In genetic epidemiology, family studies are studies of whether a disease or trait "runs in a family". In other words, they are studies aimed at detecting the presence or absence of familial aggregation for the disease or trait, in which having a family history is associated with greater risk. The family research design can also be used to estimate penetrance for a given genotype, to conduct genetic association studies, and to study potential modifiers of an individual's genetic risk.[1][2] If a family study shows that a trait is familial, this is a necessary, but not sufficient, criterion for it to be established as genetically influenced.[3]
Types
There are three main types of family studies in genetics:
Those aimed at measuring the extent of familial aggregation for a trait
Familial aggregation is the practice of combing multiple data sets of different traits and/or characteristics in a family. [4]
Family history of disease is collected in case studies, which seeks if a certain disease of one family member increases the risk of that disease being passed down to others. This could be related to either genes or environmental factors.[5]
Genetic linkage occurs when two genes on a DNA sequence on the same chromosome are inherited together. [6]
This can occur with sex linked genes with the X or Y chromosome. Although it is more common to be inherited from the X chromosome because the Y chromosome has less genes attached. [7]
Association studies aimed at detecting loci with relatively small effects on risk.[8]
Locus (loci plural) is the physical location and position of a gene or genetic marker on the chromosome. [9]
Chromosomes carry genetic information across all of it, each gene having its specific location and position. There are 40,000 to 100,000 protein coding genes across human chromosomes. [10]
