Zhen Li, Ph.D.
Affiliations: | 2018-2020 | University of California, San Diego, La Jolla, CA | |
2020- | Center for Neuroscience Research | Children's National Medical Center, Washington, DC, United States |
Area:
NeurodevelopmentWebsite:
zhenli.nameGoogle:
"Zhen Li"Mean distance: (not calculated yet)
Parents
Sign in to add mentorNenad Sestan | grad student | 2012-2017 | Yale |
Joseph G. Gleeson | post-doc | 2018-2020 | UCSD |
Tarik F. Haydar | research scientist | 2020- | Children's National Hospital |
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. |
Han Y, Han J, Li Z, et al. (2024) Identification and characterization of a novel intronic splicing mutation in CSF1R-related leukoencephalopathy. Cns Neuroscience & Therapeutics. 30: e14815 |
Li J, Wang F, Li Z, et al. (2024) Integrative multi-omics analysis identifies genetically supported druggable targets and immune cell specificity for myasthenia gravis. Journal of Translational Medicine. 22: 302 |
Chung C, Yang X, Bae T, et al. (2023) Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development. Nature Genetics |
Li Z, Klein JA, Rampam S, et al. (2022) Asynchronous excitatory neuron development in an isogenic cortical spheroid model of Down syndrome. Frontiers in Neuroscience. 16: 932384 |
Jablonska B, Adams KL, Kratimenos P, et al. (2022) Sirt2 promotes white matter oligodendrogenesis during development and in models of neonatal hypoxia. Nature Communications. 13: 4771 |
Klein JA, Li Z, Rampam S, et al. (2021) Sonic Hedgehog Pathway Modulation Normalizes Expression of Olig2 in Rostrally Patterned NPCs With Trisomy 21. Frontiers in Cellular Neuroscience. 15: 794675 |
Chai G, Szenker-Ravi E, Chung C, et al. (2021) A Human Pleiotropic Multiorgan Condition Caused by Deficient Wnt Secretion. The New England Journal of Medicine. 385: 1292-1301 |
Wang L, Li Z, Sievert D, et al. (2021) Author Correction: Loss of NARS1 impairs progenitor proliferation in cortical brain organoids and leads to microcephaly. Nature Communications. 12: 1192 |
Li Z, Tyler WA, Zeldich E, et al. (2020) Transcriptional priming as a conserved mechanism of lineage diversification in the developing mouse and human neocortex. Science Advances. 6 |
Wang L, Li Z, Sievert D, et al. (2020) Loss of NARS1 impairs progenitor proliferation in cortical brain organoids and leads to microcephaly. Nature Communications. 11: 4038 |