Ashwin Woodhoo

4.4k total citations · 1 hit paper
25 papers, 2.7k citations indexed

About

Ashwin Woodhoo is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Developmental Neuroscience. According to data from OpenAlex, Ashwin Woodhoo has authored 25 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Cellular and Molecular Neuroscience, 14 papers in Molecular Biology and 9 papers in Developmental Neuroscience. Recurrent topics in Ashwin Woodhoo's work include Nerve injury and regeneration (14 papers), Neurogenesis and neuroplasticity mechanisms (9 papers) and Hereditary Neurological Disorders (6 papers). Ashwin Woodhoo is often cited by papers focused on Nerve injury and regeneration (14 papers), Neurogenesis and neuroplasticity mechanisms (9 papers) and Hereditary Neurological Disorders (6 papers). Ashwin Woodhoo collaborates with scholars based in Spain, United Kingdom and United States. Ashwin Woodhoo's co-authors include Rhona Mirsky, Kristján R. Jessen, Peter Arthur‐Farraj, Lukas Sommer, David B. Parkinson, Axel Behrens, Alison C. Lloyd, Luke A. Noon, Ambily Bhaskaran and Daniel K. Wilton and has published in prestigious journals such as Neuron, Journal of Neuroscience and The Journal of Cell Biology.

In The Last Decade

Ashwin Woodhoo

25 papers receiving 2.6k citations

Hit Papers

c-Jun Reprograms Schwann Cells of Injured Nerves to Gener... 2012 2026 2016 2021 2012 200 400 600

Peers

Ashwin Woodhoo
Jae K. Lee United States
Zu‐Lin Chen United States
Bradley T. Lang United States
Peter Arthur‐Farraj United Kingdom
Janette M. Krum United States
Lucien J. Houenou United States
Jorge A. Pereira Switzerland
Jeffrey M. Rosenstein United States
Jae K. Lee United States
Ashwin Woodhoo
Citations per year, relative to Ashwin Woodhoo Ashwin Woodhoo (= 1×) peers Jae K. Lee

Countries citing papers authored by Ashwin Woodhoo

Since Specialization
Citations

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

Fields of papers citing papers by Ashwin Woodhoo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ashwin Woodhoo

This figure shows the co-authorship network connecting the top 25 collaborators of Ashwin Woodhoo. A scholar is included among the top collaborators of Ashwin Woodhoo 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 Ashwin Woodhoo. Ashwin Woodhoo 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.
Woodhoo, Ashwin, et al.. (2022). Application of adipose-derived mesenchymal stem cells in an in vivo model of peripheral nerve damage. Frontiers in Cellular Neuroscience. 16. 992221–992221. 5 indexed citations
2.
Pietra, Valeria La, Linda Cerofolini, Marta Varela‐Rey, et al.. (2021). HuR-targeted agents: An insight into medicinal chemistry, biophysical, computational studies and pharmacological effects on cancer models. Advanced Drug Delivery Reviews. 181. 114088–114088. 19 indexed citations
3.
Palomo-Irigoyen, Marta, et al.. (2018). Analyzing Autophagic Flux in Nerve Cultures. Methods in molecular biology. 1791. 193–206. 1 indexed citations
4.
Palomo-Irigoyen, Marta, et al.. (2018). Isolation and Purification of Primary Rodent Schwann Cells. Methods in molecular biology. 1791. 81–93. 7 indexed citations
5.
Varela‐Rey, Marta, Marta Iruarrizaga‐Lejarreta, Juan José Lozano, et al.. (2014). S-adenosylmethionine Levels Regulate the Schwann Cell DNA Methylome. Neuron. 81(5). 1024–1039. 62 indexed citations
6.
Napoli, Ilaria, Luke A. Noon, Sara Ribeiro, et al.. (2012). A Central Role for the ERK-Signaling Pathway in Controlling Schwann Cell Plasticity and Peripheral Nerve Regeneration In Vivo. Neuron. 73(4). 729–742. 317 indexed citations
7.
Arthur‐Farraj, Peter, Morwena Latouche, Daniel K. Wilton, et al.. (2012). c-Jun Reprograms Schwann Cells of Injured Nerves to Generate a Repair Cell Essential for Regeneration. Neuron. 75(4). 633–647. 632 indexed citations breakdown →
8.
Kipanyula, Maulilio J., et al.. (2012). Calcineurin–nuclear factor of activated t cells regulation of Krox‐20 expression in Schwann cells requires elevation of intracellular cyclic AMP. Journal of Neuroscience Research. 91(1). 105–115. 19 indexed citations
9.
Woodhoo, Ashwin, Marta Iruarrizaga‐Lejarreta, Naiara Beraza, et al.. (2012). Human antigen R contributes to hepatic stellate cell activation and liver fibrosis. Hepatology. 56(5). 1870–1882. 73 indexed citations
10.
Embade, Nieves, David Fernández‐Ramos, Marta Varela‐Rey, et al.. (2011). Murine double minute 2 regulates Hu antigen R stability in human liver and colon cancer through NEDDylation. Hepatology. 55(4). 1237–1248. 99 indexed citations
11.
Varela‐Rey, Marta, Nuria Martínez-López, David Fernández‐Ramos, et al.. (2010). Fatty Liver and Fibrosis in Glycine N -Methyltransferase Knockout Mice Is Prevented by Nicotinamide. Hepatology. 52(1). 105–114. 84 indexed citations
12.
Martínez-López, Nuria, Marta Varela‐Rey, David Fernández‐Ramos, et al.. (2010). Activation of LKB1-Akt Pathway Independent of Phosphoinositide 3-Kinase Plays a Critical Role in the Proliferation of Hepatocellular Carcinoma From Nonalcoholic Steatohepatitis. Hepatology. 52(5). 1621–1631. 59 indexed citations
13.
Vázquez–Chantada, Mercedes, David Fernández‐Ramos, Nieves Embade, et al.. (2010). HuR/Methyl-HuR and AUF1 Regulate the MAT Expressed During Liver Proliferation, Differentiation, and Carcinogenesis. Gastroenterology. 138(5). 1943–1953.e3. 103 indexed citations
14.
Woodhoo, Ashwin, María Beatriz Durán Alonso, Mark Turmaine, et al.. (2009). Notch controls embryonic Schwann cell differentiation, postnatal myelination and adult plasticity. Nature Neuroscience. 12(7). 839–847. 262 indexed citations
15.
Woodhoo, Ashwin & Lukas Sommer. (2008). Development of the Schwann cell lineage: From the neural crest to the myelinated nerve. Glia. 56(14). 1481–1490. 171 indexed citations
16.
Woodhoo, Ashwin, et al.. (2008). Schwann cell precursors transplanted into the injured spinal cord multiply, integrate and are permissive for axon growth. Glia. 56(12). 1263–1270. 30 indexed citations
17.
Mirsky, Rhona, Ashwin Woodhoo, David B. Parkinson, et al.. (2008). Novel signals controlling embryonic Schwann cell development, myelination and dedifferentiation. Journal of the Peripheral Nervous System. 13(2). 122–135. 170 indexed citations
18.
Woodhoo, Ashwin, Jennifer M. Gilson, Robin J.M. Franklin, et al.. (2007). Schwann cell precursors: a favourable cell for myelin repair in the Central Nervous System. Brain. 130(8). 2175–2185. 61 indexed citations
19.
D’Antonio, Maurizio, et al.. (2005). Gene profiling and bioinformatic analysis of Schwann cell embryonic development and myelination. Glia. 53(5). 501–515. 69 indexed citations
20.
Cowen, T., Ashwin Woodhoo, Keith A. Crutcher, et al.. (2003). Reduced age‐related plasticity of neurotrophin receptor expression in selected sympathetic neurons of the rat. Aging Cell. 2(1). 59–70. 19 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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