Matthew Edwards

3.0k total citations
9 papers, 119 citations indexed

About

Matthew Edwards is a scholar working on Molecular Biology, Surgery and Cellular and Molecular Neuroscience. According to data from OpenAlex, Matthew Edwards has authored 9 papers receiving a total of 119 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 1 paper in Surgery and 1 paper in Cellular and Molecular Neuroscience. Recurrent topics in Matthew Edwards's work include DNA Repair Mechanisms (3 papers), Epigenetics and DNA Methylation (3 papers) and Pluripotent Stem Cells Research (2 papers). Matthew Edwards is often cited by papers focused on DNA Repair Mechanisms (3 papers), Epigenetics and DNA Methylation (3 papers) and Pluripotent Stem Cells Research (2 papers). Matthew Edwards collaborates with scholars based in United States, United Kingdom and Israel. Matthew Edwards's co-authors include Nena J. Winand, B. J. Cooper, Deepti Pradhan, Amnon Koren, Jackie Benschop, David A. Wilkinson, Fengtang Yang, Richard Mitter, Anaid Benitez and Aengus Stewart and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Matthew Edwards

7 papers receiving 117 citations

Peers

Matthew Edwards

MB

GENET

SURGE

CB

CCM

Martin Chevarin France

Nirmal Vadgama United Kingdom

Christel Thauvin France

Newell Belnap United States

Alessia Gambadoro Italy

Andrea Hunt United States

Thomas Gstrein Austria

Ajoy Aloysius India

Karthick Natarajan Germany

Martin Chevarin France

Matthew Edwards

61 ×0.6

MB

72 ×2.8

GENET

6 ×0.3

SURGE

13 ×0.9

CB

13 ×1.1

CCM

Citations per year, relative to Matthew Edwards Matthew Edwards (= 1×) peers Martin Chevarin

Countries citing papers authored by Matthew Edwards

Since Specialization

Citations

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

Fields of papers citing papers by Matthew Edwards

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matthew Edwards

This figure shows the co-authorship network connecting the top 25 collaborators of Matthew Edwards. A scholar is included among the top collaborators of Matthew Edwards 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 Matthew Edwards. Matthew Edwards 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:

9 of 9 papers shown

1.

Scott, James N., Matthew Edwards, Xiaoling Wang, et al.. (2025). Excised DNA circles from V(D)J recombination promote relapsed leukaemia. Nature. 645(8081). 774–783.

2.

Edwards, Matthew, Ning Wang, Ido Sagi, et al.. (2024). Parent-of-origin-specific DNA replication timing is confined to large imprinted regions. Cell Reports. 43(9). 114700–114700. 1 indexed citations

3.

Edwards, Matthew, et al.. (2024). Incomplete reprogramming of DNA replication timing in induced pluripotent stem cells. Cell Reports. 43(1). 113664–113664. 3 indexed citations

4.

Kanagaraj, Radhakrishnan, Richard Mitter, Theodoros Kantidakis, et al.. (2022). Integrated genome and transcriptome analyses reveal the mechanism of genome instability in ataxia with oculomotor apraxia 2. Proceedings of the National Academy of Sciences. 119(4). 21 indexed citations

5.

Edwards, Matthew, Michael V. Zuccaro, Ido Sagi, et al.. (2021). Delayed DNA replication in haploid human embryonic stem cells. Genome Research. 31(12). 2155–2169. 6 indexed citations

6.

Wilkinson, David A., et al.. (2021). Identification of pathogenic Leptospira species and serovars in New Zealand using metabarcoding. PLoS ONE. 16(9). e0257971–e0257971. 13 indexed citations

7.

Ding, Qiliang, Matthew Edwards, Ning Wang, et al.. (2021). The genetic architecture of DNA replication timing in human pluripotent stem cells. Nature Communications. 12(1). 6746–6746. 22 indexed citations

8.

Năstase, Anca, Amit Kumar Mandal, Spyridon Gennatas, et al.. (2019). MA23.10 Low Number of Mutations and Frequent Co-Deletions of CDKN2A and IFN Type I Characterize Malignant Pleural Mesothelioma. Journal of Thoracic Oncology. 14(10). S345–S345.

9.

Winand, Nena J., et al.. (1994). Deletion of the dystrophin muscle promoter in feline muscular dystrophy. Neuromuscular Disorders. 4(5-6). 433–445. 53 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.

Explore authors with similar magnitude of impact