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Latest genomic medicine News

Establishing Genomics Australia
Complex Diagnoses Can Be Solved With New Technology
UNSW researchers lead Premier’s Prizes, including Scientist of the Year
Genomics program designed for diverse communities starts recruiting
Remote UK Regions At Risk Of Genetic Disease
Total ban on the use of adverse genetic testing results in life insurance
Cost of whole-genome sequencing approaching current routine genetic testing in blood cancer
KFSHRC Concludes Participation at AMEE 2024 in Switzerland
KFSHRC Empowers Future Healthcare Leaders with Innovative Research Programs
Editing fetal genomes is on the horizon − a medical anthropologist explains why ethical discussions with the target communities should happen sooner…
Ground-breaking study reveals previously unknown genetic causes of colorectal cancer
Manchester leads implementation of lifesaving genetic bedside stroke test
AstraZeneca announces collaboration and investment agreement with Cellectis to accelerate cell therapy and genomic medicine ambitions
Groundbreaking gene therapy trial for Hunter syndrome opens
Alexion completes purchase and licence agreement for early-stage rare disease gene therapy portfolio from Pfizer
Lifesaving bedside stroke test receives UK product safety mark
Severe Covid can alter long-term immune response
Alexion, AstraZeneca Rare Disease, enters agreement with Pfizer to acquire a portfolio of preclinical rare disease gene therapies
Genomic profiling offers hope for 23,000 cancer patients
Are we ready for gene testing and genetic medicine?
Stuttering gene. Cerebral palsy. Fast living killifish. Testing concerns
Precision medicine for Indigenous communities
Personalized Gut Microbiome Analysis for Colorectal Cancer Classification with Explainable AI
Greater Manchester secures multi-million investment to improve the diagnosis and treatment of disease to save more lives
Orkney cancer gene link revealed
Early results of gene therapy trial for ‘childhood dementia’ show promise
Genetic test to prevent newborn babies going deaf recommended by NICE
World-first genetic test for babies’ hearing wins major award
Genomics key to First Nations health equality
Rogue immune cells linked to leukaemia are key driver of a
Tumour matrix profiling gives clues to progression of some l
Renowned Dunedin Study wins Rutherford Medal
Illumina unveils NovaSeq X series to accelerate genomic discoveries
Transcript: Misha Schubert on Startup Daily 7 Sept 2022
Breakthrough For Kidney Disease Patients
Leading scientists use Genomics England data set to propose updated global guidelines to improve rare disease diagnosis