C. Sewry

1.3k total citations
33 papers, 455 citations indexed

About

C. Sewry is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, C. Sewry has authored 33 papers receiving a total of 455 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 9 papers in Cardiology and Cardiovascular Medicine and 8 papers in Genetics. Recurrent topics in C. Sewry's work include Muscle Physiology and Disorders (22 papers), Cardiomyopathy and Myosin Studies (9 papers) and Neurogenetic and Muscular Disorders Research (8 papers). C. Sewry is often cited by papers focused on Muscle Physiology and Disorders (22 papers), Cardiomyopathy and Myosin Studies (9 papers) and Neurogenetic and Muscular Disorders Research (8 papers). C. Sewry collaborates with scholars based in United Kingdom, Italy and United States. C. Sewry's co-authors include Victor Dubowitz, Francesco Muntoni, T. Voit, Heinz Jungbluth, S. Brown, Yeliz Yuva, Maria Kinali, Eugenio Mercuri, Martin Brockington and L. Feng and has published in prestigious journals such as Neurology, Annals of Neurology and Journal of the Neurological Sciences.

In The Last Decade

C. Sewry

30 papers receiving 446 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
C. Sewry United Kingdom 13 364 134 93 91 87 33 455
Carsten G. Bönnemann United States 3 304 0.8× 93 0.7× 45 0.5× 86 0.9× 48 0.6× 5 368
G. Joost Jöbsis Netherlands 8 338 0.9× 63 0.5× 88 0.9× 54 0.6× 95 1.1× 10 459
Hülya Gündeşli Türkiye 7 343 0.9× 76 0.6× 75 0.8× 55 0.6× 124 1.4× 12 417
C. Pollitt United Kingdom 7 379 1.0× 68 0.5× 136 1.5× 57 0.6× 103 1.2× 11 460
Jaya Punetha United States 11 319 0.9× 94 0.7× 51 0.5× 85 0.9× 46 0.5× 15 437
Stephanie Hirner Germany 6 341 0.9× 119 0.9× 61 0.7× 28 0.3× 104 1.2× 7 415
Takahiro Yonekawa Japan 12 186 0.5× 50 0.4× 49 0.5× 76 0.8× 40 0.5× 17 367
Francesco Muntoni United Kingdom 5 1.1k 3.1× 216 1.6× 85 0.9× 89 1.0× 171 2.0× 8 1.2k
Yiming Zheng China 13 375 1.0× 109 0.8× 133 1.4× 63 0.7× 28 0.3× 49 580
Karine Charton France 15 436 1.2× 175 1.3× 83 0.9× 63 0.7× 90 1.0× 19 485

Countries citing papers authored by C. Sewry

Since Specialization
Citations

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

Fields of papers citing papers by C. Sewry

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C. Sewry

This figure shows the co-authorship network connecting the top 25 collaborators of C. Sewry. A scholar is included among the top collaborators of C. Sewry 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 C. Sewry. C. Sewry 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.
Kiiski, K., Vilma‐Lotta Lehtokari, Adnan Y. Manzur, et al.. (2015). A Large Deletion Affecting TPM3 , Causing Severe Nemaline Myopathy. Journal of Neuromuscular Diseases. 2(4). 433–438. 11 indexed citations
2.
Zaharieva, Irina, Irene Colombo, Maria Sframeli, et al.. (2014). G.P.261. Neuromuscular Disorders. 24(9-10). 895–895. 2 indexed citations
3.
Amin, Sam, et al.. (2013). P243 – 1944 Does tuberous sclerosis complex ever involve skeletal muscle? A case for discussion. European Journal of Paediatric Neurology. 17. S120–S120.
4.
Stevens, Elizabeth, Silvia Torelli, Liang Feng, C. Sewry, & Francesco Muntoni. (2012). P15 Flow cytometry in the assessment of functional alpha-dystroglycan glycosylation in dystroglycanopathy patient fibroblasts. Neuromuscular Disorders. 22. S11–S11. 1 indexed citations
5.
Wedderburn, Lucy R., Hemlata Varsani, Brenda Banwell, et al.. (2010). VALIDATION OF A HISTOPATHOLOGICAL SCORE TOOL FOR THE MEASUREMENT OF SEVERITY IN MUSCLE BIOPSIES FROM PATIENTS WITH JUVENILE DERMATOMYOSITIS. UCL Discovery (University College London). 1 indexed citations
6.
Sewry, C., et al.. (2009). Zebra body myopathy resolved. UCL Discovery (University College London). 7 indexed citations
7.
Holt, Ian, Denis Furling, Majid Fardaei, et al.. (2008). D.P.4.10 Muscleblind-like proteins: Similarities and differences in normal and myotonic dystrophy muscle. Neuromuscular Disorders. 18(9-10). 799–799. 1 indexed citations
8.
Bertini, Enrico, Valérie Biancalana, Alessandra Bolino, et al.. (2004). 118th ENMC International Workshop on Advances in Myotubular Myopathy. 26–28 September 2003, Naarden, The Netherlands. (5th Workshop of the International Consortium on Myotubular Myopathy). Neuromuscular Disorders. 14(6). 387–396. 16 indexed citations
9.
Mercuri, Eugenio, Anne Lampe, Volker Straub, et al.. (2004). Congenital Muscular Dystrophy with Short Stature, Proximal Contractures and Distal Laxity. Neuropediatrics. 35(4). 224–229. 6 indexed citations
10.
Mercuri, Eugenio, C. Cini, Anna Pichiecchio, et al.. (2003). Muscle magnetic resonance imaging in patients with congenital muscular dystrophy and Ullrich phenotype. Neuromuscular Disorders. 13(7-8). 554–558. 57 indexed citations
11.
Kristiansen, Marianne, Gun Peggy Knudsen, Scott Tanner, et al.. (2003). X-inactivation patterns in carriers of X-linked myotubular myopathy. Neuromuscular Disorders. 13(6). 468–471. 33 indexed citations
12.
Sewry, C., et al.. (2001). alpha-dystroglycan expression and secondary merosin deficiency. UCL Discovery (University College London).
13.
Jungbluth, Heinz, Mark I. Rees, A. Manzur, et al.. (2000). An unusual case of hyperekplexia. European Journal of Paediatric Neurology. 4(2). 77–80. 7 indexed citations
14.
Philpot, J., J.M. Pennock, Frances M. Cowan, et al.. (2000). Brain magnetic resonance imaging abnormalities in merosin-positive congenital muscular dystrophy. European Journal of Paediatric Neurology. 4(3). 109–114. 15 indexed citations
15.
Villanova, Marcello, C. Sewry, Alessandro Malandrini, et al.. (1997). Immunolocalization of several laminin chains in the normal human central and peripheral nervous system.. PubMed. 29(3). 409–13. 13 indexed citations
16.
Leclerc, A., Haluk Topaloğlu, C. Sewry, et al.. (1995). Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2.. PubMed. 318(12). 1245–52. 30 indexed citations
17.
Sewry, C., Angela Clerk, J Z Heckmatt, et al.. (1991). Dystrophin abnormalities in polymyositis and dermatomyositis. Neuromuscular Disorders. 1(5). 333–339. 12 indexed citations
18.
Voït, Thomas, C. Sewry, Michael J. Dünn, & Victor Dubowitz. (1988). Binding of Ricinus communis I lectin to developing dystrophic muscle in human fetus. Journal of the Neurological Sciences. 84(2-3). 301–314. 4 indexed citations
19.
Sewry, C., T. Voit, & Victor Dubowitz. (1988). Myopathy with unique ultrastructural feature in marchinesco‐sjögren syndrome. Annals of Neurology. 24(4). 576–580. 42 indexed citations
20.
Archard, L. C., Peter J. Richardson, E. G. J. Olsen, et al.. (1987). The role of Coxsackie B viruses in the pathogenesis of myocarditis, dilated cardiomyopathy and inflammatory muscle disease.. PubMed. 53. 51–62. 22 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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