Human Genetics SIGThe ISCBFM Human Genetics SIG will promote research and enhance collaboration for studies involving human genetics. This SIG is developed to bridge collaboration between members of the ISCBFM and the International Stroke Genetics Consortium (ISGC), an international collaborative with over 150 investigators throughout the world, studying the genetics of cerebrovascular phenotypes. The ISGC, founded in 2007, meets twice per year to enable international collaboration for a large number of human genetics studies, and has successfully identified numerous loci associated with a variety of cerebrovascular phenotypes including ischemic stroke, intracerebral hemorrhage, small vessel disease, and other neuroimaging phenotypes. As increasing numbers of genome-wide significant loci are identified, collaboration with more basic investigators to understand molecular mechanisms underlying these associations will be needed. In addition, human genetics might provide translational insight into genetic findings from cellular and animal models. Thus, the Human Genetics SIG will serve as a bridge to enhance collaboration across these organizations. Mission:
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