A twin registry is a database of information about both identical twins and fraternal twins, which is often maintained by an academic institution, such as a university, or by other research institutions.
The use of twins can improve the statistical power of a genetic study by reducing the amount of genetic and/or environmental variability. [1] "Identical twins" (monozygotic (MZ) twins) share virtually all their genes with each other, and "fraternal twins" (dizygotic (DZ) twins), on average, share about 50% of their genes with each other (about the same amount of sharing as non-twin siblings). Both types of twin pairs in twin registries almost always share similar prenatal and early childhood environments as well. By determining what are called "concordance" rates for a disease or trait among identical and fraternal twin pairs, researchers can estimate whether contributing factors for that disease or trait are more likely to be hereditary, environmental, or some combination of these. A concordance rate is a statistical measure of probability - if one twin has a specific trait or disease, what is the probability that the other twin has (or will develop) that same trait or disease. In addition, with structural equation modeling and multivariate analyses of twin data, researchers can offer estimates of the extent to which allelic variants and environment may influence phenotypic traits. [1]
Some twin registries seek to cover all twins in an entire country, [1] including Sweden, [2] Denmark, [3] Norway, [4] Finland, Australia, [5] Sri Lanka [6] and the United Kingdom. [7] The Swedish Twin Registry is the largest twin database in the world, with approximately 85,000 twin pairs. [2]
Other twin registries cover a more limited geographic scope and are maintained by researchers at academic institutions, such as the Michigan State University Twin Registry, a registry of twins produced by researchers at Michigan State University, the Washington State Twin Registry, [8] a registry of twins produced by researchers at Washington State University, and the Minnesota Twin Registry project by researchers at the University of Minnesota related to the Minnesota Twin Family Study. The largest twin registry in the United States is the Mid-Atlantic Twin Registry (MATR) at Virginia Commonwealth University, which has more than 51,000 registered participants, with approximately 46,000 of these representing intact twin pairs. [1]
Many twin registries depend on the voluntary participation of twins – that is, participation in these twin registries is not compulsory, and twins must voluntarily elect whether or not to register with a twin registry (and later, whether to participate in research projects). This characteristic limitation of many twin registries leads to standard issues known as "recruitment bias" or "volunteer bias". [9] Recruitment biases include an over-inclusion of twins who share similar characteristics, [4] and over-inclusion of identical twins and female twins: [10]
Twin registries use a number of strategies to try to reduce the risk of recruitment bias. Some twin registries are "mandatory" - that is, for example, under the public health laws of Norway, all births of twins since 1967 have been recorded in a twin registry maintained by the Norwegian government. [4] By comparison, enlisting with the Australian Twin Registry is voluntary. [11] While the twin registry in Sri Lanka is based on volunteer twins, that twin registry has made extensive out-reach efforts, such as examining hospital birth records, and then making multiple follow-up efforts (including in-person visits) to find the twins and have them (or their parents) agree to be registered. [12]
Nature versus nurture is a long-standing debate in biology and society about the balance between two competing factors which determine fate: genetics (nature) and environment (nurture). The alliterative expression "nature and nurture" in English has been in use since at least the Elizabethan period and goes back to medieval French.
Twins are two offspring produced by the same pregnancy. Twins can be either monozygotic ('identical'), meaning that they develop from one zygote, which splits and forms two embryos, or dizygotic, meaning that each twin develops from a separate egg and each egg is fertilized by its own sperm cell. Since identical twins develop from one zygote, they will share the same gender, while fraternal twins may or may not. In rare cases twins can have the same mother and different fathers.
A multiple birth is the culmination of one multiple pregnancy, wherein the mother gives birth to two or more babies. A term most applicable to vertebrate species, multiple births occur in most kinds of mammals, with varying frequencies. Such births are often named according to the number of offspring, as in twins and triplets. In non-humans, the whole group may also be referred to as a litter, and multiple births may be more common than single births. Multiple births in humans are the exception and can be exceptionally rare in the largest mammals.
Twin studies are studies conducted on identical or fraternal twins. They aim to reveal the importance of environmental and genetic influences for traits, phenotypes, and disorders. Twin research is considered a key tool in behavioral genetics and in content fields, from biology to psychology. Twin studies are part of the broader methodology used in behavior genetics, which uses all data that are genetically informative – siblings studies, adoption studies, pedigree, etc. These studies have been used to track traits ranging from personal behavior to the presentation of severe mental illnesses such as schizophrenia.
Human behaviour genetics is an interdisciplinary subfield of behaviour genetics that studies the role of genetic and environmental influences on human behaviour. Classically, human behavioural geneticists have studied the inheritance of behavioural traits. The field was originally focused on determining the importance of genetic influences on human behaviour. It has evolved to address more complex questions such as: how important are genetic and/or environmental influences on various human behavioural traits; to what extent do the same genetic and/or environmental influences impact the overlap between human behavioural traits; how do genetic and/or environmental influences on behaviour change across development; and what environmental factors moderate the importance of genetic effects on human behaviour. The field is interdisciplinary, and draws from genetics, psychology, and statistics. Most recently, the field has moved into the area of statistical genetics, with many behavioural geneticists also involved in efforts to identify the specific genes involved in human behaviour, and to understand how the effects associated with these genes changes across time, and in conjunction with the environment.
Thomas J. Bouchard Jr. is an American psychologist known for his behavioral genetics studies of twins raised apart. He is professor emeritus of psychology and director of the Minnesota Center for Twin and Adoption Research at the University of Minnesota. Bouchard received his PhD from the University of California, Berkeley in 1966.
The Minnesota Center for Twin and Family Research is a series of behavioral genetic longitudinal studies of families with twin or adoptive offspring conducted by researchers at the University of Minnesota. It seeks to identify and characterize the genetic and environmental influences on the development of psychological traits.
David Thoreson Lykken was a behavioral geneticist and Professor Emeritus of Psychology and Psychiatry at the University of Minnesota. He is best known for his work on twin studies and lie detection.
Twins Days is held annually on the first full weekend in August in Twinsburg, Ohio, United States to celebrate biological twins. The event has taken place every summer since 1976 when the festival was founded by a group of Twinsburg citizens, based on a concept developed by Ray Diersing, Sage Hiller, and Ari Hiller. The first time Twins Day was proposed to city council, it was rejected; city council thought it was a bad idea. It is the largest annual gathering of twins in the world, and draws thousands of participants from all over the United States and elsewhere in the world.
In psychology, a trait is called emergenic if it is the result of a specific combination of several interacting genes. Emergenic traits will not run in families, but identical twins will share them. Traits such as "leadership", "genius" or certain mental illnesses may be emergenic. Although one may expect epigenetics to play a significant role in the phenotypic manifestation of twins reared apart, the concordance displayed between them can be attributed to emergenesis.
Concordance, as used in genetics, usually means the presence of the same trait in both members of a pair of twins. However, the strict definition is the probability that a pair of individuals will both have a certain characteristic, given that one of the pair has the characteristic. For example, twins are concordant when both have or both lack a given trait. The ideal example of concordance is that of identical twins.
The heritability of autism is the proportion of differences in expression of autism that can be explained by genetic variation; if the heritability of a condition is high, then the condition is considered to be primarily genetic. Autism has a strong genetic basis, although the genetics of autism are complex and it is unclear whether autism spectrum disorder (ASD) is explained more by multigene interactions or by rare mutations with major effects.
Research on the heritability of IQ inquires into the proportion of variance in IQ that is attributable to genetic variation within a population. Heritability, in this sense, is a mathematical estimate of how much of a trait's variation within a population can be attributed to genetic variation between individuals in that population. There has been significant controversy in the academic community about the heritability of IQ since research on the issue began in the late nineteenth century. Intelligence in the normal range is a polygenic trait, meaning that it is influenced by more than one gene, and in the case of intelligence at least 500 genes. Further, explaining the similarity in IQ of closely related persons requires careful study because environmental factors may be correlated with genetic factors.
Irving Isadore Gottesman was an American professor of psychology who devoted most of his career to the study of the genetics of schizophrenia. He wrote 17 books and more than 290 other publications, mostly on schizophrenia and behavioral genetics, and created the first academic program on behavioral genetics in the United States. He won awards such as the Hofheimer Prize for Research, the highest award from the American Psychiatric Association for psychiatric research. Lastly, Gottesman was a professor in the psychology department at the University of Minnesota, where he received his Ph.D.
Hermann Werner Siemens was a German dermatologist who first described multiple skin diseases and was one of the inventors of the twin study. Siemens' work in twin studies is influential in modern genetics and is used to address the environmental and genetic impacts upon traits. Siemens was involved in racial hygiene and affiliated with the Nazi Party.
Behavioural genetics, also referred to as behaviour genetics, is a field of scientific research that uses genetic methods to investigate the nature and origins of individual differences in behaviour. While the name "behavioural genetics" connotes a focus on genetic influences, the field broadly investigates the extent to which genetic and environmental factors influence individual differences, and the development of research designs that can remove the confounding of genes and environment. Behavioural genetics was founded as a scientific discipline by Francis Galton in the late 19th century, only to be discredited through association with eugenics movements before and during World War II. In the latter half of the 20th century, the field saw renewed prominence with research on inheritance of behaviour and mental illness in humans, as well as research on genetically informative model organisms through selective breeding and crosses. In the late 20th and early 21st centuries, technological advances in molecular genetics made it possible to measure and modify the genome directly. This led to major advances in model organism research and in human studies, leading to new scientific discoveries.
Brian J. Byrne is an Australian social scientist specializing in applied and psycholinguistics, an emeritus professor at the University of New England in Australia, and lead author of publications and articles on research in his field. Byrne was a lead researcher in the 10-year-long, $5 million National Institutes of Health study by an international team of scientists into the development of reading ability in 1,000 pairs of twins. Beginning in 2000, the study found that genetics were more important influences on reading development than environmental factors. In 2012, Byrne was appointed a lead researcher in a similar Australian study of twins.
TwinsUK, also known as TwinsUK Registry, is the biggest UK adult registry of twins in the United Kingdom, ages 16 to 98 to study the genetic and environmental aetiology of age related complex traits and diseases. Established in 1993, it is based at King's College London with an intent of aiding genetic research. The registry is used to connect researchers to volunteers.
Genome-wide complex trait analysis (GCTA) Genome-based restricted maximum likelihood (GREML) is a statistical method for variance component estimation in genetics which quantifies the total narrow-sense (additive) contribution to a trait's heritability of a particular subset of genetic variants. This is done by directly quantifying the chance genetic similarity of unrelated individuals and comparing it to their measured similarity on a trait; if two unrelated individuals are relatively similar genetically and also have similar trait measurements, then the measured genetics are likely to causally influence that trait, and the correlation can to some degree tell how much. This can be illustrated by plotting the squared pairwise trait differences between individuals against their estimated degree of relatedness. The GCTA framework can be applied in a variety of settings. For example, it can be used to examine changes in heritability over aging and development. It can also be extended to analyse bivariate genetic correlations between traits. There is an ongoing debate about whether GCTA generates reliable or stable estimates of heritability when used on current SNP data. The method is based on the outdated and false dichotomy of genes versus the environment. It also suffers from serious methodological weaknesses, such as susceptibility to population stratification.