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tongda zhang
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Genome sequencing of 320 Chinese children with epilepsy: a clinical and molecular study
D Zou, L Wang, J Liao, H Xiao, J Duan, T Zhang, J Li, Z Yin, J Zhou, ...
Brain 144 (12), 3623-3634, 2021
222021
deepMNN: deep learning-based single-cell RNA sequencing data batch correction using mutual nearest neighbors
B Zou, T Zhang, R Zhou, X Jiang, H Yang, X Jin, Y Bai
Frontiers in Genetics 12, 708981, 2021
182021
Genetic diagnosis of acute aortic dissection in South China Han population using next-generation sequencing
J Zheng, J Guo, L Huang, Q Wu, K Yin, L Wang, T Zhang, L Quan, Q Zhao, ...
International Journal of Legal Medicine 132, 1273-1280, 2018
182018
Helicobacter pylori infection affects the human gastric microbiome, as revealed by metagenomic sequencing
D Wang, T Zhang, Y Lu, C Wang, Y Wu, J Li, Y Tao, L Deng, X Zhang, ...
FEBS Open Bio 12 (6), 1188-1196, 2022
152022
Single‐cell atlas of peripheral blood mononuclear cells from pregnant women
D Chen, W Wang, L Wu, L Liang, S Wang, Y Cheng, T Zhang, C Chai, ...
Clinical and translational medicine 12 (5), e821, 2022
142022
RNA‑sequence analysis of samples from patients with idiopathic adhesive capsulitis
J Cui, T Zhang, J Xiong, W Lu, L Duan, W Zhu, D Wang
Molecular Medicine Reports 16 (5), 7665-7672, 2017
112017
Whole-genome-based Helicobacter pylori geographic surveillance: a visualized and expandable webtool
X Jiang, XU Zheng, T Zhang, Y Li, W Li, H Tan
Front. Microbiol., 2021
102021
Genomic architecture of fetal central nervous system anomalies using whole-genome sequencing
Y Yang, S Zhao, G Sun, F Chen, T Zhang, J Song, W Yang, L Wang, ...
NPJ Genomic Medicine 7 (1), 31, 2022
92022
Syntool: A novel region‐based intolerance score to single nucleotide substitution for synonymous mutations predictions based on 123,136 individuals
T Zhang, Y Wu, Z Lan, Q Shi, Y Yang, J Guo
BioMed Research International 2017 (1), 5096208, 2017
92017
Abnormal Sylvian fissure at 20–30 weeks as indicator of malformations of cortical development: role of prenatal whole‐genome sequencing
Y Liao, Y Yang, H Wen, B Wang, T Zhang, S Li
Ultrasound in Obstetrics & Gynecology 59 (4), 552-555, 2022
82022
Genotype‑phenotype analysis in Mowat‑Wilson syndrome associated with two novel and two recurrent ZEB2 variants
D Zou, L Wang, F Wen, H Xiao, J Duan, T Zhang, Z Yin, Q Dong, J Guo, ...
Experimental and therapeutic medicine 20 (6), 1-1, 2020
82020
Integrating plasma cell‐free DNA with clinical laboratory results enhances the prediction of critically ill patients with COVID‐19 at hospital admission
Y Bai, F Zheng, T Zhang, Q Luo, Y Luo, R Zhou, Y Jin, Y Shan, J Cheng, ...
Clinical and Translational Medicine 12 (7), 2022
52022
Novel compound heterozygous variants in the STIL gene identified in a Chinese family with presentation of foetal microcephaly
C Cheng, Y Yang, X Zhu, X Yu, T Zhang, F Yang, F Chen, X Chen, S Zhao, ...
European Journal of Medical Genetics 63 (12), 104091, 2020
22020
Genome sequencing combining prenatal ultrasound in the evaluation of fetal CNS structural anomalies
Y Yang, S Zhao, G Sun, F Chen, T Zhang, J Song, W Yang, L Wang, ...
medRxiv, 2020.03. 04.20031294, 2020
12020
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