Sheng‐Ping L. Hwang

1.2k total citations
51 papers, 950 citations indexed

About

Sheng‐Ping L. Hwang is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Sheng‐Ping L. Hwang has authored 51 papers receiving a total of 950 indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 13 papers in Cell Biology and 9 papers in Genetics. Recurrent topics in Sheng‐Ping L. Hwang's work include Congenital heart defects research (12 papers), Developmental Biology and Gene Regulation (11 papers) and Protist diversity and phylogeny (7 papers). Sheng‐Ping L. Hwang is often cited by papers focused on Congenital heart defects research (12 papers), Developmental Biology and Gene Regulation (11 papers) and Protist diversity and phylogeny (7 papers). Sheng‐Ping L. Hwang collaborates with scholars based in Taiwan, United States and China. Sheng‐Ping L. Hwang's co-authors include Jeng Chang, Chih‐Ching Chung, William J. Lennarz, Chang‐Jen Huang, Yi‐Chung Chen, Pung‐Pung Hwang, I-Chen Li, Li‐Jane Shih, Jacqueline S. Partin and Hsing‐Juh Lin and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Development.

In The Last Decade

Sheng‐Ping L. Hwang

51 papers receiving 937 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Sheng‐Ping L. Hwang Taiwan 19 513 195 161 124 101 51 950
Roberta Russo Italy 24 637 1.2× 200 1.0× 159 1.0× 163 1.3× 62 0.6× 74 1.6k
Shyh‐Jye Lee Taiwan 23 603 1.2× 116 0.6× 309 1.9× 69 0.6× 83 0.8× 49 1.2k
Athula H. Wikramanayake United States 25 1.5k 2.8× 76 0.4× 133 0.8× 183 1.5× 149 1.5× 51 2.1k
Federico Caicci Italy 24 1.1k 2.2× 211 1.1× 162 1.0× 81 0.7× 74 0.7× 77 2.0k
J. Ehrenfeld France 27 1.2k 2.4× 428 2.2× 121 0.8× 62 0.5× 61 0.6× 59 2.0k
Claire Larroux Australia 16 761 1.5× 202 1.0× 87 0.5× 78 0.6× 247 2.4× 18 1.6k
Uri Abdu Israel 22 672 1.3× 380 1.9× 273 1.7× 42 0.3× 174 1.7× 56 1.4k
Michael C. Schmale United States 18 208 0.4× 197 1.0× 76 0.5× 78 0.6× 107 1.1× 51 934
Éric Röttinger France 21 1.3k 2.5× 164 0.8× 161 1.0× 271 2.2× 131 1.3× 45 2.0k
Remo Sanges Italy 26 1.4k 2.6× 410 2.1× 77 0.5× 357 2.9× 238 2.4× 79 2.1k

Countries citing papers authored by Sheng‐Ping L. Hwang

Since Specialization
Citations

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

Fields of papers citing papers by Sheng‐Ping L. Hwang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sheng‐Ping L. Hwang. 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 Sheng‐Ping L. Hwang. The network helps show where Sheng‐Ping L. Hwang may publish in the future.

Co-authorship network of co-authors of Sheng‐Ping L. Hwang

This figure shows the co-authorship network connecting the top 25 collaborators of Sheng‐Ping L. Hwang. A scholar is included among the top collaborators of Sheng‐Ping L. Hwang 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 Sheng‐Ping L. Hwang. Sheng‐Ping L. Hwang 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.
Lin, Che-Yi, Mei‐Yeh Jade Lu, Jia‐Xing Yue, et al.. (2020). Molecular asymmetry in the cephalochordate embryo revealed by single-blastomere transcriptome profiling. PLoS Genetics. 16(12). e1009294–e1009294. 5 indexed citations
2.
Huang, Chang‐Jen, et al.. (2020). Zebrafish Cdx1b modulates epithalamic asymmetry by regulating ndr2 and lft1 expression. Developmental Biology. 470. 21–36. 4 indexed citations
3.
Liau, Ian, et al.. (2018). Zebrafish VCAP1X2 regulates cardiac contractility and proliferation of cardiomyocytes and epicardial cells. Scientific Reports. 8(1). 7856–7856. 7 indexed citations
4.
Her, Guor Mour, Yun‐Wen Chen, Pei‐Yi Wu, et al.. (2017). ErbB2 regulates autophagic flux to modulate the proteostasis of APP-CTFs in Alzheimer’s disease. Proceedings of the National Academy of Sciences. 114(15). E3129–E3138. 66 indexed citations
5.
Monte, Aaron, et al.. (2017). A novel stilbene-like compound that inhibits melanoma growth by regulating melanocyte differentiation and proliferation. Toxicology and Applied Pharmacology. 337. 30–38. 5 indexed citations
6.
Jiang, Yun‐Jin, Chiou‐Hwa Yuh, C.M. Wang, et al.. (2016). A Sketch of the Taiwan Zebrafish Core Facility. Zebrafish. 13(S1). S–24. 14 indexed citations
7.
Yuan, Rey-Yue, Chih‐Ming Chou, Yi‐Chung Chen, et al.. (2016). Zebrafish cyclin Dx is required for development of motor neuron progenitors and its expression is regulated by hypoxia-inducible factor 2α. Scientific Reports. 6(1). 28297–28297. 9 indexed citations
8.
9.
Chen, Yi‐Chung, et al.. (2012). Zebrafish Agr2 Is Required for Terminal Differentiation of Intestinal Goblet Cells. PLoS ONE. 7(4). e34408–e34408. 37 indexed citations
10.
Chen, Yihua, et al.. (2009). Zebrafish cdx1b regulates differentiation of various intestinal cell lineages. Developmental Dynamics. 238(5). 1021–1032. 32 indexed citations
11.
12.
Chen, Yi‐Chung, Chia‐Hsiung Cheng, Chin‐Chun Hung, et al.. (2009). Recapitulation of zebrafish sncga expression pattern and labeling the habenular complex in transgenic zebrafish using green fluorescent protein reporter gene. Developmental Dynamics. 238(3). 746–754. 29 indexed citations
13.
Lin, Chia‐Chi, Chih‐Ching Chung, Cheng-Ying Chu, et al.. (2008). Zebrafishcdx1bregulates expression of downstream factors of Nodal signaling during early endoderm formation. Development. 135(5). 941–952. 24 indexed citations
14.
Chung, Chih‐Ching, Sheng‐Ping L. Hwang, & Jeng Chang. (2008). The Identification of Three Novel Genes Involved in the Rapid-Growth Regulation in a Marine Diatom, Skeletonema costatum. Marine Biotechnology. 11(3). 356–367. 1 indexed citations
15.
Shih, Li‐Jane, et al.. (2006). Characterization of the agr2 gene, a homologue of X. laevis anterior gradient 2, from the zebrafish, Danio rerio. Gene Expression Patterns. 7(4). 452–460. 39 indexed citations
16.
Huang, Chang‐Jen, et al.. (2004). Zebrafish heparin-binding neurotrophic factor enhances neurite outgrowth during its development. Biochemical and Biophysical Research Communications. 321(2). 502–509. 6 indexed citations
17.
Hwang, Sheng‐Ping L., et al.. (2003). Evolutionary Conservation of the Bone Morphogenetic Protein 2/4 Gene between Diploblastic and Triploblastic Metazoans. Zoological studies. 42(1). 227–234. 7 indexed citations
18.
Hwang, Sheng‐Ping L., et al.. (2003). Novel pattern ofAtXloxgene expression in starfishArchaster typicusembryos. Development Growth & Differentiation. 45(1). 85–93. 7 indexed citations
19.
Hwang, Sheng‐Ping L. & William J. Lennarz. (1993). Studies on the Cellular Pathway Involved in Assembly of the Embryonic Sea Urchin Spicule. Experimental Cell Research. 205(2). 383–387. 27 indexed citations
20.
Kabakoff, Bruce, Sheng‐Ping L. Hwang, & William J. Lennarz. (1992). Characterization of post-translational modifications common to three primary mesenchyme cell-specific glycoproteins involved in sea urchin embryonic skeleton formation. Developmental Biology. 150(2). 294–305. 24 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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