Wang B - Search Results

1

Genome-wide association study of antipsychotic-induced sinus bradycardia in Chinese schizophrenia patients.

Weng S, Wang B, Li M, Chao S, Lin R, Zheng R, Yu Y, Guo S, Lin X. Weng S, et al. Among authors: wang b. PLoS One. 2021 Apr 29;16(4):e0249997. doi: 10.1371/journal.pone.0249997. eCollection 2021. PLoS One. 2021. PMID: 33914752 Free PMC article.

2

Relationship between nocturnal blood pressure variation and silent cerebral infarction in Chinese hypertensive patients.

Ma JF, Sun JL, Zhao J, Wei X, Wang BS, Fu Y. Ma JF, et al. Among authors: wang bs. J Neurol Sci. 2010 Jul 15;294(1-2):67-9. doi: 10.1016/j.jns.2010.04.002. Epub 2010 May 2. J Neurol Sci. 2010. PMID: 20439107

3

Whole-genome sequencing and RNA sequencing analysis reveals novel risk genes and differential expression patterns in hepatoblastoma.

Wang W, Zhang N, Chen L, Zhao X, Shan Y, Yang F, Wang B, Gao H, Xu M, Tang P, Qin S, Gu S. Wang W, et al. Among authors: wang b. Gene. 2024 Mar 1;897:147991. doi: 10.1016/j.gene.2023.147991. Epub 2023 Nov 14. Gene. 2024. PMID: 37972697

4

Exome sequencing identifies a novel nonsense mutation of HOXD13 in a Chinese family with synpolydactyly.

Wang B, Li N, Geng J, Wang Z, Fu Q, Wang J, Xu Y. Wang B, et al. Among authors: wang z, wang j. Congenit Anom (Kyoto). 2017 Jan;57(1):4-7. doi: 10.1111/cga.12173. Congenit Anom (Kyoto). 2017. PMID: 27254532

5

Human fetal heart specific coexpression network involves congenital heart disease/defect candidate genes.

Wang B, You G, Fu Q. Wang B, et al. Sci Rep. 2017 Apr 24;7:46760. doi: 10.1038/srep46760. Sci Rep. 2017. PMID: 28436429 Free PMC article.

6

Identification of differentially expressed miRNAs in plasma exosomes from patients with early-onset pre-eclampsia using next generation sequencing.

Wang W, Zhang W, Chen L, Wu X, Gu J, Yang F, Wang B, Qin S, Tang P. Wang W, et al. Among authors: wang b. Heliyon. 2024 Jan 26;10(3):e24543. doi: 10.1016/j.heliyon.2024.e24543. eCollection 2024 Feb 15. Heliyon. 2024. PMID: 38322831 Free PMC article.

7

Identification of the genetic basis of sporadic polydactyly in China by targeted sequencing.

Zu B, Zhang X, Xu Y, Xiang Y, Wang Z, Cai H, Wang B, You G, Fu Q. Zu B, et al. Among authors: wang z, wang b. Comput Struct Biotechnol J. 2021 Jun 9;19:3482-3490. doi: 10.1016/j.csbj.2021.06.014. eCollection 2021. Comput Struct Biotechnol J. 2021. PMID: 34194672 Free PMC article.

8

Inpatient medical cost of status epilepticus in children: A national-wide, multicenter study from China.

Wang T, Wang J, Lu G, Ding D, Yan W, Dou Y, Wang B, Zhou Y, Li T, Ma J, Zhou S, Wang Y; Chinese Pediatric Status Epilepticus Task Force. Wang T, et al. Among authors: wang j, wang y, wang b. Epilepsy Behav. 2021 Oct;123:108248. doi: 10.1016/j.yebeh.2021.108248. Epub 2021 Aug 26. Epilepsy Behav. 2021. PMID: 34455296

9

TurboID-mediated proximity labeling technologies to identify virus co-receptors.

Wang B, Yang F, Wang W, Zhao F, Sun X. Wang B, et al. Among authors: wang w. Front Cell Infect Microbiol. 2024 Jun 27;14:1371837. doi: 10.3389/fcimb.2024.1371837. eCollection 2024. Front Cell Infect Microbiol. 2024. PMID: 38994005 Free PMC article.

10

Copy number variation analysis in Chinese children with complete atrioventricular canal and single ventricle.

Zhang X, Wang B, You G, Xiang Y, Fu Q, Yu Y, Zhang X. Zhang X, et al. Among authors: wang b. BMC Med Genomics. 2021 Oct 9;14(1):243. doi: 10.1186/s12920-021-01090-y. BMC Med Genomics. 2021. PMID: 34627233 Free PMC article.

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