Using machine learning framework to identify prognostic biomarkers in neuroblastoma
Neuroblastoma is the most common solid tumor in infants and accounts for nearly 15% of all pediatric cancer-related…
Exploring the genetic and clinical landscape of clubfoot
A new publication offers an extensive examination of clubfoot, a congenital deformity known as congenital talipes equinovarus (CTEV),…
Genetic testing can guide safer chemotherapy for gastrointestinal cancer patients
For some patients with gastrointestinal (GI) cancers like colorectal and pancreatic cancer, chemotherapy can cause severe, sometimes life-threatening…
Scientists reveal how rare gene mutations drive schizophrenia risk
Uncovering how rare genetic changes disrupt brain signaling and structure, this landmark study sheds new light on the…
Researchers classify how specific genetic mutations correspond to rare disorders
The NF-κB signaling pathway plays a pivotal role in how our bodies fight infection, heal, and regulate inflammation.…
Researchers pinpoint PRMT5 as a promising target for cancer drugs
A potential target for experimental drugs that block PRMT5 – a naturally occurring enzyme some tumors rely more…
AI identifies novel gene variants linked to Alzheimer’s risk
New AI-driven research reveals how advanced machine learning models not only confirm known Alzheimer’s genes but also spot…
Into the great genome: new tracker for Australia’s genomic biodiversity
23 July 2025
News Release
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Ancient viral DNA found to regulate human gene expression
A new international study suggests that ancient viral DNA embedded in our genome, which were long dismissed as…
Exploring the genetic link between COPD and abdominal aortic aneurysm
Announcing a new article publication for Cardiovascular Innovations and Applications journal. Chronic obstructive pulmonary disease (COPD) and abdominal…