Author Thomas King reveals he has no Native heritage
Award-winning author Thomas King, after a 40-year career writing on Native American experiences, shockingly admits he has no Cherokee ancestry following a genealogical investigation.
Award-winning author Thomas King, after a 40-year career writing on Native American experiences, shockingly admits he has no Cherokee ancestry following a genealogical investigation.
Prominent Canadian author Thomas King discovers genealogist found no evidence of Cherokee ancestry after Tribal Alliance Against Frauds investigation. Read the full story.
In an extraordinary medical breakthrough, 19-month-old Oscar Sparrow from West Midlands has been identified as the only person worldwide living with a never-before-seen genetic mutation, offering new hope for rare disease research.
A mother reveals how her daughter endured cruel bullying for years before doctors discovered her weight struggles were caused by rare Bardet-Biedl syndrome, exposing the hidden reality of genetic disorders.
Groundbreaking research reveals new method to identify cancer-causing genetic changes early, potentially revolutionising preventative care and saving thousands of lives through timely intervention.
The heartbreaking story of Isabelle Tate, a young girl from England fighting Charcot-Marie-Tooth disease, a rare genetic condition threatening her ability to walk and enjoy a normal childhood.
Discover how Mad Men star John Hamm's family history reveals unexpected connections to medieval England and a remarkable journey across centuries and continents.
Exclusive: The heartbreaking story of a family coping with their daughter's rare Cri Du Chat syndrome, revealing the daily challenges and emotional toll of caring for a child with complex needs.
Royal experts question Meghan's assertion of being 43% Nigerian after DNA test reveals different ancestry results, sparking debate about truth and identity.
The NHS is rolling out a groundbreaking genetic testing programme to identify thousands of Britons with undiagnosed hereditary haemochromatosis - a dangerous iron overload condition that can cause organ damage if untreated.
Groundbreaking genetic research uncovers surprising Roman and Latin heritage in New Orleans residents, challenging conventional understanding of the city's European roots.
An investigative journey into the lives of the Whittakers, known as America's most inbred family, uncovering their isolated existence and the genetic consequences of generations of intermarriage.
From Oscar winners to pop icons, discover the surprising British heritage of famous American celebrities that will leave you utterly astonished.
Groundbreaking research from the University of Sheffield suggests vigorous exercise may accelerate motor neurone disease onset in those with predisposing genes, challenging fitness norms.
Conservative commentator Charlie Kirk's alarming claim about Utah's DNA collection practices sparks debate over genetic privacy rights and government overreach in criminal investigations.
Groundbreaking research reveals how a specific gene disrupts insulin production in the pancreas, offering new hope for millions living with diabetes worldwide.
Married at First Sight favourite Emma Barnes opens up about her devastating fertility struggles and genetic condition discovery while trying for a baby with husband Matt.
Groundbreaking research uncovers significant genetic differences that make women more vulnerable to depression, challenging long-held assumptions about mental health gender disparities.
Comedian and TV personality Rosie O'Donnell reveals she's obtained Irish citizenship, citing her opposition to Donald Trump's presidency as a key motivation behind her decision to secure an EU passport.
EastEnders actress Kellie Bright opens up about her family's emotional journey navigating her son's rare genetic disorder and the daily challenges they face.
Shocking new scientific research proposes that humanity's genetic blueprint contains evidence of extraterrestrial manipulation, challenging everything we know about human evolution.
After nearly five decades of silence, Florida authorities have finally identified the perpetrator in Susan Perkins' shocking 1978 kidnapping case, bringing long-awaited closure to her grieving family.
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.
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.