1998
DOI: 10.1289/ehp.98106817
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Genes and the environment: their impact on children's health.

Abstract: Because the human population is biologically diverse and genetically heterogeneous, it is not surprising that differences in susceptibility to disease among individuals with or without exposure to environmental agents exist. Individuals vary greatly in their susceptibility to disease. This is true of adults and children. The etiologies of many diseases of childhood are due to a combination of factors, including genetic susceptibility and environmental exposures during vulnerable periods of ,development. Genes … Show more

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Cited by 16 publications
(17 citation statements)
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“…Environmental health researchers have determined that most human disease results from a combination of environmental exposures and genetic variation (20,21). However, it is not fully understood why certain people develop disease when challenged with environmental agents and others remain healthy.…”
Section: Individual Susceptibility and Predispositionmentioning
confidence: 99%
“…Environmental health researchers have determined that most human disease results from a combination of environmental exposures and genetic variation (20,21). However, it is not fully understood why certain people develop disease when challenged with environmental agents and others remain healthy.…”
Section: Individual Susceptibility and Predispositionmentioning
confidence: 99%
“…The rationale for interaction is the hypothesis that allelic subtypes of genes that play a role in genetic or metabolic regulation influence the individual's susceptibility towards environmental agents. More recently, this interest has been extended to developmental effects as well (47). The discovery of periconceptional folic acid deficiency as a preventable cause of neural tube defects (48,49), and the investigations that followed on the role of allelic subtypes in folic acid metabolism (50,51) boosted further birth defect studies.…”
Section: Germ Cells and Genesmentioning
confidence: 99%
“…The allele differ by a single base pair change, a guanine to cytosine transversion of coding nucleotide 177, which predicts the substitution of an asparagine for a lysine in the enzyme (15). In addition to human, the ALAD cDNAs for the mouse, rat, and Escherichia coli enzymes have been isolated and sequenced (18, 19 20).…”
Section: Introductionmentioning
confidence: 99%