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Like many other medical conditions, obesity is the result of an interplay between environmental and genetic factors. [2] [3] Studies have identified variants in several genes that may contribute to weight gain and body fat distribution, although only in a few cases are genes the primary cause of obesity.
Nutritional genomics, also known as nutrigenomics, is a science studying the relationship between human genome, human nutrition and health. People in the field work toward developing an understanding of how the whole body responds to a food via systems biology, as well as single gene/single food compound relationships.
Genetic correlations are scientifically useful because genetic correlations can be analyzed over time within an individual longitudinally [41] (e.g. intelligence is stable over a lifetime, due to the same genetic influences – childhood genetically correlates = with old age [42]), or across diagnoses, allowing discovery of whether different ...
Set point theory can be construed as implying weight regulation in a wide or tight range around the set point, in a symmetric or in an asymmetric manner (i.e. treating weight gain and loss either the same or differently), and may apply to regulation of body fat levels specifically (in a multi-compartment model) or to overall body weight. Set ...
Gene–environment interaction (or genotype–environment interaction or G×E) is when two different genotypes respond to environmental variation in different ways. A norm of reaction is a graph that shows the relationship between genes and environmental factors when phenotypic differences are continuous. [1] They can help illustrate GxE ...
To support the hypothesis that core genes play a smaller than expected role, the authors describe three main observations: the heritability for complex traits is spread broadly, often uniformly, across the genome; genetic effects do not appear to be mediated by cell-type specific function; and genes in the relevant functional categories only ...
Since humans have many more genes on the X than the Y, there are many more X-linked traits than Y-linked traits. However, females carry two or more copies of the X chromosome, resulting in a potentially toxic dose of X-linked genes. [4] To correct this imbalance, mammalian females have evolved a unique mechanism of dosage compensation.
When more than one gene is involved, with or without the presence of environmental triggers, we say that the disease is the result of multifactorial inheritance. [ citation needed ] The more genes involved in the cross, the more the distribution of the genotypes will resemble a normal, or Gaussian distribution. [ 9 ]