M. Grigorova

872 total citations
17 papers, 651 citations indexed

About

M. Grigorova is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, M. Grigorova has authored 17 papers receiving a total of 651 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Cancer Research and 7 papers in Genetics. Recurrent topics in M. Grigorova's work include DNA Repair Mechanisms (7 papers), Carcinogens and Genotoxicity Assessment (7 papers) and Chromosomal and Genetic Variations (6 papers). M. Grigorova is often cited by papers focused on DNA Repair Mechanisms (7 papers), Carcinogens and Genotoxicity Assessment (7 papers) and Chromosomal and Genetic Variations (6 papers). M. Grigorova collaborates with scholars based in Netherlands, United Kingdom and Sweden. M. Grigorova's co-authors include P. Andrew Futreal, Jing Huang, Joel Greshock, Wen Wei, Michael R. Stratton, Adam P. Butler, Graham R. Bignell, Barbara Weber, Michael H. Shapero and Stephen M. Watt and has published in prestigious journals such as Genome Research, Fertility and Sterility and Mutation research. Fundamental and molecular mechanisms of mutagenesis.

In The Last Decade

M. Grigorova

16 papers receiving 621 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Grigorova Netherlands 10 414 296 241 139 60 17 651
M. Poggensee United States 7 434 1.0× 355 1.2× 142 0.6× 207 1.5× 16 0.3× 7 652
Andreas Plesch Germany 4 203 0.5× 139 0.5× 140 0.6× 122 0.9× 18 0.3× 7 384
Jane Briner United States 5 274 0.7× 296 1.0× 52 0.2× 65 0.5× 34 0.6× 7 432
Catherine S. Rodgers United Kingdom 9 145 0.4× 152 0.5× 165 0.7× 67 0.5× 46 0.8× 9 376
Mariona Terradas Spain 16 430 1.0× 236 0.8× 92 0.4× 75 0.5× 32 0.5× 31 729
Karen Eddy United States 5 572 1.4× 251 0.8× 62 0.3× 32 0.2× 55 0.9× 6 690
Silvia Viaggi Italy 15 366 0.9× 271 0.9× 40 0.2× 79 0.6× 84 1.4× 35 664
Н. П. Кулешов Russia 10 133 0.3× 97 0.3× 129 0.5× 61 0.4× 23 0.4× 17 337
Patricio González‐Hormazábal Chile 18 375 0.9× 255 0.9× 232 1.0× 63 0.5× 46 0.8× 35 718
K. Salassidis Germany 9 272 0.7× 227 0.8× 73 0.3× 73 0.5× 20 0.3× 12 482

Countries citing papers authored by M. Grigorova

Since Specialization
Citations

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

Fields of papers citing papers by M. Grigorova

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Grigorova

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

All Works

17 of 17 papers shown
1.
Maheshwari, Shamoni, Jon M. Sorenson, Ian T. Fiddes, et al.. (2020). Single-cell sequencing of genomic DNA resolves sub-clonal heterogeneity in a melanoma cell line. Communications Biology. 3(1). 318–318. 34 indexed citations
2.
Tempest, Helen G., et al.. (2010). P11 Sperm aneuploidy: When to stop counting?. Reproductive BioMedicine Online. 20. S26–S26. 1 indexed citations
3.
Thornhill, Alan R., Helen G. Tempest, M. Grigorova, et al.. (2009). A comparison of microarray methods to detect chromosomal aneuploidy in human preimplantation embryos. Fertility and Sterility. 92(3). S201–S201. 1 indexed citations
4.
Tempest, Helen G., et al.. (2009). Sperm aneuploidy: when to stop counting?. Fertility and Sterility. 92(3). S141–S142. 1 indexed citations
5.
Grigorova, M., et al.. (2005). Chromosome abnormalities in 10 lung cancer cell lines of the NCI-H series analyzed with spectral karyotyping. Cancer Genetics and Cytogenetics. 162(1). 1–9. 27 indexed citations
6.
Bignell, Graham R., Jing Huang, Joel Greshock, et al.. (2004). High-Resolution Analysis of DNA Copy Number Using Oligonucleotide Microarrays. Genome Research. 14(2). 287–295. 281 indexed citations
7.
Grigorova, M., et al.. (2004). Possible causes of chromosome instability: comparison of chromosomal abnormalities in cancer cell lines with mutations in BRCA1, BRCA2, CHK2 and BUB1. Cytogenetic and Genome Research. 104(1-4). 333–340. 33 indexed citations
8.
Hristova, Rositsa, Teodora Nikolova, M. Grigorova, et al.. (2002). Cytogenetic effects of hexavalent chromium in Bulgarian chromium platers. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 514(1-2). 29–38. 66 indexed citations
9.
10.
Natarajan, Arvind, F. Darroudi, J. Merlijn van den Berg, et al.. (2000). Biological dosimetric studies in Goiania radiation accident.
11.
Natarajan, A.T., Susy J. Santos, F. Darroudi, et al.. (1998). 137Cesium-induced chromosome aberrations analyzed by fluorescence in situ hybridization: eight years follow up of the Goiânia radiation accident victims. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 400(1-2). 299–312. 82 indexed citations
12.
Grigorova, M. & A.T. Natarajan. (1998). Relative involvement of chromosome #21 in radiation induced exchange aberrations in lymphocytes of down syndrome patients. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 404(1-2). 67–75. 7 indexed citations
13.
Grigorova, M., Yun Xiao, & A.T. Natarajan. (1997). P XIV C.3 Analysis of radiation-induced chromosome aberrations in Chinese hamster splenocytes by FISH using chromosome-specific DNA libraries. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 379(1). S136–S136. 1 indexed citations
14.
Buul, Paul P.W. van, et al.. (1995). X-ray-induced Chromosomal Aberrations and Cell Killing in Somatic and Germ Cells of theScidMouse. International Journal of Radiation Biology. 67(5). 549–555. 14 indexed citations
15.
Grigorova, M., J.J.W.A. Boei, Annemarie van Duyn-Goedhart, A.T. Natarajan, & Paul P.W. van Buul. (1995). X-ray induced translocations in bone marrow cells of scid and wild type mice detected by fluorescence in situ hybridization using mouse chromosome specific DNA libraries. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 331(1). 39–45. 10 indexed citations
16.
Buul, Paul P.W. van, et al.. (1995). Mitotic and meiotic detection of radiation-induced translocations in mouse stem cell spermatogonia using fluorescencein situ hybridization. Chromosome Research. 3(7). 427–432. 6 indexed citations
17.
Natarajan, A.T., A.S. Balajee, J.J.W.A. Boei, et al.. (1994). Recent Developments in the Assessment of Chromosomal Damage. International Journal of Radiation Biology. 66(5). 615–623. 62 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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