Associated Papers
A novel base editor SpRY-ABE8eF148A mediates efficient A-to-G base editing with a reduced off-target effect.
Li G et al.
Molecular Therapy. Nucleic Acids, 2023
Unique roles of rare variants in the genetics of complex diseases in humans.
Momozawa Y et al.
Journal of Human Genetics, 2021
Protective alleles and modifier variants in human health and disease.
Harper AR et al.
Nature Reviews. Genetics, 2015
Loss-of-function mutations in SLC30A8 protect against type 2 diabetes.
Flannick J et al.
Nature Genetics, 2014
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