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Researchers at Boston Children's, in collaboration with National Human Genome Research Institute and Mount Sinai Department of Medicine, have found variants in the human genome associated with hereditary congenital facial paresis type 1 (HCFP1).

Using Genomics to Identify Novel Therapeutic Targets for Aortic Disease #AortaEd A very well-composed review with clearcut descriptions of methodological development & conceptual pipeline for #ThoracicAorticDisease Genetics+ #MachineLearning with Population-level Phenotyped

Interested in studying neuropsychiatric disorders and/or meningeal lymphatic biology? Please see the notice below for exciting opportunities in the lab! Previous experience with patch clamp physiology and optogenetics is a big plus. Please retweet and share with your network.🙏

😮‍💨Phew - it only took 2 years but our #GWAS of influenza (40k cases, 1.31M controls) is finally out in Nature Genetics. nature.com/articles/s4158…