Gautam N. Bijur

3.4k total citations
38 papers, 3.0k citations indexed

About

Gautam N. Bijur is a scholar working on Molecular Biology, Cell Biology and Physiology. According to data from OpenAlex, Gautam N. Bijur has authored 38 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 8 papers in Cell Biology and 5 papers in Physiology. Recurrent topics in Gautam N. Bijur's work include Wnt/β-catenin signaling in development and cancer (13 papers), Mitochondrial Function and Pathology (6 papers) and Cancer-related gene regulation (6 papers). Gautam N. Bijur is often cited by papers focused on Wnt/β-catenin signaling in development and cancer (13 papers), Mitochondrial Function and Pathology (6 papers) and Cancer-related gene regulation (6 papers). Gautam N. Bijur collaborates with scholars based in United States and Belgium. Gautam N. Bijur's co-authors include Richard S. Jope, Patrizia De Sarno, Xiaohua Li, Taj D. King, Piyajit Watcharasit, Xinbin Chen, Marshall V. Williams, Anna A. Zmijewska, Gail V.W. Johnson and Ling Song and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Gautam N. Bijur

38 papers receiving 2.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gautam N. Bijur United States 27 1.9k 558 384 346 288 38 3.0k
Ling Song China 33 1.9k 1.0× 554 1.0× 531 1.4× 352 1.0× 214 0.7× 86 3.5k
Finn Olav Levy Norway 36 2.5k 1.3× 1.1k 2.0× 236 0.6× 382 1.1× 324 1.1× 131 4.1k
Sébastien Roger France 42 2.3k 1.2× 559 1.0× 192 0.5× 289 0.8× 266 0.9× 91 4.2k
Shuh Narumiya Japan 18 1.5k 0.8× 420 0.8× 659 1.7× 533 1.5× 313 1.1× 21 3.5k
Susana Solá Portugal 37 1.7k 0.9× 250 0.4× 226 0.6× 539 1.6× 547 1.9× 82 3.6k
Shao‐Hua Yang United States 41 1.6k 0.9× 752 1.3× 667 1.7× 881 2.5× 224 0.8× 89 4.5k
Wenhua Zheng China 36 2.0k 1.1× 618 1.1× 180 0.5× 565 1.6× 248 0.9× 107 3.9k
Klaus Scholich Germany 36 1.6k 0.9× 635 1.1× 181 0.5× 940 2.7× 450 1.6× 92 3.5k
Lei Ling United States 26 1.9k 1.0× 252 0.5× 182 0.5× 463 1.3× 555 1.9× 76 4.2k

Countries citing papers authored by Gautam N. Bijur

Since Specialization
Citations

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

Fields of papers citing papers by Gautam N. Bijur

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gautam N. Bijur. 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 Gautam N. Bijur. The network helps show where Gautam N. Bijur may publish in the future.

Co-authorship network of co-authors of Gautam N. Bijur

This figure shows the co-authorship network connecting the top 25 collaborators of Gautam N. Bijur. A scholar is included among the top collaborators of Gautam N. Bijur 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 Gautam N. Bijur. Gautam N. Bijur 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.
Pérez‐Costas, Emma, et al.. (2010). Light and Electron Microscopy Study of Glycogen Synthase Kinase-3β in the Mouse Brain. PLoS ONE. 5(1). e8911–e8911. 40 indexed citations
2.
Bijur, Gautam N., et al.. (2009). The basal flux of Akt in the mitochondria is mediated by heat shock protein 90. Journal of Neurochemistry. 108(5). 1289–1299. 32 indexed citations
3.
King, Taj D., et al.. (2008). Unregulated mitochondrial GSK3β activity results in NADH:Ubiquinone oxidoreductase deficiency. Neurotoxicity Research. 14(4). 367–382. 50 indexed citations
4.
Bijur, Gautam N., et al.. (2006). Akt1 is dynamically modified with O‐GlcNAc following treatments with PUGNAc and insulin‐like growth factor‐1. FEBS Letters. 580(13). 3051–3058. 69 indexed citations
5.
Sarno, Patrizia De, Gautam N. Bijur, Anna A. Zmijewska, Xiaohua Li, & Richard S. Jope. (2005). In vivo regulation of GSK3 phosphorylation by cholinergic and NMDA receptors. Neurobiology of Aging. 27(3). 413–422. 77 indexed citations
6.
Zhu, Wawa, et al.. (2004). Regulation of FOXO3a by brain-derived neurotrophic factor in differentiated human SH-SY5Y neuroblastoma cells. Molecular Brain Research. 126(1). 45–56. 58 indexed citations
7.
Bijur, Gautam N. & Richard S. Jope. (2003). Glycogen synthase kinase-3β is highly activated in nuclei and mitochondria. Neuroreport. 14(18). 2415–2419. 181 indexed citations
8.
Bijur, Gautam N. & Richard S. Jope. (2003). Rapid accumulation of Akt in mitochondria following phosphatidylinositol 3‐kinase activation. Journal of Neurochemistry. 87(6). 1427–1435. 293 indexed citations
9.
Jope, Richard S. & Gautam N. Bijur. (2002). Mood stabilizers, glycogen synthase kinase-3β and cell survival. Molecular Psychiatry. 7(S1). S35–S45. 115 indexed citations
10.
Li, Xiaohua, Gautam N. Bijur, & Richard S. Jope. (2002). Glycogen synthase kinase‐3β, mood stabilizers, and neuroprotection. Bipolar Disorders. 4(2). 137–144. 210 indexed citations
11.
Bijur, Gautam N. & Richard S. Jope. (2001). Proapoptotic Stimuli Induce Nuclear Accumulation of Glycogen Synthase Kinase-3β. Journal of Biological Chemistry. 276(40). 37436–37442. 188 indexed citations
12.
Krishnamurthy, Pavan, et al.. (2000). Transient oxidative stress in SH‐SY5Y human neuroblastoma cells results in caspase dependent and independent cell death and tau proteolysis. Journal of Neuroscience Research. 61(5). 515–523. 33 indexed citations
13.
Bijur, Gautam N., et al.. (1999). Ascorbic acid-dehydroascorbate induces cell cycle arrest at G2/M DNA damage checkpoint during oxidative stress. Environmental and Molecular Mutagenesis. 33(2). 144–152. 40 indexed citations
14.
Bijur, Gautam N., et al.. (1998). Lead and mercury mutagenesis: Role of H2O2, superoxide dismutase, and xanthine oxidase. Environmental and Molecular Mutagenesis. 31(4). 352–361. 74 indexed citations
15.
Bijur, Gautam N., Maria E. Ariza, Charles L. Hitchcock, & Marshall V. Williams. (1997). Antimutagenic and promutagenic activity of ascorbic acid during oxidative stress. Environmental and Molecular Mutagenesis. 30(3). 339–345. 51 indexed citations
16.
Gopalakrishnan, Rajaram, Christopher M. Weghorst, Teresa A. Lehman, et al.. (1997). Mutated and wild-type p53 expression and HPV integration in proliferative verrucous leukoplakia and oral squamous cell carcinoma. Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology. 83(4). 471–477. 64 indexed citations
17.
Sabourin, Carol L., et al.. (1996). Alterations in transforming growth factor-α and epidermal growth factor receptor expression during rat esophageal tumorigenesis. Molecular Carcinogenesis. 15(2). 144–153. 32 indexed citations
18.
Choban, Patricia S., Timothy E. McKnight, Louis Flancbaum, et al.. (1996). Characterization of a Murine Model of Acute Lung Injury (ALI): A Prominent Role for Interleukin-1. Journal of Investigative Surgery. 9(2). 95–109. 2 indexed citations
19.
Robertson, Fredika M., Arthur E. Pellegrini, Michael S. Ross, et al.. (1995). Interleukin‐1α gene expression during wound healing. Wound Repair and Regeneration. 3(4). 473–484. 21 indexed citations
20.
Oberyszyn, Tatiana M., Carol L. Sabourin, Gautam N. Bijur, et al.. (1993). Interleukin‐1α gene expression and localization of interleukin‐1α protein during tumor promotion. Molecular Carcinogenesis. 7(4). 238–248. 54 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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