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Latest genomic medicine News

  • Latest genomic medicine news stories and updates. What is happening today? All recent genomic medicine news and developments. Live coverage and timeline of genomic medicine. All you need to know about genomic medicine.
Global commission to pave the way for equal precision health
Research Project Promoting Patient-Specific Nucleic Acid Drug Development for Rare and Intractable Diseases (N-of-1+ Drug Development) Selected by AMED
AMA welcomes legislation ending genetic discrimination in life insurance
Snow Medical invests $24 million in three new research fellows, strengthening NSW’s biomedical research leadership
Common Genetic Cause Of Severe Epilepsy Revealed
Precision medicine helps more patients receive a genetic diagnosis
Study reveals worrying extent of imprecise gene and gene mutation naming
Helus Pharma Appoints Michael Cola as Chief Executive Officer to Lead Next Phase of Scale and Execution
Electronic Informed Consent in Research on Rare Diseases
Richard Rosenquist Brandell received recognition as Pharmaceutical Profile of the Year
New hope for children with devastating rare genetic disorder, thanks to world-first research in Manchester
What We Learned From a Decade-long Genome Cohort Study of 100,000 Japanese Individuals
Prof Kathryn North AC Named Australian Medical Research Advisory Board Chair
New Chair Of Australian Medical Research Advisory Board
Appointment Marks New Era For Medical Research Leadership
Newborn Genomic Screening Enables More Lifesaving Diagnoses
Australian Government Accelerates Genomic Medicine And Research
Babies born with DNA from three people hailed as breakthrough – but questions remain
Scientists discover genetic condition that causes paralysis following mild infections
Discovery of two new genetic disorders improves diagnoses for patients with neurodevelopmental conditions
Gene Variant Increases Risk Of Long COVID
Long-read Genome Sequencing: Transforming Genetic Diagnostics for Rare Diseases
SEK 80 million from the Government in special support for precision medicine
Investment in the BrAInChild project from the Ministry of Social Affairs – Barntumörbanken plays a key role
New Swedish Initiative to Integrate Research and Healthcare
Genetic causes of rare condition linked to hearing loss and infertility found
Transforming clinical care for children with rare genetic diseases
Embedding Genomic Research in Cancer Clinical Trials
BCNA calls out government for failing to protect Australians from genetic discrimination while showcasing its new genomics framework
Genomics Framework charts new course in cancer care for future generations
Richard Rosenquist Brandell In Newsweek
Brain scans to give crucial insight into childhood genetic disease
BCM receives $3.5 million to study telehealth genetic services for sick, underserved newborns
Genetic test for deafness in newborns to be trialled across the UK
KI Continues To Invest In Core Facilities
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

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