Genome-wide association study of schizophrenia in Ashkenazi Jews.
paper
Cited
Public
Unavailable
- Authors
- Goes, Fernando S; McGrath, John; Avramopoulos, Dimitrios; Wolyniec, Paula; Pirooznia, Mehdi; Ruczinski, Ingo; Nestadt, Gerald; Kenny, Eimear E; Vacic, Vladimir; Peters, Inga; Lencz, Todd; Darvasi, Ariel; Mulle, Jennifer G; Warren, Stephen T; Pulver, Ann E
- Year
- 2015
- Journal
- American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
- PMID
- 26198764
- DOI
- 10.1002/ajmg.b.32349
Schizophrenia is a common, clinically heterogeneous disorder associated with lifelong morbidity and early mortality. Several genetic variants associated with schizophrenia have been identified, but the majority of the heritability remains unknown. In this study, we report on a case-control sample of Ashkenazi Jews (AJ), a founder population that may provide additional insights into genetic etiology of schizophrenia. We performed a genome-wide association analysis (GWAS) of 592 cases and 505 controls of AJ ancestry ascertained in the US. Subsequently, we performed a meta-analysis with an Israeli AJ sample of 913 cases and 1640 controls, followed by a meta-analysis and polygenic risk scoring using summary results from Psychiatric GWAS Consortium 2 schizophrenia study. The U.S. AJ sample showed strong evidence of polygenic inheritance (pseudo-R(2) ∼9.7%) and a SNP-heritability estimate of 0.39 (P = 0.00046). We found no genome-wide significant associations in the U.S. sample or in the combined US/Israeli AJ meta-analysis of 1505 cases and 2145 controls. The strongest AJ specific associations (P-values in 10(-6) -10(-7) range) were in the 22q 11.2 deletion region and included the genes TBX1, GLN1, and COMT. Supportive evidence (meta P < 1 × 10(-4) ) was also found for several previously identified genome-wide significant findings, including the HLA region, CNTN4, IMMP2L, and GRIN2A. The meta-analysis of the U.S. sample with the PGC2 results provided initial genome-wide significant evidence for six new loci. Among the novel potential susceptibility genes is PEPD, a gene involved in proline metabolism, which is associated with a Mendelian disorder characterized by developmental delay and cognitive deficits.
No figures extracted from this document.
No chunks — full text not yet ingested.
No entities extracted from this document yet.
No uploaded files.
Not in any collection.
No citations found.
In this knowledge base
External
| Title | Authors | Journal | Year | Link |
|---|---|---|---|---|
| Clinical description and epigenetic profiling of a new Danish OCD case-control cohort. | Staunstrup NH et al. | — | 2026 | → |
| Elevated calneuron-1, an accessory subunit of muscarinic receptors, induces frontotemporal dysconnectivity and schizophrenia-like deficits. | Oelschlegel AM et al. | — | 2026 | → |
| Genetic evidence for causal relationship between general cognition and treatment resistance in schizophrenia. | Li C et al. | — | 2026 | → |
| Genome-wide rare copy number variations potentially associated with drug resistance in epilepsy. | Chakraborty A et al. | — | 2026 | → |
| Large-scale blood pressure GWAS accounting for gene-depression interactions in 564,680 individuals from diverse populations. | Lee S et al. | — | 2026 | → |
| Comparing Alzheimer's genes in African, European, and Amerindian induced pluripotent stem cell-derived microglia. | Moura S et al. | — | 2025 | → |
| Genetic implication of GABA<sub>B</sub> receptors in the etiology of neurological and psychiatric disorders. | Gassmann M et al. | — | 2025 | → |
| HORNET: tools to find genes with causal evidence and their regulatory networks using eQTLs. | Lorincz-Comi N et al. | — | 2025 | → |
| Integrating genetic and transcriptomic data to identify genes underlying obesity risk loci. | Xu H et al. | — | 2025 | → |
| Revealing the genetic architectures underlying organ-specific aging based on proteomic data. | Zhu RJ et al. | — | 2025 | → |
| Sex-Specific Association Between Polymorphisms in Estrogen Receptor Alpha Gene (ESR1) and Depression: A Genome-Wide Association Study of All of Us and UK Biobank Data. | Hu Y et al. | — | 2025 | → |
| SNP-associated differential methylation in <i>ARHGEF38</i>: insights into genetic-epigenetic interactions. | Kovács EHC et al. | — | 2025 | → |
| Unveiling the clinical and genetic impact of neuropsychiatric involvement in systemic lupus erythematosus. | Cha S et al. | — | 2025 | → |
| Variability of transposable elements in six genetic isolates from North-Eastern Italy and their relationship with alcohol consumption, tobacco use and BMI. | Modenini G et al. | — | 2025 | → |
| A comprehensive update on genetic inheritance, epigenetic factors, associated pathology, and recent therapeutic intervention by gene therapy in schizophrenia. | R R et al. | — | 2024 | → |
| Effects of gene dosage on cognitive ability: A function-based association study across brain and non-brain processes. | Huguet G et al. | — | 2024 | → |
| Efficient multi-phenotype genome-wide analysis identifies genetic associations for unsupervised deep-learning-derived high-dimensional brain imaging phenotypes | Guo B et al. | — | 2024 | — |
| Emerging roles of long non-coding RNAs in human epilepsy. | Yazarlou F et al. | — | 2024 | → |
| Genetics and epigenetics of diabetes and its complications in India. | Priyadarshini A et al. | — | 2024 | → |
| Genome-wide association studies and polygenic risk score phenome-wide association studies across complex phenotypes in the human phenotype project. | Levine Z et al. | — | 2024 | → |
| Genomic structural equation modeling reveals latent phenotypes in the human cortex with distinct genetic architecture. | Morey RA et al. | — | 2024 | → |
| Identification and validation of supervariants reveal novel loci associated with human white matter microstructure. | Wang S et al. | — | 2024 | → |
| Mapping drug biology to disease genetics to discover drug impacts on the human phenome. | Habib M et al. | — | 2024 | → |
| Neuronal connectivity, behavioral, and transcriptional alterations associated with the loss of MARK2. | Caiola HO et al. | — | 2024 | → |
| Sex effects on DNA methylation affect discovery in epigenome-wide association study of schizophrenia. | Tesfaye M et al. | — | 2024 | → |
| The role of cell adhesion molecule IgSF9b at the inhibitory synapse and psychiatric disease. | Clarin JD et al. | — | 2024 | → |
| Unsupervised deep representation learning enables phenotype discovery for genetic association studies of brain imaging. | Patel K et al. | — | 2024 | → |
| Brain transcriptome-wide association study implicates novel risk genes underlying schizophrenia risk. | Zhang C et al. | — | 2023 | → |
| Cognitive Impairment Associated with Schizophrenia: From Pathophysiology to Treatment. | Javitt DC | — | 2023 | → |
| Deep multimodality-disentangled association analysis network for imaging genetics in neurodegenerative diseases. | Wang T et al. | — | 2023 | → |
| DNA methylation and general psychopathology in childhood: an epigenome-wide meta-analysis from the PACE consortium. | Rijlaarsdam J et al. | — | 2023 | → |
| Genome-wide association study of brain biochemical phenotypes reveals distinct genetic architecture of Alzheimer's disease related proteins. | Oatman SR et al. | — | 2023 | → |
| Genome-wide association study of cerebellar white matter microstructure and genetic overlap with common brain disorders. | Wu BS et al. | — | 2023 | → |
| Genome-wide DNA methylation association study of recent and cumulative marijuana use in middle aged adults. | Nannini DR et al. | — | 2023 | → |
| Immp2l knockdown in male mice increases stimulus-driven instrumental behaviour but does not alter goal-directed learning or neuron density in cortico-striatal circuits in a model of Tourette syndrome and autism spectrum disorder. | Leung BK et al. | — | 2023 | → |
| Immp2l Mutation Induces Mitochondrial Membrane Depolarization and Complex III Activity Suppression after Middle Cerebral Artery Occlusion in Mice. | Ma Y et al. | — | 2023 | → |
| Ocular and neural genes jointly regulate the visuospatial working memory in ADHD children. | Zhao Y et al. | — | 2023 | → |
| 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 | → |
| Association analyses of rare variants identify two genes associated with refractive error. | Patasova K et al. | — | 2022 | → |
| Comprehensive and integrative analyses identify TYW5 as a schizophrenia risk gene. | Zhang C et al. | — | 2022 | → |
| Defining Specific Cell States of MPTP-Induced Parkinson's Disease by Single-Nucleus RNA Sequencing. | Guo Y et al. | — | 2022 | → |
| Exonic deletions in IMMP2L in schizophrenia with enhanced glycation stress subtype. | Yoshikawa A et al. | — | 2022 | → |
| Fut9 Deficiency Causes Abnormal Neural Development in the Mouse Cerebral Cortex and Retina. | Abdullah A et al. | — | 2022 | → |
| Gene-based association tests using GWAS summary statistics and incorporating eQTL. | Cao X 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 Study on Three Behaviors Tested in an Open Field in Heterogeneous Stock Rats Identifies Multiple Loci Implicated in Psychiatric Disorders. | Gunturkun MH et al. | — | 2022 | → |
| Genome-wide variants and polygenic risk scores for cognitive impairment following blood or marrow transplantation. | Sharafeldin N et al. | — | 2022 | → |
| Identifying pleiotropic genes for complex phenotypes with summary statistics from a perspective of composite null hypothesis testing. | Wang T et al. | — | 2022 | → |
| Impact of COMT, PRODH and DISC1 Genetic Variants on Cognitive Performance of Patients with Schizophrenia. | Fricke-Galindo I et al. | — | 2022 | → |
| Integration of multidimensional splicing data and GWAS summary statistics for risk gene discovery. | Ji Y et al. | — | 2022 | → |
| Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. | Bolhuis K et al. | — | 2022 | → |
| Mitochondrial Processing Peptidases-Structure, Function and the Role in Human Diseases. | Kunová N et al. | — | 2022 | → |
| Molecular mechanisms of antipsychotics - their influence on intracellular signaling pathways, and epigenetic and post-transcription processes. | Rok-Bujko P | — | 2022 | → |
| Network reconstruction for trans acting genetic loci using multi-omics data and prior information. | Hawe JS et al. | — | 2022 | → |
| Shared genetic influences on resting-state functional networks of the brain. | P O F T Guimarães J et al. | — | 2022 | → |
| The glutamate/N-methyl-d-aspartate receptor (NMDAR) model of schizophrenia at 35: On the path from syndrome to disease. | Javitt DC et al. | — | 2022 | → |
| Upper cortical layer-driven network impairment in schizophrenia. | Batiuk MY et al. | — | 2022 | → |
| A generative-discriminative framework that integrates imaging, genetic, and diagnosis into coupled low dimensional space. | Ghosal S et al. | — | 2021 | → |
| A genome-wide association study identifies a gene network associated with paranoid schizophrenia and antipsychotics-induced tardive dyskinesia. | Levchenko A 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 | → |
| A Recessively Inherited Risk Locus on Chromosome 13q22-31 Conferring Susceptibility to Schizophrenia. | Mahmood T et al. | — | 2021 | → |
| Differential DNA Methylation of the IMMP2L Gene in Families with Maternally Inherited 7q31.1 Microdeletions is Associated with Intellectual Disability and Developmental Delay. | Vasilyev SA et al. | — | 2021 | → |
| Epigenetic Age Acceleration Was Delayed in Schizophrenia. | Wu X et al. | — | 2021 | → |
| Genetic underpinnings of affective temperaments: a pilot GWAS investigation identifies a new genome-wide significant SNP for anxious temperament in ADGRB3 gene. | Gonda X et al. | — | 2021 | → |
| Genome-wide Association Analysis of Parkinson's Disease and Schizophrenia Reveals Shared Genetic Architecture and Identifies Novel Risk Loci. | Smeland OB et al. | — | 2021 | → |
| Genome-wide DNA methylation alteration in prenatally stressed Brahman heifer calves with the advancement of age. | Cilkiz KZ et al. | — | 2021 | → |
| Impact of depression and stress on placental DNA methylation in ethnically diverse pregnant women. | Tesfaye M et al. | — | 2021 | → |
| Mapping the serum proteome to neurological diseases using whole genome sequencing. | Png G et al. | — | 2021 | → |
| MHC Haplotyping of SARS-CoV-2 Patients: HLA Subtypes Are Not Associated with the Presence and Severity of COVID-19 in the Israeli Population. | Ben Shachar S et al. | — | 2021 | → |
| MicroRNAs in the Onset of Schizophrenia. | Thomas KT et al. | — | 2021 | → |
| mRNA Expression of the CUB and Sushi Multiple Domains 1 (<i>CSMD1</i>) and Its Serum Protein Level as Predictors for Psychosis in the Familial High-Risk Children and Young Adults. | Abd El Gayed EM et al. | — | 2021 | → |
| Neonatal DNA methylation and childhood low prosocial behavior: An epigenome-wide association meta-analysis. | Luo M et al. | — | 2021 | → |
| OPRD1 SNPs associated with opioid addiction are cis-eQTLs for the phosphatase and actin regulator 4 gene, PHACTR4, a mediator of cytoskeletal dynamics. | Levran O et al. | — | 2021 | → |
| Pleiotropy and Cross-Disorder Genetics Among Psychiatric Disorders. | Lee PH et al. | — | 2021 | → |
| Prox1 inhibits neurite outgrowth during central nervous system development. | Kaltezioti V et al. | — | 2021 | → |
| Regulatory genomic circuitry of human disease loci by integrative epigenomics. | Boix CA et al. | — | 2021 | → |
| Selective Activation of CNS and Reference <i>PPARGC1A</i> Promoters Is Associated with Distinct Gene Programs Relevant for Neurodegenerative Diseases. | Kwik M et al. | — | 2021 | → |
| The association of polygenic risk for schizophrenia, bipolar disorder, and depression with neural connectivity in adolescents and young adults: examining developmental and sex differences. | Meyers JL et al. | — | 2021 | → |
| "The Heidelberg Five" personality dimensions: Genome-wide associations, polygenic risk for neuroticism, and psychopathology 20 years after assessment. | Heilbronner U et al. | — | 2021 | → |
| Transcriptome-wide association analysis of brain structures yields insights into pleiotropy with complex neuropsychiatric traits. | Zhao B et al. | — | 2021 | → |
| Age dependent association of inbreeding with risk for schizophrenia in Egypt. | McClain L et al. | — | 2020 | → |
| A powerful fine-mapping method for transcriptome-wide association studies. | Wu C et al. | — | 2020 | → |
| Automated feature extraction from population wearable device data identified novel loci associated with sleep and circadian rhythms. | Li X et al. | — | 2020 | → |
| Autozygosity influences cardiometabolic disease-associated traits in the AWI-Gen sub-Saharan African study. | Ceballos FC et al. | — | 2020 | → |
| Biomarkers in Psychiatry: Concept, Definition, Types and Relevance to the Clinical Reality. | García-Gutiérrez MS et al. | — | 2020 | → |
| Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. | van der Meer D et al. | — | 2020 | → |
| Exploring the Role of Contactins across Psychological, Psychiatric and Cardiometabolic Traits within UK Biobank. | Morris J et al. | — | 2020 | → |
| Genetic Intersections of Language and Neuropsychiatric Conditions. | Koomar T et al. | — | 2020 | → |
| Genetics of Obesity in East Asians. | Sun C et al. | — | 2020 | → |
| Genome-wide association study of cognitive function in diverse Hispanics/Latinos: results from the Hispanic Community Health Study/Study of Latinos. | Jian X et al. | — | 2020 | → |
| Genomewide Association Study of Platelet Reactivity and Cardiovascular Response in Patients Treated With Clopidogrel: A Study by the International Clopidogrel Pharmacogenomics Consortium. | Verma SS et al. | — | 2020 | → |
| Genome-Wide Association Study of Suicide Death and Polygenic Prediction of Clinical Antecedents. | Docherty AR et al. | — | 2020 | → |
| Genome-wide DNA methylation analysis of heavy cannabis exposure in a New Zealand longitudinal cohort. | Osborne AJ et al. | — | 2020 | → |
| Glycobiology and schizophrenia: a biological hypothesis emerging from genomic research. | Mealer RG et al. | — | 2020 | → |
| Intragenic CNTN4 copy number variants associated with a spectrum of neurobehavioral phenotypes. | Zhang SQ et al. | — | 2020 | → |
| Long Noncoding RNA SOX2-OT: Regulations, Functions, and Roles on Mental Illnesses, Cancers, and Diabetic Complications. | Li PY et al. | — | 2020 | → |
| Network Systems Pharmacology-Based Mechanism Study on the Beneficial Effects of Vitamin D against Psychosis in Alzheimer's Disease. | Fan P et al. | — | 2020 | → |
| RBFOX1, encoding a splicing regulator, is a candidate gene for aggressive behavior. | Fernàndez-Castillo N et al. | — | 2020 | → |
| The role of environmental stress and DNA methylation in the longitudinal course of bipolar disorder. | Comes AL 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 | → |
| A decade in psychiatric GWAS research. | Horwitz T et al. | — | 2019 | → |
| Centromeric Satellite DNAs: Hidden Sequence Variation in the Human Population. | Miga KH | — | 2019 | → |
| Estimation of DNA contamination and its sources in genotyped samples. | Zajac GJM et al. | — | 2019 | → |
| Expression analysis and genotyping of DGKZ: a GWAS-derived risk gene for schizophrenia. | Alinaghi S et al. | — | 2019 | → |
| Fine-mapping scan of bipolar disorder susceptibility loci in Latino pedigrees. | Gonzalez S et al. | — | 2019 | → |
| Genetic Associations between Voltage-Gated Calcium Channels and Psychiatric Disorders. | Andrade A et al. | — | 2019 | → |
| Genetic Variation in Steroid and Xenobiotic Metabolizing Pathways and Enterolactone Excretion Before and After Flaxseed Intervention in African American and European American Women. | Chang H et al. | — | 2019 | → |
| Genome-wide association studies of alcohol dependence, DSM-IV criterion count and individual criteria. | Lai D 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 | → |
| High-throughput functional analysis of lncRNA core promoters elucidates rules governing tissue specificity. | Mattioli K et al. | — | 2019 | → |
| Identification of common genetic risk variants for autism spectrum disorder. | Grove J et al. | — | 2019 | → |
| Identification of novel genome-wide associations for suicidality in UK Biobank, genetic correlation with psychiatric disorders and polygenic association with completed suicide. | Strawbridge RJ 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 | → |
| Linking glycemic dysregulation in diabetes to symptoms, comorbidities, and genetics through EHR data mining. | Kirk IK et al. | — | 2019 | → |
| Microduplications at the 15q11.2 BP1-BP2 locus are enriched in patients with anorexia nervosa. | Chang X et al. | — | 2019 | → |
| Multivariate analysis of genome-wide data to identify potential pleiotropic genes for five major psychiatric disorders using MetaCCA. | Jia X et al. | — | 2019 | → |
| Mutations in PIK3C2A cause syndromic short stature, skeletal abnormalities, and cataracts associated with ciliary dysfunction. | Tiosano D et al. | — | 2019 | → |
| Phosphoinositides: Regulators of Nervous System Function in Health and Disease. | Raghu P et al. | — | 2019 | → |
| Retrospective Association Analysis of Longitudinal Binary Traits Identifies Important Loci and Pathways in Cocaine Use. | Wu W et al. | — | 2019 | → |
| The <i>ANKS1B</i> gene and its associated phenotypes: focus on CNS drug response. | Younis RM et al. | — | 2019 | → |
| Unravelling the genetic basis of schizophrenia and bipolar disorder with GWAS: A systematic review. | Prata DP 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 | → |
| Analysis of Association of Genetic Markers in the LUZP2 and FBXO40 Genes with the Normal Variability in Cognitive Performance in the Elderly. | Stepanov V et al. | — | 2018 | → |
| An ensemble-based likelihood ratio approach for family-based genomic risk prediction. | An H et al. | — | 2018 | → |
| Association between COMT gene polymorphisms, clinical symptoms, and cognitive functions in Han Chinese patients with schizophrenia. | Sun Z et al. | — | 2018 | → |
| Association between COMT Val158Met and psychiatric disorders: A comprehensive meta-analysis. | Taylor S | — | 2018 | → |
| Association of IMMP2L deletions with autism spectrum disorder: A trio family study and meta-analysis. | Zhang Y et al. | — | 2018 | → |
| Association of Polygenic Score for Schizophrenia and HLA Antigen and Inflammation Genes With Response to Lithium in Bipolar Affective Disorder: A Genome-Wide Association Study. | International Consortium on Lithium Genetics (ConLi+Gen) et al. | — | 2018 | → |
| Case-control studies of gene-environment interactions. When a case might not be the case. | Lobach I et al. | — | 2018 | → |
| COMT genotype is associated with plasticity in sense of body ownership: a pilot study. | Honma M et al. | — | 2018 | → |
| Genetics of self-reported risk-taking behaviour, trans-ethnic consistency and relevance to brain gene expression. | Strawbridge RJ et al. | — | 2018 | → |
| Genome-wide association studies of brain imaging phenotypes in UK Biobank. | Elliott LT et al. | — | 2018 | → |
| Genomic Deletion Involving the IMMP2L Gene in Two Cases of Autism Spectrum Disorder. | Baldan F et al. | — | 2018 | → |
| Glycosyltransferase genes that cause monogenic congenital disorders of glycosylation are distinct from glycosyltransferase genes associated with complex diseases. | Joshi HJ 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 | → |
| microRNAs Sculpt Neuronal Communication in a Tight Balance That Is Lost in Neurological Disease. | Thomas KT et al. | — | 2018 | → |
| Nutrient Sensing, Signaling and Ageing: The Role of IGF-1 and mTOR in Ageing and Age-Related Disease. | Johnson SC | — | 2018 | → |
| Polygenic Risk Scores in Clinical Psychology: Bridging Genomic Risk to Individual Differences. | Bogdan R et al. | — | 2018 | → |
| SEGtool: a specifically expressed gene detection tool and applications in human tissue and single-cell sequencing data. | Zhang Q et al. | — | 2018 | → |
| Sociogenomics in the 21<sup>st</sup> Century: An Introduction to the History and Potential of Genetically-informed Social Science. | Braudt DB | — | 2018 | → |
| Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. | Davies G et al. | — | 2018 | → |
| The immunogenetics of neurological disease. | Misra MK et al. | — | 2018 | → |
| The integrated landscape of causal genes and pathways in schizophrenia. | Ma C et al. | — | 2018 | → |
| The interaction between cannabis use and the Val158Met polymorphism of the COMT gene in psychosis: A transdiagnostic meta - analysis. | Vaessen TSJ et al. | — | 2018 | → |
| Theoretical studies of the second step of the nitric oxide synthase reaction: Electron tunneling prevents uncoupling. | Shamovsky I et al. | — | 2018 | → |
| A current view on contactin-4, -5, and -6: Implications in neurodevelopmental disorders. | Oguro-Ando A et al. | — | 2017 | → |
| Genetic Variants in CSMD1 Gene Are Associated with Cognitive Performance in Normal Elderly Population. | Stepanov V et al. | — | 2017 | → |
| Genomic Analysis of Genotype-by-Social Environment Interaction for <i>Drosophila melanogaster</i> Aggressive Behavior. | Rohde PD et al. | — | 2017 | → |
| In Search of the jüdische Typus: A Proposed Benchmark to Test the Genetic Basis of Jewishness Challenges Notions of "Jewish Biomarkers". | Elhaik E | — | 2016 | → |
| Neural correlates of reward processing in adults with 22q11 deletion syndrome. | van Duin EDA et al. | — | 2016 | → |
| Sex-specific hippocampal 5-hydroxymethylcytosine is disrupted in response to acute stress. | Papale LA et al. | — | 2016 | → |
| The Gut Microbiota and the Emergence of Autoimmunity: Relevance to Major Psychiatric Disorders. | Severance EG et al. | — | 2016 | → |