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Genetic Research

Epigenetic map creates new insights into the cause of cancer and dementia

A new project is expected to help us understand diseases such as cancer and dementia. A major partnership involving Oxford Nanopore Technologies, UK Biobank, NHS England, Genomics England, and the UK government has made this possible.

Harnessing genomic data for early disease detection

Lorna Rothery spoke to Heidi Rehm, Chair of the Global Alliance for Genomics and Health, about steps to harness quality genomic data to support disease detection and the importance of collaboration in this endeavour.

Common Agricultural Policy post-2027 strategies

Stoyan Tchoukanov, EESC member and Rapporteur for the EESC opinion on Promoting autonomous and sustainable food production, shares with us strategies for the Common Agricultural Policy post-2027.

How AI is being used to predict breast cancer survival durations

Hailey Coverson, Data Scientist at Bayezian, discusses the complexities of genomic data, accounting for biases and inaccuracies and AI’s potential in supporting clinical decisions in breast cancer care.

AI breakthrough in cancer detection

AI model named Candycrunch has been designed to transform cancer detection through advanced sugar analysis.

Stem cell therapy shows promise for hirschsprung disease

A potential new treatment avenue has appeared for individuals suffering from Hirschsprung disease, a rare condition affecting the large intestine.

Exercise considered safe for people with hypertrophic cardiomyopathy in new guidelines

Recent revisions to guidelines for people with hypertrophic cardiomyopathy (HCM) aim to clear up confusion about exercise recommendations.

Oxford Study finds blood proteins could predict cancer risk years in advance

Researchers from Oxford Population Health's Cancer Epidemiology Unit have identified specific proteins in the blood that may predict a person's risk of developing various cancers over seven years before diagnosis.

New biomarker identified for early detection of Alzheimer’s and therefore earlier diagnosis

A recent study led by the Molecular and Cellular Neurobiotechnology group at the Institute for Bioengineering of Catalonia (IBEC) and the University of Barcelona...

The truth behind ApoE4 gene variant and your risk of developing Alzheimer’s Disease

Researchers have found evidence suggesting that lifestyle factors may play a pivotal role in mitigating the risk of Alzheimer's disease, even among individuals carrying the ApoE4 gene variant.

Unlocking the mystery of SCA4: A breakthrough on a disease that was previously unknown

After years of uncertainty, researchers at the University of Utah have discovered spinocerebellar ataxia 4 (SCA4), a rare neurological disease .

Cells possess a rapid decision-making system beyond DNA

Scientists at Moffitt Cancer Center have revealed a hidden layer of cellular intelligence that questions the traditional understanding of how cells operate.

Genomic sequencing: A game changer in our fight against COVID-19 and beyond

Ron Gutman, inventor, serial healthcare and technology entrepreneur, and Stanford University adjunct professor, discusses the emergence of genomic sequencing as a vital tool in mitigating global public health threats.

Insights into autism development, treatment and management

Researchers from Japanese institutions have revealed insights into the molecular mechanisms underlying autism spectrum disorder (ASD).

Can cows create insulin? Transgenic cow opens doors for sustainable human insulin production

Researchers have successfully developed the world's first transgenic cow capable of producing human insulin in her milk.

Europe takes a step towards gene-edited crops despite patent debate

The European Parliament voted to ease regulatory oversights on crops created through gene editing, which significantly departed from its longstanding suspicion towards genetically engineered organisms.

Changing the lives of people with hereditary angioedema through gene editing therapy

The lives of those who live with hereditary angioedema, a rare genetic disorder causing severe and unpredictable swelling attacks, may be transformed.

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