Advaitha Madireddy

780 total citations
16 papers, 523 citations indexed

About

Advaitha Madireddy is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Advaitha Madireddy has authored 16 papers receiving a total of 523 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Plant Science. Recurrent topics in Advaitha Madireddy's work include DNA Repair Mechanisms (9 papers), CRISPR and Genetic Engineering (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Advaitha Madireddy is often cited by papers focused on DNA Repair Mechanisms (9 papers), CRISPR and Genetic Engineering (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Advaitha Madireddy collaborates with scholars based in United States, China and United Kingdom. Advaitha Madireddy's co-authors include Carl L. Schildkraut, Jeannine Gerhardt, William C. Drosopoulos, Xiaolei Pan, Dong Zhang, Zi Yan, Settapong T Kosiyatrakul, Pravinkumar Purushothaman, Erle S. Robertson and Subhash C. Verma and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Advaitha Madireddy

15 papers receiving 522 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Advaitha Madireddy United States 11 479 106 76 74 51 16 523
Sarah Scaglione France 7 558 1.2× 106 1.0× 91 1.2× 36 0.5× 58 1.1× 9 593
Alessandra Brambati Italy 9 526 1.1× 67 0.6× 92 1.2× 18 0.2× 56 1.1× 9 579
Andrew P. Salinger United States 8 512 1.1× 100 0.9× 35 0.5× 196 2.6× 67 1.3× 11 591
Ja-Hwan Seol United States 9 498 1.0× 57 0.5× 54 0.7× 50 0.7× 71 1.4× 9 545
Gregory D Hurlbut United States 8 390 0.8× 175 1.7× 61 0.8× 39 0.5× 15 0.3× 8 513
Sandra S. de Vries Netherlands 7 612 1.3× 209 2.0× 55 0.7× 40 0.5× 96 1.9× 7 773
Devon Chandler‐Brown United States 6 288 0.6× 73 0.7× 15 0.2× 85 1.1× 39 0.8× 9 502
Romain Groux Switzerland 7 453 0.9× 80 0.8× 30 0.4× 17 0.2× 43 0.8× 9 537
Graham J. Ray United States 4 834 1.7× 180 1.7× 51 0.7× 18 0.2× 64 1.3× 4 875
Irma Μ. Santoro United States 9 485 1.0× 85 0.8× 109 1.4× 28 0.4× 57 1.1× 12 557

Countries citing papers authored by Advaitha Madireddy

Since Specialization
Citations

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

Fields of papers citing papers by Advaitha Madireddy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Advaitha Madireddy

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

All Works

16 of 16 papers shown
1.
Ren, Haozhen, Xun Chen, Jinglin Wang, et al.. (2023). Temporal and structural patterns of hepatitis B virus integrations in hepatocellular carcinoma. Journal of Medical Virology. 95(10). e29187–e29187. 2 indexed citations
2.
Madireddy, Advaitha & Jeannine Gerhardt. (2023). Visualizing DNA replication by single-molecule analysis of replicated DNA. STAR Protocols. 4(4). 102721–102721. 1 indexed citations
3.
Giricz, Orsi, Rachel Zeig‐Owens, Kith Pradhan, et al.. (2023). 2009 – WORLD TRADE CENTER 9/11 DISASTER EXPOSURE IS ASSOCIATED WITH CLONAL HEMATOPOIESIS IN FIRST RESPONDERS AND IS CHARACTERIZED BY INNATE IMMUNE INFLAMMATION.. Experimental Hematology. 124. S41–S41.
4.
Álvarez, Silvia, Ana Carolina da Silva Almeida, Tomás Aparicio, et al.. (2022). Functional mapping of PHF6 complexes in chromatin remodeling, replication dynamics, and DNA repair. Blood. 139(23). 3418–3429. 11 indexed citations
5.
Deshpande, Madhura, Gouri J. Nanjangud, Amnon Koren, et al.. (2022). Error-prone repair of stalled replication forks drives mutagenesis and loss of heterozygosity in haploinsufficient BRCA1 cells. Molecular Cell. 82(20). 3781–3793.e7. 13 indexed citations
6.
Madireddy, Advaitha, et al.. (2022). The Cause and Consequence of Replication Stress in Adult T-Cell Leukemia. Blood. 140(Supplement 1). 11512–11512. 1 indexed citations
7.
Kang, Zhihua, Pan Fu, Allen L. Alcivar, et al.. (2021). BRCA2 associates with MCM10 to suppress PRIMPOL-mediated repriming and single-stranded gap formation after DNA damage. Nature Communications. 12(1). 5966–5966. 55 indexed citations
8.
Bacolla, Albino, William C. Drosopoulos, Settapong T Kosiyatrakul, et al.. (2021). Translesion polymerase eta both facilitates DNA replication and promotes increased human genetic variation at common fragile sites. Proceedings of the National Academy of Sciences. 118(48). 32 indexed citations
9.
Deshpande, Madhura, Ning Wang, Ryan C. O’Neil, et al.. (2020). Pluripotent stem cells with low differentiation potential contain incompletely reprogrammed DNA replication. The Journal of Cell Biology. 219(9). 13 indexed citations
10.
Ye, B. Hilda, Kith Pradhan, Ana Acuña-Villaorduña, et al.. (2019). S-Phase Progression of North American ATLL Cells Is Critically Regulated By the Proto-Oncogene BCL6 and Targetable By PARP Inhibition. Blood. 134(Supplement_1). 3779–3779. 2 indexed citations
11.
Madireddy, Advaitha & Jeannine Gerhardt. (2017). Replication Through Repetitive DNA Elements and Their Role in Human Diseases. Advances in experimental medicine and biology. 1042. 549–581. 22 indexed citations
12.
Pan, Xiaolei, et al.. (2017). FANCM, BRCA1, and BLM cooperatively resolve the replication stress at the ALT telomeres. Proceedings of the National Academy of Sciences. 114(29). E5940–E5949. 107 indexed citations
13.
Madireddy, Advaitha, Settapong T Kosiyatrakul, Emilia Herrera‐Moyano, et al.. (2016). FANCD2 Facilitates Replication through Common Fragile Sites. Molecular Cell. 64(2). 388–404. 132 indexed citations
14.
Madireddy, Advaitha, et al.. (2016). G-quadruplex-interacting compounds alter latent DNA replication and episomal persistence of KSHV. Nucleic Acids Research. 44(8). 3675–3694. 73 indexed citations
15.
Gerhardt, Jeannine, Nikica Zaninović, Qiansheng Zhan, et al.. (2014). Cis-acting DNA sequence at a replication origin promotes repeat expansion to fragile X full mutation. The Journal of Cell Biology. 206(5). 599–607. 32 indexed citations
16.
Su, Yan, Barbara Orelli, Advaitha Madireddy, Laura J. Niedernhofer, & Orlando D. Schärer. (2012). Multiple DNA Binding Domains Mediate the Function of the ERCC1-XPF Protein in Nucleotide Excision Repair. Journal of Biological Chemistry. 287(26). 21846–21855. 27 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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