Two studies published today in the American Journal of Human Genetics show the potential for genomic screening in newborns to address high rates of infant hospitalization and mortality in the United ...

A new study published in JCO Precision Oncology has identified a relatively simple method to predict the cancer patients most likely to develop severe toxicities from chemotherapy. If doctors can ...

Every year, millions of newborns undergo routine heel-prick screening, a simple test that can mean the difference between a healthy life and catastrophic disability. Now, breakthroughs in ...

San Diego – Dec. 5, 2024 – Two studies published today in the American Journal of Human Genetics show the potential for genomic screening in newborns to address high rates of infant hospitalization ...

SAN DIEGO--(BUSINESS WIRE)--Today, Fore Genomics, a leader in pediatric genetic health screening, announced a strategic partnership with Inocras, a leading innovator in whole genome sequencing (WGS) ...

When most couples plan a pregnancy, genetics rarely makes the list. Timing, finances, work schedules, these feel immediate ...

In 2023, Jill Martin took a test that changed her life. She underwent genetic testing for breast cancer and learned she had a BRCA2 mutation, which increases one’s risk of developing breast and other ...

When it came time to start a family, Sarah Elizabeth Orlando, 33, knew she would go about it differently. Before she was born, an in-utero amniocentesis had confirmed she carried the gene for fragile ...

A child born with Thalassemia Major may require blood transfusions every two to four weeks for life. In many cases, this can be prevented if both parents know their carrier status before pregnancy.