A clustered family history of breast, ovarian, and colon cancers appropriately triggered germline testing, with BRCA1 mutation status informing individualized risk stratification and counseling.

An estimated 170,000 Australians were diagnosed with cancer in 2025. Many people know the causes of cancer are partly genetic. But how do your genes, which contribute so much of what makes you you, ...

A study led by Harvard Medical School researchers shed new light on how even a single defective copy of the tumor-suppressor BRCA1 gene can increase patients’ risk of developing breast cancer.

Scientists at the University of Birmingham are a step closer to understanding the role of the gene BRCA1. Changes in this gene are associated with a high risk of developing breast and ovarian cancer.

People inherit two copies of each gene - one from each parent - an evolutionary fail-safe to ensure survival even when one of them doesn't function. For cancer-suppressor genes like BRCA1, researchers ...

The Norton & Elaine Sarnoff Center for Jewish Genetics is a supporting foundation of JUF, and is supported in part by the Michael Reese Health Trust.

A study reveals 1 in 4 Indian breast cancer patients carry inherited genetic variants beyond known BRCA genes, urging broader testing strategies.

"Here we are again. The Sidell women go through everything together," said my older sister as she looked tiny sitting in the oversized hospital chair about to have her first chemo treatment for breast ...

Association of glucagon-like peptide 1 receptor agonists with cancer risk in obesity adults with and without diabetes: A target trial emulation study. This is an ASCO Meeting Abstract from the 2025 ...

IN HER SHOES. BUT SHE’S TAKEN A HORRIBLE SITUATION AND SHE’S SOMEHOW MANAGING TO FIND A WAY TO LIVE THROUGH IT AND DO IT WITH GRACE AND INSPIRING SO MANY PEOPLE. AND WE’RE FOLLOWING THE JOURNEY OF ...