Adelina Sergueeva

1.4k total citations
26 papers, 1.0k citations indexed

About

Adelina Sergueeva is a scholar working on Cancer Research, Molecular Biology and Genetics. According to data from OpenAlex, Adelina Sergueeva has authored 26 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Cancer Research, 13 papers in Molecular Biology and 10 papers in Genetics. Recurrent topics in Adelina Sergueeva's work include Cancer, Hypoxia, and Metabolism (17 papers), High Altitude and Hypoxia (9 papers) and Hemoglobinopathies and Related Disorders (7 papers). Adelina Sergueeva is often cited by papers focused on Cancer, Hypoxia, and Metabolism (17 papers), High Altitude and Hypoxia (9 papers) and Hemoglobinopathies and Related Disorders (7 papers). Adelina Sergueeva collaborates with scholars based in Russia, United States and Germany. Adelina Sergueeva's co-authors include Victor R. Gordeuk, Galina Miasnikova, Josef T. Prchal, Lydia A. Polyakova, David W. Stockton, Sonny Ang, Daniel J. Okhotin, Gregg L. Semenza, Patrick H. Maxwell and Hua Chen and has published in prestigious journals such as Circulation, Nature Genetics and Blood.

In The Last Decade

Adelina Sergueeva

24 papers receiving 995 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Adelina Sergueeva Russia 14 541 396 326 267 264 26 1.0k
Galina Miasnikova Russia 12 532 1.0× 379 1.0× 294 0.9× 244 0.9× 257 1.0× 21 958
Betty Gardie France 15 516 1.0× 803 2.0× 172 0.5× 139 0.5× 135 0.5× 36 1.3k
Lydia A. Polyakova Russia 8 278 0.5× 195 0.5× 175 0.5× 138 0.5× 139 0.5× 9 526
Katerina Jedlickova United States 7 268 0.5× 195 0.5× 177 0.5× 128 0.5× 134 0.5× 9 505
Daniel J. Okhotin Russia 9 220 0.4× 157 0.4× 109 0.3× 106 0.4× 114 0.4× 10 406
Varsha Muralidhar United States 3 116 0.2× 387 1.0× 331 1.0× 483 1.8× 57 0.2× 5 1000
Kosei Oshima United States 6 129 0.2× 374 0.9× 413 1.3× 591 2.2× 48 0.2× 7 1.1k
Kimberly B. Zumbrennen‐Bullough United States 9 49 0.1× 282 0.7× 371 1.1× 474 1.8× 144 0.5× 9 977
Nicola M. Tomas Germany 15 87 0.2× 349 0.9× 155 0.5× 196 0.7× 61 0.2× 30 1.5k
Jan H. Marxsen Germany 11 796 1.5× 582 1.5× 42 0.1× 45 0.2× 227 0.9× 16 1.2k

Countries citing papers authored by Adelina Sergueeva

Since Specialization
Citations

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

Fields of papers citing papers by Adelina Sergueeva

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Adelina Sergueeva

This figure shows the co-authorship network connecting the top 25 collaborators of Adelina Sergueeva. A scholar is included among the top collaborators of Adelina Sergueeva 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 Adelina Sergueeva. Adelina Sergueeva 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.
Zhang, Xu, Jihyun Song, Binal N. Shah, et al.. (2023). Gene expression changes in sickle cell reticulocytes and their clinical associations. Scientific Reports. 13(1). 12864–12864.
2.
Shah, Binal N., Xu Zhang, Adelina Sergueeva, et al.. (2023). Increased transferrin protects from thrombosis in Chuvash erythrocytosis. American Journal of Hematology. 98(10). 1532–1539. 5 indexed citations
3.
Song, Jihyun, Ricardo Amaru, Adelina Sergueeva, et al.. (2018). Tibetan Enriched PKLR Variant Is Beneficial to High Altitude Adaption By Improving Oxygen Delivery. Blood. 132(Supplement 1). 1027–1027. 1 indexed citations
4.
Gordeuk, Victor R., Dominic W. Chung, Binal N. Shah, et al.. (2017). Thrombosis and Von Willebrand Factor in Chuvash Polycythemia. Blood. 130. 2377. 1 indexed citations
5.
Zhang, Xu, Binal N. Shah, Wei Zhang, et al.. (2016). A genetic variation associated with plasma erythropoietin and a non-coding transcript ofPRKAR1Ain sickle cell disease. Human Molecular Genetics. 25(20). ddw299–ddw299. 3 indexed citations
6.
Zhang, Xu, Wei Zhang, Santosh L. Saraf, et al.. (2015). Genetic polymorphism of APOB is associated with diabetes mellitus in sickle cell disease. Human Genetics. 134(8). 895–904. 13 indexed citations
7.
Zhang, Xu, Wei Zhang, Shwu‐Fan Ma, et al.. (2014). Hypoxic Response Contributes to Altered Gene Expression and Precapillary Pulmonary Hypertension in Patients With Sickle Cell Disease. Circulation. 129(16). 1650–1658. 33 indexed citations
8.
Miasnikova, Galina, Adelina Sergueeva, Lydia A. Polyakova, et al.. (2013). Effect of congenital upregulation of hypoxia inducible factors on percentage of fetal hemoglobin in the blood. Blood. 122(17). 3088–3089. 7 indexed citations
9.
Zhang, Xu, Wei Zhang, Shwu‐Fan Ma, et al.. (2013). Iron deficiency modifies gene expression variation induced by augmented hypoxia sensing. Blood Cells Molecules and Diseases. 52(1). 35–45. 18 indexed citations
10.
McClain, Donald A., Khadega A. Abuelgasim, Mehdi Nouraie, et al.. (2012). Decreased serum glucose and glycosylated hemoglobin levels in patients with Chuvash polycythemia: a role for HIF in glucose metabolism. Journal of Molecular Medicine. 91(1). 59–67. 38 indexed citations
11.
Gordeuk, Victor R., Galina Miasnikova, Adelina Sergueeva, et al.. (2011). Chuvash polycythemia VHLR200W mutation is associated with down-regulation of hepcidin expression. Blood. 118(19). 5278–5282. 40 indexed citations
12.
Miasnikova, Galina, Adelina Sergueeva, Mehdi Nouraie, et al.. (2011). The heterozygote advantage of the Chuvash polycythemia VHLR200W mutation may be protection against anemia. Haematologica. 96(9). 1371–1374. 13 indexed citations
13.
Sable, Craig, Zakari Y. Aliyu, Niti Dham, et al.. (2011). Pulmonary artery pressure and iron deficiency in patients with upregulation of hypoxia sensing due to homozygous VHLR200W mutation (Chuvash polycythemia). Haematologica. 97(2). 193–200. 18 indexed citations
14.
Yoon, Donghoon, Bumjun Kim, Daniel J. Okhotin, et al.. (2010). Increased size of solid organs in patients with Chuvash polycythemia and in mice with altered expression of HIF-1α and HIF-2α. Journal of Molecular Medicine. 88(5). 523–530. 16 indexed citations
15.
Niu, Xiaomei, Galina Miasnikova, Adelina Sergueeva, et al.. (2008). Altered cytokine profiles in patients with Chuvash polycythemia. American Journal of Hematology. 84(2). 74–78. 14 indexed citations
16.
Sergueeva, Adelina, Galina Miasnikova, Daniel J. Okhotin, et al.. (2008). Elevated homocysteine, glutathione and cysteinylglycine concentrations in patients homozygous for the Chuvash polycythemia VHL mutation. Haematologica. 93(2). 279–282. 11 indexed citations
17.
Miasnikova, Galina, Adelina Sergueeva, Lydia A. Polyakova, et al.. (2006). Endothelin-1, vascular endothelial growth factor and systolic pulmonary artery pressure in patients with Chuvash polycythemia.. PubMed. 91(6). 744–9. 59 indexed citations
18.
Gordeuk, Victor R., Adelina Sergueeva, Galina Miasnikova, et al.. (2004). Congenital disorder of oxygen sensing: association of the homozygous Chuvash polycythemia VHL mutation with thrombosis and vascular abnormalities but not tumors. Blood. 103(10). 3924–3932. 196 indexed citations
19.
Ang, Sonny, Hua Chen, Kiichi Hirota, et al.. (2002). Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia. Nature Genetics. 32(4). 614–621. 382 indexed citations
20.
Ang, Sonny, Chen Hua, Victor R. Gordeuk, et al.. (2002). Endemic Polycythemia in Russia: Mutation in the VHL Gene. Blood Cells Molecules and Diseases. 28(1). 57–62. 105 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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