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Chenqing Zheng
Chenqing Zheng
Geverifieerd e-mailadres voor mail2.sysu.edu.cn
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Genetic mechanisms of critical illness in COVID-19
E Pairo-Castineira, S Clohisey, L Klaric, AD Bretherick, K Rawlik, D Pasko, ...
Nature 591 (7848), 92-98, 2021
14532021
Mapping the human genetic architecture of COVID-19
Writing group Writing group leaders Pathak Gita A. 6 Andrews Shea J. 7 Kanai ...
Nature 600 (7889), 472-477, 2021
8422021
Whole-genome sequencing reveals host factors underlying critical COVID-19
A Kousathanas, E Pairo-Castineira, K Rawlik, A Stuckey, CA Odhams, ...
Nature 607 (7917), 97-103, 2022
3042022
GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19
E Pairo-Castineira, K Rawlik, AD Bretherick, T Qi, Y Wu, I Nassiri, ...
Nature 617 (7962), 764-768, 2023
1282023
A second update on mapping the human genetic architecture of COVID-19
M Kanai, SJ Andrews, M Cordioli, C Stevens, BM Neale, M Daly, A Ganna, ...
Nature 621 (7977), E7-E26, 2023
622023
Meta-analysis of gene expression and identification of biological regulatory mechanisms in Alzheimer's disease
L Su, S Chen, C Zheng, H Wei, X Song
Frontiers in Neuroscience 13, 633, 2019
612019
A meta-analysis of public microarray data identifies biological regulatory networks in Parkinson’s disease
L Su, C Wang, C Zheng, H Wei, X Song
BMC medical genomics 11, 1-22, 2018
442018
Genetic landscape of the ACE2 coronavirus receptor
Z Yang, E Macdonald-Dunlop, J Chen, R Zhai, T Li, A Richmond, L Klarić, ...
Circulation 145 (18), 1398-1411, 2022
342022
Network analysis of microRNAs, transcription factors, and target genes involved in axon regeneration
L Su, X Song, Z Xue, C Zheng, H Yin, H Wei
Journal of Zhejiang University. Science. B 19 (4), 293, 2018
322018
Identification of potential candidate genes and pathways in atrioventricular nodal reentry tachycardia by whole‐exome sequencing
R Luo, C Zheng, H Yang, X Chen, P Jiang, X Wu, Z Yang, X Shen, X Li
Clinical and Translational Medicine 10 (1), 238-257, 2020
192020
Variants of WNT7A and GPR124 are associated with hemorrhagic transformation following intravenous thrombolysis in ischemic stroke
S Ta, X Rong, ZN Guo, H Jin, P Zhang, F Li, Z Li, L Lin, C Zheng, Q Gu, ...
CNS Neuroscience & Therapeutics 27 (1), 71-81, 2021
172021
Demographic histories and genome-wide patterns of divergence in incipient species of shorebirds
X Wang, KH Maher, N Zhang, P Que, C Zheng, S Liu, B Wang, Q Huang, ...
Frontiers in Genetics 10, 919, 2019
152019
An analysis of abnormalities in the B cell receptor repertoire in patients with systemic sclerosis using high-throughput sequencing
X Shi, T Shao, F Huo, C Zheng, W Li, Z Jiang
PeerJ 8, e8370, 2020
142020
Low genetic diversity in captive populations of the critically endangered Blue-crowned Laughingthrush (Garrulax courtoisi) revealed by a panel of novel microsatellites
G Chen, C Zheng, N Wan, D Liu, VWK Fu, X Yang, Y Yu, Y Liu
PeerJ 7, e6643, 2019
122019
Total genetic contribution assessment across the human genome
T Li, Z Ning, Z Yang, R Zhai, C Zheng, W Xu, Y Wang, K Ying, Y Chen, ...
Nature Communications 12 (1), 2845, 2021
92021
Integrative analysis of multiomics data identifies selenium-related gene ALAD associating with keshan disease
J Huang, C Zheng, R Luo, X Cao, M Liu, Q Gu, F Li, J Li, X Wu, Z Yang, ...
Free Radical Biology and Medicine 193, 702-719, 2022
82022
Updates on Clinical and Genetic Heterogeneity of ASPM in 12 Autosomal Recessive Primary Microcephaly Families in Pakistani Population
NM Khan, B Hussain, C Zheng, A Khan, MS Masoud, Q Gu, L Qiu, ...
Frontiers in Pediatrics 9, 695133, 2021
82021
Divergent selection in low recombination regions shapes the genomic islands in two incipient shorebird species
W Zhou, N Zhang, K Huang, H Lin, J Tu, C Zheng, P Que, CY Chiang, ...
Molecular Biology and Evolution 41 (2), msae006, 2024
62024
Integrative analyses identify potential key genes and calcium-signaling pathway in familial atrioventricular nodal reentrant tachycardia using whole-exome sequencing
J Huang, R Luo, C Zheng, X Cao, Y Zhu, T He, M Liu, Z Yang, X Wu, X Li
Frontiers in Cardiovascular Medicine 9, 910826, 2022
62022
Targeted next-generation sequencing identified a known EMD mutation in a Chinese patient with Emery-Dreifuss muscular dystrophy
X Dai, C Zheng, X Chen, Y Tang, H Zhang, C Yan, H Ma, X Li
Human Genome Variation 6 (1), 42, 2019
52019
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Artikelen 1–20