Groundbreaking ONS statistics expose how parental consanguinity and substance abuse are contributing to tragic infant deaths across Britain, with experts calling for urgent public health intervention.
Exclusive investigation reveals how Russian leaders from Stalin to Putin have pursued scientific immortality through secret research programmes and controversial life-extension technologies.
Groundbreaking Cambridge research reveals how the brain's 'recycling system' fails in Alzheimer's, opening doors to revolutionary new treatments that could slow or prevent the devastating disease.
An investigation reveals how AI-generated research papers and soaring profit margins are pushing academic publishing toward breaking point, threatening scientific integrity worldwide.
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.
Revolutionary Cambridge study reveals how rogue PINK1 protein acts as 'master switch' for Parkinson's, opening new pathways for treatments that could slow or prevent disease progression.
Groundbreaking research from the Francis Crick Institute reveals how immune system activation plays crucial role in Parkinson's advancement, opening new treatment possibilities.
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.
New research explores whether a cheeky pint could actually boost your foreign language skills, challenging conventional wisdom about alcohol's effects on cognitive performance.
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 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 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.
Exclusive investigation reveals US government agency sanctioned controversial experiments transplanting human foetal tissue into lab animals, sparking fierce ethical debate.
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.