Vladislav Petyuk

16.1k total citations · 1 hit paper
118 papers, 4.8k citations indexed

About

Vladislav Petyuk is a scholar working on Molecular Biology, Spectroscopy and Physiology. According to data from OpenAlex, Vladislav Petyuk has authored 118 papers receiving a total of 4.8k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Molecular Biology, 36 papers in Spectroscopy and 34 papers in Physiology. Recurrent topics in Vladislav Petyuk's work include Advanced Proteomics Techniques and Applications (32 papers), Alzheimer's disease research and treatments (26 papers) and Mass Spectrometry Techniques and Applications (24 papers). Vladislav Petyuk is often cited by papers focused on Advanced Proteomics Techniques and Applications (32 papers), Alzheimer's disease research and treatments (26 papers) and Mass Spectrometry Techniques and Applications (24 papers). Vladislav Petyuk collaborates with scholars based in United States, Canada and Russia. Vladislav Petyuk's co-authors include Richard Smith, Weijun Qian, David Camp, Paul Piehowski, David A. Bennett, Matthew Monroe, Joshua Adkins, Navdeep Jaitly, Ronald Moore and Tao Liu and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Vladislav Petyuk

114 papers receiving 4.7k citations

Hit Papers

Nanodroplet processing pl... 2018 2026 2020 2023 2018 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vladislav Petyuk United States 39 2.8k 1.5k 962 594 276 118 4.8k
Nils J. Færgeman Denmark 45 4.3k 1.5× 540 0.4× 1.2k 1.2× 427 0.7× 483 1.8× 130 6.7k
Katrin Marcus Germany 46 3.8k 1.4× 1.5k 1.0× 1.0k 1.0× 245 0.4× 599 2.2× 247 6.3k
Loı̈c Dayon Switzerland 33 1.8k 0.7× 1.3k 0.8× 683 0.7× 222 0.4× 100 0.4× 85 3.5k
Johan Gobom Sweden 41 2.8k 1.0× 1.5k 1.0× 1.4k 1.4× 304 0.5× 358 1.3× 117 5.2k
Yuki Sugiura Japan 42 2.8k 1.0× 1.9k 1.3× 465 0.5× 204 0.3× 383 1.4× 158 5.0k
Birgit Schilling United States 52 6.2k 2.2× 1.8k 1.2× 2.1k 2.2× 258 0.4× 580 2.1× 179 10.0k
Richard D. Unwin United Kingdom 34 2.1k 0.8× 790 0.5× 640 0.7× 203 0.3× 221 0.8× 97 3.7k
Stanley M. Stevens United States 28 1.9k 0.7× 316 0.2× 611 0.6× 282 0.5× 335 1.2× 98 3.4k
Harald Köfeler Austria 38 3.9k 1.4× 1.4k 0.9× 835 0.9× 102 0.2× 206 0.7× 98 5.8k
Takahiko Shimizu Japan 48 3.8k 1.4× 228 0.2× 2.5k 2.6× 314 0.5× 357 1.3× 184 7.5k

Countries citing papers authored by Vladislav Petyuk

Since Specialization
Citations

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

Fields of papers citing papers by Vladislav Petyuk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vladislav Petyuk

This figure shows the co-authorship network connecting the top 25 collaborators of Vladislav Petyuk. A scholar is included among the top collaborators of Vladislav Petyuk 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 Vladislav Petyuk. Vladislav Petyuk 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.
Fulcher, James, Ashley N. Ives, Shinya Tasaki, et al.. (2025). Discovery of Proteoforms Associated With Alzheimer's Disease Through Quantitative Top-Down Proteomics. Molecular & Cellular Proteomics. 24(6). 100983–100983. 5 indexed citations
2.
Oveisgharan, Shahram, Lei Yu, Kátia de Paiva Lopes, et al.. (2024). G-protein coupled estrogen receptor 1, amyloid-β, and tau tangles in older adults. Communications Biology. 7(1). 569–569. 3 indexed citations
3.
Jones, Andrea A., Alfredo Ramos‐Miguel, Kristina M. Gicas, et al.. (2024). A multilayer network analysis of Alzheimer's disease pathogenesis: Roles for p‐tau, synaptic peptides, and physical activity. Alzheimer s & Dementia. 20(11). 8012–8027. 4 indexed citations
4.
Iturria‐Medina, Yasser, Simon Ducharme, Pedro Rosa‐Neto, et al.. (2022). Unified epigenomic, transcriptomic, proteomic, and metabolomic taxonomy of Alzheimer’s disease progression and heterogeneity. Science Advances. 8(46). eabo6764–eabo6764. 43 indexed citations
5.
Trumpff, Caroline, Edward Owusu-Ansah, Hans‐Ulrich Klein, et al.. (2022). Mitochondrial respiratory chain protein co-regulation in the human brain. Heliyon. 8(5). e09353–e09353. 5 indexed citations
6.
Tasaki, Shinya, Jishu Xu, Denis Avey, et al.. (2022). Inferring protein expression changes from mRNA in Alzheimer’s dementia using deep neural networks. Nature Communications. 13(1). 655–655. 49 indexed citations
7.
Yu, Lei, Yi‐Chen Hsieh, Richard V. Pearse, et al.. (2022). Association of AK4 Protein From Stem Cell–Derived Neurons With Cognitive Reserve. Neurology. 99(20). e2264–e2274. 6 indexed citations
8.
Petyuk, Vladislav, Lei Yu, Heather Olson, et al.. (2021). Proteomic Profiling of the Substantia Nigra to Identify Determinants of Lewy Body Pathology and Dopaminergic Neuronal Loss. Journal of Proteome Research. 20(5). 2266–2282. 14 indexed citations
9.
Sanford, James, Yang Wang, Joshua Hansen, et al.. (2021). Evaluation of Differential Peptide Loading on Tandem Mass Tag-Based Proteomic and Phosphoproteomic Data Quality. Journal of the American Society for Mass Spectrometry. 33(1). 17–30. 1 indexed citations
10.
Fulcher, James, Aman Makaju, Ronald Moore, et al.. (2021). Enhancing Top-Down Proteomics of Brain Tissue with FAIMS. Journal of Proteome Research. 20(5). 2780–2795. 48 indexed citations
11.
Carlyle, Becky C., Johannes Kreuzer, Sudeshna Das, et al.. (2021). Synaptic proteins associated with cognitive performance and neuropathology in older humans revealed by multiplexed fractionated proteomics. Neurobiology of Aging. 105. 99–114. 41 indexed citations
12.
Otero‐Muras, Irene, et al.. (2020). CRNT4SBML: a Python package for the detection of bistability in biochemical reaction networks. Bioinformatics. 36(12). 3922–3924. 4 indexed citations
13.
Petyuk, Vladislav, et al.. (2020). Detecting differential protein abundance by combining peptide level P -values. Molecular Omics. 16(6). 554–562. 3 indexed citations
14.
Li, Shuo, Galit Weinstein, Habil Zare, et al.. (2020). The genetics of circulating BDNF: towards understanding the role of BDNF in brain structure and function in middle and old ages. Brain Communications. 2(2). fcaa176–fcaa176. 16 indexed citations
15.
Capuano, Ana W., Robert S. Wilson, William G. Honer, et al.. (2019). Brain IGFBP-5 modifies the relation of depressive symptoms to decline in cognition in older persons. Journal of Affective Disorders. 250. 313–318. 11 indexed citations
16.
Cuesta, Rafael, Marina Gritsenko, Vladislav Petyuk, et al.. (2019). Phosphoproteome Analysis Reveals Estrogen-ER Pathway as a Modulator of mTOR Activity Via DEPTOR. Molecular & Cellular Proteomics. 18(8). 1607–1618. 22 indexed citations
17.
Tasaki, Shinya, Chris Gaiteri, Vladislav Petyuk, et al.. (2019). Genetic risk for Alzheimer’s dementia predicts motor deficits through multi-omic systems in older adults. Translational Psychiatry. 9(1). 241–241. 13 indexed citations
18.
Zhu, Ying, Paul Piehowski, Rui Zhao, et al.. (2018). Nanodroplet processing platform for deep and quantitative proteome profiling of 10–100 mammalian cells. Nature Communications. 9(1). 882–882. 417 indexed citations breakdown →
19.
Olah, Marta, Ellis Patrick, Alexandra–Chloé Villani, et al.. (2018). A transcriptomic atlas of aged human microglia. Nature Communications. 9(1). 539–539. 322 indexed citations
20.
Zheng, Xueyun, Liulin Deng, Erin Baker, et al.. (2017). Distinguishingd- andl-aspartic and isoaspartic acids in amyloid β peptides with ultrahigh resolution ion mobility spectrometry. Chemical Communications. 53(56). 7913–7916. 60 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