Ri‐Tai Huang

1.1k total citations
38 papers, 849 citations indexed

About

Ri‐Tai Huang is a scholar working on Molecular Biology, Epidemiology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Ri‐Tai Huang has authored 38 papers receiving a total of 849 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 24 papers in Epidemiology and 18 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Ri‐Tai Huang's work include Congenital heart defects research (27 papers), Congenital Heart Disease Studies (24 papers) and Tracheal and airway disorders (7 papers). Ri‐Tai Huang is often cited by papers focused on Congenital heart defects research (27 papers), Congenital Heart Disease Studies (24 papers) and Tracheal and airway disorders (7 papers). Ri‐Tai Huang collaborates with scholars based in China, Canada and Lebanon. Ri‐Tai Huang's co-authors include Song Xue, Yi‐Qing Yang, Ying‐Jia Xu, Xing‐Biao Qiu, Xing‐Yuan Liu, Xinkai Qu, Hongyu Shi, Min Zhou, Ruogu Li and Fang Yuan and has published in prestigious journals such as The American Journal of Cardiology, Gene and Heart.

In The Last Decade

Ri‐Tai Huang

37 papers receiving 839 citations

Peers

Ri‐Tai Huang
Jainy Savla United States
Jean-Pierre Gueffet France
Zhen-lei Hu China
Wilhelmina H. Bax Netherlands
Roby J. Jose Australia
Kazuwa Nakao Japan
Suvi Syväranta Finland
Hirofumi Tomimatsu Japan
Wenjian Jiang China
Takayoshi Hirota Japan
Jainy Savla United States
Ri‐Tai Huang
Citations per year, relative to Ri‐Tai Huang Ri‐Tai Huang (= 1×) peers Jainy Savla

Countries citing papers authored by Ri‐Tai Huang

Since Specialization
Citations

This map shows the geographic impact of Ri‐Tai Huang'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 Ri‐Tai Huang with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ri‐Tai Huang more than expected).

Fields of papers citing papers by Ri‐Tai Huang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ri‐Tai Huang. 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 Ri‐Tai Huang. The network helps show where Ri‐Tai Huang may publish in the future.

Co-authorship network of co-authors of Ri‐Tai Huang

This figure shows the co-authorship network connecting the top 25 collaborators of Ri‐Tai Huang. A scholar is included among the top collaborators of Ri‐Tai Huang 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 Ri‐Tai Huang. Ri‐Tai Huang is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Li, Yanjie, Juan Wang, Xingyuan Liu, et al.. (2023). Discovery of GJC1 (Cx45) as a New Gene Underlying Congenital Heart Disease and Arrhythmias. Biology. 12(3). 346–346. 10 indexed citations
2.
Wang, Zhi, Xiao-Hui Qiao, Ying‐Jia Xu, et al.. (2022). SMAD1 Loss‐of‐Function Variant Responsible for Congenital Heart Disease. BioMed Research International. 2022(1). 9916325–9916325. 9 indexed citations
3.
Xu, Ying‐Jia, Chenxi Yang, Ri‐Tai Huang, et al.. (2022). SMAD4 loss-of-function mutation predisposes to congenital heart disease. European Journal of Medical Genetics. 66(1). 104677–104677. 10 indexed citations
4.
Li, Wei, Yongyi Wang, Ri‐Tai Huang, et al.. (2022). Association of lipid metabolism-related gene promoter methylation with risk of coronary artery disease. Molecular Biology Reports. 49(10). 9373–9378. 4 indexed citations
5.
Che, Miaolin, Bo Xie, Ri‐Tai Huang, et al.. (2019). Use of Both Serum Cystatin C and Creatinine as Diagnostic Criteria for Cardiac Surgery-Associated Acute Kidney Injury and Its Correlation with Long-Term Major Adverse Events. Kidney & Blood Pressure Research. 44(3). 415–425. 5 indexed citations
6.
Xu, Ying‐Jia, Ruo‐Min Di, Xiumei Li, et al.. (2018). GATA6 loss-of-function mutation contributes to congenital bicuspid aortic valve. Gene. 663. 115–120. 36 indexed citations
7.
Schmull, Sebastian, et al.. (2017). Use of human aortic extracellular matrix as a scaffold for construction of a patient-specific tissue engineered vascular patch. Biomedical Materials. 12(6). 65006–65006. 20 indexed citations
8.
Li, Li, Juan Wang, Xingyuan Liu, et al.. (2017). HAND1 loss-of-function mutation contributes to congenital double outlet right ventricle. International Journal of Molecular Medicine. 39(3). 711–718. 17 indexed citations
9.
Qiu, Xing‐Biao, Xinkai Qu, Ruo-Gu Li, et al.. (2017). CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy. Clinical Chemistry and Laboratory Medicine (CCLM). 55(9). 1417–1425. 25 indexed citations
10.
Zhang, Min, Xing‐Yuan Liu, Ri‐Tai Huang, et al.. (2017). MESP1 loss-of-function mutation contributes to double outlet right ventricle. Molecular Medicine Reports. 16(3). 2747–2754. 10 indexed citations
11.
Qiao, Xiao-Hui, Fei Wang, Ri‐Tai Huang, et al.. (2017). MEF2C loss-of-function mutation contributes to congenital heart defects. International Journal of Medical Sciences. 14(11). 1143–1153. 31 indexed citations
12.
Xu, Ying‐Jia, Xing‐Biao Qiu, Fang Yuan, et al.. (2017). Prevalence and spectrum of NKX2.5 mutations in patients with congenital atrial septal defect and atrioventricular block. Molecular Medicine Reports. 15(4). 2247–2254. 27 indexed citations
13.
Huang, Ri‐Tai, Juan Wang, Song Xue, et al.. (2017). TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus. International Journal of Medical Sciences. 14(4). 323–332. 36 indexed citations
14.
Sun, Yu‐Min, Jun Wang, Xing‐Biao Qiu, et al.. (2016). A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis. G3 Genes Genomes Genetics. 6(4). 987–992. 40 indexed citations
15.
Lü, Caixia, Xing‐Yuan Liu, Juan Wang, et al.. (2015). A novel HAND2 loss-of-function mutation responsible for tetralogy of Fallot. International Journal of Molecular Medicine. 37(2). 445–451. 44 indexed citations
16.
Huang, Ri‐Tai, Song Xue, Ying‐Jia Xu, Min Zhou, & Yi‐Qing Yang. (2014). Somatic GATA5 mutations in sporadic tetralogy of Fallot. International Journal of Molecular Medicine. 33(5). 1227–1235. 26 indexed citations
17.
Wang, Juan, Keke Ding, Weijun Xu, et al.. (2014). A Novel NKX2.6 Mutation Associated with Congenital Ventricular Septal Defect. Pediatric Cardiology. 36(3). 646–656. 24 indexed citations
18.
Huang, Ri‐Tai, Song Xue, Ying‐Jia Xu, Min Zhou, & Yi‐Qing Yang. (2013). A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation. International Journal of Molecular Medicine. 31(5). 1119–1126. 54 indexed citations
19.
Xue, Song, et al.. (2012). Meta-analysis of clinical studies comparing coronary artery bypass grafting with percutaneous coronary intervention in patients with end-stage renal disease. European Journal of Cardio-Thoracic Surgery. 43(3). 459–467. 37 indexed citations
20.
Huang, Ri‐Tai, Song Xue, Ying‐Jia Xu, & Yi‐Qing Yang. (2012). Somatic mutations in the GATA6 gene underlie sporadic tetralogy of Fallot. International Journal of Molecular Medicine. 31(1). 51–58. 34 indexed citations

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Jainy Savla Breakdown of academic impact, for papers by Jean-Pierre Gueffet Breakdown of academic impact, for papers by Zhen-lei Hu Breakdown of academic impact, for papers by Wilhelmina H. Bax Breakdown of academic impact, for papers by Roby J. Jose Breakdown of academic impact, for papers by Kazuwa Nakao Breakdown of academic impact, for papers by Suvi Syväranta Breakdown of academic impact, for papers by Hirofumi Tomimatsu Breakdown of academic impact, for papers by Wenjian Jiang Breakdown of academic impact, for papers by Takayoshi Hirota
Rankless by CCL
2026