ArticleBehavior genetics2015
Estimation of Genetic Relationships Between Individuals Across Cohorts and Platforms: Application to Childhood Height.
Article in Behavior genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.
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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.
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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.
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Who cites it
12 citing papers in PubMed, 2 syntheses or guidelines pooled it.
- Genome-wide Association Meta-analysis of Childhood and Adolescent Internalizing Symptoms.Journal of the American Academy of Child and Adolescent Psychiatry · 2022Pooled it
- A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Pediatric Cohorts.Journal of the American Academy of Child and Adolescent Psychiatry · 2016Pooled it
- Genetic evidence for a large overlap and potential bidirectional causal effects between resilience and well-being.Neurobiology of stress · 2021Article
- Onset of Preclinical Alzheimer Disease in Monozygotic Twins.Annals of neurology · 2021Article
- Empirical comparisons of multiple Mendelian randomization approaches in the presence of assortative mating.International journal of epidemiology · 2020Article
- Maternal and paternal effects on offspring internalizing problems: Results from genetic and family-based analyses.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2020Article
- Heritability estimates for 361 blood metabolites across 40 genome-wide association studies.Nature communications · 2020Review
- A Genetic Investigation of the Well-Being Spectrum.Behavior genetics · 2019Article
- The moderating role of SES on genetic differences in educational achievement in the Netherlands.NPJ science of learning · 2019Article
- The EMIF-AD PreclinAD study: study design and baseline cohort overview.Alzheimer's research & therapy · 2018Article
- Predicting loneliness with polygenic scores of social, psychological and psychiatric traits.Genes, brain, and behavior · 2018Article
- Dopaminergic Genetic Variants and Voluntary Externally Paced Exercise Behavior.Medicine and science in sports and exercise · 2018Article
Corrections and comments
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Authors and funding
13 authors.
Funding
Abstract
Combining genotype data across cohorts increases power to estimate the heritability due to common single nucleotide polymorphisms (SNPs), based on analyzing a Genetic Relationship Matrix (GRM). However, the combination of SNP data across multiple cohorts may lead to stratification, when for example, different genotyping platforms are used. In the current study, we address issues of combining SNP data from different cohorts, the Netherlands Twin Register (NTR) and the Generation R (GENR) study. Both cohorts include children of Northern European Dutch background (N = 3102 + 2826, respectively) who were genotyped on different platforms. We explore imputation and phasing as a tool and compare three GRM-building strategies, when data from two cohorts are (1) just combined, (2) pre-combined and cross-platform imputed and (3) cross-platform imputed and post-combined. We test these three strategies with data on childhood height for unrelated individuals (N = 3124, average age 6.7 years) to explore their effect on SNP-heritability estimates and compare results to those obtained from the independent studies. All combination strategies result in SNP-heritability estimates with a standard error smaller than those of the independent studies. We did not observe significant difference in estimates of SNP-heritability based on various cross-platform imputed GRMs. SNP-heritability of childhood height was on average estimated as 0.50 (SE = 0.10). Introducing cohort as a covariate resulted in ≈2 % drop. Principal components (PCs) adjustment resulted in SNP-heritability estimates of about 0.39 (SE = 0.11). Strikingly, we did not find significant difference between cross-platform imputed and combined GRMs. All estimates were significant regardless the use of PCs adjustment. Based on these analyses we conclude that imputation with a reference set helps to increase power to estimate SNP-heritability by combining cohorts of the same ethnicity genotyped on different platforms. However, important factors should be taken into account such as remaining cohort stratification after imputation and/or phenotypic heterogeneity between and within cohorts. Whether one should use imputation, or just combine the genotype data, depends on the number of overlapping SNPs in relation to the total number of genotyped SNPs for both cohorts, and their ability to tag all the genetic variance related to the specific trait of interest.
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