Tapahsama Banerjee

711 total citations
11 papers, 265 citations indexed

About

Tapahsama Banerjee is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Tapahsama Banerjee has authored 11 papers receiving a total of 265 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Genetics and 1 paper in Pathology and Forensic Medicine. Recurrent topics in Tapahsama Banerjee's work include DNA Repair Mechanisms (8 papers), BRCA gene mutations in cancer (7 papers) and CRISPR and Genetic Engineering (5 papers). Tapahsama Banerjee is often cited by papers focused on DNA Repair Mechanisms (8 papers), BRCA gene mutations in cancer (7 papers) and CRISPR and Genetic Engineering (5 papers). Tapahsama Banerjee collaborates with scholars based in United States. Tapahsama Banerjee's co-authors include Jeffrey D. Parvin, Lea M. Starita, Stanley Fields, Shweta Kotian, Jay Shendure, Justin Gullingsrud, Michael A. Freitas, Xiaoyan Guan, Ainsley Lockhart and Karuppaiyah Selvendiran and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and PLoS ONE.

In The Last Decade

Tapahsama Banerjee

11 papers receiving 265 citations

Peers

Tapahsama Banerjee
Raymond Che United States
Christian Pistore Italy
Alice Fletcher United Kingdom
Stacey E. P. Joosten Netherlands
Kavitta Sivanandan Malaysia
Asuka Hira Japan
Brian J. Orelli United States
Hanan Khoury-Haddad Israel
Andrew Perez United States
Mae A. Goldgraben United Kingdom
Raymond Che United States
Tapahsama Banerjee
Citations per year, relative to Tapahsama Banerjee Tapahsama Banerjee (= 1×) peers Raymond Che

Countries citing papers authored by Tapahsama Banerjee

Since Specialization
Citations

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

Fields of papers citing papers by Tapahsama Banerjee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tapahsama Banerjee

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

All Works

11 of 11 papers shown
1.
Banerjee, Tapahsama, et al.. (2023). DNA repair function scores for 2172 variants in the BRCA1 amino-terminus. PLoS Genetics. 19(8). e1010739–e1010739. 2 indexed citations
2.
Banerjee, Tapahsama, Nahum Smith, Wenfang Liu, et al.. (2023). Multiplexed assay of variant effect reveals residues of functional importance in the BRCA1 coiled-coil and serine cluster domains. PLoS ONE. 18(11). e0293422–e0293422. 1 indexed citations
3.
Banerjee, Tapahsama, et al.. (2022). The functional impact of BRCA1 BRCT domain variants using multiplexed DNA double-strand break repair assays. The American Journal of Human Genetics. 109(4). 618–630. 8 indexed citations
4.
Banerjee, Tapahsama, Jie Ning, Fernanda Martins Rodrigues, et al.. (2019). Functional analysis of BARD1 missense variants in homology-directed repair and damage sensitivity. PLoS Genetics. 15(3). e1008049–e1008049. 22 indexed citations
5.
Starita, Lea M., Tapahsama Banerjee, Justin Gullingsrud, et al.. (2018). A Multiplex Homology-Directed DNA Repair Assay Reveals the Impact of More Than 1,000 BRCA1 Missense Substitution Variants on Protein Function. The American Journal of Human Genetics. 103(4). 498–508. 78 indexed citations
6.
Banerjee, Tapahsama, et al.. (2017). HDAC10 as a potential therapeutic target in ovarian cancer. Gynecologic Oncology. 144(3). 613–620. 38 indexed citations
7.
Nair, Sreejith J., Xiaowen Zhang, Huai-Chin Chiang, et al.. (2016). Genetic suppression reveals DNA repair-independent antagonism between BRCA1 and COBRA1 in mammary gland development. Nature Communications. 7(1). 10913–10913. 17 indexed citations
8.
Banerjee, Tapahsama, et al.. (2015). The chromatin scaffold protein SAFB1 localizes SUMO-1 to the promoters of ribosomal protein genes to facilitate transcription initiation and splicing. Nucleic Acids Research. 43(7). 3605–3613. 26 indexed citations
9.
Arora, Mansi, et al.. (2015). RING1A and BMI1 bookmark active genes via ubiquitination of chromatin-associated proteins. Nucleic Acids Research. 44(5). 2136–2144. 19 indexed citations
10.
Banerjee, Tapahsama, et al.. (2015). Functional Analysis of BARD1 Missense Variants in Homology-Directed Repair of DNA Double Strand Breaks. Human Mutation. 36(12). 1205–1214. 24 indexed citations
11.
Kotian, Shweta, Tapahsama Banerjee, Ainsley Lockhart, et al.. (2014). NUSAP1 influences the DNA damage response by controlling BRCA1 protein levels. Cancer Biology & Therapy. 15(5). 533–543. 30 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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2026