Tokhir Dadaev

7.3k total citations
20 papers, 784 citations indexed

About

Tokhir Dadaev is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Molecular Biology. According to data from OpenAlex, Tokhir Dadaev has authored 20 papers receiving a total of 784 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 7 papers in Pulmonary and Respiratory Medicine and 6 papers in Molecular Biology. Recurrent topics in Tokhir Dadaev's work include Genetic Associations and Epidemiology (7 papers), Prostate Cancer Treatment and Research (7 papers) and BRCA gene mutations in cancer (6 papers). Tokhir Dadaev is often cited by papers focused on Genetic Associations and Epidemiology (7 papers), Prostate Cancer Treatment and Research (7 papers) and BRCA gene mutations in cancer (6 papers). Tokhir Dadaev collaborates with scholars based in United Kingdom, United States and Japan. Tokhir Dadaev's co-authors include Zsofia Kote‐Jarai, Rosalind A. Eeles, Edward J. Saunders, Daniel Leongamornlert, Michelle Guy, Chee Goh, Malgorzata Tymrakiewicz, Rosemary Wilkinson, Elena Castro and Koveela Govindasami and has published in prestigious journals such as Journal of Clinical Oncology, Bioinformatics and Cancer Research.

In The Last Decade

Tokhir Dadaev

18 papers receiving 774 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tokhir Dadaev United Kingdom 11 510 288 288 279 178 20 784
Chee Goh United Kingdom 10 586 1.1× 307 1.1× 329 1.1× 296 1.1× 218 1.2× 20 894
Malgorzata Tymrakiewicz United Kingdom 5 386 0.8× 224 0.8× 231 0.8× 224 0.8× 139 0.8× 9 599
Koveela Govindasami United Kingdom 9 318 0.6× 178 0.6× 175 0.6× 158 0.6× 110 0.6× 14 484
Irene Rainville United States 11 198 0.4× 158 0.5× 121 0.4× 138 0.5× 146 0.8× 22 423
Bastien Nguyen United States 13 446 0.9× 214 0.7× 116 0.4× 454 1.6× 384 2.2× 24 870
A‐Yong Cao China 12 83 0.2× 199 0.7× 238 0.8× 272 1.0× 260 1.5× 40 606
Etienne Rouleau France 11 219 0.4× 131 0.5× 49 0.2× 303 1.1× 291 1.6× 39 547
Anna Johnson United States 14 244 0.5× 165 0.6× 63 0.2× 95 0.3× 90 0.5× 38 408
Małgorzata Stawicka Poland 10 99 0.2× 254 0.9× 376 1.3× 345 1.2× 306 1.7× 17 693
Kerry Kingham United States 14 102 0.2× 333 1.2× 648 2.3× 172 0.6× 343 1.9× 31 1.0k

Countries citing papers authored by Tokhir Dadaev

Since Specialization
Citations

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

Fields of papers citing papers by Tokhir Dadaev

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tokhir Dadaev

This figure shows the co-authorship network connecting the top 25 collaborators of Tokhir Dadaev. A scholar is included among the top collaborators of Tokhir Dadaev 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 Tokhir Dadaev. Tokhir Dadaev 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.
Saunders, Edward J., Tokhir Dadaev, Mark N. Brook, et al.. (2024). Identification of Genes with Rare Loss of Function Variants Associated with Aggressive Prostate Cancer and Survival. European Urology Oncology. 7(2). 248–257. 3 indexed citations
2.
Brook, Mark N., Holly Ní Raghallaigh, Koveela Govindasami, et al.. (2022). Family History of Prostate Cancer and Survival Outcomes in the UK Genetic Prostate Cancer Study. European Urology. 83(3). 257–266. 10 indexed citations
3.
Nyberg, Tommy, Mark N. Brook, Andrew Lee, et al.. (2022). CanRisk-Prostate: A Comprehensive, Externally Validated Risk Model for the Prediction of Future Prostate Cancer. Journal of Clinical Oncology. 41(5). 1092–1104. 21 indexed citations
4.
Saunders, Edward J., et al.. (2021). Prostate cancer risk in men of differing genetic ancestry and approaches to disease screening and management in these groups. British Journal of Cancer. 126(10). 1366–1373. 17 indexed citations
5.
6.
Conti, David V., Burcu F. Darst, Edward J. Saunders, et al.. (2020). Abstract PO-146: Multiethnic GWAS meta-analysis identifies novel variants and informs genetic risk prediction for prostate cancer across populations. Cancer Epidemiology Biomarkers & Prevention. 29(12_Supplement). PO–146.
7.
Leongamornlert, Daniel, Edward J. Saunders, Sarah Wakerell, et al.. (2019). Germline DNA Repair Gene Mutations in Young-onset Prostate Cancer Cases in the UK: Evidence for a More Extensive Genetic Panel. European Urology. 76(3). 329–337. 36 indexed citations
8.
Nyberg, Tommy, Koveela Govindasami, Goska Leslie, et al.. (2018). Homeobox B13 G84E Mutation and Prostate Cancer Risk. European Urology. 75(5). 834–845. 30 indexed citations
9.
Mijušković, Martina, Edward J. Saunders, Daniel Leongamornlert, et al.. (2018). Rare germline variants in DNA repair genes and the angiogenesis pathway predispose prostate cancer patients to develop metastatic disease. British Journal of Cancer. 119(1). 96–104. 31 indexed citations
10.
Eeles, Rosalind A., Daniel Leongamornlert, Edward J. Saunders, et al.. (2018). DNA repair gene panel mutations in young onset prostate cancer cases in the.. Journal of Clinical Oncology. 36(6_suppl). 18–18. 4 indexed citations
11.
Castro, Elena, Christos Mikropoulos, Elizabeth Bancroft, et al.. (2016). The PROFILE Feasibility Study: Targeted Screening of Men With a Family History of Prostate Cancer. The Oncologist. 21(6). 716–722. 26 indexed citations
12.
Castro, Elena, Sarah Jugurnauth-Little, Fátima Al‐Shahrour, et al.. (2015). High burden of copy number alterations and c-MYC amplification in prostate cancer from BRCA2 germline mutation carriers. Annals of Oncology. 26(11). 2293–2300. 25 indexed citations
13.
Dadaev, Tokhir, Daniel Leongamornlert, Edward J. Saunders, Rosalind A. Eeles, & Zsofia Kote‐Jarai. (2015). LocusExplorer: a user-friendly tool for integrated visualization of human genetic association data and biological annotations. Bioinformatics. 32(6). 949–951. 6 indexed citations
14.
Leongamornlert, Daniel, Edward J. Saunders, Tokhir Dadaev, et al.. (2014). Frequent germline deleterious mutations in DNA repair genes in familial prostate cancer cases are associated with advanced disease. British Journal of Cancer. 110(6). 1663–1672. 109 indexed citations
15.
Kote‐Jarai, Zsofia, Edward J. Saunders, Daniel Leongamornlert, et al.. (2013). Abstract 2546: Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression.. Cancer Research. 73(8_Supplement). 2546–2546. 4 indexed citations
16.
Castro, Elena, David Olmos, Chee Goh, et al.. (2013). Effect of germ-line BRCA mutations in biochemical relapse and survival after treatment for localized prostate cancer.. Journal of Clinical Oncology. 31(6_suppl). 29–29. 2 indexed citations
17.
Leongamornlert, Daniel, Nadiya Mahmud, Malgorzata Tymrakiewicz, et al.. (2012). Germline BRCA1 mutations increase prostate cancer risk. British Journal of Cancer. 106(10). 1697–1701. 201 indexed citations
18.
Castro, Elena, David Olmos, Chee Goh, et al.. (2012). BRCA carrier status as an independent prognostic factor associated with earlier biochemical relapse in local prostate cancer.. Journal of Clinical Oncology. 30(15_suppl). 1545–1545. 1 indexed citations
19.
Kote‐Jarai, Zsofia, Daniel Leongamornlert, Edward J. Saunders, et al.. (2011). BRCA2 is a moderate penetrance gene contributing to young-onset prostate cancer: implications for genetic testing in prostate cancer patients. British Journal of Cancer. 105(8). 1230–1234. 256 indexed citations
20.
Castro, Elena, Chee Goh, David Olmos, et al.. (2011). Correlation of germ-line BRCA2 mutations with aggressive prostate cancer and outcome.. Journal of Clinical Oncology. 29(15_suppl). 1517–1517. 2 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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