The Generation Study, which is now available at Nottingham University Hospitals (NUH) NHS Trust, tests for more than 200 rare ...

Routine newborn screening (NBS) has transformed early disease detection. However, traditional biochemical tests limit the range of conditions that can be identified at birth. Next-generation ...

Patients will be able to find out whether they have genes linked to cancer using a world-leading tool developed by the NHS.

SAN DIEGO--(BUSINESS WIRE)--Today, Fore Genomics, a leader in pediatric genetic health screening, announced a strategic partnership with Inocras, a leading innovator in whole genome sequencing (WGS) ...

Preterm babies face greater health risks from the moment they are born. Their organs, immune systems, and metabolic pathways are not fully developed, making them more vulnerable to complications.

Expanded partnership to help increase patient access to critical genetic screening services including genetic counseling and test result turnaround time "Genetic screening is a vital part of fertility ...

Background: During the past two decades, the attention of public health has been drawn to premarital genetic screening (PGS) programs to reduce birth defects and avoid genetic disorders. In Jordan, ...

Leading genomic health experts from Monash University are calling for urgent government funding to progress the development ...

Routine genetic testing for maturity-onset diabetes of the young (MODY) could be cost-effective or even save money, depending on the price of the test and the prevalence of MODY in the population ...

Studying over 100,000 embryos revealed genetic factors behind chromosome segregation issues that lead to aneuploidy, ...