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Leading scientists from around the globe are working at the Clemson University Center for Human Genetics to advance our understanding of the fundamental principles by which genetic and environmental factors determine and predict both healthy traits and susceptibility to disease in humans.
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Newsletter of the Center for Human Genetics at Clemson...
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Active research projects in the Center investigate the roles...
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Systems genetics of the Drosophila metabolome. Genome Res...
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The Center for Human Genetics is located in Self Regional Hall, a 17,000 square foot facility located on the campus of the Greenwood Genetic Center. The facility is designed to promote a collaborative interactive environment with open office space for graduate students, postdoctoral fellows and research staff.
Active research projects in the Center investigate the roles of gene regulation, post-translational modification and structural variation in common and rare diseases; develop more powerful models for genotype-phenotype prediction; and utilize systems genetics approaches in cellular and animal models to more fully understand the genome-wide ...
13 Απρ 2021 · The National Institutes of Health (NIH) has tasked Clemson University with unlocking these genetic codes through a new $10.6 million grant to establish the Center of Biomedical Research Excellence (COBRE) in Human Genetics in collaboration with the Greenwood Genetic Center (GGC).
1 Μαρ 2019 · Groundbreaking geneticist Trudy Mackay joined Clemson in 2018 as director of the University’s Center for Human Genetics and is building a team of researchers working to significantly advance our understanding of genetic disorders.
Genetics and genomics underlie precision healthcare and promise innovations in disease prevention, early detection, diagnostics, and treatment that require different ways of providing health care and conducting research.
8 Οκτ 2018 · Trudy Mackay and Robert Anholt of Clemson University’s Center for Human Genetics have received $1.87 million from the National Institutes of Health to advance research aimed at significantly increasing our fundamental understanding of the complex roles molecular variations play in human disease.