heritability phenotype
Evidence from:
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Related entities (17)
Mentioned in (47)
Papers in which this entity is mentioned.
- Specificity, length and luck drive gene rankings in association studies. (2026)
- Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI. (2024)
- BridgePRS leverages shared genetic effects across ancestries to increase polygenic risk score portability. (2024)
- Principles and methods for transferring polygenic risk scores across global populations. (2024)
- Biobank-scale methods and projections for sparse polygenic prediction from machine learning. (2023)
- Guidelines for Evaluating the Comparability of Down-Sampled GWAS Summary Statistics. (2023)
- Polygenic scoring accuracy varies across the genetic ancestry continuum. (2023)
- The Genetic Architecture of Obsessive-Compulsive Disorder: Contribution of Liability to OCD From Alleles Across the Frequency Spectrum. (2022)
- Mother-child similarity in brain morphology: A comparison of structural characteristics of the brain's reading network. (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)
- Shared genetic architecture across psychiatric disorders. (2021)
- Intergenerational transmission of the patterns of functional and structural brain networks. (2021)
- Polygenic prediction via Bayesian regression and continuous shrinkage priors. (2019)
- Genomic structural equation modelling provides insights into the multivariate genetic architecture of complex traits. (2019)
- Reliability and validity of an internalizing symptom scale based on the adolescent and adult Semi-Structured Assessment for the Genetics of Alcoholism (SSAGA). (2019)
- Heritability of obsessive-compulsive trait dimensions in youth from the general population. (2018)
- Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. (2018)
- LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis. (2017)
- Detecting Genomic Signatures of Natural Selection with Principal Component Analysis: Application to the 1000 Genomes Data. (2016)
- Genetic and environmental influences interact with age and sex in shaping the human methylome. (2016)
- The heritability of alcohol use disorders: a meta-analysis of twin and adoption studies. (2015)
- What twin studies tell us about the heritability of brain development, morphology, and function: a review. (2015)
- Quantitative tract-based white matter heritability in twin neonates. (2015)
- The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. (2014)
- Heritability and genomics of gene expression in peripheral blood. (2014)
- Heritability and molecular-genetic basis of resting EEG activity: a genome-wide association study. (2014)
- Intersubject variability of and genetic effects on the brain's functional connectivity during infancy. (2014)
- Genetic influences on brain developmental trajectories on neuroimaging studies: from infancy to young adulthood. (2014)
- Linear mixed-effects modeling approach to FMRI group analysis. (2013)
- Population-specificity of human DNA methylation. (2012)
- White matter heritability using diffusion tensor imaging in neonatal brains. (2012)
- Sex differences and developmental stability in genetic and environmental influences on psychoactive substance consumption from early adolescence to young adulthood. (2011)
- An Interdisciplinary Approach to Studying Gene-Environment Interactions: From Twin Studies to Gene Identification and Back. (2011)
- Human aggression across the lifespan: genetic propensities and environmental moderators. (2011)
- A population-based twin study of the genetic and environmental relationship of major depression, regular tobacco use and nicotine dependence. (2011)
- Distribution of allele frequencies and effect sizes and their interrelationships for common genetic susceptibility variants. (2011)
- Genetic control over the resting brain. (2010)
- Cortical thickness or grey matter volume? The importance of selecting the phenotype for imaging genetics studies. (2010)
- Structural MRI of pediatric brain development: what have we learned and where are we going? (2010)
- The genetic interpretation of area under the ROC curve in genomic profiling. (2010)
- Finding the missing heritability of complex diseases. (2009)
- Differences in genetic and environmental influences on the human cerebral cortex associated with development during childhood and adolescence. (2009)
- Dramatic increase in heritability of cognitive development from early to middle childhood: an 8-year longitudinal study of 8,700 pairs of twins. (2009)
- The future of genetics in psychology and psychiatry: microarrays, genome-wide association, and non-coding RNA. (2009)
- New insights into the genetics of addiction. (2009)
- The changing impact of genes and environment on brain development during childhood and adolescence: initial findings from a neuroimaging study of pediatric twins. (2008)
- Variance decomposition using an IRT measurement model. (2007)
Merged raw entities (3)
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 |
|---|---|---|---|
| heritability | phenotype | 46 | 89 |
| h2 | phenotype | 3 | 4 |
| estimated heritability | phenotype | — | — |