David Read

489 total citations
8 papers, 341 citations indexed

About

David Read is a scholar working on Molecular Biology, Plant Science and Neurology. According to data from OpenAlex, David Read has authored 8 papers receiving a total of 341 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Plant Science and 1 paper in Neurology. Recurrent topics in David Read's work include CRISPR and Genetic Engineering (4 papers), Chromosomal and Genetic Variations (4 papers) and Genomics and Chromatin Dynamics (4 papers). David Read is often cited by papers focused on CRISPR and Genetic Engineering (4 papers), Chromosomal and Genetic Variations (4 papers) and Genomics and Chromatin Dynamics (4 papers). David Read collaborates with scholars based in United Kingdom, Germany and Netherlands. David Read's co-authors include Ian R. Adams, Wendy A. Bickmore, Madapura M. Pradeepa, Robert S. Illingworth, Chris Hunter, Eugenio Fava, Pierluigi Nicotera, David Dinsdale, Laura Berliocchi and Marcel Leist and has published in prestigious journals such as Genes & Development, The Journal of Cell Biology and Human Molecular Genetics.

In The Last Decade

David Read

8 papers receiving 338 citations

Peers

David Read

MB

PS

GENET

CMN

NEURO

Dalia Ghoneim United States

Sofia Madsen Sweden

Nichole Owen United States

Ivana Ivković France

Julie Ni United States

Délara Sabéran‐Djoneidi France

Colin P. Florian United States

Valerie Podhraski Austria

Rashmi U. Pathak India

Alexander Samoshkin United States

Dalia Ghoneim United States

David Read

277 ×1.0

MB

32 ×0.5

PS

125 ×2.4

GENET

31 ×0.6

CMN

18 ×0.6

NEURO

Citations per year, relative to David Read David Read (= 1×) peers Dalia Ghoneim

Countries citing papers authored by David Read

Since Specialization

Citations

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

Fields of papers citing papers by David Read

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Read

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

All Works

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8 of 8 papers shown

1.

Reichmann, Judith, Lisa Lister, James H. Crichton, et al.. (2020). Tex19.1 inhibits the N-end rule pathway and maintains acetylated SMC3 cohesin and sister chromatid cohesion in oocytes. The Journal of Cell Biology. 219(5). 7 indexed citations

2.

Crichton, James H., David Read, & Ian R. Adams. (2018). Defects in meiotic recombination delay progression through pachytene in Tex19.1−/− mouse spermatocytes. Chromosoma. 127(4). 437–459. 8 indexed citations

3.

Crichton, James H., Christopher J. Playfoot, Marie MacLennan, et al.. (2017). Tex19.1 promotes Spo11-dependent meiotic recombination in mouse spermatocytes. PLoS Genetics. 13(7). e1006904–e1006904. 20 indexed citations

4.

MacLennan, Marie, Marta García-Cañadas, Judith Reichmann, et al.. (2017). Mobilization of LINE-1 retrotransposons is restricted by Tex19.1 in mouse embryonic stem cells. eLife. 6. 62 indexed citations

5.

Taylor, Gillian C.A., Dinesh C. Soares, Shelagh Boyle, et al.. (2016). Condensin II mutation causes T-cell lymphoma through tissue-specific genome instability. Genes & Development. 30(19). 2173–2186. 33 indexed citations

6.

Illingworth, Robert S., David Read, Chris Hunter, et al.. (2015). The E3 ubiquitin ligase activity of RING1B is not essential for early mouse development. Genes & Development. 29(18). 1897–1902. 116 indexed citations

7.

Reichmann, Judith, James P. Reddington, David Read, et al.. (2013). The genome-defence gene Tex19.1 suppresses LINE-1 retrotransposons in the placenta and prevents intra-uterine growth retardation in mice. Human Molecular Genetics. 22(9). 1791–1806. 30 indexed citations

8.

Berliocchi, Laura, Eugenio Fava, Marcel Leist, et al.. (2005). Botulinum neurotoxin C initiates two different programs for neurite degeneration and neuronal apoptosis. The Journal of Cell Biology. 168(4). 607–618. 65 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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