bipolar disorder phenotype
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Related entities (44)
Mentioned in (58)
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)
- Associations between common genetic variants and income provide insights about the socio-economic health gradient. (2025)
- Massively parallel reporter assay investigates shared genetic variants of eight psychiatric disorders. (2025)
- Genome-wide association testing beyond SNPs. (2025)
- Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder. (2025)
- Parent-of-origin effects on complex traits in up to 236,781 individuals. (2025)
- Parenting by individuals with fetal alcohol spectrum disorders and neurobehavioral outcomes in their offspring. (2024)
- Clinical, genomic, and neurophysiological correlates of lifetime suicide attempts among individuals with alcohol dependence. (2024)
- CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods. (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)
- The Human Phenotype Ontology in 2024: phenotypes around the world. (2024)
- Adverse childhood experiences in children with fetal alcohol spectrum disorders and their effects on behavior. (2023)
- Human 3D brain organoids: steering the demolecularization of brain and neurological diseases. (2023)
- Current considerations for fetal alcohol spectrum disorders: identification to intervention. (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)
- Stability and change in the interpretation of facial emotions in fetal alcohol spectrum disorders from childhood to adolescence. (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)
- Parsing genetically influenced risk pathways: genetic loci impact problematic alcohol use via externalizing and specific risk. (2022)
- Prenatal alcohol exposure and mental health at midlife: A preliminary report on two longitudinal cohorts. (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)
- Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction. (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)
- A Prospective Comparison of Bipolar I and II Subjects With and Without Comorbid Alcohol Dependence From the COGA Dataset. (2020)
- Exploring the relationship between polygenic risk for cannabis use, peer cannabis use and the longitudinal course of cannabis involvement. (2019)
- Linking genes, circuits, and behavior: network connectivity as a novel endophenotype of externalizing. (2019)
- Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. (2019)
- Ethanol activates immune response in lymphoblastoid cells. (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)
- The Impact of Peer Substance Use and Polygenic Risk on Trajectories of Heavy Episodic Drinking Across Adolescence and Emerging Adulthood. (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)
- The PsychENCODE project. (2015)
- A gene-based association method for mapping traits using reference transcriptome data. (2015)
- What Happens When Children with Fetal Alcohol Spectrum Disorders Become Adults? (2015)
- Candidate gene-environment interaction research: reflections and recommendations. (2015)
- Genome-wide association study of nicotine dependence in American populations: identification of novel risk loci in both African-Americans and European-Americans. (2015)
- Comorbidity of severe psychotic disorders with measures of substance use. (2014)
- Genetic influences on alcohol use across stages of development: GABRA2 and longitudinal trajectories of drunkenness from adolescence to young adulthood. (2014)
- Using genetic information from candidate gene and genome-wide association studies in risk prediction for alcohol dependence. (2014)
- A genome-wide association study of alcohol-dependence symptom counts in extended pedigrees identifies C15orf53. (2013)
- Copy number variations in 6q14.1 and 5q13.2 are associated with alcohol dependence. (2012)
- Longevity candidate genes and their association with personality traits in the elderly. (2012)
- White matter microstructural alterations in children with prenatal methamphetamine/polydrug exposure. (2012)
- AID/APOBEC cytosine deaminase induces genome-wide kataegis. (2012)
- Genomic regions identified by overlapping clusters of nominally-positive SNPs from genome-wide studies of alcohol and illegal substance dependence. (2011)
- Evidence for genes on chromosome 2 contributing to alcohol dependence with conduct disorder and suicide attempts. (2010)
- Tackling the widespread and critical impact of batch effects in high-throughput data. (2010)
- ToppGene Suite for gene list enrichment analysis and candidate gene prioritization. (2009)
- 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 (18)
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 |
|---|---|---|---|
| bipolar disorder | phenotype | 259 | 827 |
| bipolar affective disorder | phenotype | 6 | 8 |
| bipolar | phenotype | 5 | 6 |
| bipolar illness | phenotype | 5 | 7 |
| bipolar disorders | phenotype | 4 | 4 |
| bipolar patients | phenotype | 1 | 1 |
| bipolar (depressive phase) | phenotype | — | — |
| bipolar disorder subjects | phenotype | — | — |
| bipolar sample | phenotype | — | — |
| bipolar subjects | phenotype | — | — |
| early-onset bd | phenotype | — | — |
| f30-f31 | phenotype | — | — |
| icd-10 f31 | phenotype | — | — |
| icd-8 296 | phenotype | — | — |
| icd-9 296[2-7] | phenotype | — | — |
| manic-depressive disorder | phenotype | — | — |
| manic-depressive illness | phenotype | — | — |
| manic–depressive illness | phenotype | — | — |