Inger Tappin

1.2k total citations
16 papers, 915 citations indexed

About

Inger Tappin is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Inger Tappin has authored 16 papers receiving a total of 915 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 3 papers in Cell Biology and 3 papers in Genetics. Recurrent topics in Inger Tappin's work include DNA Repair Mechanisms (11 papers), Genomics and Chromatin Dynamics (6 papers) and DNA and Nucleic Acid Chemistry (3 papers). Inger Tappin is often cited by papers focused on DNA Repair Mechanisms (11 papers), Genomics and Chromatin Dynamics (6 papers) and DNA and Nucleic Acid Chemistry (3 papers). Inger Tappin collaborates with scholars based in United States, China and South Korea. Inger Tappin's co-authors include Jerard Hurwitz, Vladimir P. Bermudez, Andrea Farina, Young‐Hoon Kang, Ze’ev A. Ronai, Serge Y. Fuchs, Joon-Kyu Lee, Yoshimasa Maniwa, Keiko Ozato and Kyoko Yokomori and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Inger Tappin

16 papers receiving 904 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Inger Tappin United States 16 840 157 150 121 102 16 915
Arkaitz Ibarra United States 11 1.0k 1.2× 127 0.8× 155 1.0× 87 0.7× 143 1.4× 13 1.2k
Nicole Hustedt Switzerland 10 923 1.1× 236 1.5× 186 1.2× 105 0.9× 101 1.0× 11 1.0k
Ozan Aygün United States 10 750 0.9× 112 0.7× 118 0.8× 72 0.6× 100 1.0× 12 882
XiaoZhe Wang United States 10 850 1.0× 226 1.4× 186 1.2× 107 0.9× 209 2.0× 12 958
Katsuya Takenaka Japan 11 794 0.9× 191 1.2× 262 1.7× 80 0.7× 173 1.7× 15 952
Claudia Kerzendorfer Austria 14 666 0.8× 174 1.1× 90 0.6× 147 1.2× 102 1.0× 16 779
Courtney A. Lovejoy United States 10 806 1.0× 255 1.6× 108 0.7× 101 0.8× 108 1.1× 14 891
Nicholas S. Y. Ting Canada 10 744 0.9× 232 1.5× 107 0.7× 117 1.0× 109 1.1× 14 850
William F. Mueller United States 13 669 0.8× 137 0.9× 150 1.0× 145 1.2× 71 0.7× 23 830
William A. Michaud United States 13 657 0.8× 163 1.0× 192 1.3× 58 0.5× 125 1.2× 21 824

Countries citing papers authored by Inger Tappin

Since Specialization
Citations

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

Fields of papers citing papers by Inger Tappin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Inger Tappin

This figure shows the co-authorship network connecting the top 25 collaborators of Inger Tappin. A scholar is included among the top collaborators of Inger Tappin 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 Inger Tappin. Inger Tappin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

16 of 16 papers shown
1.
Wu, Kenneth, Robert Chong, Qing Yu, et al.. (2016). Suramin inhibits cullin-RING E3 ubiquitin ligases. Proceedings of the National Academy of Sciences. 113(14). E2011–8. 44 indexed citations
2.
Chong, Robert, Kenneth Wu, Donald E. Spratt, et al.. (2014). Pivotal role for the ubiquitin Y59-E51 loop in lysine 48 polyubiquitination. Proceedings of the National Academy of Sciences. 111(23). 8434–8439. 22 indexed citations
3.
Sneeden, Jessica L., Sara Grossi, Inger Tappin, Jerard Hurwitz, & Wolf‐Dietrich Heyer. (2013). Reconstitution of recombination-associated DNA synthesis with human proteins. Nucleic Acids Research. 41(9). 4913–4925. 44 indexed citations
4.
Kang, Young‐Hoon, et al.. (2013). Human Tim-Tipin complex affects the biochemical properties of the replicative DNA helicase and DNA polymerases. Proceedings of the National Academy of Sciences. 110(7). 2523–2527. 55 indexed citations
5.
Kang, Young‐Hoon, Andrea Farina, Vladimir P. Bermudez, et al.. (2013). Interaction between human Ctf4 and the Cdc45/Mcm2-7/GINS (CMG) replicative helicase. Proceedings of the National Academy of Sciences. 110(49). 19760–19765. 39 indexed citations
6.
Kang, Young‐Hoon, et al.. (2012). Properties of the human Cdc45/Mcm2-7/GINS helicase complex and its action with DNA polymerase ε in rolling circle DNA synthesis. Proceedings of the National Academy of Sciences. 109(16). 6042–6047. 108 indexed citations
7.
Yardimci, Hasan, Xindan Wang, A.B. Loveland, et al.. (2012). Bypass of a protein barrier by a replicative DNA helicase. Nature. 492(7428). 205–209. 74 indexed citations
8.
Bermudez, Vladimir P., Andrea Farina, Torahiko L. Higashi, et al.. (2012). In vitro loading of human cohesin on DNA by the human Scc2-Scc4 loader complex. Proceedings of the National Academy of Sciences. 109(24). 9366–9371. 35 indexed citations
9.
Bermudez, Vladimir P., et al.. (2011). Studies on Human DNA Polymerase ϵ and GINS Complex and Their Role in DNA Replication. Journal of Biological Chemistry. 286(33). 28963–28977. 70 indexed citations
10.
Bermudez, Vladimir P., Andrea Farina, Inger Tappin, & Jerard Hurwitz. (2010). Influence of the Human Cohesion Establishment Factor Ctf4/AND-1 on DNA Replication. Journal of Biological Chemistry. 285(13). 9493–9505. 49 indexed citations
11.
Tappin, Inger, Robert W. Lim, Bin Lü, et al.. (2010). Differential regulation of full-length genome and a single-stranded 7S DNA along the cell cycle in human mitochondria. Nucleic Acids Research. 38(19). 6466–6476. 24 indexed citations
12.
Yamoah, Kosj, Kenneth Wu, Inger Tappin, et al.. (2005). Proximity-induced activation of human Cdc34 through heterologous dimerization. Proceedings of the National Academy of Sciences. 102(42). 15053–15058. 34 indexed citations
13.
Fien, Karen, Young‐Sik Cho, Joon-Kyu Lee, et al.. (2004). Primer Utilization by DNA Polymerase α-Primase Is Influenced by Its Interaction with Mcm10p. Journal of Biological Chemistry. 279(16). 16144–16153. 68 indexed citations
14.
Bermudez, Vladimir P., Yoshimasa Maniwa, Inger Tappin, et al.. (2003). The alternative Ctf18-Dcc1-Ctf8-replication factor C complex required for sister chromatid cohesion loads proliferating cell nuclear antigen onto DNA. Proceedings of the National Academy of Sciences. 100(18). 10237–10242. 106 indexed citations
15.
Bermudez, Vladimir P., Stuart A. MacNeill, Inger Tappin, & Jerard Hurwitz. (2002). The Influence of the Cdc27 Subunit on the Properties of theSchizosaccharomyces pombe DNA Polymerase δ. Journal of Biological Chemistry. 277(39). 36853–36862. 44 indexed citations
16.
Fuchs, Serge Y., Inger Tappin, & Ze’ev A. Ronai. (2000). Stability of the ATF2 Transcription Factor Is Regulated by Phosphorylation and Dephosphorylation. Journal of Biological Chemistry. 275(17). 12560–12564. 99 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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