Duanxiang Li

3.6k total citations
31 papers, 2.7k citations indexed

About

Duanxiang Li is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Orthopedics and Sports Medicine. According to data from OpenAlex, Duanxiang Li has authored 31 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Cardiology and Cardiovascular Medicine, 16 papers in Molecular Biology and 3 papers in Orthopedics and Sports Medicine. Recurrent topics in Duanxiang Li's work include Cardiomyopathy and Myosin Studies (21 papers), Cardiovascular Effects of Exercise (13 papers) and RNA Research and Splicing (9 papers). Duanxiang Li is often cited by papers focused on Cardiomyopathy and Myosin Studies (21 papers), Cardiovascular Effects of Exercise (13 papers) and RNA Research and Splicing (9 papers). Duanxiang Li collaborates with scholars based in United States, Canada and China. Duanxiang Li's co-authors include Ray E. Hershberger, Nadine Norton, Jill D. Siegfried, Linda L. Bachinski, Ana Morales, Jorge Gonzalez‐Quintana, Óscar González‐Lorenzo, Jessica D. Kushner, Rita Hill and Robert Roberts and has published in prestigious journals such as Journal of Biological Chemistry, Circulation and Journal of the American College of Cardiology.

In The Last Decade

Duanxiang Li

30 papers receiving 2.7k citations

Peers

Duanxiang Li

CCM

GENET

SURGE

Karin Y. van Spaendonck‐Zwarts Netherlands

Brenda Gerull Germany

Barbara McDonough United States

Alessandra Rampazzo Italy

Florence Kyndt France

Jared M. Evans United States

Magdaléna Harakaľová Netherlands

Judy U. Earley United States

Jonathan T. Lu United States

Elisabeth M. Lodder Netherlands

Karin Y. van Spaendonck‐Zwarts Netherlands

Duanxiang Li

1.4k ×0.7

CCM

847 ×0.6

202 ×1.0

GENET

154 ×0.8

346 ×2.0

SURGE

Citations per year, relative to Duanxiang Li Duanxiang Li (= 1×) peers Karin Y. van Spaendonck‐Zwarts

Countries citing papers authored by Duanxiang Li

Since Specialization

Citations

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

Fields of papers citing papers by Duanxiang Li

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Duanxiang Li. 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 Duanxiang Li. The network helps show where Duanxiang Li may publish in the future.

Co-authorship network of co-authors of Duanxiang Li

This figure shows the co-authorship network connecting the top 25 collaborators of Duanxiang Li. A scholar is included among the top collaborators of Duanxiang Li 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 Duanxiang Li. Duanxiang Li 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

Siegfried, Jill D., Mark Hofmeyer, Evadnie Rampersaud, et al.. (2013). Temporal Relationship of Conduction System Disease and Ventricular Dysfunction in LMNA Cardiomyopathy. Journal of Cardiac Failure. 19(4). 233–239. 39 indexed citations

Norton, Nadine, Duanxiang Li, & Ray E. Hershberger. (2012). Next-generation sequencing to identify genetic causes of cardiomyopathies. Current Opinion in Cardiology. 27(3). 214–220. 32 indexed citations

Norton, Nadine, Jill D. Siegfried, Duanxiang Li, & Ray E. Hershberger. (2011). Assessment of LMNA Copy Number Variation in 58 Probands with Dilated Cardiomyopathy. Clinical and Translational Science. 4(5). 351–352. 12 indexed citations

Norton, Nadine, Duanxiang Li, Mark J. Rieder, et al.. (2011). Genome-wide Studies of Copy Number Variation and Exome Sequencing Identify Rare Variants in BAG3 as a Cause of Dilated Cardiomyopathy. The American Journal of Human Genetics. 88(3). 273–282. 262 indexed citations

Pinto, José R., Jill D. Siegfried, Michelle S. Parvatiyar, et al.. (2011). Functional Characterization of TNNC1 Rare Variants Identified in Dilated Cardiomyopathy. Journal of Biological Chemistry. 286(39). 34404–34412. 48 indexed citations

Rampersaud, Evadnie, Jill D. Siegfried, Nadine Norton, et al.. (2011). Rare variant mutations identified in pediatric patients with dilated cardiomyopathy. Progress in Pediatric Cardiology. 31(1). 39–47. 51 indexed citations

Li, Duanxiang, Ana Morales, Jorge Gonzalez‐Quintana, et al.. (2010). Identification of Novel Mutations in RBM20 in Patients with Dilated Cardiomyopathy. Clinical and Translational Science. 3(3). 90–97. 143 indexed citations

Morales, Ana, José R. Pinto, Jill D. Siegfried, et al.. (2010). Late Onset Sporadic Dilated Cardiomyopathy Caused by a Cardiac Troponin T Mutation. Clinical and Translational Science. 3(5). 219–226. 9 indexed citations

Li, Duanxiang, et al.. (2010). SCN5A Rare Variants in Familial Dilated Cardiomyopathy Decrease Peak Sodium Current Depending on the Common Polymorphism H558R and Common Splice Variant Q1077del. Clinical and Translational Science. 3(6). 287–294. 39 indexed citations

10.

Hershberger, Ray E., Sharie B. Parks, Jessica D. Kushner, et al.. (2009). Clinical and Functional Characterization of TNNT2 Mutations Identified in Patients with Dilated Cardiomyopathy. Circulation. 2(4). 1 indexed citations

11.

Hershberger, Ray E., Sharie B. Parks, Jessica D. Kushner, et al.. (2008). Coding Sequence Mutations Identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 Patients with Familial or Idiopathic Dilated Cardiomyopathy. Clinical and Translational Science. 1(1). 21–26. 148 indexed citations

12.

Jerosch‐Herold, Michael, David C. Sheridan, Jessica D. Kushner, et al.. (2008). Cardiac magnetic resonance imaging of myocardial contrast uptake and blood flow in patients affected with idiopathic or familial dilated cardiomyopathy. American Journal of Physiology-Heart and Circulatory Physiology. 295(3). H1234–H1242. 161 indexed citations

13.

Parks, Sharie B., Jessica D. Kushner, Deirdre Nauman, et al.. (2008). Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy. American Heart Journal. 156(1). 161–169. 186 indexed citations

14.

Li, Duanxiang, Sharie B. Parks, Jessica D. Kushner, et al.. (2006). Mutations of Presenilin Genes in Dilated Cardiomyopathy and Heart Failure. The American Journal of Human Genetics. 79(6). 1030–1039. 139 indexed citations

15.

Sidhu, Jasvinder, Duanxiang Li, Zhinong Wang, et al.. (2004). 839-5 Two transgenic animal models expressing human troponin T gene mutations: One exhibiting dilated cardiomyopathy (W141) and the other exhibiting hypertrophic cardiomyopathy (Q92). Journal of the American College of Cardiology. 43(5). A216–A216. 1 indexed citations

16.

Li, Duanxiang, Linda L. Bachinski, & Robert Roberts. (2001). Genomic Organization and Isoform-Specific Tissue Expression of Human NAPOR (CUGBP2) as a Candidate Gene for Familial Arrhythmogenic Right Ventricular Dysplasia. Genomics. 74(3). 396–401. 41 indexed citations

17.

Natarajan, Aruna, Hiroyuki Yamagishi, Ferhaan Ahmad, et al.. (2001). Human eHAND, but not dHAND, is Down-regulated in Cardiomyopathies. Journal of Molecular and Cellular Cardiology. 33(9). 1607–1614. 30 indexed citations

18.

Li, Duanxiang, Óscar González‐Lorenzo, Linda L. Bachinski, & Robert Roberts. (2000). Human protein tyrosine phosphatase-like gene: expression profile, genomic structure, and mutation analysis in families with ARVD. Gene. 256(1-2). 237–243. 29 indexed citations

19.

Li, Duanxiang, Paula E. Burch, Óscar González‐Lorenzo, et al.. (2000). Molecular Cloning, Expression Analysis, and Chromosome Mapping of WDR6, a Novel Human WD-Repeat Gene. Biochemical and Biophysical Research Communications. 274(1). 117–123. 13 indexed citations

20.

Li, Duanxiang, Ferhaan Ahmad, Martin J. Gardner, et al.. (2000). The Locus of a Novel Gene Responsible for Arrhythmogenic Right-Ventricular Dysplasia Characterized by Early Onset and High Penetrance Maps to Chromosome 10p12-p14. The American Journal of Human Genetics. 66(1). 148–156. 91 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.

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