Ruth M. Arkell

4.4k total citations
57 papers, 2.7k citations indexed

About

Ruth M. Arkell is a scholar working on Molecular Biology, Genetics and Rehabilitation. According to data from OpenAlex, Ruth M. Arkell has authored 57 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 16 papers in Genetics and 9 papers in Rehabilitation. Recurrent topics in Ruth M. Arkell's work include Developmental Biology and Gene Regulation (16 papers), Wound Healing and Treatments (9 papers) and Congenital heart defects research (8 papers). Ruth M. Arkell is often cited by papers focused on Developmental Biology and Gene Regulation (16 papers), Wound Healing and Treatments (9 papers) and Congenital heart defects research (8 papers). Ruth M. Arkell collaborates with scholars based in Australia, United Kingdom and United States. Ruth M. Arkell's co-authors include R. S. P. Beddington, Allison J. Cowin, Andrew J. Copp, Patrick Tam, Patrick M. Nolan, Andy Greenfield, Pam Siggers, Steve D. M. Brown, Zlatko Kopecki and Ian C. Gray and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Ruth M. Arkell

56 papers receiving 2.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ruth M. Arkell Australia 27 2.2k 773 354 175 169 57 2.7k
Concepción Rodrı́guez Esteban United States 34 4.0k 1.9× 749 1.0× 361 1.0× 420 2.4× 165 1.0× 48 4.9k
Cynthia A. Loomis United States 25 1.8k 0.8× 450 0.6× 429 1.2× 232 1.3× 226 1.3× 55 2.8k
Huiqing Zhou Netherlands 35 2.1k 1.0× 853 1.1× 204 0.6× 136 0.8× 155 0.9× 96 3.1k
Sigmar Stricker Germany 36 2.6k 1.2× 825 1.1× 286 0.8× 259 1.5× 175 1.0× 74 3.5k
Tomasz Wilanowski Poland 22 1.4k 0.7× 355 0.5× 315 0.9× 129 0.7× 98 0.6× 46 1.9k
Francesca Gualandi Italy 32 2.1k 1.0× 531 0.7× 252 0.7× 247 1.4× 342 2.0× 115 2.8k
Hans G. Dauwerse Netherlands 25 2.1k 1.0× 1.2k 1.6× 333 0.9× 237 1.4× 520 3.1× 43 3.5k
Maria A. Ciemerych Poland 28 2.4k 1.1× 489 0.6× 546 1.5× 662 3.8× 122 0.7× 92 3.3k
Jyotsna Dhawan India 26 1.8k 0.8× 424 0.5× 369 1.0× 344 2.0× 109 0.6× 56 2.3k
Sheila M. Bell United States 25 1.4k 0.6× 392 0.5× 177 0.5× 380 2.2× 196 1.2× 42 2.3k

Countries citing papers authored by Ruth M. Arkell

Since Specialization
Citations

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

Fields of papers citing papers by Ruth M. Arkell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ruth M. Arkell. 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 Ruth M. Arkell. The network helps show where Ruth M. Arkell may publish in the future.

Co-authorship network of co-authors of Ruth M. Arkell

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

All Works

20 of 20 papers shown
1.
Roome, R. Brian, Archana Yadav, Diana Nardini, et al.. (2026). Ontogeny of the spinal cord dorsal horn. Science. 391(6781). eadx5781–eadx5781. 1 indexed citations
2.
3.
Ali, Radiya G., et al.. (2021). WNT-responsive SUMOylation of ZIC5 promotes murine neural crest cell development, having multiple effects on transcription. Journal of Cell Science. 134(9). 13 indexed citations
4.
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Arkell, Ruth M., et al.. (2018). ZIC2 in Holoprosencephaly. Advances in experimental medicine and biology. 1046. 269–299. 14 indexed citations
6.
Gainkam, Lea Olive Tchouate, et al.. (2016). Zic2mutation causes holoprosencephaly via disruption of NODAL signalling. Human Molecular Genetics. 25(18). 3946–3959. 25 indexed citations
7.
Arkell, Ruth M., Nicolas Fossat, & Patrick Tam. (2013). Wnt signalling in mouse gastrulation and anterior development: new players in the pathway and signal output. Current Opinion in Genetics & Development. 23(4). 454–460. 41 indexed citations
8.
Ali, Radiya G., Tamsin E. M. Jones, Damian Adams, et al.. (2011). Mouse strains for the ubiquitous or conditional overexpression of the Flii gene. genesis. 49(8). 681–688. 15 indexed citations
9.
Kopecki, Zlatko, Geraldine M. O’Neill, Ruth M. Arkell, & Allison J. Cowin. (2011). Regulation of Focal Adhesions by Flightless I Involves Inhibition of Paxillin Phosphorylation via a Rac1-Dependent Pathway. Journal of Investigative Dermatology. 131(7). 1450–1459. 31 indexed citations
10.
Arkell, Ruth M., et al.. (2010). Regeneration of Hair Follicles Is Modulated by Flightless I (Flii) in a Rodent Vibrissa Model. Journal of Investigative Dermatology. 131(4). 838–847. 14 indexed citations
11.
Adams, Damian, Nadira Ruzehaji, Xanthe L. Strudwick, et al.. (2009). Attenuation of Flightless I, an actin-remodelling protein, improves burn injury repair via modulation of transforming growth factor (TGF)-β1 and TGF-β3. British Journal of Dermatology. 161(2). 326–336. 42 indexed citations
12.
Warr, Nick, et al.. (2008). Zic2 -associated holoprosencephaly is caused by a transient defect in the organizer region during gastrulation. Human Molecular Genetics. 17(19). 2986–2996. 76 indexed citations
13.
Mallon, Ann‐Marie, Laurens Wilming, James Gilbert, et al.. (2004). Organization and Evolution of a Gene-Rich Region of the Mouse Genome: A 12.7-Mb Region Deleted in the Del(13)Svea36H Mouse. Genome Research. 14(10a). 1888–1901. 23 indexed citations
14.
Davies, Jennifer R., et al.. (2004). Overlapping and distinct expression domains of Zic2 and Zic3 during mouse gastrulation. Gene Expression Patterns. 4(5). 505–511. 56 indexed citations
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Bogani, Debora, Nick Warr, Jennifer R. Davies, et al.. (2004). New semidominant mutations that affect mouse development. genesis. 40(2). 109–117. 22 indexed citations
17.
Siggers, Pam, et al.. (2003). Zic2 is required for neural crest formation and hindbrain patterning during mouse development. Developmental Biology. 264(2). 391–406. 94 indexed citations
18.
Curtin, John A., Elizabeth Quint, Vicky Tsipouri, et al.. (2003). Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse. Current Biology. 13(13). 1129–1133. 485 indexed citations
19.
Grimmond, Sean M., et al.. (2001). Expression of a novel mammalian epidermal growth factor-related gene during mouse neural development. Mechanisms of Development. 102(1-2). 209–211. 45 indexed citations
20.
Sheardown, Steven A., Sarah M. Duthie, Colette M. Johnston, et al.. (1997). Stabilization of Xist RNA Mediates Initiation of X Chromosome Inactivation. Cell. 91(1). 99–107. 207 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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