Yun Li
Affiliations: | 2018- | Molecular Genetics | University of Toronto, Toronto, ON, Canada |
Area:
Stem cells, Autism, OrganoidsGoogle:
"Yun Li"Mean distance: 16.14 (cluster 31) | S | N | B | C | P |
Parents
Sign in to add mentorLuis Parada | grad student | 2002-2008 | UT Southwestern |
Rudolf Jaenisch | post-doc | 2009-2017 | MIT |
BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
Wang WX, Douglas TR, Zhang H, et al. (2023) Universal, label-free, single-molecule visualization of DNA origami nanodevices across biological samples using origamiFISH. Nature Nanotechnology |
Ahmed M, Muffat J, Li Y. (2023) Understanding neural development and diseases using CRISPR screens in human pluripotent stem cell-derived cultures. Frontiers in Cell and Developmental Biology. 11: 1158373 |
Bhattacharya A, Choi WWY, Muffat J, et al. (2021) Modeling developmental brain diseases using human pluripotent stem cell-derived brain organoids - progress and perspective. Journal of Molecular Biology. 167386 |
Dhaliwal N, Choi WWY, Muffat J, et al. (2021) Modeling PTEN overexpression-induced microcephaly in human brain organoids. Molecular Brain. 14: 131 |
Tian A, Muffat J, Li Y. (2020) Studying Human Neurodevelopment and Diseases Using 3D Brain Organoids. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 40: 1186-1193 |
Li Y, Muffat J, Omer Javed A, et al. (2019) Genome-wide CRISPR screen for Zika virus resistance in human neural cells. Proceedings of the National Academy of Sciences of the United States of America |
Omer Javed A, Li Y, Muffat J, et al. (2018) Microcephaly Modeling of Kinetochore Mutation Reveals a Brain-Specific Phenotype. Cell Reports. 25: 368-382.e5 |
Muffat J, Li Y, Omer A, et al. (2018) Human induced pluripotent stem cell-derived glial cells and neural progenitors display divergent responses to Zika and dengue infections. Proceedings of the National Academy of Sciences of the United States of America |
Mellios N, Feldman DA, Sheridan SD, et al. (2018) Human cerebral organoids reveal deficits in neurogenesis and neuronal migration in MeCP2-deficient neural progenitors. Molecular Psychiatry. 23: 791 |
Liu XS, Wu H, Krzisch M, et al. (2018) Rescue of Fragile X Syndrome Neurons by DNA Methylation Editing of the FMR1 Gene. Cell |