schizophrenia phenotype
Evidence from:
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Related entities (71)
Mentioned in (106)
Papers in which this entity is mentioned.
- Infant subcortical brain volumes associated with maternal obesity and diabetes: a large multicohort human study. (2026)
- Mapping the genetic landscape across 14 psychiatric disorders. (2026)
- Regional cerebellum volume anomalies and associated cognitive function in children with fetal alcohol spectrum disorders. (2026)
- Associations between common genetic variants and income provide insights about the socio-economic health gradient. (2025)
- Concordance between male- and female-specific GWAS results helps define underlying genetic architecture of complex traits. (2025)
- Integrated single-cell multiomic profiling of caudate nucleus suggests key mechanisms in alcohol use disorder. (2025)
- Intranasal Administration of KCNN2 Blocking Peptide Improves Deficits in Cognitive Flexibility in Mouse Model of Fetal Alcohol Spectrum Disorders. (2025)
- Multi-omic quantitative trait loci link tandem repeat size variation to gene regulation in human brain. (2025)
- Massively parallel reporter assay investigates shared genetic variants of eight psychiatric disorders. (2025)
- Integrated single-cell multiomic profiling of caudate nucleus suggests key mechanisms in alcohol use disorder. (2025)
- Genome-wide association testing beyond SNPs. (2025)
- Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder. (2025)
- Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank. (2024)
- Childhood trauma is associated with developmental trajectories of EEG coherence, alcohol-related outcomes, and PTSD symptoms. (2024)
- Clinical, genomic, and neurophysiological correlates of lifetime suicide attempts among individuals with alcohol dependence. (2024)
- A global multicohort study to map subcortical brain development and cognition in infancy and early childhood. (2024)
- Detection and analysis of complex structural variation in human genomes across populations and in brains of donors with psychiatric disorders. (2024)
- Recent advances in polygenic scores: translation, equitability, methods and FAIR tools. (2024)
- Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder. (2024)
- Human 3D brain organoids: steering the demolecularization of brain and neurological diseases. (2023)
- Pitfalls of predicting age-related traits by polygenic risk scores. (2023)
- Predicting Alcohol-Related Memory Problems in Older Adults: A Machine Learning Study with Multi-Domain Features. (2023)
- Associations Between Cannabis Use, Polygenic Liability for Schizophrenia, and Cannabis-related Experiences in a Sample of Cannabis Users. (2023)
- Genetic Influences on the Developing Young Brain and Risk for Neuropsychiatric Disorders. (2023)
- Multi-trait genome-wide association study of opioid addiction: OPRM1 and beyond. (2022)
- mutations, genetic mosaicism and human disease. (2022)
- Item-Level Genome-Wide Association Study of the Alcohol Use Disorders Identification Test in Three Population-Based Cohorts. (2022)
- Lack of Evidence for a Relationship Between Salivary CRP and Women's Sexual Desire: An Investigation Across Clinical and Healthy Samples. (2022)
- Research Review: A guide to computing and implementing polygenic scores in developmental research. (2022)
- Parsing genetically influenced risk pathways: genetic loci impact problematic alcohol use via externalizing and specific risk. (2022)
- Evidence for long-lasting alterations in the fecal microbiota following prenatal alcohol exposure. (2022)
- Large-scale collaboration in ENIGMA-EEG: A perspective on the meta-analytic approach to link neurological and psychiatric liability genes to electrophysiological brain activity. (2021)
- Prenatal Adversity Alters the Epigenetic Profile of the Prefrontal Cortex: Sexually Dimorphic Effects of Prenatal Alcohol Exposure and Food-Related Stress. (2021)
- Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. (2021)
- Whole-genome analysis reveals the contribution of non-coding de novo transposon insertions to autism spectrum disorder. (2021)
- Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction. (2021)
- Genetic association study of childhood aggression across raters, instruments, and age. (2021)
- SPOTlight: seeded NMF regression to deconvolute spatial transcriptomics spots with single-cell transcriptomes. (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. (2021)
- Predicting risk for Alcohol Use Disorder using longitudinal data with multimodal biomarkers and family history: a machine learning study. (2021)
- Polygenic risk scores: from research tools to clinical instruments. (2020)
- Immune network dysregulation associated with child neurodevelopmental delay: modulatory role of prenatal alcohol exposure. (2020)
- Tutorial: a guide to performing polygenic risk score analyses. (2020)
- The mutational constraint spectrum quantified from variation in 141,456 humans. (2020)
- A Prospective Comparison of Bipolar I and II Subjects With and Without Comorbid Alcohol Dependence From the COGA Dataset. (2020)
- Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits. (2020)
- Polygenic prediction via Bayesian regression and continuous shrinkage priors. (2019)
- Element-centric clustering comparison unifies overlaps and hierarchy. (2019)
- Exploring the relationship between polygenic risk for cannabis use, peer cannabis use and the longitudinal course of cannabis involvement. (2019)
- Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. (2019)
- Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
- The mutational constraint spectrum quantified from variation in 141,456 humans (2019)
- Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
- Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. (2019)
- Genome-wide association studies of alcohol dependence, DSM-IV criterion count and individual criteria. (2019)
- Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. (2019)
- Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. (2018)
- Effects of prenatal alcohol exposure (PAE): insights into FASD using mouse models of PAE. (2018)
- Implications of altered maternal cytokine concentrations on infant outcomes in children with prenatal alcohol exposure. (2018)
- Meta-Analysis of Genetic Influences on Initial Alcohol Sensitivity. (2018)
- Altered maternal immune networks are associated with adverse child neurodevelopment: Impact of alcohol consumption during pregnancy. (2018)
- Sex differences in associations between white matter microstructure and gonadal hormones in children and adolescents with prenatal alcohol exposure. (2017)
- The Impact of Peer Substance Use and Polygenic Risk on Trajectories of Heavy Episodic Drinking Across Adolescence and Emerging Adulthood. (2017)
- Vitamin D Deficiency in Pregnant Ukrainian Women: Effects of Alcohol Consumption on Vitamin D Status. (2017)
- Cortical gyrification is abnormal in children with prenatal alcohol exposure. (2017)
- The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies. (2017)
- Genetic correlates of the development of theta event related oscillations in adolescents and young adults. (2017)
- Epigenetics studies of fetal alcohol spectrum disorder: where are we now? (2017)
- Longitudinal changes in pubertal maturation and white matter microstructure. (2017)
- Genome-wide Association Study of Cannabis Dependence Severity, Novel Risk Variants, and Shared Genetic Risks. (2016)
- New insights into the generation and role of de novo mutations in health and disease. (2016)
- KAT2B polymorphism identified for drug abuse in African Americans with regulatory links to drug abuse pathways in human prefrontal cortex. (2016)
- Assessing the Independent and Joint Effects of Unmedicated Prenatal Depressive Symptoms and Alcohol Consumption in Pregnancy and Infant Neurodevelopmental Outcomes. (2016)
- Polygenic risk for alcohol dependence associates with alcohol consumption, cognitive function and social deprivation in a population-based cohort. (2016)
- The PsychENCODE project. (2015)
- Eyeblink Classical Conditioning in Alcoholism and Fetal Alcohol Spectrum Disorders. (2015)
- Atypical cortical gyrification in adolescents with histories of heavy prenatal alcohol exposure. (2015)
- Peroxisome proliferator-activated receptors α and γ are linked with alcohol consumption in mice and withdrawal and dependence in humans. (2015)
- Candidate gene-environment interaction research: reflections and recommendations. (2015)
- Gender modulates the development of theta event related oscillations in adolescents and young adults. (2015)
- A Long-Term Longitudinal Examination of the Effect of Early Onset of Alcohol and Drug Use on Later Alcohol Abuse. (2015)
- Genome-wide association study of nicotine dependence in American populations: identification of novel risk loci in both African-Americans and European-Americans. (2015)
- Genetic linkage analysis in the age of whole-genome sequencing. (2015)
- Comorbidity of severe psychotic disorders with measures of substance use. (2014)
- Maternal and neonatal plasma microRNA biomarkers for fetal alcohol exposure in an ovine model. (2014)
- Genetic influences on alcohol use across stages of development: GABRA2 and longitudinal trajectories of drunkenness from adolescence to young adulthood. (2014)
- Diminishing return for increased Mappability with longer sequencing reads: implications of the k-mer distributions in the human genome. (2014)
- Using genetic information from candidate gene and genome-wide association studies in risk prediction for alcohol dependence. (2014)
- Common biological networks underlie genetic risk for alcoholism in African- and European-American populations. (2013)
- A genome-wide association study of alcohol-dependence symptom counts in extended pedigrees identifies C15orf53. (2013)
- Magnetic resonance microscopy-based analyses of the neuroanatomical effects of gestational day 9 ethanol exposure in mice. (2013)
- The aggregate effect of dopamine genes on dependence symptoms among cocaine users: cross-validation of a candidate system scoring approach. (2012)
- Copy number variations in 6q14.1 and 5q13.2 are associated with alcohol dependence. (2012)
- Large-scale objective phenotyping of 3D facial morphology. (2012)
- White matter microstructural alterations in children with prenatal methamphetamine/polydrug exposure. (2012)
- Ethanol-induced face-brain dysmorphology patterns are correlative and exposure-stage dependent. (2012)
- A longitudinal study of the long-term consequences of drinking during pregnancy: heavy in utero alcohol exposure disrupts the normal processes of brain development. (2012)
- A framework for variation discovery and genotyping using next-generation DNA sequencing data. (2011)
- A practical approach to incidental findings in neuroimaging research. (2011)
- Gene-environment interaction in psychological traits and disorders. (2011)
- Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion. (2011)
- Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. (2011)
- Diffusion tensor imaging of the cerebellum and eyeblink conditioning in fetal alcohol spectrum disorder. (2011)
- Prenatal alcohol exposure alters the patterns of facial asymmetry. (2010)
- Brain signatures of monetary loss and gain: outcome-related potentials in a single outcome gambling task. (2009)
- Copy-number-variation and copy-number-alteration region detection by cumulative plots. (2009)
Merged raw entities (24)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| schizophrenia | phenotype | 543 | 2354 |
| schizophrenia patients | cohort | 35 | 59 |
| patients with schizophrenia | cohort | 18 | 27 |
| schizophrenic patients | cohort | 10 | 14 |
| family history of schizophrenia | phenotype | 2 | 4 |
| schizophrenic | phenotype | 2 | 2 |
| f20 | phenotype | 1 | 1 |
| sch | phenotype | 1 | 2 |
| schizophrenic patients | phenotype | 1 | 1 |
| sczd | phenotype | 1 | 9 |
| adult schizophrenia brains | phenotype | — | — |
| dsm-iii-r schizophrenia | phenotype | — | — |
| genetic or clinical risk for schizophrenia | phenotype | — | — |
| individuals with schizophrenia | phenotype | — | — |
| mim 181500 | phenotype | — | — |
| patients with schizophrenia | phenotype | — | — |
| schizophrenia cohort | phenotype | — | — |
| schizophrenia diagnosis | phenotype | — | — |
| schizophrenia-like illness | phenotype | — | — |
| schizophrenia-like symptoms | phenotype | — | — |
| schizophrenia patients | phenotype | — | — |
| schizophrenia subjects | phenotype | — | — |
| schizophrenia susceptibility | phenotype | — | — |
| schizophrenics | phenotype | — | — |