Roopesh Anand

2.3k total citations
23 papers, 1.4k citations indexed

About

Roopesh Anand is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, Roopesh Anand has authored 23 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 6 papers in Oncology and 5 papers in Cancer Research. Recurrent topics in Roopesh Anand's work include DNA Repair Mechanisms (22 papers), CRISPR and Genetic Engineering (17 papers) and Carcinogens and Genotoxicity Assessment (5 papers). Roopesh Anand is often cited by papers focused on DNA Repair Mechanisms (22 papers), CRISPR and Genetic Engineering (17 papers) and Carcinogens and Genotoxicity Assessment (5 papers). Roopesh Anand collaborates with scholars based in Switzerland, United Kingdom and United States. Roopesh Anand's co-authors include Petr Ćejka, Lepakshi Ranjha, Elda Cannavò, Angelo Taglialatela, Jen‐Wei Huang, Alberto Ciccia, Giuseppe Leuzzi, Vincenzo Costanzo, Raúl Rabadán and Brynn Levy and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Roopesh Anand

23 papers receiving 1.4k citations

Peers

Countries citing papers authored by Roopesh Anand

Since Specialization

Citations

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

Fields of papers citing papers by Roopesh Anand

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roopesh Anand

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	The APE2 nuclease is essential for DNA double-strand break repair by microhomology-mediated end joining 2023 ·Molecular Cell ·Hubert Fleury, (unknown), (unknown), Roopesh Anand, (unknown), (unknown), (unknown), Kerri A. Ball, Bruce Proctor, Ondrej Beláň, (unknown), Raquel Ortega, Benjamin Dodd, (unknown), (unknown), Justin Leung, Simon J. Boulton, Nausica Arnoult	24
2	Visualization of direct and diffusion-assisted RAD51 nucleation by full-length human BRCA2 protein 2023 ·Molecular Cell ·Ondrej Beláň, (unknown), Lucas Kuhlen, Roopesh Anand, Artur Kaczmarczyk, Dominika T. Gruszka, Hasan Yardimci, Xiaodong Zhang, David Rueda, Stephen C. West, Simon J. Boulton	14
3	Structure and function of the RAD51B–RAD51C–RAD51D–XRCC2 tumour suppressor 2023 ·Nature ·(unknown), Chih‐Chao Liang, Ondrej Beláň, Simone Kunzelmann, Sarah Maslen, Monica C. Rodrigo-Brenni, Roopesh Anand, Mark Skehel, Simon J. Boulton, Stephen C. West	37
4	POLQ seals post-replicative ssDNA gaps to maintain genome stability in BRCA-deficient cancer cells 2022 ·Molecular Cell ·Ondrej Beláň, (unknown), (unknown), Roopesh Anand, Aleksandra Vančevska, Joana Neves, Vera Grinkevich, Graeme Hewitt, Sandra Segura‐Bayona, Roberto Bellelli, Helen M.R. Robinson, Geoff S. Higgins, Graeme C.M. Smith, Stephen C. West, David Rueda, Simon J. Boulton	72
5	MRE11-RAD50-NBS1 Complex Is Sufficient to Promote Transcription by RNA Polymerase II at Double-Strand Breaks by Melting DNA Ends 2021 ·Cell Reports ·Sheetal Sharma, Roopesh Anand, Xuzhu Zhang, Sofia Francia, Flavia Michelini, Alessandro Galbiati, Hannah Williams, Daryl A. Ronato, Jean‐Yves Masson, Eli Rothenberg, Petr Ćejka, Fabrizio d’Adda di Fagagna	45
6	HELQ is a dual-function DSB repair enzyme modulated by RPA and RAD51 2021 ·Nature ·Roopesh Anand, (unknown), Ondrej Beláň, Matthew D. Newton, Aleksandra Vančevska, Artur Kaczmarczyk, Tohru Takaki, David Rueda, Simon N. Powell, Simon J. Boulton	44
7	Single-molecule analysis reveals cooperative stimulation of Rad51 filament nucleation and growth by mediator proteins 2021 ·Molecular Cell ·Ondrej Beláň, Consuelo Barroso, Artur Kaczmarczyk, Roopesh Anand, (unknown), Nicola O’Reilly, Matthew D. Newton, (unknown), Radoslav I. Enchev, Enrique Martínez-Pérez, David Rueda, Simon J. Boulton	53
8	Mechanism of mitotic recombination: insights from C. elegans 2021 ·Current Opinion in Genetics & Development ·Ondrej Beláň, Roopesh Anand, Simon J. Boulton	5
9	CtIP promotes the motor activity of DNA2 to accelerate long-range DNA end resection 2020 ·Proceedings of the National Academy of Sciences ·Ilaria Ceppi, Sean Howard, (unknown), Cosimo Pinto, Roopesh Anand, Ralf Seidel, Petr Ćejka	58
10	MCM8IP activates the MCM8-9 helicase to promote DNA synthesis and homologous recombination upon DNA damage 2020 ·Nature Communications ·Jen‐Wei Huang, Ananya Acharya, Angelo Taglialatela, Tarun S. Nambiar, Raquel Cuella-Martin, Giuseppe Leuzzi, Samuel B. Hayward, (unknown), Gregory J. Brunette, Roopesh Anand, Rajesh K. Soni, Nathan L Clark, Kara A. Bernstein, Petr Ćejka, Alberto Ciccia	33
11	The internal region of CtIP negatively regulates DNA end resection 2020 ·Nucleic Acids Research ·Sean Howard, Ilaria Ceppi, Roopesh Anand, Roger Geiger, Petr Ćejka	13
12	Competing interaction partners modulate the activity of Sgs1 helicase during DNA end resection 2019 ·The EMBO Journal ·(unknown), (unknown), Maryna Levikova, Peter Daldrop, Roopesh Anand, Petr Ćejka, Ralf Seidel	22
13	NBS1 promotes the endonuclease activity of the MRE11‐RAD50 complex by sensing CtIP phosphorylation 2019 ·The EMBO Journal ·Roopesh Anand, (unknown), (unknown), Sean Howard, Lepakshi Ranjha, Manuel Stucki, Petr Ćejka	66
14	Methods to Study DNA End Resection II: Biochemical Reconstitution Assays 2018 ·Methods in enzymology on CD-ROM/Methods in enzymology ·Cosimo Pinto, Roopesh Anand, Petr Ćejka	16
15	Methods to Study DNA End Resection I: Recombinant Protein Purification 2018 ·Methods in enzymology on CD-ROM/Methods in enzymology ·Roopesh Anand, Cosimo Pinto, Petr Ćejka	26
16	Restoration of Replication Fork Stability in BRCA1- and BRCA2-Deficient Cells by Inactivation of SNF2-Family Fork Remodelers 2017 ·Molecular Cell ·Angelo Taglialatela, Silvia Álvarez, Giuseppe Leuzzi, Vincenzo Sannino, Lepakshi Ranjha, Jen‐Wei Huang, Chioma J. Madubata, Roopesh Anand, Brynn Levy, Raúl Rabadán, Petr Ćejka, Vincenzo Costanzo, Alberto Ciccia	310
17	The Mre11-Nbs1 Interface Is Essential for Viability and Tumor Suppression 2017 ·Cell Reports ·Jun Hyun Kim, (unknown), Roopesh Anand, Claire Wyman, Petr Ćejka, John H.J. Petrini	35
18	RECQL4 Promotes DNA End Resection in Repair of DNA Double-Strand Breaks 2016 ·Cell Reports ·Huiming Lu, Raghavendra A. Shamanna, Guido Keijzers, Roopesh Anand, Lene Juel Rasmussen, Petr Ćejka, Deborah L. Croteau, Vilhelm A. Bohr	74
19	Phosphorylated CtIP Functions as a Co-factor of the MRE11-RAD50-NBS1 Endonuclease in DNA End Resection 2016 ·Molecular Cell ·Roopesh Anand, Lepakshi Ranjha, Elda Cannavò, Petr Ćejka	248
20	The Saccharomyces cerevisiae Mlh1-Mlh3 Heterodimer Is an Endonuclease That Preferentially Binds to Holliday Junctions 2014 ·Journal of Biological Chemistry ·Lepakshi Ranjha, Roopesh Anand, Petr Ćejka	96

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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