Albert M. Cheh

1.4k total citations
21 papers, 922 citations indexed

About

Albert M. Cheh is a scholar working on Molecular Biology, Cancer Research and Health, Toxicology and Mutagenesis. According to data from OpenAlex, Albert M. Cheh has authored 21 papers receiving a total of 922 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 5 papers in Cancer Research and 4 papers in Health, Toxicology and Mutagenesis. Recurrent topics in Albert M. Cheh's work include DNA and Nucleic Acid Chemistry (8 papers), Carcinogens and Genotoxicity Assessment (5 papers) and DNA Repair Mechanisms (3 papers). Albert M. Cheh is often cited by papers focused on DNA and Nucleic Acid Chemistry (8 papers), Carcinogens and Genotoxicity Assessment (5 papers) and DNA Repair Mechanisms (3 papers). Albert M. Cheh collaborates with scholars based in United States, Japan and Australia. Albert M. Cheh's co-authors include Jane M. Sayer, J. B. Neilands, Donald M. Jerina, Bruce E. Dale, Nirmal Uppugundla, Shishir P. S. Chundawat, Leonardo da Costa Sousa, Venkatesh Balan, Umesh P. Agarwal and Giovanni Bellesia and has published in prestigious journals such as Science, Journal of the American Chemical Society and Journal of Biological Chemistry.

In The Last Decade

Albert M. Cheh

21 papers receiving 862 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Albert M. Cheh United States 14 353 276 220 217 194 21 922
Irene Witte Germany 19 298 0.8× 103 0.4× 301 1.4× 246 1.1× 20 0.1× 44 927
Jinglin Tian China 15 268 0.8× 210 0.8× 53 0.2× 114 0.5× 107 0.6× 28 868
Yoshikuni Yakabe Japan 16 172 0.5× 58 0.2× 98 0.4× 351 1.6× 59 0.3× 33 793
Reinhard Kreiling Germany 19 107 0.3× 145 0.5× 189 0.9× 357 1.6× 34 0.2× 28 1.2k
Zuzana Magdolénová Norway 14 173 0.5× 260 0.9× 180 0.8× 289 1.3× 156 0.8× 17 1.2k
Abdul Jabar Pakistan 10 160 0.5× 157 0.6× 57 0.3× 251 1.2× 213 1.1× 15 870
Markus Schulz Germany 13 104 0.3× 124 0.4× 180 0.8× 255 1.2× 62 0.3× 19 787
Hiroyuki Sawanishi Japan 16 306 0.9× 71 0.3× 188 0.9× 155 0.7× 19 0.1× 86 850
Mehran Pazirandeh United States 13 447 1.3× 143 0.5× 32 0.1× 118 0.5× 35 0.2× 20 842
Genevieve M. Fent United States 8 181 0.5× 394 1.4× 29 0.1× 122 0.6× 402 2.1× 10 1.1k

Countries citing papers authored by Albert M. Cheh

Since Specialization
Citations

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

Fields of papers citing papers by Albert M. Cheh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Albert M. Cheh. 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 Albert M. Cheh. The network helps show where Albert M. Cheh may publish in the future.

Co-authorship network of co-authors of Albert M. Cheh

This figure shows the co-authorship network connecting the top 25 collaborators of Albert M. Cheh. A scholar is included among the top collaborators of Albert M. Cheh 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 Albert M. Cheh. Albert M. Cheh 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.
Humpula, James F., Nirmal Uppugundla, Ramin Vismeh, et al.. (2013). Probing the nature of AFEX-pretreated corn stover derived decomposition products that inhibit cellulase activity. Bioresource Technology. 152. 38–45. 15 indexed citations
2.
Chundawat, Shishir P. S., Giovanni Bellesia, Nirmal Uppugundla, et al.. (2011). Restructuring the Crystalline Cellulose Hydrogen Bond Network Enhances Its Depolymerization Rate. Journal of the American Chemical Society. 133(29). 11163–11174. 302 indexed citations
3.
Sayer, Jane M., Haruhiko Yagi, Heiko Kroth, et al.. (2005). Error-prone Translesion Synthesis by Human DNA Polymerase η on DNA-containing Deoxyadenosine Adducts of 7,8-Dihydroxy-9,10-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene. Journal of Biological Chemistry. 280(48). 39684–39692. 15 indexed citations
4.
Kroth, Heiko, Jane M. Sayer, Chikahide Masutani, et al.. (2002). Preferential Misincorporation of Purine Nucleotides by Human DNA Polymerase η Opposite Benzo[a]pyrene 7,8-Diol 9,10-Epoxide Deoxyguanosine Adducts. Journal of Biological Chemistry. 277(14). 11765–11771. 77 indexed citations
7.
Cheh, Albert M., Farida Latif, Richard Fishel, et al.. (1994). DNA Strand Breaks Induced by Configurationally Isomeric Hydrocarbon Diol Epoxides. Drug Metabolism Reviews. 26(1-2). 287–299. 7 indexed citations
8.
Lakshman, Mahesh K., Wei Xiao, Jane M. Sayer, Albert M. Cheh, & Donald M. Jerina. (1994). Synthesis and Assignment of Absolute Configuration to the N6-Deoxyadenosine Adducts Resulting from Cis and Trans Ring-Opening of Phenanthrene 9,10-Oxide. The Journal of Organic Chemistry. 59(7). 1755–1760. 8 indexed citations
9.
Cheh, Albert M., Anju Chadha, Jane M. Sayer, et al.. (1993). Structures of covalent nucleoside adducts formed from adenine, guanine, and cytosine bases of DNA and the optically active bay-region 3,4-diol 1,2-epoxides of benz[a]anthracene. The Journal of Organic Chemistry. 58(15). 4013–4022. 16 indexed citations
10.
Chadha, Anju, et al.. (1991). Covalent Bonding of Bay-Region Diol Epoxides to Nucleic Acids. Advances in experimental medicine and biology. 283. 533–553. 83 indexed citations
11.
Cheh, Albert M., Haruhiko Yagi, & Donald M. Jerina. (1990). Stereoselective release of polycyclic aromatic hydrocarbon-deoxyadenosine adducts from DNA by the phosphorus-32 postlabeling and deoxyribonuclease I/snake venom phosphodiesterase digestion methods. Chemical Research in Toxicology. 3(6). 545–550. 17 indexed citations
12.
Chadha, Anju, Jane M. Sayer, Herman J. C. Yeh, et al.. (1989). Structures of covalent nucleoside adducts formed from adenine, guanine, and cytosine bases of DNA and the optically active bay-region 3,4-diol 1,2-epoxides of dibenz[a,j]anthracene. Journal of the American Chemical Society. 111(14). 5456–5463. 32 indexed citations
13.
Cheh, Albert M.. (1986). Mutagen production by chlorination of methylated α,β-unsaturated ketones. Mutation Research/Genetic Toxicology. 169(1-2). 1–9. 6 indexed citations
14.
Cheh, Albert M., et al.. (1985). Production of mutagenic artifacts by the action of residual chlorine on xad-4 resin. Journal of Chromatography A. 325(1). 95–102. 9 indexed citations
15.
Cheh, Albert M. & Robert E. Carlson. (1981). Determination of potentially mutagenic and carcinogenic electrophiles in environmental samples. Analytical Chemistry. 53(7). 1001–1006. 33 indexed citations
16.
Cheh, Albert M., et al.. (1980). A comparison of the ability of frog and rat S‐9 to activate promutagens in the Ames test. Environmental Mutagenesis. 2(4). 487–508. 7 indexed citations
17.
Cheh, Albert M., et al.. (1980). Nonvolatile Mutagens in Drinking Water: Production by Chlorination and Destruction by Sulfite. Science. 207(4426). 90–92. 145 indexed citations
18.
Wood, John M., et al.. (1978). Mechanisms for the biomethylation of metals and metalloids.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 37(1). 16–21. 27 indexed citations
19.
Ridley, William P., et al.. (1977). Recent studies on biomethylation and demethylation of toxic elements.. Environmental Health Perspectives. 19. 43–46. 21 indexed citations
20.
Cheh, Albert M. & J. B. Neilands. (1973). Zinc, an essential metal ion for beef liver δ-aminolevulinate dehydratase. Biochemical and Biophysical Research Communications. 55(4). 1060–1063. 69 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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