Germline genetic screening can identify whether a patient with cancer has inherited genetic alterations in a gene or genes ...

Universal germline genetic testing of nearly 40,000 patients with solid tumors detected a substantial proportion of inherited gene variants that would have been missed by the standard germline testing ...

Among patients with cancer with a genetic variant that increases the risk for hereditary cancers, personalized support ...

Florida has launched a newborn genomic screening pilot program designed to test babies for more than 900 genetic conditions, ...

The number of treatments for rare genetic disorders is expected to increase sharply in the next several years.

Xytex today announced the expansion of its donor screening protocol to include hereditary cancer genetic testing, as the first donor candidates screened under the expanded protocol near completion of ...

New study suggests that settlement of the Pacific occurred in a migration process with what the authors call a series of ...

MyOme today announced CASRcade, a cascade genetic testing program sponsored by BridgeBio for families affected by Autosomal Dominant Hypocalcemia Type 1 (ADH1), a rare condition, yet a common genetic ...

Researchers at LMU Munich, the Max Planck Institute of Biochemistry, and Helmholtz Munich developed and published SPARCS on October 8, 2026, a microscopy-based CRISPR screening method that uses ...

A nationwide reproductive carrier screening program in Singapore using a customized 112-gene panel has identified at-risk ...

She had just diagnosed our 11-year-old daughter, Maya, with Nicolaides-Baraitser syndrome, a genetic condition so rare there ...

First-degree relatives—parents, siblings and children—of cancer patients who received personalized support and navigation services throughout the genetic testing process were significantly more likely ...