With Strand Life Sciences, Reliance is pushing genetic testing toward the mainstream. Incumbents, regulators and doctors are ...

A team of Indian researchers has identified a rare USP18 gene mutation linked to recurrent neurological decline in ...

In Armenia, outdated diagnostic systems lead to 90% of amniocentesis procedures being unnecessary, forcing many pregnant ...

Today at the San Antonio Breast Cancer Symposium (SABCS), researchers presented the initial findings from a major multi-year collaboration between the ECOG-ACRIN Cancer Research Group (ECOG-ACRIN) and ...

Exact Sciences Corp. , a leading provider of cancer screening and diagnostic tests, today announced the first clinical study results from its Oncodetect® molecular residual disease (MRD) test in ...

BENGALURU: A team of doctors in Bengaluru has identified a previously unknown KDM6B gene variant in a 10-year-old boy struggling with autism and developmental delays. The child, who also had Attention ...

Indian researchers have identified a rare USP18 gene mutation linked to recurrent neurological decline in children. The rare USP18 gene mutation offers crucial insights into a neurological disorder ...

A retrospective real-world analysis presented at the 2025 ASH Annual Meeting and Exposition showed that circulating tumor DNA (ctDNA) detected at the end of treatment (EOT) was a prognostic indicator ...

Health experts say the proposed Assisted Reproductive Technology Bill could close gaps by enforcing genetic screening, donor ...

Challenging federal funding cuts, minimal residual disease, and a busy field of CAR T-cell candidates characterized this year ...