Anutosh Chakraborty

2.7k total citations
36 papers, 2.2k citations indexed

About

Anutosh Chakraborty is a scholar working on Molecular Biology, Cell Biology and Epidemiology. According to data from OpenAlex, Anutosh Chakraborty has authored 36 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 11 papers in Cell Biology and 8 papers in Epidemiology. Recurrent topics in Anutosh Chakraborty's work include Endoplasmic Reticulum Stress and Disease (7 papers), Pancreatic function and diabetes (7 papers) and Cellular transport and secretion (5 papers). Anutosh Chakraborty is often cited by papers focused on Endoplasmic Reticulum Stress and Disease (7 papers), Pancreatic function and diabetes (7 papers) and Cellular transport and secretion (5 papers). Anutosh Chakraborty collaborates with scholars based in United States, India and Poland. Anutosh Chakraborty's co-authors include Solomon H. Snyder, Seyun Kim, Mengge Zhou, David J. Tweardy, Qing Zeng, Stephanie D. Drenning, Jennifer R. Grandis, Krishna R. Juluri, Adele M. Snowman and Michael A. Koldobskiy and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Anutosh Chakraborty

36 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Anutosh Chakraborty United States	23	1.3k	619	529	313	246	36	2.2k
Tania Maffucci United Kingdom	27	1.8k 1.3×	321 0.5×	723 1.4×	193 0.6×	356 1.4×	52	2.6k
Keren Paz United States	21	1.7k 1.3×	560 0.9×	701 1.3×	323 1.0×	248 1.0×	33	2.6k
Bruno Ségui France	31	1.6k 1.2×	637 1.0×	444 0.8×	726 2.3×	207 0.8×	90	2.8k
Elena Tibaldi Italy	30	1.4k 1.0×	466 0.8×	390 0.7×	514 1.6×	97 0.4×	65	2.5k
Masayoshi Yada Japan	17	2.1k 1.6×	863 1.4×	446 0.8×	287 0.9×	212 0.9×	45	3.1k
Domenico Grieco Italy	26	1.9k 1.4×	608 1.0×	575 1.1×	158 0.5×	108 0.4×	42	2.6k
Sejeong Shin United States	21	1.6k 1.2×	541 0.9×	369 0.7×	223 0.7×	89 0.4×	30	2.2k
Antonis S. Zervos United States	25	2.8k 2.1×	492 0.8×	414 0.8×	392 1.3×	100 0.4×	40	3.6k
Stephen R. James United Kingdom	13	2.6k 1.9×	282 0.5×	502 0.9×	324 1.0×	288 1.2×	19	3.2k
Sang-Oh Yoon United States	21	2.0k 1.5×	584 0.9×	393 0.7×	240 0.8×	161 0.7×	30	2.8k

Countries citing papers authored by Anutosh Chakraborty

Since Specialization

Citations

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

Fields of papers citing papers by Anutosh Chakraborty

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anutosh Chakraborty

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Chakraborty, Molee, et al.. (2023). The IP6K Inhibitor LI-2242 Ameliorates Diet-Induced Obesity, Hyperglycemia, and Hepatic Steatosis in Mice by Improving Cell Metabolism and Insulin Signaling. Biomolecules. 13(5). 868–868. 8 indexed citations

Chakraborty, Molee, Jinsong Zhang, Kelly D. Pyles, et al.. (2023). Ube4A maintains metabolic homeostasis and facilitates insulin signaling in vivo. Molecular Metabolism. 75. 101767–101767. 4 indexed citations

Ghoshal, S. P., et al.. (2022). Whole Body Ip6k1 Deletion Protects Mice from Age-Induced Weight Gain, Insulin Resistance and Metabolic Dysfunction. International Journal of Molecular Sciences. 23(4). 2059–2059. 7 indexed citations

Zhou, Yubai, Molee Chakraborty, Chunfang Gu, et al.. (2022). Development of Novel IP6K Inhibitors for the Treatment of Obesity and Obesity-Induced Metabolic Dysfunctions. Journal of Medicinal Chemistry. 65(9). 6869–6887. 21 indexed citations

Chakraborty, Molee, Barbara Ulmasov, Kyle S. McCommis, et al.. (2021). Pleiotropic actions of IP6K1 mediate hepatic metabolic dysfunction to promote nonalcoholic fatty liver disease and steatohepatitis. Molecular Metabolism. 54. 101364–101364. 15 indexed citations

Chakraborty, Anutosh, et al.. (2020). Targeting the Inositol Pyrophosphate Biosynthetic Enzymes in Metabolic Diseases. Molecules. 25(6). 1403–1403. 31 indexed citations

Boregowda, Siddaraju V., S. P. Ghoshal, Cori N. Booker, et al.. (2017). IP6K1 Reduces Mesenchymal Stem/Stromal Cell Fitness and Potentiates High Fat Diet-Induced Skeletal Involution. Stem Cells. 35(8). 1973–1983. 23 indexed citations

Ghoshal, S. P., Qingzhang Zhu, Alice Asteian, et al.. (2016). TNP [N2-(m-Trifluorobenzyl), N6-(p-nitrobenzyl)purine] ameliorates diet induced obesity and insulin resistance via inhibition of the IP6K1 pathway. Molecular Metabolism. 5(10). 903–917. 47 indexed citations

Ghoshal, S. P., Richa Tyagi, Qingzhang Zhu, & Anutosh Chakraborty. (2016). Inositol hexakisphosphate kinase-1 interacts with perilipin1 to modulate lipolysis. The International Journal of Biochemistry & Cell Biology. 78. 149–155. 29 indexed citations

10.

Zhu, Qingzhang, S. P. Ghoshal, Ana P. C. Rodrigues, et al.. (2016). Adipocyte-specific deletion of Ip6k1 reduces diet-induced obesity by enhancing AMPK-mediated thermogenesis. Journal of Clinical Investigation. 126(11). 4273–4288. 73 indexed citations

11.

Zhu, Qingzhang, et al.. (2016). Global IP6K1 deletion enhances temperature modulated energy expenditure which reduces carbohydrate and fat induced weight gain. Molecular Metabolism. 6(1). 73–85. 38 indexed citations

12.

Chakraborty, Anutosh, et al.. (2013). Inositol hexakisphosphate kinase-1 regulates behavioral responses via GSK3 signaling pathways. Molecular Psychiatry. 19(3). 284–293. 44 indexed citations

13.

Chakraborty, Anutosh, Krishna Patil, Shatavisha Dasgupta, et al.. (2012). Incidence of CMV-HCV coinfection in renal transplant recipient. BMJ Case Reports. 2012. bcr1220115314–bcr1220115314. 5 indexed citations

14.

Kim, Seyun, Sangwon F. Kim, David Maag, et al.. (2011). Amino Acid Signaling to mTOR Mediated by Inositol Polyphosphate Multikinase. Cell Metabolism. 13(2). 215–221. 113 indexed citations

15.

Prasad, Amit, Yonghui Jia, Anutosh Chakraborty, et al.. (2011). Inositol hexakisphosphate kinase 1 regulates neutrophil function in innate immunity by inhibiting phosphatidylinositol-(3,4,5)-trisphosphate signaling. Nature Immunology. 12(8). 752–760. 79 indexed citations

16.

Chakraborty, Anutosh, Michael A. Koldobskiy, Nicholas T. Bello, et al.. (2010). Inositol Pyrophosphates Inhibit Akt Signaling, Thereby Regulating Insulin Sensitivity and Weight Gain. Cell. 143(6). 897–910. 296 indexed citations

17.

Mustafa, Asif K., Damian B. van Rossum, Randen L. Patterson, et al.. (2009). Glutamatergic regulation of serine racemase via reversal of PIP2 inhibition. Proceedings of the National Academy of Sciences. 106(8). 2921–2926. 52 indexed citations

18.

Bhandari, Rashna, Anutosh Chakraborty, & Solomon H. Snyder. (2007). Inositol Pyrophosphate Pyrotechnics. Cell Metabolism. 5(5). 321–323. 13 indexed citations

19.

Grandis, Jennifer R., Stephanie D. Drenning, Anutosh Chakraborty, et al.. (1998). Requirement of Stat3 but not Stat1 activation for epidermal growth factor receptor- mediated cell growth In vitro.. Journal of Clinical Investigation. 102(7). 1385–1392. 441 indexed citations

20.

Chakraborty, Anutosh & Hemanta K. Majumder. (1991). An ATP-independent catenating enzyme from the kinetoplast hemoflagellate Leishmaniadonovani. Biochemical and Biophysical Research Communications. 180(1). 279–285. 18 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.

Explore authors with similar magnitude of impact