Olga Ilkayeva

34.9k total citations · 6 hit papers
208 papers, 19.4k citations indexed

About

Olga Ilkayeva is a scholar working on Molecular Biology, Physiology and Epidemiology. According to data from OpenAlex, Olga Ilkayeva has authored 208 papers receiving a total of 19.4k indexed citations (citations by other indexed papers that have themselves been cited), including 133 papers in Molecular Biology, 99 papers in Physiology and 33 papers in Epidemiology. Recurrent topics in Olga Ilkayeva's work include Adipose Tissue and Metabolism (67 papers), Metabolomics and Mass Spectrometry Studies (52 papers) and Diet and metabolism studies (47 papers). Olga Ilkayeva is often cited by papers focused on Adipose Tissue and Metabolism (67 papers), Metabolomics and Mass Spectrometry Studies (52 papers) and Diet and metabolism studies (47 papers). Olga Ilkayeva collaborates with scholars based in United States, Canada and Australia. Olga Ilkayeva's co-authors include Christopher B. Newgard, James R. Bain, Deborah M. Muoio, Robert D. Stevens, Timothy R. Koves, Michael J. Muehlbauer, Brett R. Wenner, Robert Stevens, Robert C. Noland and Svati H. Shah and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Olga Ilkayeva

201 papers receiving 19.2k citations

Hit Papers

A Branched-Chain Amino Ac... 2008 2026 2014 2020 2009 2008 2010 2013 2016 500 1000 1.5k 2.0k

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Olga Ilkayeva 11.0k 8.4k 3.6k 1.9k 1.8k 208 19.4k
Deborah M. Muoio 8.9k 0.8× 8.2k 1.0× 2.6k 0.7× 1.6k 0.9× 1.7k 0.9× 133 16.1k
James R. Bain 8.9k 0.8× 6.9k 0.8× 2.7k 0.8× 1.3k 0.7× 2.6k 1.4× 211 16.9k
Jason R.B. Dyck 10.4k 0.9× 6.3k 0.7× 2.7k 0.8× 2.5k 1.3× 3.2k 1.8× 298 21.3k
Sander M. Houten 7.5k 0.7× 4.4k 0.5× 2.9k 0.8× 1.3k 0.7× 2.6k 1.4× 157 14.0k
Hubert Vidal 11.4k 1.0× 10.5k 1.3× 6.2k 1.7× 3.0k 1.6× 2.6k 1.4× 346 25.3k
Marc K. Hellerstein 5.3k 0.5× 5.9k 0.7× 3.8k 1.0× 3.2k 1.7× 2.4k 1.3× 297 19.1k
Brian N. Finck 8.8k 0.8× 5.7k 0.7× 4.0k 1.1× 1.9k 1.0× 2.2k 1.2× 191 17.9k
Sander Kersten 11.6k 1.1× 8.5k 1.0× 6.1k 1.7× 3.9k 2.1× 2.6k 1.4× 228 25.3k
Gregory R. Steinberg 12.3k 1.1× 8.8k 1.0× 6.2k 1.7× 3.3k 1.8× 4.7k 2.6× 246 23.5k
Francesc Villarroya 6.2k 0.6× 8.2k 1.0× 4.6k 1.3× 900 0.5× 1.1k 0.6× 308 15.3k

Countries citing papers authored by Olga Ilkayeva

Since Specialization
Citations

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

Fields of papers citing papers by Olga Ilkayeva

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Olga Ilkayeva

This figure shows the co-authorship network connecting the top 25 collaborators of Olga Ilkayeva. A scholar is included among the top collaborators of Olga Ilkayeva 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 Olga Ilkayeva. Olga Ilkayeva 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.
Fee, Brian E., Lanette Fee, Yazan Alwarawrah, et al.. (2024). Type I interferon signaling and peroxisomal dysfunction contribute to enhanced inflammatory cytokine production in IRGM1-deficient macrophages. Journal of Biological Chemistry. 300(11). 107883–107883.
2.
Ilkayeva, Olga, Jeffrey I. Everitt, James V. Alvarez, et al.. (2024). Optical imaging reveals chemotherapy-induced metabolic reprogramming of residual disease and recurrence. Science Advances. 10(14). eadj7540–eadj7540. 5 indexed citations
3.
Osazuwa‐Peters, Oyomoare L., April Deveaux, Michael J. Muehlbauer, et al.. (2024). Racial Differences in Vaginal Fluid Metabolites and Association with Systemic Inflammation Markers among Ovarian Cancer Patients: A Pilot Study. Cancers. 16(7). 1259–1259. 4 indexed citations
4.
Rowland, Leslie A., Adı́lson Guilherme, Felipe Henriques, et al.. (2023). De novo lipogenesis fuels adipocyte autophagosome and lysosome membrane dynamics. Nature Communications. 14(1). 1362–1362. 28 indexed citations
5.
Regan, Jessica A., Robert J. Mentz, Jennifer B. Green, et al.. (2023). Mitochondrial metabolites predict adverse cardiovascular events in individuals with diabetes. JCI Insight. 8(17). 9 indexed citations
6.
Bhatt, Dhaval P., Christine A. Mills, Kristin A. Anderson, et al.. (2022). Deglutarylation of glutaryl-CoA dehydrogenase by deacylating enzyme SIRT5 promotes lysine oxidation in mice. Journal of Biological Chemistry. 298(4). 101723–101723. 13 indexed citations
7.
Hernández‐Saavedra, Diego, Christina A. Markunas, Hirokazu Takahashi, et al.. (2022). Maternal Exercise and Paternal Exercise Induce Distinct Metabolite Signatures in Offspring Tissues. Diabetes. 71(10). 2094–2105. 10 indexed citations
8.
Wagner, Gregory R., Kristin A. Anderson, Scott B. Crown, et al.. (2022). Statin therapy inhibits fatty acid synthase via dynamic protein modifications. Nature Communications. 13(1). 2542–2542. 18 indexed citations
9.
Fan, Liyan, David R. Sweet, Domenick A. Prosdocimo, et al.. (2021). Muscle Krüppel-like factor 15 regulates lipid flux and systemic metabolic homeostasis. Journal of Clinical Investigation. 131(4). 20 indexed citations
10.
Liu, Yu, Alan Kuang, James R. Bain, et al.. (2021). Maternal Metabolites Associated With Gestational Diabetes Mellitus and a Postpartum Disorder of Glucose Metabolism. The Journal of Clinical Endocrinology & Metabolism. 106(11). 3283–3294. 17 indexed citations
11.
Chang, Hao-Wei, Nathan P. McNulty, Martin L. Hibberd, et al.. (2021). Gut microbiome contributions to altered metabolism in a pig model of undernutrition. Proceedings of the National Academy of Sciences. 118(21). 18 indexed citations
12.
Hershberger, Kathleen A., John P. Rooney, Rakesh Bodhicharla, et al.. (2021). Early-life mitochondrial DNA damage results in lifelong deficits in energy production mediated by redox signaling in Caenorhabditis elegans. Redox Biology. 43. 102000–102000. 17 indexed citations
13.
Choi, Béatrice S.-Y., Noëmie Daniel, Vanessa P. Houde, et al.. (2021). Feeding diversified protein sources exacerbates hepatic insulin resistance via increased gut microbial branched-chain fatty acids and mTORC1 signaling in obese mice. Nature Communications. 12(1). 3377–3377. 78 indexed citations
14.
Levine, Daniel C., Hee‐Kyung Hong, Jonathan Cedernaes, et al.. (2021). NADH inhibition of SIRT1 links energy state to transcription during time-restricted feeding. Nature Metabolism. 3(12). 1621–1632. 50 indexed citations
15.
Liu, Yu, Alan Kuang, Octavious Talbot, et al.. (2020). Metabolomic and genetic associations with insulin resistance in pregnancy. Diabetologia. 63(9). 1783–1795. 32 indexed citations
16.
Lowe, William L., James R. Bain, Michael Nodzenski, et al.. (2017). Maternal BMI and Glycemia Impact the Fetal Metabolome. Diabetes Care. 40(7). 902–910. 83 indexed citations
17.
White, Phillip J., Amanda L. Lapworth, Jie An, et al.. (2016). Branched-chain amino acid restriction in Zucker-fatty rats improves muscle insulin sensitivity by enhancing efficiency of fatty acid oxidation and acyl-glycine export. Molecular Metabolism. 5(7). 538–551. 202 indexed citations
18.
Burkewitz, Kristopher, Ianessa Morantte, Heather J. Weir, et al.. (2015). Neuronal CRTC-1 Governs Systemic Mitochondrial Metabolism and Lifespan via a Catecholamine Signal. Cell. 160(5). 842–855. 139 indexed citations
19.
Michalek, Ryan D., Valerie A. Gerriets, Amanda Nichols, et al.. (2011). Estrogen-related receptor-α is a metabolic regulator of effector T-cell activation and differentiation. Proceedings of the National Academy of Sciences. 108(45). 18348–18353. 169 indexed citations
20.
Wang, May-Yun, Lijun Chen, Gregory O. Clark, et al.. (2010). Leptin therapy in insulin-deficient type I diabetes. Proceedings of the National Academy of Sciences. 107(11). 4813–4819. 262 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

Rankless by CCL
2026