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Cascade testing: Can health systems be involved in informing relatives of genetic test results? Check out the experience of KP WA Research relative notification program. karger.com/phg/article/do…

Machine learning has revolutionized the way genomic data are analyzed and interpreted. This Nature Reviews Genetics collection explores how machine learning has contributed valuable insights into genetic variation and disease mechanisms. nature.com/collections/sm…

"Although seven drugs have already been approved in the USA for the treatment of DMD, only one has been approved in Europe. Ultimately, it is the patients, their families and the payers who decide whether marginally effective drugs are worth the cost." nature.com/articles/s4159…

“I’m speechless. I like machine learning and artificial intelligence networks as much as the next person, but hard to see this is a physics discovery.” AI comes to the Nobels. nature.com/articles/d4158…

Copy number variation (CNV) is an important source of heritability with downstream applications such as polygenic risk scoring and drug target identification. An informative Nature Reviews Genetics review on the use of CNV in genome wide association studies. nature.com/articles/s4157…

Development of a Breast Cancer Risk Prediction Model Integrating Monogenic, Polygenic, and Epidemiologic Risk. Via Cancer Epidemiology, Biomarkers & Prevention aacrjournals.org/cebp/article-a…

Transcriptomics is an emerging tool in research to predict toxicological hazards. An informative Nature Reviews Genetics review on progress in toxicogenomics to protect human health. nature.com/articles/s4157…

This large-scale evaluation study underscores the importance of a genetic diagnosis in children with severe developmental disorders to ensure timely referral, enable appropriate care, and to access relevant patient support groups. Genetics in Medicine Open sciencedirect.com/science/articl…

Rigorous evaluation of the utility of EHR-based screening tools for Familial hypercholesterolemia is needed to ensure their effectiveness in healthcare settings.Check out our recent JACC Journals manuscript! jacc.org/doi/10.1016/j.… Muin J. Khoury @NHLBI_Translate Family Heart Foundation

An informative Genetics in Medicine review of 10 years of ClinGen as a global effort to define the clinical relevance of genes and variants for medical and research use. sciencedirect.com/science/articl…

Precision public health in action: global genomic surveillance of monkeypox virus. Via nature nature.com/articles/s4159…

A collection of articles on genomic testing in low and middle income countries. Via European Journal of Human Genetics nature.com/articles/s4143…

From Genes to Public Health: The journey continues on bluesky!

After 40 years at the Centers for Disease Control and Prevention, and more than 25 years in public health genomics, I am retiring at the end of 2024. What a privilege and an honor it has been! But the journey from genes to public health continues.

Public Health Genomics 2025: The End of the Beginning (Again)! linkedin.com/posts/muin-j-k…

April 1 was a sad day at CDC! linkedin.com/posts/muin-j-k…

Public health genomics in the United States: 1998-2025. Via LinkedIn linkedin.com/posts/muin-j-k…

From genetic epidemiology to public health genomics and precision public health: Looking back, looking ahead. Via Karger Publishers karger.com/phg/article/28…

From genes to public health 1996: the beginning of the journey! Via AJPH ajph.aphapublications.org/doi/10.2105/AJ…

From Genes to Public Health: Am Emerging Opportunity for the Administration for Healthy America! linkedin.com/posts/muin-j-k…