Genetic modification enhances “living drugs” for blood cancers
CAR T cells are patient-derived, genetically engineered immune cells. They are “living drugs” and constitute a milestone in…
Genomic study reveals colonial and Indigenous contributions to modern South Africans
A genomic analysis of over 1,200 people from across South Africa reveals how colonial-era European, Indigenous Khoe-San peoples,…
Scientists uncover 53 genetic clues that shape math ability beyond IQ
An exciting new study reveals the hidden genetic architecture of quantitative ability, showing how brain wiring and signaling…
PacBio Targets Carrier Screening, Aims to Simplify Genetic Testing
PacBio is known in the genomics space for its HiFi sequencing technology—which provides long, highly accurate reads. But…
Low dose of aspirin cuts recurrence risk in colorectal cancer with genetic mutation
A Swedish-led research team at Karolinska Institutet and Karolinska University Hospital has shown in a new randomized clinical…
Empowerment Through DNA Knowledge – Saucon Source
Jessica Burke of Allentown remembered she previously signed up to participate in the St. Luke’s DNA Answers research…
New genetic test redefines diagnosis and management of hereditary pancreatitis
A new genetic test developed at Mayo Clinic is redefining how clinicians diagnose and manage hereditary pancreatitis. Pancreatitis, inflammation…
Rare ABCA7 gene variants linked to Alzheimer’s risk
A new study from MIT neuroscientists reveals how rare variants of a gene called ABCA7 may contribute to…
Study uncovers three-way relationships between gut fungi, genetics and disease risk
A new genome-wide study uncovers evidence of the first three-way relationships between human genetic variation, variation in the…
BlueGenesLab Expands Genetic Panel to Include Three New GLP-1-Related Genes
SCOTTSDALE, Ariz., Sept. 08, 2025 (GLOBE NEWSWIRE) — BlueGenesLab, a precision genomics company headquartered in Scottsdale, Arizona, today…
Preclinical Data Spotlights Gene with Therapeutic Potential for Barth Syndrome
Barth Syndrome is a rare X-linked genetic condition caused by a mutation in the Tafazzin gene, which is…
Gene expression maps explain why diseases often occur together
By grouping patients based on gene activity, scientists show that shared molecular pathways, especially immune-related ones, help explain…