Evan Reid

7.6k total citations
59 papers, 3.8k citations indexed

About

Evan Reid is a scholar working on Cellular and Molecular Neuroscience, Neurology and Cell Biology. According to data from OpenAlex, Evan Reid has authored 59 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Cellular and Molecular Neuroscience, 21 papers in Neurology and 18 papers in Cell Biology. Recurrent topics in Evan Reid's work include Hereditary Neurological Disorders (40 papers), Neurological diseases and metabolism (21 papers) and Cellular transport and secretion (16 papers). Evan Reid is often cited by papers focused on Hereditary Neurological Disorders (40 papers), Neurological diseases and metabolism (21 papers) and Cellular transport and secretion (16 papers). Evan Reid collaborates with scholars based in United Kingdom, United States and France. Evan Reid's co-authors include James W. Connell, Cahir J. O’Kane, Craig Blackstone, J. Paul Luzio, Christopher M. Sanderson, Andrew Dearlove, David C. Rubinsztein, Matthew Seaman, Thomas L. Edwards and Rachel Allison and has published in prestigious journals such as The Lancet, Nature Communications and Nature Genetics.

In The Last Decade

Evan Reid

58 papers receiving 3.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Evan Reid United Kingdom 32 2.0k 1.6k 1.3k 966 635 59 3.8k
Gregory A. Cox United States 38 891 0.5× 497 0.3× 3.3k 2.5× 248 0.3× 617 1.0× 82 4.4k
Klaus Wagner Austria 23 856 0.4× 528 0.3× 1.5k 1.1× 437 0.5× 464 0.7× 61 2.9k
Jan Senderek Germany 37 1.4k 0.7× 670 0.4× 2.2k 1.7× 503 0.5× 194 0.3× 92 3.9k
Stephan Kröger Germany 31 1.0k 0.5× 962 0.6× 2.2k 1.7× 299 0.3× 138 0.2× 63 3.5k
Dennis Dooijes Netherlands 38 598 0.3× 304 0.2× 3.2k 2.5× 289 0.3× 438 0.7× 110 5.7k
Véronique Rogemond France 46 1.8k 0.9× 659 0.4× 1.3k 1.0× 260 0.3× 163 0.3× 112 5.4k
Elizabeth C. Engle United States 39 631 0.3× 799 0.5× 1.9k 1.5× 283 0.3× 183 0.3× 112 4.4k
Patrick N. Anderson United Kingdom 37 2.4k 1.2× 283 0.2× 1.4k 1.1× 261 0.3× 128 0.2× 84 3.8k
Mario Soriano‐Navarro Spain 30 899 0.5× 390 0.2× 1.8k 1.4× 385 0.4× 612 1.0× 47 3.7k
Elisa Barbarese United States 37 816 0.4× 662 0.4× 3.1k 2.4× 379 0.4× 214 0.3× 67 4.3k

Countries citing papers authored by Evan Reid

Since Specialization
Citations

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

Fields of papers citing papers by Evan Reid

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Evan Reid

This figure shows the co-authorship network connecting the top 25 collaborators of Evan Reid. A scholar is included among the top collaborators of Evan Reid 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 Evan Reid. Evan Reid 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.
Zlamalova, Eliska, et al.. (2024). Atlastin-1 regulates endosomal tubulation and lysosomal proteolysis in human cortical neurons. Neurobiology of Disease. 199. 106556–106556.
2.
Synofzik, Matthis, Elena I. Rugarli, Evan Reid, & Rebecca Schüle. (2023). Ataxia and spastic paraplegia in mitochondrial disease. Handbook of clinical neurology. 194. 79–98. 4 indexed citations
3.
Majumder, Piyali, et al.. (2022). AP-4 regulates neuronal lysosome composition, function, and transport via regulating export of critical lysosome receptor proteins at the trans-Golgi network. Molecular Biology of the Cell. 33(12). ar102–ar102. 17 indexed citations
4.
Bourinaris, Thomas, Damian Smedley, Valentina Cipriani, et al.. (2020). Identification of UBAP1 mutations in juvenile hereditary spastic paraplegia in the 100,000 Genomes Project. European Journal of Human Genetics. 28(12). 1763–1768. 11 indexed citations
5.
Connell, James W., et al.. (2019). ESCRT-III-associated proteins and spastin inhibit protrudin-dependent polarised membrane traffic. Cellular and Molecular Life Sciences. 77(13). 2641–2658. 21 indexed citations
6.
Connell, James W., Rachel Allison, & Evan Reid. (2016). Quantitative Gait Analysis Using a Motorized Treadmill System Sensitively Detects Motor Abnormalities in Mice Expressing ATPase Defective Spastin. PLoS ONE. 11(3). e0152413–e0152413. 17 indexed citations
7.
Hensiek, Anke, Stephen Kirker, & Evan Reid. (2014). Diagnosis, investigation and management of hereditary spastic paraplegias in the era of next-generation sequencing. Journal of Neurology. 262(7). 1601–1612. 44 indexed citations
8.
Schiel, John A., et al.. (2011). Endocytic membrane fusion and buckling-induced microtubule severing mediate cell abscission. Journal of Cell Science. 124(9). 1411–1424. 88 indexed citations
9.
Lumb, Jennifer H., James W. Connell, Rachel Allison, & Evan Reid. (2011). The AAA ATPase spastin links microtubule severing to membrane modelling. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1823(1). 192–197. 57 indexed citations
10.
Hopkins, T.G., Eamonn R. Maher, Evan Reid, & Stefan J. Marciniak. (2011). Recurrent pneumothorax. The Lancet. 377(9777). 1624–1624. 8 indexed citations
11.
Smith, Bradley, Steve Bevan, Caroline Vance, et al.. (2009). Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra‐familial variability in age of onset and complex phenotype. Clinical Genetics. 75(5). 485–489. 18 indexed citations
12.
Wang, Xinnan, et al.. (2007). Drosophila spichthyin inhibits BMP signaling and regulates synaptic growth and axonal microtubules. Nature Neuroscience. 10(2). 177–185. 143 indexed citations
13.
Moumoulidis, Ioannis, Patrick Axon, David Baguley, & Evan Reid. (2007). A review on the genetics of otosclerosis. Clinical Otolaryngology. 32(4). 239–247. 27 indexed citations
14.
Marini, Carla, Davide Mei, Teresa Temudo, et al.. (2007). Idiopathic Epilepsies with Seizures Precipitated by Fever and SCN1A Abnormalities. Epilepsia. 48(9). 1678–1685. 132 indexed citations
15.
Valdmanis, Paul N., Inge A. Meijer, Annie Reynolds, et al.. (2006). Mutations in the KIAA0196 Gene at the SPG8 Locus Cause Hereditary Spastic Paraplegia. The American Journal of Human Genetics. 80(1). 152–161. 141 indexed citations
16.
Blumen, Sergiu C., Saif Abu‐Mouch, David Negus, et al.. (2003). A locus for complicated hereditary spastic paraplegia maps to chromosome 1q24‐q32. Annals of Neurology. 54(6). 796–803. 31 indexed citations
17.
Proukakis, Christos, Michaela Auer‐Grumbach, Klaus Wagner, et al.. (2003). Screening of patients with hereditary spastic paraplegia reveals seven novel mutations in theSPG4 (Spastin) gene. Human Mutation. 21(2). 170–170. 25 indexed citations
18.
Reid, Evan. (2003). Science in motion: common molecular pathological themes emerge in the hereditary spastic paraplegias: Table 1. Journal of Medical Genetics. 40(2). 81–86. 123 indexed citations
19.
Reid, Evan, Mark Kloos, Allison E. Ashley‐Koch, et al.. (2002). A Kinesin Heavy Chain (KIF5A) Mutation in Hereditary Spastic Paraplegia (SPG10). The American Journal of Human Genetics. 71(5). 1189–1194. 377 indexed citations
20.

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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