C. Sewry

2.0k total citations
14 papers, 546 citations indexed

About

C. Sewry is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, C. Sewry has authored 14 papers receiving a total of 546 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 4 papers in Genetics and 4 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in C. Sewry's work include Muscle Physiology and Disorders (8 papers), Neurogenetic and Muscular Disorders Research (4 papers) and Cardiomyopathy and Myosin Studies (3 papers). C. Sewry is often cited by papers focused on Muscle Physiology and Disorders (8 papers), Neurogenetic and Muscular Disorders Research (4 papers) and Cardiomyopathy and Myosin Studies (3 papers). C. Sewry collaborates with scholars based in United Kingdom, United States and Germany. C. Sewry's co-authors include Michael G. Hanna, Janice L. Holton, David Hilton‐Jones, M. Parton, Rosaline C. M. Quinlivan, Francesco Muntoni, Stefen Brady, Waney Squier, Susan Treves and Sylvie Ducreux and has published in prestigious journals such as Journal of Biological Chemistry, Neurology and BMJ Open.

In The Last Decade

C. Sewry

13 papers receiving 539 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 11 382 170 122 103 69 14 546
Francesco Laschena Italy 12 419 1.1× 72 0.4× 192 1.6× 172 1.7× 104 1.5× 18 534
P Ottaviani Italy 9 401 1.0× 74 0.4× 202 1.7× 154 1.5× 107 1.6× 19 516
Keiji Chida Japan 9 203 0.5× 167 1.0× 77 0.6× 92 0.9× 59 0.9× 23 468
Erik P. Rader United States 13 608 1.6× 26 0.2× 96 0.8× 78 0.8× 36 0.5× 28 791
Sanna Huovinen Finland 15 347 0.9× 63 0.4× 176 1.4× 95 0.9× 145 2.1× 32 498
Robert‐Yves Carlier France 12 253 0.7× 52 0.3× 132 1.1× 103 1.0× 93 1.3× 37 546
Gudrun Schreiber Germany 9 312 0.8× 15 0.1× 87 0.7× 36 0.3× 81 1.2× 17 549
Henk Veldman Netherlands 16 182 0.5× 57 0.3× 83 0.7× 163 1.6× 44 0.6× 20 484
M. Osborn United Kingdom 9 291 0.8× 44 0.3× 95 0.8× 81 0.8× 76 1.1× 13 495
Mary S. Carvalho Brazil 11 215 0.6× 31 0.2× 65 0.5× 42 0.4× 42 0.6× 27 267

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

14 of 14 papers shown
1.
Munot, Pinki, Silvia Torelli, Adnan Manzur, et al.. (2021). TRAPPC11 ‐related muscular dystrophy with hypoglycosylation of alpha‐dystroglycan in skeletal muscle and brain. Neuropathology and Applied Neurobiology. 48(2). e12771–e12771. 17 indexed citations
2.
Udd, Bjarne, Werner Stenzel, Anders Oldfors, et al.. (2019). 1st ENMC European meeting: The EURO-NMD pathology working group Recommended Standards for Muscle Pathology Amsterdam, The Netherlands, 7 December 2018. Neuromuscular Disorders. 29(6). 483–485. 34 indexed citations
3.
Phadke, Rahul, Anna Sárközy, Emily C. Oates, et al.. (2019). P.236Myofibres with subsarcolemmal rims and/or central aggregates of mitochondria (SRCAM) are prevalent in congenital titinopathies. Neuromuscular Disorders. 29. S135–S135.
4.
Sframeli, Maria, Anna Sárközy, Marta Bértoli, et al.. (2017). Congenital muscular dystrophies in the UK population: Clinical and molecular spectrum of a large cohort diagnosed over a 12-year period. Neuromuscular Disorders. 27(9). 793–803. 65 indexed citations
5.
Dastgir, Jahannaz, Anne Rutkowski, Ke Yan, et al.. (2015). Common Data Elements for Muscle Biopsy Reporting. Archives of Pathology & Laboratory Medicine. 140(1). 51–65. 16 indexed citations
6.
Brady, Stefen, Waney Squier, C. Sewry, et al.. (2014). A retrospective cohort study identifying the principal pathological features useful in the diagnosis of inclusion body myositis. BMJ Open. 4(4). e004552–e004552. 70 indexed citations
7.
Whyte, Tamieka, Philip L. Beales, Daniel P. S. Osborn, et al.. (2014). G.P.154. Neuromuscular Disorders. 24(9-10). 847–848. 1 indexed citations
8.
Maddison, Paul, Maxwell S. Damian, C. Sewry, et al.. (2012). Clinical and Myopathological Characteristics of Desminopathy Caused by a Mutation in Desmin Tail Domain. European Neurology. 68(5). 279–286. 6 indexed citations
9.
Scoto, Mariacristina, Sebahattin Çirak, R. Mein, et al.. (2011). SEPN1 -related myopathies. Neurology. 76(24). 2073–2078. 57 indexed citations
10.
Forrest, Katharine, Safa Al‐Sarraj, C. Sewry, et al.. (2010). Infantile onset myofibrillar myopathy due to recessive CRYAB mutations. Neuromuscular Disorders. 21(1). 37–40. 36 indexed citations
11.
Hilton‐Jones, David, et al.. (2010). Inclusion body myositis. Neuromuscular Disorders. 20(2). 142–147. 80 indexed citations
12.
Jungbluth, Heinz, Alan H. Beggs, Carsten G. Bönnemann, et al.. (2004). 111th ENMC International Workshop on Multi-minicore Disease. 2nd International MmD Workshop, 9–11 November 2002, Naarden, The Netherlands. Neuromuscular Disorders. 14(11). 754–766. 21 indexed citations
13.
Ducreux, Sylvie, Francesco Zorzato, Clemens R. Müller, et al.. (2004). Effect of Ryanodine Receptor Mutations on Interleukin-6 Release and Intracellular Calcium Homeostasis in Human Myotubes from Malignant Hyperthermia-susceptible Individuals and Patients Affected by Central Core Disease. Journal of Biological Chemistry. 279(42). 43838–43846. 81 indexed citations
14.

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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