Xiaochang Zhang, Ph.D

Affiliations: 
2018- Department of Human Genetics University of Chicago, Chicago, IL 
Area:
Brain development and disorders
Website:
https://genes.uchicago.edu/directory/xiaochang-zhang-phd
Google:
"Xiaochang Zhang"
Mean distance: 14.59 (cluster 11)
 
SNBCP

Children

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Irena Feng research assistant 2018-2019
Xinran Feng grad student 2018-2020 Chicago
Cai Qi post-doc Chicago
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Publications

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Yang Y, Yang R, Kang B, et al. (2023) Single-cell long-read sequencing in human cerebral organoids uncovers cell-type-specific and autism-associated exons. Cell Reports. 42: 113335
Yang R, Feng X, Arias-Cavieres A, et al. (2023) Upregulation of SYNGAP1 expression in mice and human neurons by redirecting alternative splicing. Neuron
Qi C, Feng I, Costa AR, et al. (2021) Variants in ADD1 cause intellectual disability, corpus callosum dysgenesis, and ventriculomegaly in humans. Genetics in Medicine : Official Journal of the American College of Medical Genetics
Ruan X, Kang B, Qi C, et al. (2021) Progenitor cell diversity in the developing mouse neocortex. Proceedings of the National Academy of Sciences of the United States of America. 118
Lim ET, Uddin M, De Rubeis S, et al. (2020) Publisher Correction: Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder. Nature Neuroscience
Coulter ME, Musaev D, DeGennaro EM, et al. (2020) Regulation of human cerebral cortical development by EXOC7 and EXOC8, components of the exocyst complex, and roles in neural progenitor cell proliferation and survival. Genetics in Medicine : Official Journal of the American College of Medical Genetics
Lim ET, Uddin M, De Rubeis S, et al. (2017) Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder. Nature Neuroscience
Zhang X, Chen MH, Wu X, et al. (2016) Cell-Type-Specific Alternative Splicing Governs Cell Fate in the Developing Cerebral Cortex. Cell. 166: 1147-1162.e15
Jamuar SS, Lam AT, Kircher M, et al. (2014) Somatic mutations in cerebral cortical malformations. The New England Journal of Medicine. 371: 733-43
Zhang X, Ling J, Barcia G, et al. (2014) Mutations in QARS, encoding glutaminyl-tRNA synthetase, cause progressive microcephaly, cerebral-cerebellar atrophy, and intractable seizures. American Journal of Human Genetics. 94: 547-58
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