Elizabeth Wraige

3.9k total citations
51 papers, 1.2k citations indexed

About

Elizabeth Wraige is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Elizabeth Wraige has authored 51 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 10 papers in Cellular and Molecular Neuroscience and 10 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Elizabeth Wraige's work include Muscle Physiology and Disorders (8 papers), Blood Coagulation and Thrombosis Mechanisms (8 papers) and Neurogenetic and Muscular Disorders Research (6 papers). Elizabeth Wraige is often cited by papers focused on Muscle Physiology and Disorders (8 papers), Blood Coagulation and Thrombosis Mechanisms (8 papers) and Neurogenetic and Muscular Disorders Research (6 papers). Elizabeth Wraige collaborates with scholars based in United Kingdom, United States and Canada. Elizabeth Wraige's co-authors include Vijeya Ganesan, Heinz Jungbluth, Andrew A. Mallick, Fenella J. Kirkham, Hannah B Edwards, Penny Fallon, Tony McShane, Tammy Hedderly, Finbar O’Callaghan and Evangeline Wassmer and has published in prestigious journals such as Neurology, PEDIATRICS and Annals of Neurology.

In The Last Decade

Elizabeth Wraige

50 papers receiving 1.2k citations

Peers

Elizabeth Wraige
Daniel P. Stein United States
Elizabeth Wraige
Citations per year, relative to Elizabeth Wraige Elizabeth Wraige (= 1×) peers Daniel P. Stein

Countries citing papers authored by Elizabeth Wraige

Since Specialization
Citations

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

Fields of papers citing papers by Elizabeth Wraige

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elizabeth Wraige

This figure shows the co-authorship network connecting the top 25 collaborators of Elizabeth Wraige. A scholar is included among the top collaborators of Elizabeth Wraige 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 Elizabeth Wraige. Elizabeth Wraige 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.
Sárközy, Anna, Mário Sá, Deborah Ridout, et al.. (2023). Long-term Natural History of Pediatric Dominant and Recessive RYR1 -Related Myopathy. Neurology. 101(15). e1495–e1508. 4 indexed citations
2.
McKevitt, Christopher, Marta Topor, Andrew A. Mallick, et al.. (2018). Seeking normality: Parents' experiences of childhood stroke. Child Care Health and Development. 45(1). 89–95. 14 indexed citations
3.
Gordon, Anne, et al.. (2018). Self-reported needs after pediatric stroke. European Journal of Paediatric Neurology. 22(5). 791–796. 5 indexed citations
4.
Jungbluth, Heinz, et al.. (2016). Treatment with Zoledronic Acid in Children with Duchenne Muscular Dystrophy. 86. 1 indexed citations
5.
Rosch, Richard, Alasdair Bamford, Yael Hacohen, et al.. (2014). Guillain‐Barré syndrome associated with CASPR2 antibodies: two paediatric cases. Journal of the Peripheral Nervous System. 19(3). 246–249. 16 indexed citations
6.
Dlamini, Nomazulu, Dragana Josifova, Simon Paine, et al.. (2013). Clinical and neuropathological features of X-linked spinal muscular atrophy (SMAX2) associated with a novel mutation in the UBA1 gene. Neuromuscular Disorders. 23(5). 391–398. 40 indexed citations
7.
Mallick, Andrew A., Vijeya Ganesan, Fenella J. Kirkham, et al.. (2013). Childhood arterial ischaemic stroke incidence, presenting features, and risk factors: a prospective population-based study. The Lancet Neurology. 13(1). 35–43. 229 indexed citations
8.
Lim, Ming, Michael Absoud, Conal Austin, et al.. (2013). Outcome of children with acetylcholine receptor (AChR) antibody positive juvenile myasthenia gravis following thymectomy. Neuromuscular Disorders. 24(1). 25–30. 24 indexed citations
9.
Dowling, James J., Suzanne Lillis, Haiyan Zhou, et al.. (2011). King–Denborough syndrome with and without mutations in the skeletal muscle ryanodine receptor (RYR1) gene. Neuromuscular Disorders. 21(6). 420–427. 72 indexed citations
10.
Tang, Shan, et al.. (2011). Beneficial use of steroids in hereditary neuropathy with liability to pressure palsy. Developmental Medicine & Child Neurology. 54(2). 183–186. 6 indexed citations
11.
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
12.
Dlamini, Nomazulu, Miranda Splitt, Ata Siddiqui, et al.. (2009). Generalized arterial calcification of infancy: Phenotypic spectrum among three siblings including one case without obvious arterial calcifications. American Journal of Medical Genetics Part A. 149A(3). 456–460. 21 indexed citations
13.
Baird, Gillian, et al.. (2008). QUESTION 3. Archives of Disease in Childhood. 93(11). 998–999. 4 indexed citations
14.
Cheuk, Daniel KL, et al.. (2007). Surgery for scoliosis in Duchenne muscular dystrophy. Cochrane Database of Systematic Reviews. CD005375–CD005375. 18 indexed citations
15.
Kerr, Tim, Dragana Josifova, K. Bushby, et al.. (2006). Congenital arthrogryposis and dilated cardiomyopathy associated with a R644C substitution in the Lamin A/C gene. Developmental Medicine & Child Neurology. 48. 29–29. 3 indexed citations
16.
Wraige, Elizabeth, et al.. (2003). Ischaemic stroke subtypes in children and adults. Developmental Medicine & Child Neurology. 45(4). 229–232. 16 indexed citations
17.
Wraige, Elizabeth, Cother Hajat, Wajanat Jan, et al.. (2003). Ischaemic stroke subtypes in children and adults. Developmental Medicine & Child Neurology. 45(4). 229–32. 14 indexed citations
18.
Wraige, Elizabeth, et al.. (2003). Arterial dissection complicating tonsillectomy. Developmental Medicine & Child Neurology. 45(9). 638–9. 11 indexed citations
19.
Wraige, Elizabeth. (2002). Investigation of daytime wetting: when is spinal cord imaging indicated?. Archives of Disease in Childhood. 87(2). 151–155. 9 indexed citations
20.
Wraige, Elizabeth. (2002). Idiopathic intracranial hypertension: is papilloedema inevitable?. Archives of Disease in Childhood. 87(3). 223–224. 23 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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