ArticlePLoS genetics2011
Common variants show predicted polygenic effects on height in the tails of the distribution, except in extremely short individuals.
Article in PLoS genetics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
35 citing papers in PubMed.
- A heritability-optimized method for functional prioritization of rare coding variants in complex traits.Nature genetics · 2026Article
- Article
- Identification and analysis of individuals who deviate from their genetically-predicted phenotype.PLoS genetics · 2023Article
- Identification and analysis of individuals who deviate from their genetically-predicted phenotype.bioRxiv : the preprint server for biology · 2023Article
- Your height affects your health: genetic determinants and health-related outcomes in Taiwan.BMC medicine · 2022Article
- Whole Exome Sequencing in Healthy Individuals of Extreme Constitution Types Reveals Differential Disease Risk: A Novel Approach towards Predictive Medicine.Journal of personalized medicine · 2022Article
- Review
- Pygmalion in the Genes? On the potentially negative impacts of polygenic scores for educational attainment.Social psychology of education : an international journal · 2021Article
- Common maternal and fetal genetic variants show expected polygenic effects on risk of small- or large-for-gestational-age (SGA or LGA), except in the smallest 3% of babies.PLoS genetics · 2020Article
- Article
- Predicting Polygenic Risk of Psychiatric Disorders.Biological psychiatry · 2019Review
- Genetic architecture of human thinness compared to severe obesity.PLoS genetics · 2019Article
- Insights and Implications of Genome-Wide Association Studies of Height.The Journal of clinical endocrinology and metabolism · 2018Review
- Individual and shared effects of social environment and polygenic risk scores on adolescent body mass index.Scientific reports · 2018Article
- Elevated Body Mass Index is Associated with Increased Integration and Reduced Cohesion of Sensory-Driven and Internally Guided Resting-State Functional Brain Networks.Cerebral cortex (New York, N.Y. : 1991) · 2018Article
- Common DNA Variants Accurately Rank an Individual of Extreme Height.International journal of genomics · 2018Article
- Genetic variations at the human growth hormone receptor (GHR) gene locus are associated with idiopathic short stature.Journal of cellular and molecular medicine · 2017Article
- Genome-wide compound heterozygote analysis highlights alleles associated with adult height in Europeans.Human genetics · 2017Article
- The Biology of Stature.The Journal of pediatrics · 2016Article
- Variations in the high-mobility group-A2 gene (HMGA2) are associated with idiopathic short stature.Pediatric research · 2016Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
18 authors.
Funding
Abstract
Common genetic variants have been shown to explain a fraction of the inherited variation for many common diseases and quantitative traits, including height, a classic polygenic trait. The extent to which common variation determines the phenotype of highly heritable traits such as height is uncertain, as is the extent to which common variation is relevant to individuals with more extreme phenotypes. To address these questions, we studied 1,214 individuals from the top and bottom extremes of the height distribution (tallest and shortest ∼1.5%), drawn from ∼78,000 individuals from the HUNT and FINRISK cohorts. We found that common variants still influence height at the extremes of the distribution: common variants (49/141) were nominally associated with height in the expected direction more often than is expected by chance (p<5×10⁻²⁸), and the odds ratios in the extreme samples were consistent with the effects estimated previously in population-based data. To examine more closely whether the common variants have the expected effects, we calculated a weighted allele score (WAS), which is a weighted prediction of height for each individual based on the previously estimated effect sizes of the common variants in the overall population. The average WAS is consistent with expectation in the tall individuals, but was not as extreme as expected in the shortest individuals (p<0.006), indicating that some of the short stature is explained by factors other than common genetic variation. The discrepancy was more pronounced (p<10⁻⁶) in the most extreme individuals (height<0.25 percentile). The results at the extreme short tails are consistent with a large number of models incorporating either rare genetic non-additive or rare non-genetic factors that decrease height. We conclude that common genetic variants are associated with height at the extremes as well as across the population, but that additional factors become more prominent at the shorter extreme.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.