Human Genetics – the science of how our genomes function, vary, and shape our unique, individual characteristics – is a rapidly expanding field with major implications for medical and fundamental research, clinical practice, and many other areas. In this course, students will learn about the principles of human genetics & genomics at the levels of molecules, cells, individuals, and populations. Topics include patterns of inheritance; the molecular causes and biochemical basis of genetic disorders; disease gene identification; the origin and distribution of human genetic variation; genetic influences on common, complex diseases; epigenetics and regulation of gene expression; genomic technologies for understanding human genomes; cancer genetics; behavioral genetics; human ancestry and evolution; applications such as genetic screening, genetic counseling, and gene therapy; and ethical questions raised by emerging abilities to edit the human genome, modify the human germline, and many more. prereq: Biol 4003 or instructor consent
Gopher Grades is maintained by Social Coding with data from Summer 2017 to Summer 2024 provided by the Office of Institutional Data and Research
Privacy Policy