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Cheng Wang
Cheng Wang
Beckman Research Institute of City of Hope
Verified email at coh.org
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Cited by
Year
Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis
C Wang, Y Li, L Shi, J Ren, M Patti, T Wang, JRM de Oliveira, MJ Sobrido, ...
Nature genetics 44 (3), 254-256, 2012
4142012
Gain-of-function mutations in SCN11A cause familial episodic pain
XY Zhang, J Wen, W Yang, C Wang, L Gao, LH Zheng, T Wang, K Ran, ...
The American Journal of Human Genetics 93 (5), 957-966, 2013
2042013
ApoE-isoform-dependent SARS-CoV-2 neurotropism and cellular response
C Wang, M Zhang, G Garcia, E Tian, Q Cui, X Chen, G Sun, J Wang, ...
Cell stem cell 28 (2), 331-342. e5, 2021
1822021
Modeling human cytomegalovirus-induced microcephaly in human iPSC-derived brain organoids
G Sun, F Chiuppesi, X Chen, C Wang, E Tian, J Nguyen, M Kha, D Trinh, ...
Cell Reports Medicine 1 (1), 2020
792020
Targeting PUS7 suppresses tRNA pseudouridylation and glioblastoma tumorigenesis
Q Cui, K Yin, X Zhang, P Ye, X Chen, J Chao, H Meng, J Wei, D Roeth, ...
Nature cancer 2 (9), 932-949, 2021
742021
Comparative transcriptomic analysis of SARS-CoV-2 infected cell model systems reveals differential innate immune responses
G Sun, Q Cui, G Garcia Jr, C Wang, M Zhang, V Arumugaswami, ...
Scientific Reports 11 (1), 17146, 2021
262021
Murine Placental‐Fetal Phosphate Dyshomeostasis Caused by an Xpr1 Deficiency Accelerates Placental Calcification and Restricts Fetal Growth in Late Gestation
X Xu, X Li, H Sun, Z Cao, R Gao, T Niu, Y Wang, T Ma, R Chen, C Wang, ...
Journal of Bone and Mineral Research 35 (1), 116-129, 2020
182020
PiT2 regulates neuronal outgrowth through interaction with microtubule-associated protein 1B
XX Ma, X Li, P Yi, C Wang, J Weng, L Zhang, X Xu, H Sun, S Feng, K Liu, ...
Scientific Reports 7 (1), 17850, 2017
162017
A PDGFB mutation causes paroxysmal nonkinesigenic dyskinesia with brain calcification
C Wang, X Ma, X Xu, B Huang, H Sun, L Li, M Zhang, JY Liu
Movement disorders: official journal of the Movement Disorder Society 32 (7 …, 2017
152017
A PRRT2 variant in a Chinese family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures results in loss of interaction with STX1B
H Ma, S Feng, X Deng, L Wang, S Zeng, C Wang, X Ma, H Sun, R Chen, ...
Epilepsia 59 (8), 1621-1630, 2018
122018
Astrocytic response mediated by the CLU risk allele inhibits OPC proliferation and myelination in a human iPSC model
Z Liu, J Chao, C Wang, G Sun, D Roeth, W Liu, X Chen, L Li, E Tian, ...
Cell reports 42 (8), 2023
92023
A Novel CDH1 Mutation Causing Reduced E-Cadherin Dimerization Is Associated with Nonsyndromic Cleft Lip With or Without Cleft Palate
S Du, Y Yang, P Yi, J Luo, T Liu, R Chen, C Liu, T Ma, Y Li, C Wang, ...
Genetic Testing and Molecular Biomarkers 23 (11), 759-765, 2019
82019
Identification of compound heterozygous mutations in GNPTG in three siblings of a Chinese family with mucolipidosis type III gamma
Y Gao, K Yang, S Xu, C Wang, J Liu, Z Zhang, M Yuan, X Luo, M Liu, ...
Molecular Genetics and Metabolism 102 (1), 107-109, 2011
82011
Compound screen identifies the small molecule Q34 as an inhibitor of SARS-CoV-2 infection
Q Cui, G Garcia, M Zhang, C Wang, H Li, T Zhou, G Sun, ...
Iscience 25 (1), 2022
52022
p. His16Arg of STXBP1 (MUNC18-1) Associated with syntaxin 3B causes autosomal dominant congenital nystagmus
Y Li, L Jiang, L Wang, C Wang, C Liu, A Guo, M Liu, L Zhang, C Ma, ...
Frontiers in Cell and Developmental Biology 8, 591781, 2020
42020
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