Bo Wang

发表

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

Qi-hua Fu, Bo Wang, Guoling You, 2017, Scientific Reports.

DNA methylation and cis-regulation of gene expression by prostate cancer risk SNPs

James Y. Dai, J. Stanford, E. Ostrander, 2020, PLoS genetics.

Identification of miRNA–mRNA–TFs Regulatory Network and Crucial Pathways Involved in Tetralogy of Fallot

Qi-hua Fu, Bo Wang, Guoling You, 2020, Frontiers in Genetics.

Sexual difference of small RNA expression in Tetralogy of Fallot

Qi-hua Fu, Bo Wang, Guocheng Shi, 2018, Scientific Reports.

Rare Copy Number Variation Analysis in Chinese Children of Complete Atrioventricular Canal and Single Ventricle

Bo Wang, Guoling You, Xingyu Zhang, 2021 .

A Novel Missense Mutation of GATA4 in a Chinese Family with Congenital Heart Disease

Jian Wang, Bo Wang, K. Sun, 2016, PloS one.

Copy number variation-associated lncRNAs may contribute to the etiologies of congenital heart disease

Bo Wang, M. Qi, Xingyu Zhang, 2023, Communications Biology.

Mutational screening of GLI3, SHH, preZRS, and ZRS in 102 Chinese children with nonsyndromic polydactyly

Bo Wang, Yun-lan Xu, Ying Xiang, 2017, Developmental dynamics : an official publication of the American Association of Anatomists.

Accurate diagnosis of spinal muscular atrophy and 22q11.2 deletion syndrome using limited deoxynucleotide triphosphates and high-resolution melting

Bo Wang, Guoling You, Xiaoqing Zhang, 2018, BMC Genomics.

Exome Sequencing Identified a Novel FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly

Bo Wang, Guoling You, Zhigang Wang, 2017, International journal of molecular sciences.

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

Bo Wang, Guoling You, Zhigang Wang, 2021, Computational and structural biotechnology journal.

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

Jian Wang, Bo Wang, Niu Li, 2017, Congenital anomalies.

SORBS2 is a genetic factor contributing to cardiac malformation of 4q deletion syndrome

Bo Wang, Guoling You, Huiwen Chen, 2020, bioRxiv.

SORBS2 is a genetic factor contributing to cardiac malformation of 4q deletion syndrome patients

Bo Wang, Guoling You, Huiwen Chen, 2021, eLife.

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

Bo Wang, Guoling You, Xingyu Zhang, 2021, BMC medical genomics.

Vigorous Physical Activity Is Associated with Lower Risk of Metastatic–Lethal Progression in Prostate Cancer and Hypomethylation in the CRACR2A Gene

James Y. Dai, J. Stanford, J. Wright, 2018, Cancer Epidemiology, Biomarkers & Prevention.

15q11.2 deletion is enriched in patients with total anomalous pulmonary venous connection

Bo Wang, Guocheng Shi, Huiwen Chen, 2020, Journal of Medical Genetics.

FGD5-AS1 Is a Hub lncRNA ceRNA in Hearts With Tetralogy of Fallot Which Regulates Congenital Heart Disease Genes Transcriptionally and Epigenetically

Bo Wang, Zhuoming Xu, Xingyu Zhang, 2021, Frontiers in Cell and Developmental Biology.

A novel GJA1 mutation identified by whole exome sequencing in a Chinese family with autosomal dominant syndactyly.

Bo Wang, Guoling You, Zhaojing Zheng, 2016, Clinica chimica acta; international journal of clinical chemistry.

Sexual difference of small RNA expression in Tetralogy of Fallot

Bo Wang, Guocheng Shi, Zhongqun Zhu, 2018, Scientific Reports.

Integrated analysis of copy number variation-associated lncRNAs identifies candidates contributing to the etiologies of congenital kidney anomalies

Bo Wang, M. Qi, Xingyu Zhang, 2023, Communications biology.

Long Noncoding RNA lnc-TSSK2-8 Activates Canonical Wnt/β-Catenin Signaling Through Small Heat Shock Proteins HSPA6 and CRYAB

Bo Wang, Zhuoming Xu, M. Qi, 2021, Frontiers in Cell and Developmental Biology.