hearing loss | GenomeWeb

hearing loss

Researchers from Taiwan followed dozens of children who screened positive for deafness-related genotypes at birth, identifying those with hearing loss over six years.

This Week in PLOS

In PLOS this week: GWAS links gene to noise-induced hearing loss in mice, population genetics of malaria parasites, and more.

By testing hundreds of children with brain tumors who were treated with cisplatin, researchers identified risk variants related to cisplatin ototoxicity.

In preparation for the launch, the laboratory is currently exploring the test in a clinical research setting and is hoping to sequence its first genome next month.

University of Iowa and Baylor College of Medicine researchers reported that they have developed and tested a method that uses target enrichment and massively parallel sequencing to find variants behind non-syndromic hearing loss.

In PLOS this week: role for Notch signaling in congenital heart disease, sciatica risk variants, and more.

Researchers in China have used the CRISPR/Cas9 genome editing approach to alter the length of hair fibers in cashmere goats.

According to ScienceInsider, the Scripps Research Institute and the California Institute for Biomedical Research are merging.

National Cancer Institute researchers didn't report severe adverse events to Food and Drug Administration in a timely manner, the Wall Street Journal reports.