Florida has launched a newborn genomic screening pilot program designed to test babies for more than 900 genetic conditions, making it the first state-funded initiative of its kind in the nation.

Dr. Lamas, a contributing Opinion writer, is a pulmonary and critical care physician at Brigham and Women’s Hospital in Boston. See more of our coverage in your search results.Encuentra más de nuestra ...

New guidance co-led by University of Otago researchers could help more people with suspected inherited diseases receive a ...

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

EVANS, Ga., Oct. 5, 2026 /PRNewswire/ -- Xytex today announced the expansion of its donor screening protocol to include hereditary cancer genetic testing, as the first donor candidates screened under ...

Oregon will soon begin enrolling families in a nationwide research study that tests whether genome sequencing can be added to ...

One in eight women will receive a breast cancer diagnosis in their lifetime. But the journey isn’t the same for everyone. When it comes to a diagnosis or a treatment ...

C EGFR T790M gene variant face roughly 25 times the lung cancer risk of noncarriers, according to the largest-yet study of ...