The discovery of a pancreatic gene found to be specific to only humans and apes may aid in the understanding and treatment of type 1 diabetes...
Researchers have identified four new breast-cancer-associated genes that have the potential to help improve clinical screening for women at risk...
Genetic variants previously thought to cause premature menopause are unlikely to be solely responsible for the condition, researchers have revealed...
Artificial Intelligence technology could use retinal scans to aid clinicians in diagnosing rare inherited eye conditions...
A rare gene mutation that may increase risk of breast cancer, has been identified in women of Polish descent...
A genetic link between unexplained infertility and diseases such as cancer, heart disease and Parkinson's disease in women has been discovered...
A large-scale genetic analysis has identified ten genes that increase a person's susceptibility to Crohn's disease, expanding scientist's understanding of this complex condition...
Genetic screening in most couples reveals just five percent of the genetic risk of their child developing a severe neurodevelopmental disorder...
The Royal College of Obstetricians and Gynaecologists hosted a free webinar on Genomics in Perinatal Medicine, which was a helpful walk-through of technical and practical aspects of whole exome sequencing in antenatal care, alongside ethical issues and parental perspectives…
Analysis of recently released exome sequence data has identified an association between rare genetic variants and cardiometabolic diseases, such as diabetes and heart failure...
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