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Editorial
. 2019 Jun 13;10(6):450.
doi: 10.3390/genes10060450.

Identification of Disease Risk DNA Variations is Shaping the Future of Precision Health

Affiliations
Editorial

Identification of Disease Risk DNA Variations is Shaping the Future of Precision Health

Walid D Fakhouri et al. Genes (Basel). .

Abstract

In recent years, the knowledge generated by decoding the human genome has allowed groundbreaking genetic research to better understand genomic architecture and heritability in healthy and disease states. The vast amount of data generated over time and yet to be generated provides the basis for translational research towards the development of preventive and therapeutic strategies for many conditions. In this special issue, we highlight the discoveries of disease-associated and protective DNA variations in common human diseases and developmental disorders.

Keywords: alternative splicing and mRNA stability; alternative transcriptional start site; coding DNA variations; genomic evolution; noncoding DNA variations; post-transcriptional and -translational regulation.

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Conflict of interest statement

The authors declare no conflicts of interest.

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References

    1. Lindblad-Toh K., Garber M., Zuk O., Lin M.F., Parker B.J., Washietl S., Kheradpour P., Ernst J., Jordan G., Mauceli E., et al. A high-resolution map of human evolutionary constraint using 29 mammals. Nature. 2011;478:476–482. doi: 10.1038/nature10530. - DOI - PMC - PubMed
    1. Maurano M.T., Humbert R., Rynes E., Thurman R.E., Haugen E., Wang H., Reynolds A.P., Sandstrom R., Qu H., Brody J., et al. Systematic localization of common disease-associated variation in regulatory DNA. Science. 2012;337:1190–1195. doi: 10.1126/science.1222794. - DOI - PMC - PubMed
    1. Ward L.D., Kellis M. Interpreting noncoding genetic variation in complex traits and human disease. Nat. Biotechnol. 2012;30:1095–1106. doi: 10.1038/nbt.2422. - DOI - PMC - PubMed
    1. Manocha S., Farokhnia N., Khosropanah S., Bertol J.W., Santiago J.J., Fakhouri W.D. Systematic review of hormonal and genetic factors involved in the nonsyndromic disorders of the lower jaw. Dev. Dyn. 2019;248:162–172. doi: 10.1002/dvdy.8. - DOI - PubMed
    1. Williams M.A., Biguetti C., Romero-Bustillos M., Maheshwari K., Dinckan N., Cavalla F., Liu X., Silva R., Akyalcin S., Uyguner Z.O., et al. Colorectal Cancer-Associated Genes Are Associated with Tooth Agenesis and May Have a Role in Tooth Development. Sci. Rep. 2018;8:2979. doi: 10.1038/s41598-018-21368-z. - DOI - PMC - PubMed

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