Fred E. Indig

4.6k total citations
55 papers, 3.5k citations indexed

About

Fred E. Indig is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Fred E. Indig has authored 55 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 13 papers in Cell Biology and 9 papers in Cellular and Molecular Neuroscience. Recurrent topics in Fred E. Indig's work include DNA Repair Mechanisms (15 papers), Mitochondrial Function and Pathology (5 papers) and Neuropeptides and Animal Physiology (5 papers). Fred E. Indig is often cited by papers focused on DNA Repair Mechanisms (15 papers), Mitochondrial Function and Pathology (5 papers) and Neuropeptides and Animal Physiology (5 papers). Fred E. Indig collaborates with scholars based in United States, Israel and Switzerland. Fred E. Indig's co-authors include Dennis D. Taub, Ashani T. Weeraratna, Myriam Gorospe, Michael P. O’Connell, Jennifer L. Martindale, Xiaoling Yang, Vilhelm A. Bohr, Geppino Falco, Martin Latterich and Mark H. Ginsberg and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Fred E. Indig

55 papers receiving 3.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fred E. Indig United States 31 2.5k 550 542 535 403 55 3.5k
Mirko H. H. Schmidt Germany 36 2.5k 1.0× 550 1.0× 780 1.4× 647 1.2× 312 0.8× 73 4.5k
Senén Vilaró Spain 39 2.0k 0.8× 795 1.4× 438 0.8× 739 1.4× 380 0.9× 108 4.3k
Pär Gerwins Sweden 33 2.4k 1.0× 467 0.8× 597 1.1× 597 1.1× 296 0.7× 60 4.1k
Karl N. Miller United States 19 2.1k 0.8× 717 1.3× 588 1.1× 688 1.3× 744 1.8× 24 3.8k
S. Patricia Becerra United States 39 2.7k 1.1× 542 1.0× 438 0.8× 179 0.3× 251 0.6× 93 4.1k
Aiguo Shen China 32 2.3k 0.9× 328 0.6× 620 1.1× 683 1.3× 267 0.7× 179 3.6k
Kazunori Akimoto Japan 29 2.5k 1.0× 931 1.7× 320 0.6× 422 0.8× 258 0.6× 72 3.4k
Taro Okada Japan 29 3.6k 1.5× 1.2k 2.2× 350 0.6× 310 0.6× 671 1.7× 64 4.8k
Marina Macı́as-Silva Mexico 23 2.3k 0.9× 229 0.4× 322 0.6× 499 0.9× 147 0.4× 74 3.1k
François-Xavier Claret United States 17 3.2k 1.3× 606 1.1× 687 1.3× 964 1.8× 163 0.4× 20 4.1k

Countries citing papers authored by Fred E. Indig

Since Specialization
Citations

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

Fields of papers citing papers by Fred E. Indig

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fred E. Indig. 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 Fred E. Indig. The network helps show where Fred E. Indig may publish in the future.

Co-authorship network of co-authors of Fred E. Indig

This figure shows the co-authorship network connecting the top 25 collaborators of Fred E. Indig. A scholar is included among the top collaborators of Fred E. Indig 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 Fred E. Indig. Fred E. Indig 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.
Thakur, Bhushan, Haiqing Fu, Christophe E. Redon, et al.. (2022). Convergence of SIRT1 and ATR signaling to modulate replication origin dormancy. Nucleic Acids Research. 50(9). 5111–5128. 14 indexed citations
2.
Cui, Jing, Jingcheng Zhou, Weiqing He, et al.. (2022). Targeting selenoprotein H in the nucleolus suppresses tumors and metastases by Isovalerylspiramycin I. Journal of Experimental & Clinical Cancer Research. 41(1). 126–126. 20 indexed citations
3.
Jang, Sang‐Min, Jenny F. Nathans, Haiqing Fu, et al.. (2020). The RepID–CRL4 ubiquitin ligase complex regulates metaphase to anaphase transition via BUB3 degradation. Nature Communications. 11(1). 24–24. 27 indexed citations
4.
Wnorowski, Artur, Rajib Paul, Robert P. Wersto, et al.. (2017). Concurrent activation of β 2 -adrenergic receptor and blockage of GPR55 disrupts pro-oncogenic signaling in glioma cells. Cellular Signalling. 36. 176–188. 11 indexed citations
5.
Noh, Ji Heon, Kyoung Mi Kim, Kotb Abdelmohsen, et al.. (2016). HuR and GRSF1 modulate the nuclear export and mitochondrial localization of the lncRNARMRP. Genes & Development. 30(10). 1224–1239. 183 indexed citations
6.
Eitan, Erez, Ronald S. Petralia, Ya-Xian Wang, et al.. (2016). Probing extracellular Sonic hedgehog in neurons. Biology Open. 5(8). 1086–1092. 11 indexed citations
7.
Singh, N., et al.. (2015). The development of mitochondrial membrane affinity chromatography columns for the study of mitochondrial transmembrane proteins. Analytical Biochemistry. 484. 154–161. 8 indexed citations
8.
Chen, Kuang‐Hueih, Asish Dasgupta, Jinhui Ding, et al.. (2013). Role of mitofusin 2 (Mfn2) in controlling cellular proliferation. The FASEB Journal. 28(1). 382–394. 93 indexed citations
9.
Paul, Rajib, Artur Wnorowski, Isabel González‐Mariscal, et al.. (2013). (R,R′)-4′-methoxy-1-naphthylfenoterol targets GPR55-mediated ligand internalization and impairs cancer cell motility. Biochemical Pharmacology. 87(4). 547–561. 18 indexed citations
10.
Krzysik-Walker, Susan M., Isabel González‐Mariscal, Morten Scheibye‐Knudsen, Fred E. Indig, & Michel Bernier. (2012). The Biarylpyrazole Compound AM251 Alters Mitochondrial Physiology via Proteolytic Degradation of ERRα. Molecular Pharmacology. 83(1). 157–166. 8 indexed citations
11.
Zalzman, Michal, Geppino Falco, Lioudmila V. Sharova, et al.. (2010). Zscan4 regulates telomere elongation and genomic stability in ES cells. Nature. 464(7290). 858–863. 336 indexed citations
12.
O’Connell, Michael P., Jennifer L. Fiori, Fred E. Indig, et al.. (2009). Wnt5A Activates the Calpain-Mediated Cleavage of Filamin A. Journal of Investigative Dermatology. 129(7). 1782–1789. 58 indexed citations
13.
Baatar, Dolgor, Purevdorj B. Olkhanud, Valerie Wells, et al.. (2009). Tregs utilize β-galactoside-binding protein to transiently inhibit PI3K/p21ras activity of human CD8+ T cells to block their TCR-mediated ERK activity and proliferation. Brain Behavior and Immunity. 23(7). 1028–1037. 15 indexed citations
14.
Dissanayake, Samudra K., Michael S. Wade, Carrie E. Johnson, et al.. (2007). The Wnt5A/Protein Kinase C Pathway Mediates Motility in Melanoma Cells via the Inhibition of Metastasis Suppressors and Initiation of an Epithelial to Mesenchymal Transition. Journal of Biological Chemistry. 282(23). 17259–17271. 294 indexed citations
15.
D’Souza, Theresa, Fred E. Indig, & Patrice J. Morin. (2007). Phosphorylation of claudin-4 by PKCε regulates tight junction barrier function in ovarian cancer cells. Experimental Cell Research. 313(15). 3364–3375. 75 indexed citations
16.
Imam, Syed Z., Fred E. Indig, Wen‐Hsing Cheng, et al.. (2007). Cockayne syndrome protein B interacts with and is phosphorylated by c-Abl tyrosine kinase. Nucleic Acids Research. 35(15). 4941–4951. 18 indexed citations
17.
Leotlela, Poloko D., Michael S. Wade, Paul H. Duray, et al.. (2006). Claudin-1 overexpression in melanoma is regulated by PKC and contributes to melanoma cell motility. Oncogene. 26(26). 3846–3856. 137 indexed citations
18.
Ahn, Byungchan, Jeanine A. Harrigan, Fred E. Indig, David M. Wilson, & Vilhelm A. Bohr. (2004). Regulation of WRN Helicase Activity in Human Base Excision Repair. Journal of Biological Chemistry. 279(51). 53465–53474. 70 indexed citations
19.
Lopreiato, Joseph, et al.. (2003). DNA Damage Modulates Nucleolar Interaction of the Werner Protein with the AAA ATPase p97/VCP. Molecular Biology of the Cell. 14(10). 4221–4229. 67 indexed citations
20.
Indig, Fred E., et al.. (1998). Organelle Membrane Fusion: A Novel Function for the Syntaxin Homolog Ufe1p in ER Membrane Fusion. Cell. 92(5). 611–620. 130 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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