Karun Mutreja

1.7k total citations · 1 hit paper
11 papers, 1.0k citations indexed

About

Karun Mutreja is a scholar working on Oncology, Molecular Biology and Surgery. According to data from OpenAlex, Karun Mutreja has authored 11 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Oncology, 5 papers in Molecular Biology and 2 papers in Surgery. Recurrent topics in Karun Mutreja's work include DNA Repair Mechanisms (5 papers), CRISPR and Genetic Engineering (4 papers) and Cancer Cells and Metastasis (3 papers). Karun Mutreja is often cited by papers focused on DNA Repair Mechanisms (5 papers), CRISPR and Genetic Engineering (4 papers) and Cancer Cells and Metastasis (3 papers). Karun Mutreja collaborates with scholars based in United States, Switzerland and Canada. Karun Mutreja's co-authors include Massimo Lopes, Ralph Zellweger, Matteo Berti, Raquel Herrador, Damian Dalcher, Alessandro Vindigni, Jonas Schmid, Sebastian Ursich, Pavel Janščák and André Nussenzweig and has published in prestigious journals such as Nature Communications, The Journal of Cell Biology and The EMBO Journal.

In The Last Decade

Karun Mutreja

9 papers receiving 1.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Rad51-mediated replication fork reversal is a global response to genotoxic treatments in human cells

2015 521 citations Ralph Zellweger, Damian Dalcher et al. The Journal of Cell Biology profile →

Peers

Karun Mutreja

MB

ONCOL

CR

GENET

CB

Arne Nedergaard Kousholt Denmark

Gurushankar Chandramouly United States

Vincenzo Sannino Italy

Anita Cheng United States

Hervé Técher France

Niraj Joshi Canada

Velibor Savic United Kingdom

Morgane Macheret Switzerland

Mengtan Xing Norway

Giuseppe Leuzzi United States

Arne Nedergaard Kousholt Denmark

Karun Mutreja

850 ×0.9

MB

372 ×1.0

ONCOL

104 ×0.7

CR

144 ×1.2

GENET

102 ×0.9

CB

Citations per year, relative to Karun Mutreja Karun Mutreja (= 1×) peers Arne Nedergaard Kousholt

Countries citing papers authored by Karun Mutreja

Since Specialization

Citations

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

Fields of papers citing papers by Karun Mutreja

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karun Mutreja

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

All Works

Sort: Min cites: Since: Top N: Style:

11 of 11 papers shown

1.

Abubakar, Mustapha, Shaoqi Fan, Alyssa Klein, et al.. (2025). Spatially Resolved Single-Cell Morphometry of Benign Breast Disease Biopsy Images Uncovers Quantitative Cytomorphometric Features Predictive of Subsequent Invasive Breast Cancer Risk. Modern Pathology. 38(7). 100767–100767.

2.

Abubakar, Mustapha, Alyssa Klein, Shaoqi Fan, et al.. (2023). Host, reproductive, and lifestyle factors in relation to quantitative histologic metrics of the normal breast. Breast Cancer Research. 25(1). 97–97. 6 indexed citations

3.

Synnott, Naoise C., Maria Luana Poeta, Manuela Costantini, et al.. (2021). Characterizing the tumor microenvironment in rare renal cancer histological types. The Journal of Pathology Clinical Research. 8(1). 88–98. 9 indexed citations

4.

González‐Acosta, Daniel, Karun Mutreja, Susana Llanos, et al.. (2021). PrimPol‐mediated repriming facilitates replication traverse of DNA interstrand crosslinks. The EMBO Journal. 40(14). e106355–e106355. 47 indexed citations

5.

Abubakar, Mustapha, Jing Zhang, Thomas U. Ahearn, et al.. (2021). Tumor-Associated Stromal Cellular Density as a Predictor of Recurrence and Mortality in Breast Cancer: Results from Ethnically Diverse Study Populations. Cancer Epidemiology Biomarkers & Prevention. 30(7). 1397–1407. 11 indexed citations

6.

Koerner, Mara V.A., Katir Patel, Mustapha Abubakar, et al.. (2020). Abstract 386: Design and application of an 8-plex multiplex immunofluorescence panel for deep phenotypic profiling of the tumor microenvironment using InSituPlex technology. Cancer Research. 80(16_Supplement). 386–386.

7.

Mutreja, Karun, Jana Krietsch, Jeannine Hess, et al.. (2018). ATR-Mediated Global Fork Slowing and Reversal Assist Fork Traverse and Prevent Chromosomal Breakage at DNA Interstrand Cross-Links. Cell Reports. 24(10). 2629–2642.e5. 98 indexed citations

8.

Zellweger, Ralph, Nagaraja Chappidi, Matteo Berti, et al.. (2017). Replication fork reversal triggers fork degradation in BRCA2-defective cells. Nature Communications. 8(1). 859–859. 283 indexed citations

9.

Mutreja, Karun, Lepakshi Ranjha, Ralph Zellweger, et al.. (2016). The MMS22L–TONSL heterodimer directly promotes RAD51‐dependent recombination upon replication stress. The EMBO Journal. 35(23). 2584–2601. 57 indexed citations

10.

Zellweger, Ralph, Damian Dalcher, Karun Mutreja, et al.. (2015). Rad51-mediated replication fork reversal is a global response to genotoxic treatments in human cells. The Journal of Cell Biology. 208(5). 563–579. 521 indexed citations breakdown →

11.

Pfister, Thomas D., Lynda Dieckman, Robert J. Kinders, et al.. (2013). Abstract 5544: Development of recombinant transcription factor proteins and antibodies for application in clinical immunoassays.. Cancer Research. 73(8_Supplement). 5544–5544. 2 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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