Testing toddlers for inherited heart disease
Blood test at birth could reveal genetic high cholesterol levels, potentially preventing heart problems developing in the future
The life of a cell
From the 17th century to the latest Nobel Prize winner - could we now be closer than ever in our understanding of the building blocks of all life?
The need for diversity in genomic data
Genomic research calls for broader genetic representation to ensure future healthcare could be truly personalised
The first ‘three-parent baby’ – of many?
Birth of baby boy with DNA from three parents puts ethical debate on mitochondrial transfer technique back in the spotlight
Liquid biopsy – a new era in personalised medicine?
Examining the promises and challenges of exciting advances taking place in genetic testing, aiming to improve diagnosis and reduce patient risk
Gene editing meets gene therapy
Despite continued ethical debate, latest advances in gene editing technologies are poised to transform patient treatment
A shot of young blood: from the divine to epigenomics
Exploring the evolution of the blood transfusion, from 17th century experiments to cell rejuvenating potential of new treatments
Examining liquid biopsy in cancer management
Less-invasive method touted as potentially revolutionary for cancer care – could this mean the end for tissue biopsies?
Congenital heart disease study reveals inheritance factor
Examining the genetic roots of cardiac conditions and how further research could bring benefits to patients
Genomics and intellectual disability
Looking into the future of genetic testing for developmental disorders and the promise of genomic insight yet to come
Harnessing the benefits of genomic data
Data sharing review puts focus on challenges surrounding use of patient information for healthcare research
The genetics of obesity
Latest genomic research explores genetic risk of excessive weight gain - are the causes of obesity environmental or is the answer in our DNA?