Genetic testing for hereditary arrhythmia and cardiomyopathy in an area with known founder effects on local genetic variants ...

As genetic and biomarker tests become more common, so do new therapies that target specific tumor types and may lead to ...

Testing is recommended for those with personal and family histories of several types of cancer — including pancreatic and ...

March is Cerebral Palsy Awareness Month. Dr. Paul Kruszka is Chief Medical Officer at GeneDx, a commercial laboratory ...

Our goals are to expand access to genomic testing and develop cutting-edge genomic testing to help more families get answers ...

Researchers at the University of Washington and Seattle Children's found that using exclusion-based criteria to refer infants for genetic testing in the NICU led to more diagnoses and at earlier ages.

The latest research led from Manchester could revolutionize the diagnosis of Perrault syndrome, a rare genetic condition that ...

High-throughput genetic testing identifies 25% more rare disease risks, empowering families with early detection & prevention. Learn more this World Rare Disease Day!

The following is a summary of "Diagnosis, screening, and follow-up of patients with familial interstitial lung disease: ...

Representative Gus Bilirakis (R-FL) has introduced a bipartisan, bicameral bill to improve access to molecular diagnostic testing for rare cancer patients. N ...

It's estimated 65,000 New Zealand are already living with the eye disease glaucoma, but are totally unaware. Early stage glaucoma has no symptoms until damage has already been caused. But if caught ...