Margaret M. Mc Gee

2.3k total citations · 1 hit paper
38 papers, 1.8k citations indexed

About

Margaret M. Mc Gee is a scholar working on Molecular Biology, Cell Biology and Organic Chemistry. According to data from OpenAlex, Margaret M. Mc Gee has authored 38 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 9 papers in Cell Biology and 8 papers in Organic Chemistry. Recurrent topics in Margaret M. Mc Gee's work include Extracellular vesicles in disease (8 papers), Microtubule and mitosis dynamics (7 papers) and Cancer therapeutics and mechanisms (6 papers). Margaret M. Mc Gee is often cited by papers focused on Extracellular vesicles in disease (8 papers), Microtubule and mitosis dynamics (7 papers) and Cancer therapeutics and mechanisms (6 papers). Margaret M. Mc Gee collaborates with scholars based in Ireland, United States and Italy. Margaret M. Mc Gee's co-authors include Kieran Brennan, Alfonso Blanco, Yunjie Wu, Ciarán Richardson, S. P. Fitzgerald, Katrin Martin, Jeff O’Sullivan, Daniela M. Zisterer, Giuseppe Campiani and W. Eugene Knox and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and PLoS ONE.

In The Last Decade

Margaret M. Mc Gee

38 papers receiving 1.8k citations

Hit Papers

A comparison of methods for the isolation and separation ... 2020 2026 2022 2024 2020 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Margaret M. Mc Gee Ireland 19 1.3k 435 261 228 176 38 1.8k
Shuang Liu China 25 1.3k 1.0× 488 1.1× 343 1.3× 193 0.8× 96 0.5× 83 2.2k
Lurong Zhang China 25 1.3k 1.0× 246 0.6× 281 1.1× 248 1.1× 85 0.5× 66 2.2k
Jijun Cheng United States 24 1.1k 0.9× 403 0.9× 217 0.8× 188 0.8× 109 0.6× 32 1.6k
Susan A. Brooks United Kingdom 29 1.8k 1.4× 511 1.2× 419 1.6× 610 2.7× 206 1.2× 88 2.7k
Marcin Poręba Poland 28 1.4k 1.1× 390 0.9× 659 2.5× 328 1.4× 355 2.0× 68 2.2k
Søren Skov Jensen Denmark 16 1.7k 1.3× 440 1.0× 111 0.4× 198 0.9× 63 0.4× 17 2.1k
Paulina Kasperkiewicz Poland 22 906 0.7× 301 0.7× 395 1.5× 279 1.2× 294 1.7× 43 1.5k
Srikumar M. Raja United States 27 1.3k 1.0× 247 0.6× 359 1.4× 684 3.0× 104 0.6× 37 2.4k
Carlo Mischiati Italy 28 1.3k 1.0× 176 0.4× 193 0.7× 193 0.8× 318 1.8× 98 2.1k
Florian Rothweiler Germany 23 1.1k 0.8× 241 0.6× 562 2.2× 105 0.5× 95 0.5× 56 2.0k

Countries citing papers authored by Margaret M. Mc Gee

Since Specialization
Citations

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

Fields of papers citing papers by Margaret M. Mc Gee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Margaret M. Mc Gee

This figure shows the co-authorship network connecting the top 25 collaborators of Margaret M. Mc Gee. A scholar is included among the top collaborators of Margaret M. Mc Gee 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 Margaret M. Mc Gee. Margaret M. Mc Gee 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.
Brennan, Kieran, et al.. (2025). Menstrual blood serum extracellular vesicles reveal novel molecular biomarkers and potential endotypes of unexplained infertility. Scientific Reports. 15(1). 11974–11974. 3 indexed citations
2.
Brennan, Kieran, et al.. (2025). Proteomic signature of menstrual blood mesenchymal stromal cells and their extracellular vesicles in women with unexplained infertility. Reproductive BioMedicine Online. 51(4). 104980–104980. 4 indexed citations
4.
García-Posadas, Laura, et al.. (2023). Isolation and Characterization of Human Conjunctival Mesenchymal Stromal Cells and Their Extracellular Vesicles. Investigative Ophthalmology & Visual Science. 64(12). 38–38. 6 indexed citations
5.
Brennan, Kieran, et al.. (2022). Investigation of canine extracellular vesicles in diffuse large B-cell lymphomas. PLoS ONE. 17(9). e0274261–e0274261. 12 indexed citations
6.
Brennan, Kieran, Katrin Martin, S. P. Fitzgerald, et al.. (2020). A comparison of methods for the isolation and separation of extracellular vesicles from protein and lipid particles in human serum. Scientific Reports. 10(1). 1039–1039. 641 indexed citations breakdown →
7.
Casey, Jillian P., Kieran Brennan, Paul McGettigan, et al.. (2016). Recessive NEK9 mutation causes a lethal skeletal dysplasia with evidence of cell cycle and ciliary defects. Human Molecular Genetics. 25(9). 1824–1835. 33 indexed citations
8.
Gee, Margaret M. Mc. (2015). Targeting the Mitotic Catastrophe Signaling Pathway in Cancer. Mediators of Inflammation. 2015(1). 146282–146282. 166 indexed citations
9.
Annibali, Daniela, Jonathan R. Whitfield, Emilia Favuzzi, et al.. (2014). Myc inhibition is effective against glioma and reveals a role for Myc in proficient mitosis. Nature Communications. 5(1). 4632–4632. 145 indexed citations
10.
Gee, Margaret M. Mc, et al.. (2012). The peptidyl prolyl isomerase cyclophilin A localizes at the centrosome and the midbody and is required for cytokinesis. Cell Cycle. 11(7). 1340–1353. 24 indexed citations
12.
Fichtner, Iduna, Clara Pampillón, Nigel J. Sweeney, et al.. (2007). Substituted titanocenes induce caspase-dependent apoptosis in human epidermoid carcinoma cells in vitro and exhibit antitumour activity in vivo. British Journal of Cancer. 97(9). 1234–1241. 47 indexed citations
14.
Mulligan, Jude M., Lisa M. Greene, Suzanne M. Cloonan, et al.. (2006). Identification of Tubulin as the Molecular Target of Proapoptotic Pyrrolo-1,5-benzoxazepines. Molecular Pharmacology. 70(1). 60–70. 52 indexed citations
15.
Gee, Margaret M. Mc, Lisa M. Greene, Vito Nacci, et al.. (2004). Selective Induction of Apoptosis by PBOX-6 in Leukemia Cells occurs via the JNK Dependent Phosphorylation and Inactivation of Bcl-2 and Bcl-XL. 1 indexed citations
17.
Gee, Margaret M. Mc, Edel M. Hyland, Giuseppe Campiani, et al.. (2002). Caspase‐3 is not essential for DNA fragmentation in MCF‐7 cells during apoptosis induced by the pyrrolo‐1,5‐benzoxazepine, PBOX‐6. FEBS Letters. 515(1-3). 66–70. 95 indexed citations
18.
Zisterer, Daniela M., Margaret M. Mc Gee, Giuseppe Campiani, et al.. (2001). Pyrrolo-1,5-benzoxazepines: a new class of apoptotic agents. Biochemical Society Transactions. 29(6). 704–704. 7 indexed citations
19.
Sheahan, B. J., et al.. (1998). The Semliki Forest virus vector induces p53-independent apoptosis.. Journal of General Virology. 79(10). 2405–2410. 73 indexed citations
20.
Gee, Margaret M. Mc & W. Eugene Knox. (1971). Phosphate-Activated Isoenzymes of Glutaminasein Rat Liver and Kidney. Enzyme. 12(5). 618–621. 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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