In PNAS this week: sequencing analysis of Brooklyn measles cases, conserved neural transcriptional features that coincide with monogamy, and more.
The molecular test detects a form of herpes virus that can infect newborns and cause deafness.
The study provided whole-exome diagnostic sequencing for 106 newborns with hearing loss while also offering optional screening results for genes associated with childhood-onset conditions.
Investigators from the school will use the funding to continue a research program applying genomics to hearing loss screening and treatment.
The £550,000 award is part of a larger multi-partner grant to develop and implement a point-of-care test to avoid antibiotic-related hearing loss in newborns.
CBC News reports that a genetic study of hearing is relying on Newfoundland's founder population.
At the ACMG meeting, Cynthia Morton said that several projects, including her team’s SEQaBOO study, are exploring the utility of genomic testing in newborn hearing screening.
A Harvard-led team used genome editing to prevent inherited deafness in mice.
In Nature this week: genome-editing to treat hearing loss in mice, juvenile myelomonocytic leukemia subgroups, and more.
In PLOS this week: HIV-1 genetic diversity in Bangalore; gene variants and noise-induced hearing loss; and more.
Researchers are refining a tool to predict a woman's risk of developing breast cancer, according to the Guardian.
According to Stat News, the partial government shutdown in the US could soon affect the ability of the Food and Drug Administration to review new drugs.
In PNAS this week: gypsy moth genome sequenced, phylogenomic analysis of Polyneopterans, and more.
CNN reports that people's genes tend to have a greater influence on their risk of developing disease than their environment, but it varies by phenotype.