Mónika Göőz

2.4k total citations
60 papers, 1.8k citations indexed

About

Mónika Göőz is a scholar working on Molecular Biology, Oncology and Epidemiology. According to data from OpenAlex, Mónika Göőz has authored 60 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 10 papers in Oncology and 8 papers in Epidemiology. Recurrent topics in Mónika Göőz's work include Mitochondrial Function and Pathology (11 papers), Helicobacter pylori-related gastroenterology studies (7 papers) and ATP Synthase and ATPases Research (6 papers). Mónika Göőz is often cited by papers focused on Mitochondrial Function and Pathology (11 papers), Helicobacter pylori-related gastroenterology studies (7 papers) and ATP Synthase and ATPases Research (6 papers). Mónika Göőz collaborates with scholars based in United States, Russia and Hungary. Mónika Göőz's co-authors include Pal Göőz, Adam J. Smolka, John R. Raymond, Louis M. Luttrell, Charles E. Hammond, Aleksander Baldys, John J. Lemasters, Eduardo N. Maldonado, Arindam Saha and Steffen Backert and has published in prestigious journals such as Journal of Biological Chemistry, Gastroenterology and PLoS ONE.

In The Last Decade

Mónika Göőz

60 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mónika Göőz United States 24 754 317 313 282 185 60 1.8k
Michael Seed United Kingdom 22 610 0.8× 210 0.7× 327 1.0× 325 1.2× 123 0.7× 53 1.9k
Yuki Tanaka Japan 22 1.0k 1.4× 517 1.6× 434 1.4× 336 1.2× 169 0.9× 120 2.6k
Chiara Foglieni Italy 26 905 1.2× 222 0.7× 247 0.8× 187 0.7× 106 0.6× 61 2.0k
Huseyin Mehmet United Kingdom 25 1.2k 1.6× 178 0.6× 351 1.1× 313 1.1× 218 1.2× 52 2.6k
Elena Toniato Italy 24 688 0.9× 174 0.5× 674 2.2× 330 1.2× 137 0.7× 87 2.0k
Robert Moumdjian Canada 29 784 1.0× 470 1.5× 443 1.4× 415 1.5× 343 1.9× 65 3.0k
Li Zhu China 26 953 1.3× 131 0.4× 310 1.0× 165 0.6× 116 0.6× 91 2.1k
Kayoko Higuchi Japan 25 791 1.0× 568 1.8× 207 0.7× 392 1.4× 248 1.3× 117 2.2k
Michele Reibaldi Italy 35 950 1.3× 132 0.4× 321 1.0× 175 0.6× 134 0.7× 258 4.3k
Michael K. Jones United States 24 766 1.0× 382 1.2× 203 0.6× 237 0.8× 156 0.8× 56 1.7k

Countries citing papers authored by Mónika Göőz

Since Specialization
Citations

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

Fields of papers citing papers by Mónika Göőz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mónika Göőz

This figure shows the co-authorship network connecting the top 25 collaborators of Mónika Göőz. A scholar is included among the top collaborators of Mónika Göőz 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 Mónika Göőz. Mónika Göőz 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.
2.
Göőz, Mónika, et al.. (2025). CD45+/ Col I+ Fibrocytes: Major source of collagen in the fibrotic lung, but not in passaged fibroblast cultures. Matrix Biology. 136. 87–101. 1 indexed citations
3.
Pérez, Sandra, Mónika Göőz, & Eduardo N. Maldonado. (2024). Mitochondrial Dysfunction and Metabolic Disturbances Induced by Viral Infections. Cells. 13(21). 1789–1789. 6 indexed citations
4.
Dimou, Anastasios, Yuri K. Peterson, Mónika Göőz, et al.. (2020). Neuropilin-2b facilitates resistance to tyrosine kinase inhibitors in non–small cell lung cancer. Journal of Thoracic and Cardiovascular Surgery. 162(2). 463–473. 5 indexed citations
5.
Helke, Kristi L., et al.. (2019). Effects of vagus nerve stimulation are mediated in part by TrkB in a parkinson’s disease model. Behavioural Brain Research. 373. 112080–112080. 20 indexed citations
6.
Salim, Sohail Abdul, et al.. (2018). Baclofen-induced neurotoxicity in patients with compromised renal function: Review. International Journal of Clinical Pharmacology and Therapeutics. 56(10). 467–475. 7 indexed citations
7.
Ghatak, Shibnath, Vincent Hascall, Roger R. Markwald, et al.. (2017). Transforming growth factor β1 (TGFβ1)-induced CD44V6-NOX4 signaling in pathogenesis of idiopathic pulmonary fibrosis. Journal of Biological Chemistry. 292(25). 10490–10519. 70 indexed citations
8.
Fang, Diana, Kareem A. Heslop, David N. DeHart, et al.. (2017). Oxidative Stress Induced by Vdac Opening in Cancer Cells Depends on Cytosolic Free Tubulin and is Blocked by ROS Scavenging and Suppression of Superoxide Formation by Complex III. Biophysical Journal. 112(3). 324a–324a. 1 indexed citations
9.
Maldonado, Eduardo N., David N. DeHart, Diana Fang, et al.. (2016). Oxidative Stress and JNK Activation cause Mitochondrial Dysfunction and Cell Death in Hepatocarcinoma after VDAC-Tubulin Antagonists. Biophysical Journal. 110(3). 470a–470a. 1 indexed citations
10.
Navar, L. Gabriel, et al.. (2013). Diabetes Care Its Association With Glycosylated Hemoglobin Level. The American Journal of the Medical Sciences. 347(3). 245–247. 5 indexed citations
11.
Zhang, Zhi‐Ren, Wenfeng Chu, Bin‐Lin Song, et al.. (2013). TRPP2 and TRPV4 Form an EGF-Activated Calcium Permeable Channel at the Apical Membrane of Renal Collecting Duct Cells. PLoS ONE. 8(8). e73424–e73424. 51 indexed citations
12.
Saigusa, Takamitsu, Brian J. Siroky, Mónika Göőz, et al.. (2011). Collecting duct cells that lack normal cilia have mislocalized vasopressin-2 receptors. American Journal of Physiology-Renal Physiology. 302(7). F801–F808. 22 indexed citations
13.
Navar, L. Gabriel, et al.. (2011). Automated Reporting of Estimated Glomerular Filtration Rate Alters Referral Patterns to a Nephrology Clinic. The American Journal of the Medical Sciences. 342(3). 218–220. 3 indexed citations
14.
Navar, L. Gabriel, et al.. (2010). ADAM-17 Is Activated by the Mitogenic Protein Kinase ERK in a Model of Kidney Fibrosis. The American Journal of the Medical Sciences. 339(2). 105–107. 20 indexed citations
15.
Göőz, Mónika. (2010). ADAM-17: the enzyme that does it all. Critical Reviews in Biochemistry and Molecular Biology. 45(2). 146–169. 331 indexed citations
16.
17.
Garnovskaya, Maria N., et al.. (2009). Epidermal growth factor activates Na+/H+ exchanger in podocytes through a mechanism that involves Janus kinase and calmodulin. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1793(7). 1174–1181. 44 indexed citations
18.
Göőz, Pal, Mónika Göőz, Aleksander Baldys, & Stanley Hoffman. (2009). ADAM-17 regulates endothelial cell morphology, proliferation, and in vitro angiogenesis. Biochemical and Biophysical Research Communications. 380(1). 33–38. 46 indexed citations
19.
Saha, Arindam, Charles E. Hammond, Mónika Göőz, & Adam J. Smolka. (2007). IL-1β modulation of H,K-ATPase α-subunit gene transcription inHelicobacter pyloriinfection. American Journal of Physiology-Gastrointestinal and Liver Physiology. 292(4). G1055–G1061. 22 indexed citations
20.
Göőz, Mónika, et al.. (2000). Helicobacter pylori stimulates secretion of matrix metalloproteinases (MMPS) and their inhibitors from human gastric epithelial cells. Gastroenterology. 118(4). A740–A740. 1 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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