Mridula Nambiar

2.0k total citations
28 papers, 1.5k citations indexed

About

Mridula Nambiar is a scholar working on Molecular Biology, Organic Chemistry and Plant Science. According to data from OpenAlex, Mridula Nambiar has authored 28 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 5 papers in Organic Chemistry and 4 papers in Plant Science. Recurrent topics in Mridula Nambiar's work include DNA Repair Mechanisms (15 papers), DNA and Nucleic Acid Chemistry (9 papers) and RNA Interference and Gene Delivery (6 papers). Mridula Nambiar is often cited by papers focused on DNA Repair Mechanisms (15 papers), DNA and Nucleic Acid Chemistry (9 papers) and RNA Interference and Gene Delivery (6 papers). Mridula Nambiar collaborates with scholars based in India, United States and United Kingdom. Mridula Nambiar's co-authors include Sathees C. Raghavan, Bibha Choudhary, Gerald R. Smith, Vijayalakshmi Kari, Gunaseelan Goldsmith, Subhas S. Karki, Sujeet Kumar, Mrinal Srivastava, Kishore K. Chiruvella and C. V. Kavitha and has published in prestigious journals such as Cell, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Mridula Nambiar

28 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mridula Nambiar India 20 1.1k 244 202 172 150 28 1.5k
Masataka Tsuda Japan 19 1.1k 1.0× 174 0.7× 388 1.9× 81 0.5× 223 1.5× 49 1.4k
Krisztina Pongracz United States 23 1.2k 1.0× 122 0.5× 102 0.5× 70 0.4× 299 2.0× 38 1.6k
Marie‐Josèphe Giraud‐Panis France 28 1.9k 1.7× 118 0.5× 311 1.5× 183 1.1× 85 0.6× 49 2.3k
Stéphane Vispé France 16 952 0.8× 102 0.4× 243 1.2× 52 0.3× 139 0.9× 23 1.1k
Noriko Shimazaki Japan 18 984 0.9× 51 0.2× 192 1.0× 136 0.8× 171 1.1× 33 1.2k
Jessica Marinello Italy 20 1.4k 1.2× 174 0.7× 302 1.5× 72 0.4× 302 2.0× 29 1.7k
J. Retèl Netherlands 22 1.3k 1.1× 129 0.5× 269 1.3× 223 1.3× 202 1.3× 54 1.6k
Maria Hägg Olofsson Sweden 17 1.2k 1.0× 107 0.4× 472 2.3× 49 0.3× 247 1.6× 26 1.7k
Chunlai Nie China 22 796 0.7× 90 0.4× 293 1.5× 53 0.3× 169 1.1× 57 1.3k
Hidesuke Fukazawa Japan 23 882 0.8× 163 0.7× 329 1.6× 37 0.2× 131 0.9× 50 1.6k

Countries citing papers authored by Mridula Nambiar

Since Specialization
Citations

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

Fields of papers citing papers by Mridula Nambiar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mridula Nambiar

This figure shows the co-authorship network connecting the top 25 collaborators of Mridula Nambiar. A scholar is included among the top collaborators of Mridula Nambiar 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 Mridula Nambiar. Mridula Nambiar 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.
Nieuwenhuijze, Annemarie van, Pushpinder Bawa, Mrinal Srivastava, et al.. (2021). MicroRNA miR-29c regulates RAG1 expression and modulates V(D)J recombination during B cell development. Cell Reports. 36(2). 109390–109390. 23 indexed citations
2.
Smith, Gerald R. & Mridula Nambiar. (2020). New Solutions to Old Problems: Molecular Mechanisms of Meiotic Crossover Control. Trends in Genetics. 36(5). 337–346. 20 indexed citations
3.
Nambiar, Mridula, et al.. (2019). Distributing meiotic crossovers for optimal fertility and evolution. DNA repair. 81. 102648–102648. 16 indexed citations
4.
Nambiar, Mridula & Gerald R. Smith. (2018). Pericentromere-Specific Cohesin Complex Prevents Meiotic Pericentric DNA Double-Strand Breaks and Lethal Crossovers. Molecular Cell. 71(4). 540–553.e4. 33 indexed citations
5.
Nambiar, Mridula & Gerald R. Smith. (2016). Repression of harmful meiotic recombination in centromeric regions. Seminars in Cell and Developmental Biology. 54. 188–197. 72 indexed citations
6.
Ma, Lijuan, Neta Milman, Mridula Nambiar, & Gerald R. Smith. (2015). Two separable functions of Ctp1 in the early steps of meiotic DNA double-strand break repair. Nucleic Acids Research. 43(15). 7349–7359. 11 indexed citations
7.
Nambiar, Mridula, et al.. (2015). Detection of G-Quadruplex DNA Using Primer Extension as a Tool. PLoS ONE. 10(3). e0119722–e0119722. 24 indexed citations
8.
Nambiar, Mridula, et al.. (2012). Potential G-quadruplex formation at breakpoint regions of chromosomal translocations in cancer may explain their fragility. Genomics. 100(2). 72–80. 66 indexed citations
9.
Srivastava, Mrinal, Mridula Nambiar, Sheetal Sharma, et al.. (2012). An Inhibitor of Nonhomologous End-Joining Abrogates Double-Strand Break Repair and Impedes Cancer Progression. Cell. 151(7). 1474–1487. 297 indexed citations
10.
Nambiar, Mridula & Sathees C. Raghavan. (2012). Mechanism of Fragility at BCL2 Gene Minor Breakpoint Cluster Region during t(14;18) Chromosomal Translocation. Journal of Biological Chemistry. 287(12). 8688–8701. 40 indexed citations
11.
Nambiar, Mridula & Sathees C. Raghavan. (2012). Chromosomal translocations among the healthy human population: implications in oncogenesis. Cellular and Molecular Life Sciences. 70(8). 1381–1392. 30 indexed citations
12.
Karki, Subhas S., Panjamurthy Kuppusamy, Sujeet Kumar, et al.. (2011). Synthesis and biological evaluation of novel 2-aralkyl-5-substituted-6-(4′-fluorophenyl)-imidazo[2,1-b][1,3,4]thiadiazole derivatives as potent anticancer agents. European Journal of Medicinal Chemistry. 46(6). 2109–2116. 87 indexed citations
13.
Nambiar, Mridula, et al.. (2011). How does DNA break during chromosomal translocations?. Nucleic Acids Research. 39(14). 5813–5825. 103 indexed citations
14.
Shahabuddin, M., et al.. (2010). A novel structural derivative of natural alkaloid ellipticine, MDPSQ, induces necrosis in leukemic cells. Investigational New Drugs. 29(4). 523–533. 23 indexed citations
15.
Nambiar, Mridula, Gunaseelan Goldsmith, Balaji T. Moorthy, et al.. (2010). Formation of a G-quadruplex at the BCL2 major breakpoint region of the t(14;18) translocation in follicular lymphoma. Nucleic Acids Research. 39(3). 936–948. 108 indexed citations
16.
17.
Shahabuddin, M., et al.. (2009). A novel DNA intercalator, butylamino-pyrimido[4′,5′:4,5]selenolo(2,3-b)quinoline, induces cell cycle arrest and apoptosis in leukemic cells. Investigational New Drugs. 28(1). 35–48. 47 indexed citations
18.
Nambiar, Mridula & Sathees C. Raghavan. (2009). Prevalence and analysis of t(14;18) and t(11;14) chromosomal translocations in healthy Indian population. Annals of Hematology. 89(1). 35–43. 18 indexed citations
19.
Nambiar, Mridula, et al.. (2008). Amplification of chromosomal translocation junctions from paraffin-embedded tissues of follicular lymphoma patients. Biomedical Materials. 3(3). 34103–34103. 2 indexed citations
20.
Chiruvella, Kishore K., et al.. (2008). Methyl angolensate, a natural tetranortriterpenoid induces intrinsic apoptotic pathway in leukemic cells. FEBS Letters. 582(29). 4066–4076. 68 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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