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

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 ...

The inherited mutation substantially increases the chance of developing lung cancer, including in people who don't smoke.

Among cancer patients who received personalized support and navigation services from experts throughout the genetic testing ...

Smoking is one of the biggest contributors to lung cancer, but anywhere from 10-20% of cases in the U.S. each year are diagnosed in people who never smoked. In a new study published in Science, ...

A genetic mutation that raises lung cancer risk was much more common among those born in Southeastern states than elsewhere ...

Integrating new AI screening tools for BRCA and HRD breast-cancer mutations into routine care could lead to earlier detection, more precise treatment, and lives saved. If they are aware of the threat, ...

Identification of a specific genetic mutation in patients with non-small-cell lung cancer (NSCLC) helps clinicians select the best treatment option. Potential NSCLC patients usually undergo invasive ...

Mayo Clinic researchers report encouraging early results from an experimental therapy targeting the genetic cause of a rare ...

The two sisters opened up about their mom’s journey with cancer on their Netflix series, ‘Earle Meets World’ ...

One rare inherited mutation raised lung cancer risk more than smoking did, and the effect was strongest in people who never ...

Among cancer patients who received personalized support and navigation services from experts throughout the genetic testing process, their first-degree relatives – parents, siblings and children – ...