Henian Cao

5.7k total citations · 1 hit paper
70 papers, 3.8k citations indexed

About

Henian Cao is a scholar working on Molecular Biology, Surgery and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Henian Cao has authored 70 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 27 papers in Surgery and 18 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Henian Cao's work include Nuclear Structure and Function (17 papers), Pancreatic function and diabetes (16 papers) and Lipid metabolism and disorders (15 papers). Henian Cao is often cited by papers focused on Nuclear Structure and Function (17 papers), Pancreatic function and diabetes (16 papers) and Lipid metabolism and disorders (15 papers). Henian Cao collaborates with scholars based in Canada, United States and United Kingdom. Henian Cao's co-authors include Robert A. Hegele, Jian Wang, Bernard Zinman, Anthony J. Hanley, Stewart B. Harris, Adam D. McIntyre, Matthew R. Ban, Carol M. Anderson, John F. Robinson and Jacqueline S. Dron and has published in prestigious journals such as Journal of Biological Chemistry, The Journal of Clinical Endocrinology & Metabolism and Diabetes.

In The Last Decade

Henian Cao

70 papers receiving 3.7k citations

Hit Papers

Nuclear lamin A/C R482Q mutation in Canadian kindreds wit... 2000 2026 2008 2017 2000 100 200 300 400 500
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy
    2000 534 citations Henian Cao Human Molecular Genetics profile →

Peers

Henian Cao
Richard J. Coward United Kingdom
Tova Chajek‐Shaul Israel
Isao Ebihara Japan
D. J. Galton United Kingdom
Markus Bitzer United States
Elisabeth Widén Finland
Sabrina Prudente Italy
Hironori Yamasaki Japan
Kelly A. Volcik United States
F. Sandhofer Austria
Richard J. Coward United Kingdom
Henian Cao
Citations per year, relative to Henian Cao Henian Cao (= 1×) peers Richard J. Coward

Countries citing papers authored by Henian Cao

Since Specialization
Citations

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

Fields of papers citing papers by Henian Cao

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Henian Cao

This figure shows the co-authorship network connecting the top 25 collaborators of Henian Cao. A scholar is included among the top collaborators of Henian Cao 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 Henian Cao. Henian Cao 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.
Dron, Jacqueline S., Allison A. Dilliott, Adam D. McIntyre, et al.. (2020). Ancestry-specific profiles of genetic determinants of severe hypertriglyceridemia. Journal of clinical lipidology. 15(1). 88–96. 10 indexed citations
2.
Berberich, Amanda J., Jian Wang, Henian Cao, et al.. (2020). Simplifying Detection of Copy-Number Variations in Maturity-Onset Diabetes of the Young. Canadian Journal of Diabetes. 45(1). 71–77. 4 indexed citations
3.
Dron, Jacqueline S., Jian Wang, Adam D. McIntyre, Henian Cao, & Robert A. Hegele. (2020). The polygenic nature of mild-to-moderate hypertriglyceridemia. Journal of clinical lipidology. 14(1). 28–34.e2. 32 indexed citations
4.
Dron, Jacqueline S., Amanda J. Berberich, Jian Wang, et al.. (2020). Combined hyperlipidemia is genetically similar to isolated hypertriglyceridemia. Journal of clinical lipidology. 15(1). 79–87. 21 indexed citations
5.
Dron, Jacqueline S., Jian Wang, Cécile Low‐Kam, et al.. (2017). Polygenic determinants in extremes of high-density lipoprotein cholesterol. Journal of Lipid Research. 58(11). 2162–2170. 47 indexed citations
6.
Iacocca, Michael A., Jian Wang, Jacqueline S. Dron, et al.. (2017). Use of next-generation sequencing to detect LDLR gene copy number variation in familial hypercholesterolemia. Journal of Lipid Research. 58(11). 2202–2209. 60 indexed citations
7.
Brahm, Amanda J., Grace Wang, Jian Wang, et al.. (2016). Genetic Confirmation Rate in Clinically Suspected Maturity-Onset Diabetes of the Young. Canadian Journal of Diabetes. 40(6). 555–560. 14 indexed citations
8.
Farhan, Sali M.K., Allison A. Dilliott, Mahdi Ghani, et al.. (2016). The ONDRISeq panel: custom-designed next-generation sequencing of genes related to neurodegeneration. npj Genomic Medicine. 1(1). 16032–16032. 15 indexed citations
9.
Hegele, Robert A., Matthew R. Ban, Brooke A. Kennedy, et al.. (2009). A polygenic basis for four classical Fredrickson hyperlipoproteinemia phenotypes that are characterized by hypertriglyceridemia. Human Molecular Genetics. 18(21). 4189–4194. 74 indexed citations
10.
Cao, Henian, et al.. (2008). Heterozygous CAV1 frameshift mutations (MIM 601047) in patients with atypical partial lipodystrophy and hypertriglyceridemia. Lipids in Health and Disease. 7(1). 3–3. 115 indexed citations
11.
Hegele, Robert A., et al.. (2006). Sequencing of the Reannotated LMNB2 Gene Reveals Novel Mutations in Patients with Acquired Partial Lipodystrophy. The American Journal of Human Genetics. 79(2). 383–389. 147 indexed citations
12.
Hegele, Robert A., Bernard Zinman, Anthony J. Hanley, et al.. (2003). Genes, environment and Oji-Cree type 2 diabetes. Clinical Biochemistry. 36(3). 163–170. 39 indexed citations
13.
Dai, Erbin, Haiyan Guan, Liying Liu, et al.. (2003). Serp-1, a Viral Anti-inflammatory Serpin, Regulates Cellular Serine Proteinase and Serpin Responses to Vascular Injury. Journal of Biological Chemistry. 278(20). 18563–18572. 46 indexed citations
14.
Cao, Henian & Robert A. Hegele. (2000). Human aryl hydrocarbon receptor nuclear translocator gene (ARNT) D/N511 polymorphism. Journal of Human Genetics. 45(2). 92–93. 13 indexed citations
15.
16.
Cao, Henian & Robert A. Hegele. (2000). Human C-reactive protein (CRP) 1059G/C polymorphism. Journal of Human Genetics. 45(2). 100–101. 69 indexed citations
17.
Cao, Henian & Robert A. Hegele. (2000). Human cathepsin S gene (CTSS) promoter −25G/A polymorphism. Journal of Human Genetics. 45(2). 94–95. 6 indexed citations
18.
Hegele, Robert A., Kenneth Y. Kwan, Stewart B. Harris, et al.. (2000). NAT2 polymorphism associated with plasma glucose concentration in Canadian Oji-Cree. Pharmacogenetics. 10(3). 233–238. 14 indexed citations
19.
Cao, Henian & Robert A. Hegele. (2000). Human hepatocyte nuclear factor-1β (HNF1B) 1968A/G polymorphism. Journal of Human Genetics. 45(2). 98–99. 1 indexed citations
20.
Fehlner‐Gardiner, Christine, Henian Cao, Linda Jackson‐Boeters, et al.. (1999). Characterization of a functional relationship between hepatocyte growth factor and mouse bone marrow-derived mast cells. Differentiation. 65(1). 27–42. 9 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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