Exclusive: As heart attack and stroke cases surge among people in their 50s, a leading cardiologist shares the crucial warning signs most people miss. Discover how to protect your heart health today.
A UK family shares their emotional journey as their newborn son battles a rare neonatal disease, facing months of uncertainty and fighting for answers in the NHS system.
Exclusive investigation reveals how Mark and Rebecca Black, raised as brother and sister in Scotland, discovered they were biological parents and entered into a secret marriage that stunned their community.
Groundbreaking research from UK scientists revolutionises fertility treatment by transforming skin cells into viable human eggs, offering new hope for infertility and genetic disorders.
The emotional journey of a family who fought for answers after noticing developmental delays in their son, culminating in a rare MICPCH syndrome diagnosis.
Thousands of British women carrying the BRCA1 gene mutation face increased ovarian cancer risk. New NHS programme offers regular blood tests to detect early signs.
Austin police employ groundbreaking DNA technology to identify alleged bicycle thief who left genetic evidence on snack wrapper at crime scene
Exclusive: The heart-wrenching story of a mother's battle to save her daughter, Arianna, from the ultra-rare GRIN1 gene mutation, a condition so uncommon it affects just a handful of people globally.
A revolutionary new drug, pridopidine, has shown significant promise in slowing the progression of Huntington's disease, offering new hope to UK families affected by the genetic condition.
Groundbreaking medical research from UCL and University College London Hospitals has successfully lowered levels of the toxic protein that causes Huntington's disease using an innovative genetic therapy injected into the spinal fluid.
The Trump administration has released a divisive report suggesting environmental factors are the primary cause of autism, drawing immediate condemnation from leading researchers and autism advocacy groups who warn it could dangerously misdirect public hea
The parents of a baby girl born without eyes due to an incredibly rare genetic condition share their emotional journey and determination to give their daughter the best life possible.
Groundbreaking US court ruling forces Tylenol manufacturers to pay £1.5 billion in compensation after scientific evidence confirms prenatal painkiller use increases autism risk by 20%.
Groundbreaking research from Queen's University Belfast uncovers the true genetic origins of the Irish people, tracing ancient DNA back to mass migrations from the Middle East and Eastern Europe.
An East Sussex mother's heart-wrenching account of her son's ultra-rare GRIN2B condition, which causes extreme violence, property destruction, and a desperate fight for support.
Groundbreaking study reveals the remarkable genetic adaptations of the Turkana people, offering new insights into human evolution and survival in one of Africa's most unforgiving landscapes.
Jade, 33, went for a routine blood test expecting nothing unusual. Weeks later, she received a life-altering diagnosis of Hereditary Angioedema (HAE) - a rare genetic disorder with no cure. Her story highlights the importance of recognising unusual sympto
A landmark study from the Natural History Museum reveals how British DNA is reshaping our understanding of African genetic history, uncovering centuries of migration and diversity.
Scientists crack the genetic code of the Anopheles funestus mosquito, a major malaria vector in Africa, paving the way for innovative genetic control strategies to combat the deadly disease.
Exclusive: A teenager's life has been defined by unimaginable pain and hospital isolation due to the cruel genetic condition sickle cell disease, robbing her of a normal childhood and future dreams.
Groundbreaking genetic research brings the dream of resurrecting the extinct dodo bird one step closer to reality. Scientists achieve a major milestone in sequencing its genome, sparking both excitement and ethical debate.
A revolutionary AI system developed by UK researchers can now forecast an individual's genetic risk for over 1000 conditions, transforming preventive healthcare and early diagnosis.
A UK mother's extraordinary bond with her newborn daughter has captured hearts worldwide after the baby was born with an identical facial birthmark. This rare genetic phenomenon defies odds and celebrates the unique beauty of family connections.
World Athletics President Seb Coe calls for a major shift towards genetic and biological testing to create a more robust anti-doping system and ensure a level playing field for all athletes.
Groundbreaking research from the University of Oxford shows a dramatic decline in teen pregnancies across the UK. However, the study exposes a troubling reality: girls from the most deprived backgrounds remain disproportionately at risk, highlighting a de
In a landmark medical breakthrough, a UK patient is living well with a genetically modified pig kidney. This NHS-backed procedure at a top US hospital could revolutionise organ transplantation and slash waiting lists.
The Seattle Police Department is under fire from the ACLU for allegedly building a 'covert DNA database' by collecting genetic material from hundreds of individuals, including a disproportionate number of Native Americans, without consent or criminal char
Exclusive: A major forensic breakthrough using advanced DNA technology has provided a crucial link in the infamous Gilgo Beach serial killings investigation, potentially unmasking a suspect in the Long Island murder mystery that has haunted the US for ove
Algerian boxing champion Imane Khelif launches a formal appeal against her disqualification from the Women's World Boxing Championships over disputed genetic sex test results, challenging the sport's gender policies.