Sergei Zhuk

549 total citations
18 papers, 296 citations indexed

About

Sergei Zhuk is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Epidemiology. According to data from OpenAlex, Sergei Zhuk has authored 18 papers receiving a total of 296 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Cardiology and Cardiovascular Medicine and 5 papers in Epidemiology. Recurrent topics in Sergei Zhuk's work include Cardiomyopathy and Myosin Studies (4 papers), Epigenetics and DNA Methylation (2 papers) and Congenital Heart Disease Studies (2 papers). Sergei Zhuk is often cited by papers focused on Cardiomyopathy and Myosin Studies (4 papers), Epigenetics and DNA Methylation (2 papers) and Congenital Heart Disease Studies (2 papers). Sergei Zhuk collaborates with scholars based in Russia, Sweden and Austria. Sergei Zhuk's co-authors include Anna Kostareva, Anna Malashicheva, О. М. Моисеева, Ulrich Elling, Maria Novatchkova, Georg Michlits, Gintautas Vainorius, Martin Aichinger, Thomas R. Burkard and Dominic Hoepfner and has published in prestigious journals such as Nature Methods, Science Advances and Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease.

In The Last Decade

Sergei Zhuk

17 papers receiving 292 citations

Peers

Sergei Zhuk

CCM

PRM

EPIDE

SURGE

Florian Priller Germany

Katyayani Sukhavasi Estonia

Ragini Phansalkar United States

Tilman Ziegler Germany

Hadil El‐Sammak Germany

Martje Tönjes Germany

Ketty Kessler France

Subreena Simrick United Kingdom

G. Vuagniaux Switzerland

Sonisha Warren United States

Florian Priller Germany

Sergei Zhuk

234 ×1.2

33 ×0.6

CCM

34 ×0.6

PRM

50 ×0.9

EPIDE

30 ×0.8

SURGE

Citations per year, relative to Sergei Zhuk Sergei Zhuk (= 1×) peers Florian Priller

Countries citing papers authored by Sergei Zhuk

Since Specialization

Citations

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

Fields of papers citing papers by Sergei Zhuk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sergei Zhuk

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

All Works

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18 of 18 papers shown

Zhuk, Sergei, et al.. (2025). The clinical and genetic spectrum of pediatric hypertrophic cardiomyopathy manifesting before one year of age. Pediatric Research. 98(4). 1301–1312.

Zlotina, Anna, et al.. (2024). Characterization of pathogenic genetic variants in Russian patients with primary ciliary dyskinesia using gene panel sequencing and transcript analysis. Orphanet Journal of Rare Diseases. 19(1). 310–310. 1 indexed citations

Smolina, Natalia, Sergei Zhuk, Giuseppe Faggian, et al.. (2023). Desmin mutations impact the autophagy flux in C2C12 cell in mutation-specific manner. Cell and Tissue Research. 393(2). 357–375. 4 indexed citations

Hagelkrüys, Astrid, Jasmin Taubenschmid, Anoop Kavirayani, et al.. (2022). The HUSH complex controls brain architecture and protocadherin fidelity. Science Advances. 8(44). eabo7247–eabo7247. 16 indexed citations

Sjöberg, Gunnar, Sergei Zhuk, S. I. Tarnovskaya, et al.. (2022). Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood. Orphanet Journal of Rare Diseases. 17(1). 358–358. 7 indexed citations

Никитин, А. Г., et al.. (2022). Case Report: Two New Cases of Autosomal-Recessive Hypertrophic Cardiomyopathy Associated With TRIM63-Compound Heterozygous Variant. Frontiers in Genetics. 13. 743472–743472. 8 indexed citations

Лебедев, Д. С., Л. Б. Митрофанова, Sergei Zhuk, et al.. (2021). Case Reports: Emery-Dreifuss Muscular Dystrophy Presenting as a Heart Rhythm Disorders in Children. Frontiers in Cardiovascular Medicine. 8. 668231–668231. 3 indexed citations

Лебедев, Д. С., et al.. (2021). RBM20-Associated Ventricular Arrhythmias in a Patient with Structurally Normal Heart. Genes. 12(1). 94–94. 7 indexed citations

Zhuk, Sergei, et al.. (2018). Monocytes with Oncogenic Mutation JAK2 V617F as a Tool for Studies of the Pathogenic Mechanisms of Myelofibrosis. Bulletin of Experimental Biology and Medicine. 164(4). 569–575. 1 indexed citations

10.

Michlits, Georg, Maria Hubmann, Gintautas Vainorius, et al.. (2017). CRISPR-UMI: single-cell lineage tracing of pooled CRISPR–Cas9 screens. Nature Methods. 14(12). 1191–1197. 85 indexed citations

11.

Savvateeva, Maria V., et al.. (2017). Murine and human hematopoietic progenitor cultures grown on stromal layers expressing Notch ligands. Molecular Biology. 51(2). 313–322. 5 indexed citations

12.

Savvateeva, Maria V., et al.. (2017). [Murine and human hematopoietic progenitor cultures grown on stromal layers expressing Notch ligands].. PubMed. 51(2). 356–366. 2 indexed citations

13.

Kostina, Aleksandra, O. B. Irtyuga, О. М. Моисеева, et al.. (2016). Notch-dependent EMT is attenuated in patients with aortic aneurysm and bicuspid aortic valve. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1862(4). 733–740. 58 indexed citations

14.

Pivovarova‐Ramich, Olga, Silke Hornemann, Sandra Weimer, et al.. (2015). Regulation of nutrition-associated receptors in blood monocytes of normal weight and obese humans. Peptides. 65. 12–19. 22 indexed citations

15.

Pivovarova‐Ramich, Olga, Christian von Loeffelholz, Iryna Ilkavets, et al.. (2015). Modulation of insulin degrading enzyme activity and liver cell proliferation. Cell Cycle. 14(14). 2293–2300. 32 indexed citations

16.

Tatarinova, Tatiana V., Natalia Smolina, Sergei Zhuk, et al.. (2014). Variants in theNOTCH1Gene in Patients with Aortic Coarctation. Congenital Heart Disease. 9(5). 391–396. 41 indexed citations

17.

Orlov, Sergey, et al.. (2010). Roles of ZF5 and CGGBP-20 transcription factors in regulating expression of human FMR1 gene responsible for fragile X-syndrome. Cell and Tissue Biology. 4(1). 54–62. 1 indexed citations

18.

Orlov, Sergey, et al.. (2009). [The role of ZF5 and CGGBP-20 transcription factors in expression regulation of human FMR1 gene responsible for X-fragile syndrome].. PubMed. 51(12). 1005–12. 3 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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