Silicon Valley's embryo testing sparks ethics debate
A groundbreaking yet contentious embryo screening method in Silicon Valley is sparking ethical debates. Could this redefine parenthood?
A groundbreaking yet contentious embryo screening method in Silicon Valley is sparking ethical debates. Could this redefine parenthood?
Researchers in Colorado have genetically engineered rabbits with eerie tentacle-like appendages sprouting from their heads, sparking ethical debates and scientific fascination.
Groundbreaking DNA research uncovers unexpected British ancestry in modern Mexicans, tracing back to 16th-century colonisers and African slaves.
A heartbroken mother reveals her four-year-old son's eerie premonition before he tragically passed away from a rare genetic condition.
A provocative exhibition in Paris features portraits created using strangers' DNA, raising ethical questions about privacy and art.
Kathleen Folbigg, once dubbed 'Australia's worst female serial killer', has been pardoned after new scientific evidence cast doubt on her convictions. Discover the full story behind this shocking case.
A woman's life was turned upside down after a DNA test revealed her father wasn't biologically related to her. Read her emotional journey of discovery.
A toddler initially treated for a fever was later diagnosed with a rare genetic illness. Doctors now hope a £500,000 treatment can slow the disease's progression.
New research reveals potential genetic markers linked to chronic fatigue syndrome, offering hope for better diagnosis and treatment.
A groundbreaking study has identified key genetic markers linked to Myalgic Encephalomyelitis (ME/CFS), offering new hope for understanding this debilitating condition.
Former Geordie Shore star Aaron Chalmers and his ex-partner Talia Oatway reveal their son Oakley's battle with Apert Syndrome, a rare genetic condition.
Scientists have identified key genetic markers linked to chronic fatigue syndrome, offering new hope for diagnosis and treatment.
A journalist recounts their unsettling encounter with the Whittaker family, known as one of America's most inbred families, revealing their struggles and the harsh realities of genetic isolation.
A rare genetic condition means some individuals never experience hunger, leading to unique health challenges and lifestyle adjustments. Discover their fascinating stories.
Actor David Suchet shares his family's journey with tuberous sclerosis, a rare genetic condition affecting his grandson, to raise awareness and support research.
Renowned actor David Suchet shares his family's journey with tuberous sclerosis, advocating for greater awareness and research into the rare genetic condition.
Beloved actor David Suchet reveals his grandson's battle with a rare genetic disease, sharing the family's emotional journey and raising awareness for the condition.
A family's terrifying ordeal with heart attacks has prompted vital health checks, revealing a hidden genetic condition.
A baby boy's persistent crying was dismissed as colic before a devastating diagnosis revealed a rare genetic disorder. His parents share their emotional story.
Discover how the MyHeritage DNA test kit can help you explore your genetic roots with detailed ethnicity estimates and family matching features.
A father emotionally shares his family's struggle with his daughter's rare genetic disorder during an appearance on ITV's This Morning, raising awareness and touching viewers' hearts.
Groundbreaking research reveals why certain individuals avoided COVID-19 infection entirely, pointing to a remarkable genetic advantage that kept them safe.
A mother's harrowing 999 call reveals the NHS crisis as her 12-year-old son with a rare genetic disorder is left without a hospital bed for days.
A revolutionary genetic test may soon predict obesity risk years before symptoms appear, offering hope for early intervention and prevention.
After years of uncertainty, a determined mother finally uncovers the truth behind her daughter's baffling health condition—a rare genetic disorder that had eluded doctors for years.
A groundbreaking DNA test may soon help identify children at risk of obesity early, offering parents and doctors a chance to intervene before health issues arise.
The UK's groundbreaking mitochondrial donation IVF technique marks a significant but careful step in genetic innovation, offering hope to families affected by mitochondrial diseases.
The UK has become the first country to officially approve a groundbreaking IVF technique that incorporates DNA from three individuals, aiming to prevent genetic disorders in babies.
A groundbreaking IVF procedure has successfully prevented mitochondrial disease in eight babies, marking a significant milestone in genetic medicine.
A grieving mother shares her devastating story after losing her daughter to mitochondrial disease, a rare and often misunderstood condition.