Contribution of rare and common variants determine complex diseases-Hirschsprung disease as a modelAlves, M. M., Sribudiani, Y., Brouwer, R. W. W., Amiel, J., Antinolo, G., Borrego, S., Ceccherini, I., Chakravarti, A., Fernandez, R. M., Garcia-Barcelo, M-M., Griseri, P., Lyonnet, S., Tam, P. K., van IJcken, W. F. J., Eggen, B. J. L., te Meerman, G. J. & Hofstra, R. M. W., 1-Oct-2013, In : Developmental Biology. 382, 1, p. 320-329 10 p.
Research output: Contribution to journal › Article › Academic › peer-review
Finding genes for complex diseases has been the goal of many genetic studies. Most of these studies have been successful by searching for genes and mutations in rare familial cases, by screening candidate genes and by performing genome wide association studies. However, only a small fraction of the total genetic risk for these complex genetic diseases can be explained by the identified mutations and associated genetic loci. In this review we focus on Hirschsprung disease (HSCR) as an example of a complex genetic disorder. We describe the genes identified in this congenital malformation and postulate that both common 'low penetrant' variants in combination with rare or private 'high penetrant' variants determine the risk on HSCR, and likely, on other complex diseases. We also discuss how new technological advances can be used to gain further insights in the genetic background of complex diseases. Finally, we outline a few steps to develop functional assays in order to determine the involvement of these variants in disease development. (C) 2013 Elsevier Inc. All rights reserved.
|Number of pages||10|
|Publication status||Published - 1-Oct-2013|
- Hirschsprung disease, Rare variants, GWAS, Next generation sequencing, Systems biology, Functional assays, GENOME-WIDE ASSOCIATION, ENTERIC NERVOUS-SYSTEM, CENTRAL HYPOVENTILATION SYNDROME, SMAD-INTERACTING PROTEIN-1, SHAH-WAARDENBURG SYNDROME, RECEPTOR TYROSINE KINASE, RET PROTOONCOGENE, NEURAL CREST, ENDOTHELIN-3 GENE, MULTIGENIC INHERITANCE