Cheryl Longman

4.8k total citations
46 papers, 1.2k citations indexed

About

Cheryl Longman is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Cheryl Longman has authored 46 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 14 papers in Cellular and Molecular Neuroscience and 8 papers in Genetics. Recurrent topics in Cheryl Longman's work include Muscle Physiology and Disorders (14 papers), Genetic Neurodegenerative Diseases (14 papers) and Mitochondrial Function and Pathology (9 papers). Cheryl Longman is often cited by papers focused on Muscle Physiology and Disorders (14 papers), Genetic Neurodegenerative Diseases (14 papers) and Mitochondrial Function and Pathology (9 papers). Cheryl Longman collaborates with scholars based in United Kingdom, United States and Türkiye. Cheryl Longman's co-authors include Martin Brockington, S. Brown, Francesco Muntoni, Silvia Torelli, Eugenio Mercuri, S. Robb, Francesco Muntoni, Richard Petty, Mark Hamilton and Caroline A. Sewry and has published in prestigious journals such as PLoS ONE, Neurology and Human Molecular Genetics.

In The Last Decade

Cheryl Longman

45 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cheryl Longman United Kingdom 16 907 263 183 180 158 46 1.2k
Susana Quijano‐Roy France 18 1.0k 1.1× 233 0.9× 276 1.5× 379 2.1× 88 0.6× 32 1.2k
Luca Bello Italy 21 1.0k 1.1× 270 1.0× 285 1.6× 249 1.4× 136 0.9× 84 1.4k
Phillipa J. Lamont Australia 19 1.0k 1.1× 366 1.4× 173 0.9× 354 2.0× 172 1.1× 61 1.3k
M. Mayer France 21 1.0k 1.2× 172 0.7× 333 1.8× 153 0.8× 152 1.0× 49 1.5k
Kenzo Hamano Japan 11 720 0.8× 261 1.0× 80 0.4× 71 0.4× 141 0.9× 23 1.0k
C. Ortez Spain 15 422 0.5× 146 0.6× 121 0.7× 154 0.9× 118 0.7× 76 691
Joachim Schessl Germany 22 622 0.7× 386 1.5× 165 0.9× 265 1.5× 69 0.4× 43 1.2k
Lucia Galli Italy 22 947 1.0× 200 0.8× 72 0.4× 133 0.7× 544 3.4× 57 1.4k
Daisuke Furutama Japan 18 743 0.8× 520 2.0× 165 0.9× 133 0.7× 47 0.3× 36 1.2k
Yuzo Tanabe Japan 19 912 1.0× 184 0.7× 62 0.3× 76 0.4× 197 1.2× 40 1.3k

Countries citing papers authored by Cheryl Longman

Since Specialization
Citations

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

Fields of papers citing papers by Cheryl Longman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cheryl Longman

This figure shows the co-authorship network connecting the top 25 collaborators of Cheryl Longman. A scholar is included among the top collaborators of Cheryl Longman 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 Cheryl Longman. Cheryl Longman 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.
Edwards, Rachel, Eve Miller‐Hodges, Dawn O’Sullivan, et al.. (2025). Late-onset multiple-acyl-CoA-dehydrogenase deficiency-like condition: a case series from the West of Scotland. Neuromuscular Disorders. 49. 105343–105343. 4 indexed citations
2.
Sárközy, Anna, Pinki Munot, William Stewart, et al.. (2023). Glycogen storage disease type IV without detectable polyglucosan bodies: importance of broad gene panels. Neuromuscular Disorders. 33(9). 98–105. 1 indexed citations
3.
Hamilton, Mark, António Atalaia, John McLean, et al.. (2022). Clinical and neuroradiological correlates of sleep in myotonic dystrophy type 1. Neuromuscular Disorders. 32(5). 377–389. 8 indexed citations
4.
Mroczek, Magdalena, Cheryl Longman, Maria Elena Farrugia, et al.. (2022). FXR1-related congenital myopathy: expansion of the clinical and genetic spectrum. Journal of Medical Genetics. 59(11). 1069–1074. 3 indexed citations
5.
Hamilton, Mark, John McLean, Sarah A. Cumming, et al.. (2022). Masseter muscle volume as a disease marker in adult-onset myotonic dystrophy type 1. Neuromuscular Disorders. 32(11-12). 893–902. 1 indexed citations
6.
Cumming, Sarah A., Gillian Stevens, Saif Razvi, et al.. (2020). A DM1 patient with CCG variant repeats: Reaching the diagnosis. Neuromuscular Disorders. 31(3). 232–238. 1 indexed citations
7.
Petty, Richard, Maria Eugenicos, Mark Hamilton, et al.. (2019). The prevalence of faecal incontinence in myotonic dystrophy type 1. Neuromuscular Disorders. 29(7). 562–566. 10 indexed citations
8.
Cumming, Sarah A., Mark Hamilton, Helen Gregory, et al.. (2018). De novo repeat interruptions are associated with reduced somatic instability and mild or absent clinical features in myotonic dystrophy type 1. European Journal of Human Genetics. 26(11). 1635–1647. 69 indexed citations
9.
Ullmann, Urielle, L. D'Argenzio, Shrey Mathur, et al.. (2018). ECEL1 gene related contractural syndrome: Long-term follow-up and update on clinical and pathological aspects. Neuromuscular Disorders. 28(9). 741–749. 10 indexed citations
10.
Hamilton, Mark, Sarah A. Cumming, Helen Gregory, et al.. (2017). Elevated plasma levels of cardiac troponin-I predict left ventricular systolic dysfunction in patients with myotonic dystrophy type 1: A multicentre cohort follow-up study. PLoS ONE. 12(3). e0174166–e0174166. 29 indexed citations
11.
Hilton‐Jones, David, Cheryl Longman, Richard Petty, et al.. (2012). Modafinil for excessive daytime sleepiness in myotonic dystrophy type 1 – The patients’ perspective. Neuromuscular Disorders. 22(7). 597–603. 25 indexed citations
12.
McGowan, Ruth, Sarah J. Ross, Susan Holloway, et al.. (2012). Results of Duchenne muscular dystrophy family screening in practice: leaks rather than cascades?. Clinical Genetics. 83(2). 187–190. 6 indexed citations
13.
Rankin, Julia, Michaela Auer‐Grumbach, Warwick Bagg, et al.. (2008). Extreme phenotypic diversity and nonpenetrance in families with the LMNA gene mutation R644C. American Journal of Medical Genetics Part A. 146A(12). 1530–1542. 80 indexed citations
14.
Clement, Emma, Caroline Godfrey, Jenny Tan, et al.. (2008). Mild POMGnT1 Mutations Underlie a Novel Limb-Girdle Muscular Dystrophy Variant. Archives of Neurology. 65(1). 137–41. 57 indexed citations
15.
Winnepenninckx, Birgitta, Cheryl Longman, Ronald S. Murray, et al.. (2007). The molecular basis of the folate-sensitive fragile site FRA11A at 11q13. Cytogenetic and Genome Research. 119(1-2). 9–14. 20 indexed citations
16.
Brockington, Martin, Silvia Torelli, Paola Prandini, et al.. (2005). Localization and functional analysis of the LARGE family of glycosyltransferases: significance for muscular dystrophy. Human Molecular Genetics. 14(5). 657–665. 78 indexed citations
17.
Mercuri, Eugenio & Cheryl Longman. (2005). Congenital Muscular Dystrophy. Pediatric Annals. 34(7). 560–568. 11 indexed citations
18.
Mercuri, Eugenio, Sonia Messina, Maria Kinali, et al.. (2003). Congenital form of spinal muscular atrophy predominantly affecting the lower limbs: a clinical and muscle MRI study. Neuromuscular Disorders. 14(2). 125–129. 28 indexed citations
19.
Dinçer, Pervin, Yeliz Yuva, Beril Talim, et al.. (2003). A novel form of recessive limb girdle muscular dystrophy with mental retardation and abnormal expression of α-dystroglycan. Neuromuscular Disorders. 13(10). 771–778. 32 indexed citations
20.
Longman, Cheryl, Margo Whiteford, David Koppel, et al.. (2003). Craniosynostosis associated with intracranial calcification: a novel recessive syndrome. Clinical Dysmorphology. 12(4). 215–220. 2 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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