Genetic Epidemiology, Translational Neurogenomics, Psychiatric Genetics and Statistical Genetics Laboratories investigate the pattern of disease in families, particularly identical and non-identical twins, to assess the relative importance of genes and environment in a variety of important health problems.
QIMR Home Page
GenEpi Home Page
About GenEpi
Publications
Contacts
Research
Staff Index
Collaborators
Software Tools
Computing Resources
Studies
Search
GenEpi Intranet
PMID
370072
TITLE
Model-fitting approaches to the analysis of human behaviour.
ABSTRACT
Model-fitting methods are now prominent in the analysis of human behavioural variation. Various ways of specifying models have been proposed. These are identical in their simplest form but differ in the emphasis given to more subtle sources of variation. The biometrical genetical approach allows flexibility in the specification of non-additive factors. Given additivity, the approach of path analysis may be used to specify several environmental models in the presence of assortative mating. In many cases the methods should yield identical conclusions. Several statistical methods have been proposed for parameter estimation and hypothesis testing. The most suitable rely on the method of maximum likelihood for the estimation of variance and covariance components. Any multifactorial model can be formulated in these terms. The choice of method will depend chiefly on the design of the experiment and the ease with which a data summary can be obtained without significant loss of information. Examples are given in which the causes of variation show different degrees of detectable complexity. A variety of experimental designs yield behavioural data which illustrate the contribution of additive and non-additive genetical effects, the mating system, sibling and cultural effects, the interaction of genetical effects with age and sex. The discrimination between alternative hypotheses is often difficult. The extension of the approach to the analysis of multiple measurements and discontinuous traits is considered.
DATE PUBLISHED
1978 Dec
HISTORY
PUBSTATUS PUBSTATUSDATE
pubmed 1978/12/01
medline 1978/12/01 00:01
entrez 1978/12/01 00:00
AUTHORS
NAME COLLECTIVENAME LASTNAME FORENAME INITIALS AFFILIATION AFFILIATIONINFO
Eaves LJ Eaves L J LJ
Last KA Last K A KA
Young PA Young P A PA
Martin NG Martin N G NG
INVESTIGATORS
JOURNAL
VOLUME: 41
ISSUE: 3
TITLE: Heredity
ISOABBREVIATION: Heredity (Edinb)
YEAR: 1978
MONTH: Dec
DAY:
MEDLINEDATE:
SEASON:
CITEDMEDIUM: Print
ISSN: 0018-067X
ISSNTYPE: Print
MEDLINE JOURNAL
MEDLINETA: Heredity (Edinb)
COUNTRY: England
ISSNLINKING: 0018-067X
NLMUNIQUEID: 0373007
PUBLICATION TYPE
PUBLICATIONTYPE TEXT
Journal Article
Review
COMMENTS AND CORRECTIONS
GRANTS
GENERAL NOTE
KEYWORDS
MESH HEADINGS
DESCRIPTORNAME QUALIFIERNAME
Adoption
Environment
Female
Genetics, Behavioral
Genetics, Medical
Genotype
Humans
Mathematics
Models, Biological
Pedigree
Phenotype
Pregnancy
Twins
SUPPLEMENTARY MESH
GENE SYMBOLS
CHEMICALS
OTHER ID's