobiology of schizophrenia: new findings from the structure to the molecules].	Schmitt A et al.	—	2015	→
Neuronal migration abnormalities and its possible implications for schizophrenia.	Muraki K et al.	—	2015	→
New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis.	Lee SH et al.	—	2015	→
New discoveries in schizophrenia genetics reveal neurobiological pathways: A review of recent findings.	Kotlar AV et al.	—	2015	→
Nodal centrality of functional network in the differentiation of schizophrenia.	Cheng H et al.	—	2015	→
Non-coding genetic variants in human disease.	Zhang F et al.	—	2015	→
Noncoding RNAs and neurobehavioral mechanisms in psychiatric disease.	Kocerha J et al.	—	2015	→
Overview of genetic research in anorexia nervosa: The past, the present and the future.	Brandys MK et al.	—	2015	→
Path from schizophrenia genomics to biology: gene regulation and perturbation in neurons derived from induced pluripotent stem cells and genome editing.	Duan J	—	2015	→
Polygenic risk scores in bipolar disorder subgroups.	Aminoff SR et al.	—	2015	→
Polygenic risk scores in imaging genetics: Usefulness and applications.	Dima D et al.	—	2015	→
Psychopathological manifestations of joint hypermobility and joint hypermobility syndrome/ Ehlers-Danlos syndrome, hypermobility type: The link between connective tissue and psychological distress revised.	Sinibaldi L et al.	—	2015	→
Recognition deficits in mice carrying mutations of genes encoding BLOC-1 subunits pallidin or dysbindin.	Spiegel S et al.	—	2015	→
Reduced protein synthesis in schizophrenia patient-derived olfactory cells.	English JA et al.	—	2015	→
Resequencing and association analysis of coding regions at twenty candidate genes suggest a role for rare risk variation at AKAP9 and protective variation at NRXN1 in schizophrenia susceptibility.	Suárez-Rama JJ et al.	—	2015	→
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Schizophrenia and psychoneuroimmunology: an integrative view.	Sperner-Unterweger B et al.	—	2015	→
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Schizophrenia risk variants modulate white matter volume across the psychosis spectrum: evidence from two independent cohorts.	Oertel-Knöchel V et al.	—	2015	→
Seasonality shows evidence for polygenic architecture and genetic correlation with schizophrenia and bipolar disorder.	Byrne EM et al.	—	2015	→
Secondary association of PDLIM5 with paranoid schizophrenia in Emirati patients.	Moselhy H et al.	—	2015	→
Shared additive genetic influences on DSM-IV criteria for alcohol dependence in subjects of European ancestry.	Palmer RH et al.	—	2015	→
Significant expansion of the REST/NRSF cistrome in human versus mouse embryonic stem cells: potential implications for neural development.	Rockowitz S et al.	—	2015	→
Systematic Integration of Brain eQTL and GWAS Identifies ZNF323 as a Novel Schizophrenia Risk Gene and Suggests Recent Positive Selection Based on Compensatory Advantage on Pulmonary Function.	Luo XJ et al.	—	2015	→
The cortical thickness phenotype of individuals with DISC1 translocation resembles schizophrenia.	Doyle OM et al.	—	2015	→
The effects of the CACNA1C rs1006737 A/G on affective startle modulation in healthy males.	Pasparakis E et al.	—	2015	→
The emerging picture of autism spectrum disorder: genetics and pathology.	Chen JA et al.	—	2015	→
The Fourth Law of Behavior Genetics.	Chabris CF et al.	—	2015	→
The Genotype and Phenotype (GaP) registry: a living biobank for the analysis of quantitative traits.	Gregersen PK et al.	—	2015	→
The GSK3B gene confers risk for both major depressive disorder and schizophrenia in the Han Chinese population.	Chen J et al.	—	2015	→
The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease.	Groza T et al.	—	2015	→
The impact of genome wide supported microRNA-137 (MIR137) risk variants on frontal and striatal white matter integrity, neurocognitive functioning, and negative symptoms in schizophrenia.	Kuswanto CN et al.	—	2015	→
The impact of NMDA receptor hypofunction on GABAergic neurons in the pathophysiology of schizophrenia.	Cohen SM et al.	—	2015	→
The importance of endophenotypes in schizophrenia research.	Braff DL	—	2015	→
The NVL gene confers risk for both major depressive disorder and schizophrenia in the Han Chinese population.	Wang M et al.	—	2015	→
The Physiology, Pathology, and Pharmacology of Voltage-Gated Calcium Channels and Their Future Therapeutic Potential.	Zamponi GW et al.	—	2015	→
The proteome of schizophrenia.	Nascimento JM et al.	—	2015	→
The Psychiatric Genomics Consortium Posttraumatic Stress Disorder Workgroup: Posttraumatic Stress Disorder Enters the Age of Large-Scale Genomic Collaboration.	Logue MW et al.	—	2015	→
Therapeutic Targets for Neurodevelopmental Disorders Emerging from Animal Models with Perinatal Immune Activation.	Ibi D et al.	—	2015	→
The relationship between schizophrenia and rheumatoid arthritis revisited: genetic and epidemiological analyses.	Euesden J et al.	—	2015	→
The role of schizotypy in the study of the etiology of schizophrenia spectrum disorders.	Barrantes-Vidal N et al.	—	2015	→
The schizophrenia risk gene product miR-137 alters presynaptic plasticity.	Siegert S et al.	—	2015	→
The Use of Induced Pluripotent Stem Cell Technology to Advance Autism Research and Treatment.	Acab A et al.	—	2015	→
Transcriptome outlier analysis implicates schizophrenia susceptibility genes and enriches putatively functional rare genetic variants.	Duan J et al.	—	2015	→
Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma.	Swaminathan B et al.	—	2015	→
Variation in Dopamine D2 and Serotonin 5-HT2A Receptor Genes is Associated with Working Memory Processing and Response to Treatment with Antipsychotics.	Blasi G et al.	—	2015	→
White matter abnormalities of microstructure and physiological noise in schizophrenia.	Cheng H et al.	—	2015	→
White Matter Lesion Progression: Genome-Wide Search for Genetic Influences.	Hofer E et al.	—	2015	→
A genetic variant in 12q13, a possible risk factor for bipolar disorder, is associated with depressive state, accounting for stressful life events.	Shimasaki A et al.	—	2014	→
An Overview of the Association between Schizotypy and Dopamine.	Mohr C et al.	—	2014	→