| Literature DB >> 29477192 |
Lam C Tsoi1, Matthew T Patrick2, James T Elder3.
Abstract
Complex cutaneous disorders result from the combined effect of many different genes and environmental factors, with individual genetic variants often having only a modest effect on disease risk. The ability to examine large numbers of samples is required for correlating genetic variants with diseases/traits. Technological advances in high-throughput genotyping, along with mapping of the human genome and its associated inter-individual variation, have allowed genetic variants to be analyzed at high density in large case-control cohorts for many diseases, including several major skin diseases. These genome-wide association studies focus on showing differences in the frequencies of variants between case and control groups, rather than co-transmission of a variant and disease through a family, as is done in linkage studies. In this review, we provide overall guidance for genome-wide association study analysis and interpreting the results. Additionally, we discuss challenges and future directions for genome-wide association studies, focusing on translation of findings to provide biological and clinical implications for dermatology.Entities:
Mesh:
Year: 2018 PMID: 29477192 PMCID: PMC5903459 DOI: 10.1016/j.jid.2018.01.004
Source DB: PubMed Journal: J Invest Dermatol ISSN: 0022-202X Impact factor: 8.551