Rang Xu

807 total citations
43 papers, 624 citations indexed

About

Rang Xu is a scholar working on Molecular Biology, Epidemiology and Genetics. According to data from OpenAlex, Rang Xu has authored 43 papers receiving a total of 624 indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 18 papers in Epidemiology and 10 papers in Genetics. Recurrent topics in Rang Xu's work include Congenital heart defects research (23 papers), Congenital Heart Disease Studies (17 papers) and Coronary Artery Anomalies (5 papers). Rang Xu is often cited by papers focused on Congenital heart defects research (23 papers), Congenital Heart Disease Studies (17 papers) and Coronary Artery Anomalies (5 papers). Rang Xu collaborates with scholars based in China, United States and Hong Kong. Rang Xu's co-authors include Haitao Bai, Chun Wang, Kun Sun, Jian Lu, Shengfang Ge, Zhongwei Cao, Ping Zhang, Yuejuan Xu, Fen Li and Jian Huang and has published in prestigious journals such as Nature Communications, PLoS ONE and Scientific Reports.

In The Last Decade

Rang Xu

40 papers receiving 620 citations

Peers

Countries citing papers authored by Rang Xu

Since Specialization

Citations

This map shows the geographic impact of Rang Xu's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Rang Xu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rang Xu more than expected).

Fields of papers citing papers by Rang Xu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rang Xu. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Rang Xu. The network helps show where Rang Xu may publish in the future.

Co-authorship network of co-authors of Rang Xu

This figure shows the co-authorship network connecting the top 25 collaborators of Rang Xu. A scholar is included among the top collaborators of Rang Xu based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Rang Xu. Rang Xu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Variants in FOXC1 and FOXC2 identified in patients with conotruncal heart defects 2024 ·Genomics ·Wei Wei, (unknown), Fen Li, Kun Sun, Xuechao Jiang, Rang Xu	0
2	Analysis of pathogenic variants in 605 Chinese children with non-syndromic cardiac conotruncal defects based on targeted sequencing 2023 ·Genomics ·(unknown), (unknown), (unknown), (unknown), Huiying Wang, Qihua Fu, Fen Li, Rang Xu, Chen Sun, (unknown), Kun Sun	1
3	Identification of FOXH1 mutations in patients with sporadic conotruncal heart defect 2020 ·Clinical Genetics ·Wei Wei, (unknown), Fen Li, Kun Sun, Xuechao Jiang, Rang Xu	6
4	Novel In-Frame Deletion Mutation in NOTCH1 in a Chinese Sporadic Case of Adams–Oliver Syndrome 2020 ·DNA and Cell Biology ·(unknown), Ling Yang, (unknown), Rang Xu, Yurong Wu	3
5	Diagnostic yield of additional exome sequencing after the detection of long continuous stretches of homozygosity (LCSH) in SNP arrays 2020 ·Journal of Human Genetics ·Yanjie Fan, Lili Wang, Yu Sun, Ting Xu, Zhuwen Gong, (unknown), Wenjuan Qiu, Lili Liang, Bing Xiao, Huiwen Zhang, Lianshu Han, Fujun Lin, Rang Xu, Xuefan Gu, Yongguo Yu	2
6	Tet inactivation disrupts YY1 binding and long-range chromatin interactions during embryonic heart development 2019 ·Nature Communications ·Shaohai Fang, Jia Li, Yang Xiao, Minjung Lee, Lei Guo, Wei Han, Tingting Li, Matthew C. Hill, Tingting Hong, (unknown), Rang Xu, Ping Zhang, Fen Wang, Jiang Chang, Yubin Zhou, Deqiang Sun, James F. Martin, Yun Huang	59
7	Genetic Analyses Identified a SALL4 Gene Mutation Associated with Holt–Oram Syndrome 2018 ·DNA and Cell Biology ·(unknown), Chen Sun, Kun Sun, Rang Xu, Yurong Wu	6
8	A loss-of-function mutation p.T52S in RIPPLY3 is a potential predisposing genetic risk factor for Chinese Han conotruncal heart defect patients without the 22q11.2 deletion/duplication 2018 ·Journal of Translational Medicine ·(unknown), (unknown), Qingjie Wang, Xiaoqing Zhang, Fen Li, Qihua Fu, Rang Xu, Yu Yu, (unknown), Yuejuan Xu, Kun Sun	2
9	Duplication and Deletion of 22q11 Associated with Anomalous Pulmonary Venous Connection 2017 ·Pediatric Cardiology ·(unknown), (unknown), Chunjie Liu, Chen Sun, Fen Li, Kun Sun, Rang Xu	5
10	In Silico Analyses Reveal the Relationship Between SIX1/EYA1 Mutations and Conotruncal Heart Defects 2017 ·Pediatric Cardiology ·(unknown), Lijuan Xu, (unknown), Chen Sun, Rang Xu	4
11	CITED2 Mutations in Conserved Regions Contribute to Conotruncal Heart Defects in Chinese Children 2017 ·DNA and Cell Biology ·(unknown), Pu Tian, Yang Liu, (unknown), Rang Xu	11
12	Copy Number Variants and Exome Sequencing Analysis in Six Pairs of Chinese Monozygotic Twins Discordant for Congenital Heart Disease 2017 ·Twin Research and Human Genetics ·Yuejuan Xu, Tingting Li, Pu Tian, (unknown), Fei Long, Chen Sun, Kun Sun, Rang Xu	11
13	Identification of candidate genes for congenital heart defects on proximal chromosome 8p 2016 ·Scientific Reports ·Tingting Li, Chunjie Liu, Yuejuan Xu, Qianqian Guo, Chen Sun, Kun Sun, Rang Xu	8
14	Exome Sequencing Identifies a Novel MYH7 p.G407C Mutation Responsible for Familial Hypertrophic Cardiomyopathy 2014 ·DNA and Cell Biology ·Qianqian Guo, Yuejuan Xu, Xike Wang, Ying Guo, Rang Xu, Kun Sun, Chen Sun	3
15	Duplication and Deletion of CFC1 Associated with Heterotaxy Syndrome 2014 ·DNA and Cell Biology ·(unknown), Fei Long, Liping Wang, Yuejuan Xu, (unknown), LI Fen, Chen Sun, Kun Sun, Rang Xu	6
16	Identification of two novel GATA6 mutations in patients with nonsyndromic conotruncal heart defects 2014 ·Molecular Medicine Reports ·Xike Wang, Wei Ji, Jian Wang, (unknown), Ying Guo, Rang Xu, Chen Sun, Kun Sun	21
17	A Potential Relationship among Beta-Defensins Haplotype, SOX7 Duplication and Cardiac Defects 2013 ·PLoS ONE ·Fei Long, Xike Wang, Shaohai Fang, Yuejuan Xu, Kun Sun, Chen Sun, Rang Xu	11
18	MicroRNA-21 regulates the sensitivity of diffuse large B-cell lymphoma cells to the CHOP chemotherapy regimen 2012 ·International Journal of Hematology ·Haitao Bai, (unknown), Chong Deng, Xiaoyu Yang, Chun Wang, Rang Xu	61
19	Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus 2011 ·BMC Medical Genetics ·Yuejuan Xu, Jian Wang, Rang Xu, (unknown), (unknown), (unknown), Liming Bao, Jie Shen, Qihua Fu, Fen Li, Kun Sun	23
20	Sp1 and Sp3 regulate basal transcription of the survivin gene 2007 ·Biochemical and Biophysical Research Communications ·Rang Xu, Ping Zhang, Jian Huang, Shengfang Ge, Jian Lu, (unknown)	81

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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