Shing H. Zhan

2.5k total citations
30 papers, 1.2k citations indexed

About

Shing H. Zhan is a scholar working on Molecular Biology, Genetics and Ecology. According to data from OpenAlex, Shing H. Zhan has authored 30 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 12 papers in Genetics and 7 papers in Ecology. Recurrent topics in Shing H. Zhan's work include Chromosomal and Genetic Variations (6 papers), Genetic diversity and population structure (5 papers) and Genomics and Phylogenetic Studies (4 papers). Shing H. Zhan is often cited by papers focused on Chromosomal and Genetic Variations (6 papers), Genetic diversity and population structure (5 papers) and Genomics and Phylogenetic Studies (4 papers). Shing H. Zhan collaborates with scholars based in Canada, United States and Taiwan. Shing H. Zhan's co-authors include Itay Mayrose, Michael S. Barker, Sarah P. Otto, Loren H. Rieseberg, Carl J. Rothfels, Yujia A. Chan, Steven J.M. Jones, Anthony P. Fejes, Yaoqing Shen and Benjamin E. Deverman and has published in prestigious journals such as Science, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Shing H. Zhan

30 papers receiving 1.2k citations

Peers

Shing H. Zhan
André Pires‐daSilva United States
Julien Roux Switzerland
Yemin Lan United States
Ran Zhao China
Anaïs F. Bardet France
Ben‐Yang Liao Taiwan
Aiqing Li China
Anqi Zhu United States
Scott E. Baird United States
J.A. Luty United States
André Pires‐daSilva United States
Shing H. Zhan
Citations per year, relative to Shing H. Zhan Shing H. Zhan (= 1×) peers André Pires‐daSilva

Countries citing papers authored by Shing H. Zhan

Since Specialization
Citations

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

Fields of papers citing papers by Shing H. Zhan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shing H. Zhan. 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 Shing H. Zhan. The network helps show where Shing H. Zhan may publish in the future.

Co-authorship network of co-authors of Shing H. Zhan

This figure shows the co-authorship network connecting the top 25 collaborators of Shing H. Zhan. A scholar is included among the top collaborators of Shing H. Zhan 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 Shing H. Zhan. Shing H. Zhan 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
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Román‐Palacios, Cristian, et al.. (2021). Animal chromosome counts reveal a similar range of chromosome numbers but with less polyploidy in animals compared to flowering plants. Journal of Evolutionary Biology. 34(8). 1333–1339. 21 indexed citations
4.
Chen, Albert T., et al.. (2021). COVID-19 CG enables SARS-CoV-2 mutation and lineage tracking by locations and dates of interest. eLife. 10. 71 indexed citations
5.
Chan, Yujia A. & Shing H. Zhan. (2021). The Emergence of the Spike Furin Cleavage Site in SARS-CoV-2. Molecular Biology and Evolution. 39(1). 46 indexed citations
6.
Zhan, Shing H., Sepideh Massoumi Alamouti, Brian Kwok, et al.. (2021). Target capture sequencing of SARS-CoV-2 genomes using the ONETest Coronaviruses Plus. Diagnostic Microbiology and Infectious Disease. 101(3). 115508–115508. 3 indexed citations
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Zhan, Shing H., et al.. (2020). Hidden introductions of freshwater red algae via the aquarium trade exposed by DNA barcodes. Environmental DNA. 3(2). 481–491. 4 indexed citations
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Zhan, Shing H., et al.. (2019). Aggregated Dendrograms for Visual Comparison between Many Phylogenetic Trees. IEEE Transactions on Visualization and Computer Graphics. 26(9). 2732–2747. 9 indexed citations
10.
Mandáková, Terezie, et al.. (2017). Multispeed genome diploidization and diversification after an ancient allopolyploidization. Molecular Ecology. 26(22). 6445–6462. 47 indexed citations
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Zhan, Shing H., et al.. (2016). Phylogenetic evidence for cladogenetic polyploidization in land plants. American Journal of Botany. 103(7). 1252–1258. 24 indexed citations
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Qadir, Mohammed A., et al.. (2014). ChildSeq-RNA. Journal of Molecular Diagnostics. 16(3). 361–370. 21 indexed citations
13.
Demos, Michelle, Clara DM van Karnebeek, Colin J.D. Ross, et al.. (2014). A novel recurrent mutation in ATP1A3 causes CAPOS syndrome. Orphanet Journal of Rare Diseases. 9(1). 15–15. 135 indexed citations
14.
Greenway, Steven C., Ross McLeod, Stacey Hume, et al.. (2013). Exome Sequencing Identifies a Novel Variant in ACTC1 Associated With Familial Atrial Septal Defect. Canadian Journal of Cardiology. 30(2). 181–187. 29 indexed citations
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Zhan, Shing H., et al.. (2013). Data from: Comparative analysis reveals that polyploidy does not decelerate diversification in fish. Data Archiving and Networked Services (DANS). 1 indexed citations
16.
Doherty, Dan, Albert E. Chudley, Gail Coghlan, et al.. (2012). GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome. The American Journal of Human Genetics. 91(1). 209–209. 2 indexed citations
17.
Doherty, Dan, Albert E. Chudley, Gail Coghlan, et al.. (2012). GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome. The American Journal of Human Genetics. 90(6). 1088–1093. 81 indexed citations
18.
Kane, Nolan C., Michael S. Barker, Shing H. Zhan, & Loren H. Rieseberg. (2011). Molecular Evolution across the Asteraceae: Micro- and Macroevolutionary Processes. Molecular Biology and Evolution. 28(12). 3225–3235. 17 indexed citations
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Gibson, William T., Rebecca L. Hood, Shing H. Zhan, et al.. (2011). Mutations in EZH2 Cause Weaver Syndrome. The American Journal of Human Genetics. 90(1). 110–118. 196 indexed citations
20.
Xiang, Hua, Ming Li, Fei Yang, et al.. (2008). Fine mapping of Ekp-1, a locus associated with silkworm (Bombyx mori) proleg development. Heredity. 100(5). 533–540. 13 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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