Abstract
The Y chromosome is the most gene-deficient chromosome in the human genome (though not the smallest chromosome) and has largely been sequestered away from large-scale studies of the effects of genetics on human health. Here I review the literature, focusing on the last 2 years, for recent evidence of the role of the Y chromosome in protecting from or contributing to disease. Although many studies have focused on Y chromosome gene copy number and variants in fertility, the role of the Y chromosome in human health is now known to extend too many other conditions including the development of multiple cancers and Alzheimer's disease. I further include the discussion of current technology and methods for analyzing Y chromosome variation. The true role of the Y chromosome and associated genetic variants in human disease will only become clear when the Y chromosome is integrated into larger studies of human genetic variation, rather than being analyzed in isolation.
| Original language | English (US) |
|---|---|
| Pages (from-to) | R296-R300 |
| Journal | Human molecular genetics |
| Volume | 30 |
| Issue number | 2 |
| DOIs | |
| State | Published - Oct 15 2021 |
ASJC Scopus subject areas
- Molecular Biology
- Genetics
- Genetics(clinical)
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