Reflections on the field of human genetics: A call for increased disease genetics theory

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Abstract

Development of human genetics theoretical models and the integrationof those models with experiment and statistical evaluation are criticalfor scientific progress. This perspective argues that increased effort in disease genetics theory, complementing experimental, and statistical efforts, will escalate the unraveling of molecular etiologies of complexdiseases. In particular, the development of new, realistic disease genetics models will help elucidate complex disease pathogenesis, and the predicted patterns in genetic data made by these models will enable the concurrent, more comprehensive statistical testing of multiple aspects of disease genetics predictions, thereby better identifying disease loci. By theoretical human genetics, I intend to encompass all investigations devoted to modeling the heritable architecture underlying disease traits and studies of the resulting principles and dynamics of such models. Hence, the scope of theoretical disease genetics work includes constructionand analysis of models describing how disease-predisposing alleles (1) arise, (2) are transmitted across families and populations, and (3) interact with other risk and protective alleles across both the genome and environmental factors to produce disease states. Theoretical work improves insight into viable genetic models of diseases consistent with empirical results from linkage, transmission, and association studies as well as population genetics. Furthermore, understanding the patterns of genetic data expected under realistic disease models will enable more powerfulapproaches to discover disease-predisposing alleles and additional heritable factors important in common diseases. In spite of the pivotal roleof disease genetics theory, such investigation is not particularly vibrant.

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APA

Schrodi, S. J. (2016). Reflections on the field of human genetics: A call for increased disease genetics theory. Frontiers in Genetics, 7(JUN). https://doi.org/10.3389/fgene.2016.00106

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