extended twin design
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2018 ◽  
Vol 21 (3) ◽  
pp. 163-178 ◽  
Author(s):  
Brad Verhulst ◽  
Michael C. Neale ◽  
Lindon J. Eaves ◽  
Sarah E. Medland ◽  
Andrew C. Heath ◽  
...  

Drinking alcohol is a normal behavior in many societies, and prior studies have demonstrated it has both genetic and environmental sources of variation. Using two very large samples of twins and their first-degree relatives (Australia ≈ 20,000 individuals from 8,019 families; Virginia ≈ 23,000 from 6,042 families), we examine whether there are differences: (1) in the genetic and environmental factors that influence four interrelated drinking behaviors (quantity, frequency, age of initiation, and number of drinks in the last week), (2) between the twin-only design and the extended twin design, and (3) the Australian and Virginia samples. We find that while drinking behaviors are interrelated, there are substantial differences in the genetic and environmental architectures across phenotypes. Specifically, drinking quantity, frequency, and number of drinks in the past week have large broad genetic variance components, and smaller but significant environmental variance components, while age of onset is driven exclusively by environmental factors. Further, the twin-only design and the extended twin design come to similar conclusions regarding broad-sense heritability and environmental transmission, but the extended twin models provide a more nuanced perspective. Finally, we find a high level of similarity between the Australian and Virginian samples, especially for the genetic factors. The observed differences, when present, tend to be at the environmental level. Implications for the extended twin model and future directions are discussed.


2013 ◽  
Vol 10 (4) ◽  
pp. 1090-1099 ◽  
Author(s):  
Katarina Alanko ◽  
Benny Salo ◽  
Andreas Mokros ◽  
Pekka Santtila

2011 ◽  
Vol 14 (2) ◽  
pp. 119-128 ◽  
Author(s):  
Inge L.C. van Soelen ◽  
Rachel M. Brouwer ◽  
Marieke van Leeuwen ◽  
René S. Kahn ◽  
Hilleke E. Hulshoff Pol ◽  
...  

The longitudinal stability of IQ is well-documented as is its increasing heritability with age. In a longitudinal twin study, we addressed the question to what extent heritability and stability differ for full scale (FSIQ), verbal (VIQ), and performance IQ (PIQ) in childhood (age 9–11 years), and early adolescence (age 12–14 years). Genetic and environmental influences and correlations over time were evaluated in an extended twin design, including Dutch twins and their siblings. Intelligence was measured by the Wechsler Intelligence Scale for children — Third version (WISC III). Heritability in childhood was 34% for FSIQ, 37% for VIQ, and 64% for PIQ, and increased up to 65%, 51%, and 72% in early adolescence. The influence of common environment decreased between childhood and early adolescence from explaining 43% of the phenotypic variance for FSIQ to 18% and from 42% for VIQ to 26%. For PIQ common environmental influences did not play a role, either in childhood or in early adolescence. The stability in FSIQ and VIQ across the 3-year interval (rp) was .72 for both measures and was explained by genetic and common environmental correlations across time (FSIQ, rg= .96, rc= 1.0; VIQ, rg=.78, rc= 1.0). Stability of PIQ (rp=.56) was lower and was explained by genetic influences (rg= .90). These results confirm the robust findings of increased heritability of general cognitive abilities during the transition from childhood to adolescence. Interestingly, results for PIQ differ from those for FSIQ and VIQ, in that no significant contribution of environment shared by siblings from the same family was detected.


2008 ◽  
Vol 199 (1) ◽  
pp. 43.e1-43.e5 ◽  
Author(s):  
Zachary A.-F. Kistka ◽  
Emily A. DeFranco ◽  
Lannie Ligthart ◽  
Gonneke Willemsen ◽  
Jevon Plunkett ◽  
...  

2007 ◽  
Vol 197 (6) ◽  
pp. S199
Author(s):  
Emily Defranco ◽  
Zachary Kistka ◽  
Lannie Ligthart ◽  
Gonneke Willemsen ◽  
Jevon Plunkett ◽  
...  

2006 ◽  
Vol 36 (2) ◽  
pp. 229-237 ◽  
Author(s):  
R. D. Stoel ◽  
E. J. C. De Geus ◽  
D. I. Boomsma

Hypertension ◽  
2005 ◽  
Vol 45 (1) ◽  
pp. 80-85 ◽  
Author(s):  
Nina Kupper ◽  
Gonneke Willemsen ◽  
Harriëtte Riese ◽  
Daniëlle Posthuma ◽  
Dorret I. Boomsma ◽  
...  

1987 ◽  
Vol 36 (1) ◽  
pp. 29-39 ◽  
Author(s):  
D.I. Boomsma ◽  
P.C.M. Molenaar

AbstractWhen the univariate twin design is extended by including parents of twins, it is possible to assess additive genetic effects in the presence of assortative mating and genotype-environment correlation, the effects of parental influence, as well as the extent of residual shared environmental influences. The analysis of data obtained in such an extended twin design can be carried out by means of constrained maximum likelihood confirmatory factor analysis. Specifically, the structural model underlying this design can be represented as a LISREL model with nonlinear constraints. This representation offers the possibility to consider extended multivariate twin designs involving common genetic and environmental factors. The proposed method will be illustrated with applications to simulated and real data.


1984 ◽  
Vol 33 (2) ◽  
pp. 287-301 ◽  
Author(s):  
C.S. Haley

AbstractPhenotypic variation in human population may contain contributions from a number of different sex-associated genetic influences. These influences include maternal effects, the effects of sex-linked loci, and the effects of sex-limited autosomally linked loci. The families produced by MZ and DZ twins provide statistics which permit the detection and estimation of these effects. In particular, they provide statistics derived from various types of age-matched half-sibs and cousins in addition to those derived from the more usually studied full-sib or parent-offspring relationships. Specific models for genetic maternal effects, sex-linkage and sex-limitation are used to explore the use of extended twin design for the detection of and the discrimination between various sex-associated effects. The sample sizes required to detect maternal effects and sex-linkage were considered for some simple cases and it is concluded that comparison derived from the progeny of twins will often provide better tests for these effects than those derived from parent-offspring comparison.


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