2004
DOI: 10.1093/bmb/ldh012
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Human genetic variation and health: new assessment approaches based on ethnogenetic layering

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Cited by 31 publications
(20 citation statements)
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“…Parra et al 2003;Jackson 2004;Helgason et al 2005). Geographic ancestry has also in many instances been considered a useful device for making inferences about an individual's ancestry, which may help to predict whether a person carries specific genetic risk factors that influence health (cf.…”
Section: Discussionmentioning
confidence: 99%
“…Parra et al 2003;Jackson 2004;Helgason et al 2005). Geographic ancestry has also in many instances been considered a useful device for making inferences about an individual's ancestry, which may help to predict whether a person carries specific genetic risk factors that influence health (cf.…”
Section: Discussionmentioning
confidence: 99%
“…Assessing 400 years of genetic variation data should allow for the observation of any microethnic substructure (Microethnic substructure refers to within group population stratification that is the result of local patterns of social and cultural identity. Microethnic substructure occurs within macroethnic (i.e., socio‐racial) groupings; Jackson, 2004, 2008) and the identification of relevant polymorphisms contributing to the etiology of HTN and stroke in this group. The historically recent 400 years of the transatlantic trade in enslaved Africans from West and West Central Africa and their transport to the Americas via the Middle Passage may have exposed these forced migrants to selection for electrolyte conservation (Jackson, 1991).…”
Section: Resultsmentioning
confidence: 99%
“…This different form of behavioral change has shown equally capable of influencing genetic change, and the persistence of type 2 diabetes. One must remember that diet, along with subsistence, infectious disease, and other sociocultural and environmental filters must be given the attention they deserve in the study of any worldly distributed disorder (Jackson, 2004). Both these filters-by their ability to fill the gap and complicate the pathway between a coded genotype and an expressed phenotype-and the regional subtleties already described have a lot to tell us if we are willing to listen.…”
Section: An Analogymentioning
confidence: 99%