A recent article published in Cell Death Discovery has explored digestive symptoms of COVID-19 and the potentially pathogenic route of […]
Researchers at The Ohio State University have developed an integrated database known as scREAD – single-cell RNA-Seq database for Alzheimer’s […]
A new genetics service known as WINGS (Wales Infants’ and Children’s Genome Service) was launched last week. The service aims […]
Jo Balfour, one of the founding members and current Operations Manager at Cambridge Rare Disease Network (CRDN), has collaborated with […]
A study has found that rare genetic alterations in the TLR7 gene may have predisposed two sets of brothers who […]
Autism spectrum disorder (ASD) affects one in 54 children in the US and is associated with a heritability between 50-90%. […]
The current COVID-19 pandemic has revealed that increased age and the presence of co-existing health conditions, such as cancer, cardiovascular, […]
Since the discovery of the CRISPR-Cas9 system in 2012, the potential of editing genes for improved agricultural output and treatment […]
A recent article published in Nature, describes a breakthrough in our knowledge of the human genome with the first gapless, […]
A new single-cell study has found that aneuploidy is common in early-stage human embryos, a finding that may have implications […]
