Sheng-Shung Cheng

1.4k total citations
37 papers, 1.1k citations indexed

About

Sheng-Shung Cheng is a scholar working on Pollution, Building and Construction and Biomedical Engineering. According to data from OpenAlex, Sheng-Shung Cheng has authored 37 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Pollution, 19 papers in Building and Construction and 9 papers in Biomedical Engineering. Recurrent topics in Sheng-Shung Cheng's work include Anaerobic Digestion and Biogas Production (19 papers), Wastewater Treatment and Nitrogen Removal (17 papers) and Biofuel production and bioconversion (9 papers). Sheng-Shung Cheng is often cited by papers focused on Anaerobic Digestion and Biogas Production (19 papers), Wastewater Treatment and Nitrogen Removal (17 papers) and Biofuel production and bioconversion (9 papers). Sheng-Shung Cheng collaborates with scholars based in Taiwan, Japan and Poland. Sheng-Shung Cheng's co-authors include I‐Cheng Tseng, Jer‐Horng Wu, Shiue-Lin Li, Ta‐Chen Lin, Yoichi Kamagata, Hideki Harada, Yanling Qiu, Akiyoshi Ohashi, Hiroyuki Imachi and Yuji Sekiguchi and has published in prestigious journals such as Applied and Environmental Microbiology, Journal of Hazardous Materials and Bioresource Technology.

In The Last Decade

Sheng-Shung Cheng

37 papers receiving 1.1k 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-Shung Cheng Taiwan 19 560 469 263 236 211 37 1.1k
Jana Zábranská Czechia 21 617 1.1× 715 1.5× 228 0.9× 346 1.5× 156 0.7× 39 1.6k
Thérèse Mahony Ireland 22 736 1.3× 928 2.0× 285 1.1× 308 1.3× 305 1.4× 34 1.6k
Jan Sipma Netherlands 18 551 1.0× 385 0.8× 241 0.9× 476 2.0× 346 1.6× 27 1.5k
Akiko Miya Japan 14 349 0.6× 186 0.4× 148 0.6× 273 1.2× 154 0.7× 28 799
Maoan Du China 18 534 1.0× 225 0.5× 371 1.4× 283 1.2× 93 0.4× 29 1.4k
José M. Carvajal‐Arroyo Belgium 22 880 1.6× 212 0.5× 682 2.6× 261 1.1× 242 1.1× 31 1.5k
A. J. Cavaleiro Portugal 18 447 0.8× 932 2.0× 194 0.7× 320 1.4× 253 1.2× 49 1.3k
Jeong-Hoon Park South Korea 11 289 0.5× 483 1.0× 393 1.5× 212 0.9× 81 0.4× 17 900
Andreia F. Salvador Portugal 17 361 0.6× 649 1.4× 371 1.4× 252 1.1× 179 0.8× 44 1.2k
Colin Wardman United States 6 323 0.6× 704 1.5× 786 3.0× 256 1.1× 190 0.9× 6 1.3k

Countries citing papers authored by Sheng-Shung Cheng

Since Specialization
Citations

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

Fields of papers citing papers by Sheng-Shung Cheng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sheng-Shung Cheng. 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-Shung Cheng. The network helps show where Sheng-Shung Cheng may publish in the future.

Co-authorship network of co-authors of Sheng-Shung Cheng

This figure shows the co-authorship network connecting the top 25 collaborators of Sheng-Shung Cheng. A scholar is included among the top collaborators of Sheng-Shung Cheng 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-Shung Cheng. Sheng-Shung Cheng 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, Shiue-Lin, Jui-Hung Yen, Kenji Kano, et al.. (2018). Using metabolic charge production in the tricarboxylic acid cycle (QTCA) to evaluate the extracellular-electron-transfer performances of Shewanella spp.. Bioelectrochemistry. 124. 119–126. 5 indexed citations
2.
Li, Shiue-Lin, et al.. (2017). A metabolic-activity-detecting approach to life detection: Restoring a chemostat from stop-feeding using a rapid bioactivity assay. Bioelectrochemistry. 118. 147–153. 8 indexed citations
3.
Li, Shiue-Lin, et al.. (2017). Amylolysis is predominated by cell-surface-bound hydrolase during anaerobic fermentation under mesophilic conditions. Journal of Bioscience and Bioengineering. 125(4). 432–438. 7 indexed citations
7.
Cheng, Sheng-Shung, et al.. (2011). Bio-hydrogen behavior of suspended and attached microorganisms in anaerobic fluidized bed. International Journal of Hydrogen Energy. 36(14). 8800–8808. 6 indexed citations
8.
Li, Shiue-Lin, Stefano Freguia, Shiu‐Mei Liu, et al.. (2010). Effects of oxygen on Shewanella decolorationis NTOU1 electron transfer to carbon-felt electrodes. Biosensors and Bioelectronics. 25(12). 2651–2656. 27 indexed citations
9.
Cheng, Sheng-Shung, et al.. (2010). Process recovery of biohydrogenation in a pilot plant from methanogens invasion. International Journal of Hydrogen Energy. 36(14). 8779–8784. 13 indexed citations
10.
Lin, Ta‐Chen, et al.. (2009). Ex situ bioremediation of oil-contaminated soil. Journal of Hazardous Materials. 176(1-3). 27–34. 110 indexed citations
11.
Wang, Yu‐Hsuan, et al.. (2009). Starch hydrolysis characteristics of hydrogen producing sludge in thermophilic hydrogen fermentor fed with kitchen waste. International Journal of Hydrogen Energy. 34(17). 7435–7440. 15 indexed citations
12.
Tsujimura, Seiya, et al.. (2007). Self-excreted mediator from Escherichia coli K-12 for electron transfer to carbon electrodes. Applied Microbiology and Biotechnology. 76(6). 1439–1446. 63 indexed citations
13.
Cheng, Sheng-Shung, et al.. (2006). Escherichia coli-catalyzed bioelectrochemical oxidation of acetate in the presence of mediators. Bioelectrochemistry. 69(1). 74–81. 13 indexed citations
14.
Qiu, Yanling, Yuji Sekiguchi, Satoshi Hanada, et al.. (2006). Pelotomaculum terephthalicum sp. nov. and Pelotomaculum isophthalicum sp. nov.: two anaerobic bacteria that degrade phthalate isomers in syntrophic association with hydrogenotrophic methanogens. Archives of Microbiology. 185(3). 172–182. 90 indexed citations
15.
Qiu, Yanling, Yuji Sekiguchi, Hiroyuki Imachi, et al.. (2004). Identification and Isolation of Anaerobic, Syntrophic Phthalate Isomer-Degrading Microbes from Methanogenic Sludges Treating Wastewater from Terephthalate Manufacturing. Applied and Environmental Microbiology. 70(3). 1617–1626. 73 indexed citations
16.
Qiu, Yanling, Yuji Sekiguchi, Hiroyuki Imachi, et al.. (2003). Sporotomaculum syntrophicum sp. nov., a novel anaerobic, syntrophic benzoate-degrading bacterium isolated from methanogenic sludge treating wastewater from terephthalate manufacturing. Archives of Microbiology. 179(4). 242–249. 39 indexed citations
17.
Wu, Jer‐Horng, Wen‐Tso Liu, I‐Cheng Tseng, & Sheng-Shung Cheng. (2001). Characterization of a 4-Methylbenzoate-Degrading Methanogenic Consortium as Determined by Small-Subunit rDNA Sequence Analysis.. Journal of Bioscience and Bioengineering. 91(5). 449–455. 35 indexed citations
18.
Lay, Jiunn‐Jyi & Sheng-Shung Cheng. (1998). Influence of Hydraulic Loading Rate on UASB Reactor Treating Phenolic Wastewater. Journal of Environmental Engineering. 124(9). 829–837. 18 indexed citations
19.
Cheng, Sheng-Shung, et al.. (1991). The Influence of Glucose Supplement on the Degradation of Catechol. Water Science & Technology. 23(7-9). 1201–1209. 25 indexed citations
20.
Kim, Byung R., et al.. (1986). Adsorption, desorption, and bioregeneration in an anaerobic, granular activated carbon reactor for the removal of phenol. Journal of Water Pollution Control Federation. 58(1). 35–40. 23 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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