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:
Neurodevelopment
Website:
zhenli.name
Google:
"Zhen Li"
Mean distance: (not calculated yet)
 

Parents

Sign in to add mentor
Nenad 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

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
See more...