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| 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 | 206 | 2013 |
| 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 | 188 | 2021 |
| 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 | 81 | 2020 |
| 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 | 80 | 2021 |
| 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 | 26 | 2021 |
| 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 | 18 | 2020 |
| 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 | 17 | 2017 |
| 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 | 16 | 2017 |
| 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 | 12 | 2018 |
| 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 | 11 | 2023 |
| 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 | 9 | 2019 |
| 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 | 9 | 2011 |
| 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 | 5 | 2022 |
| 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 | 5 | 2020 |
yanhong shi在 coh.org 的电子邮件经过验证
