Andrei Golovko

3.5k total citations · 2 hit papers
22 papers, 2.7k citations indexed

About

Andrei Golovko is a scholar working on Molecular Biology, Surgery and Oncology. According to data from OpenAlex, Andrei Golovko has authored 22 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Surgery and 5 papers in Oncology. Recurrent topics in Andrei Golovko's work include RNA modifications and cancer (5 papers), Drug Transport and Resistance Mechanisms (4 papers) and Cancer-related molecular mechanisms research (4 papers). Andrei Golovko is often cited by papers focused on RNA modifications and cancer (5 papers), Drug Transport and Resistance Mechanisms (4 papers) and Cancer-related molecular mechanisms research (4 papers). Andrei Golovko collaborates with scholars based in United States, Ukraine and China. Andrei Golovko's co-authors include Harry R. Davis, Glen Tetzloff, Lizbeth Hoos, Nicholas Murgolo, Ming Zeng, Luquan Wang, Li-Ji Zhu, S. Altmann, Sai Prasad N. Iyer and Maureen Maguire and has published in prestigious journals such as Science, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Andrei Golovko

21 papers receiving 2.6k citations

Hit Papers

Niemann-Pick C1 Like 1 Protein Is Critical for Intestinal... 2003 2026 2010 2018 2004 2003 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andrei Golovko United States 12 1.3k 1.2k 639 510 399 22 2.7k
Raymond E. Soccio United States 21 734 0.6× 1.9k 1.6× 378 0.6× 52 0.1× 339 0.8× 26 3.0k
Hueng-Sik Choi South Korea 31 886 0.7× 2.5k 2.2× 949 1.5× 77 0.2× 697 1.7× 67 4.4k
E. Doran United Kingdom 13 761 0.6× 2.1k 1.8× 275 0.4× 48 0.1× 596 1.5× 16 2.8k
Holger Doege United States 17 472 0.4× 1.2k 1.1× 165 0.3× 84 0.2× 383 1.0× 18 2.2k
Arthur R. Buckley United States 32 166 0.1× 1.2k 1.1× 767 1.2× 107 0.2× 581 1.5× 76 2.8k
Barbara Batetta Italy 23 393 0.3× 600 0.5× 184 0.3× 78 0.2× 238 0.6× 63 1.8k
Sergio A. Lamprecht Israel 27 173 0.1× 871 0.8× 466 0.7× 461 0.9× 285 0.7× 64 2.8k
A. Trentalance Italy 23 405 0.3× 826 0.7× 250 0.4× 68 0.1× 258 0.6× 72 1.9k
Charles W. Garner United States 25 710 0.6× 1.8k 1.5× 220 0.3× 57 0.1× 478 1.2× 46 2.6k
Marion B. Sewer United States 30 227 0.2× 1.0k 0.9× 300 0.5× 99 0.2× 404 1.0× 47 2.1k

Countries citing papers authored by Andrei Golovko

Since Specialization
Citations

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

Fields of papers citing papers by Andrei Golovko

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrei Golovko

This figure shows the co-authorship network connecting the top 25 collaborators of Andrei Golovko. A scholar is included among the top collaborators of Andrei Golovko 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 Andrei Golovko. Andrei Golovko 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.
Ye, Xiangcang, Zeyu Liu, Zheng Shen, et al.. (2023). Nutrient-Sensing Ghrelin Receptor in Macrophages Modulates Bisphenol A-Induced Intestinal Inflammation in Mice. Genes. 14(7). 1455–1455. 8 indexed citations
2.
Chen, Jingshu, Sui Ke, James J. Cai, et al.. (2022). Ablation of long noncoding RNA MALAT1 activates antioxidant pathway and alleviates sepsis in mice. Redox Biology. 54. 102377–102377. 26 indexed citations
3.
Golovko, Andrei, et al.. (2020). DISTANT METASTASIS TO THE THYROID GLAND: CLINICAL REVIEW. SHILAP Revista de lepidopterología. 105–113. 1 indexed citations
4.
Golovko, Andrei, et al.. (2019). Parathyroid carcinoma: a case report. Experimental Oncology. 41(1). 72–75. 3 indexed citations
5.
Chen, Jingshu, Lei Zhong, Jing Wu, et al.. (2018). A Murine Pancreatic Islet Cell-based Screening for Diabetogenic Environmental Chemicals. Journal of Visualized Experiments. 6 indexed citations
6.
Chen, Jingshu, Sui Ke, Jing Wu, et al.. (2018). Long noncoding RNA MALAT1 regulates generation of reactive oxygen species and the insulin responses in male mice. Biochemical Pharmacology. 152. 94–103. 59 indexed citations
7.
Cheng, Yating, Parisa Imanirad, Indira Jutooru, et al.. (2018). Role of metastasis-associated lung adenocarcinoma transcript-1 (MALAT-1) in pancreatic cancer. PLoS ONE. 13(2). e0192264–e0192264. 39 indexed citations
8.
Chen, Jingshu, Lei Zhong, Jing Wu, et al.. (2018). A Murine Pancreatic Islet Cell-based Screening for Diabetogenic Environmental Chemicals. Journal of Visualized Experiments. 1 indexed citations
10.
Fietz, Daniela, Alberto Sánchez‐Guijo, Michaela F. Hartmann, et al.. (2017). Sodium-dependent organic anion transporter ( Slc10a6−/− ) knockout mice show normal spermatogenesis and reproduction, but elevated serum levels for cholesterol sulfate. The Journal of Steroid Biochemistry and Molecular Biology. 179. 45–54. 9 indexed citations
11.
Miard, Stéphanie, Philippe Joubert, Sophie Carter, et al.. (2017). Absence of Malat1 does not prevent DEN-induced hepatocarcinoma in mice. Oncology Reports. 37(4). 2153–2160. 9 indexed citations
12.
Cui, Hongmei, Xinsheng Gu, Jingshu Chen, et al.. (2017). Pregnane X receptor regulates the AhR/Cyp1A1 pathway and protects liver cells from benzo-[α]-pyrene-induced DNA damage. Toxicology Letters. 275. 67–76. 29 indexed citations
13.
Golovko, Andrei, Bo-Jhih Guan, Benjamin Morpurgo, et al.. (2016). The eIF2A knockout mouse. Cell Cycle. 15(22). 3115–3120. 23 indexed citations
14.
Hong, Lan, Galya Vassileva, Li Liu, et al.. (2009). GPR119 is required for physiological regulation of glucagon-like peptide-1 secretion but not for metabolic homeostasis. Journal of Endocrinology. 201(2). 219–230. 132 indexed citations
15.
Zhang, Qing, Ping Qiu, Jason S. Simon, et al.. (2007). P518/Qrfp sequence polymorphisms in SAMP6 osteopenic mouse. Genomics. 90(5). 629–635. 16 indexed citations
16.
Vassileva, Galya, Andrei Golovko, Susan J. Abbondanzo, et al.. (2006). Targeted deletion of Gpbar1 protects mice from cholesterol gallstone formation. Biochemical Journal. 398(3). 423–430. 229 indexed citations
17.
Kowalski, Timothy J., Brian D. Spar, Mandy J. Maguire, et al.. (2005). Transgenic overexpression of neuromedin U promotes leanness and hypophagia in mice. Journal of Endocrinology. 185(1). 151–164. 59 indexed citations
18.
Reich, Eva‐Pia, Long Cui, Catherine Pugliese‐Sivo, et al.. (2005). Blocking ion channel KCNN4 alleviates the symptoms of experimental autoimmune encephalomyelitis in mice. European Journal of Immunology. 35(4). 1027–1036. 78 indexed citations
19.
Altmann, S., Harry R. Davis, Li-Ji Zhu, et al.. (2004). Niemann-Pick C1 Like 1 Protein Is Critical for Intestinal Cholesterol Absorption. Science. 303(5661). 1201–1204. 1393 indexed citations breakdown →
20.
Hedrick, Joseph A., Galya Vassileva, Susan J. Abbondanzo, et al.. (2003). The KiSS-1 receptor GPR54 is essential for the development of the murine reproductive system. Biochemical and Biophysical Research Communications. 312(4). 1357–1363. 542 indexed citations breakdown →

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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