Catherine DeVile

2.1k total citations
36 papers, 1.1k citations indexed

About

Catherine DeVile is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Catherine DeVile has authored 36 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 7 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Catherine DeVile's work include Connective tissue disorders research (10 papers), Bone fractures and treatments (5 papers) and Metabolism and Genetic Disorders (3 papers). Catherine DeVile is often cited by papers focused on Connective tissue disorders research (10 papers), Bone fractures and treatments (5 papers) and Metabolism and Genetic Disorders (3 papers). Catherine DeVile collaborates with scholars based in United Kingdom, India and Sweden. Catherine DeVile's co-authors include R Stanhope, David Grant, Richard Hayward, Ashok Vellodi, Elin Haf Davies, Margaret Timmons, Markus Ries, Chris Harris, Lucinda Carr and Ivo N. van Schaik and has published in prestigious journals such as The Lancet, PLoS ONE and Neurology.

In The Last Decade

Catherine DeVile

36 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Catherine DeVile United Kingdom	17	274	236	224	183	182	36	1.1k
Caroline Sevin France	20	551 2.0×	444 1.9×	268 1.2×	358 2.0×	120 0.7×	54	1.4k
Gail J. Mick United States	12	206 0.8×	229 1.0×	107 0.5×	324 1.8×	44 0.2×	45	1.1k
Parayil Sankaran Bindu India	19	386 1.4×	170 0.7×	80 0.4×	48 0.3×	77 0.4×	92	1.1k
Carolina Fischinger Moura de Souza Brazil	19	507 1.9×	427 1.8×	183 0.8×	40 0.2×	132 0.7×	110	1.2k
Stephanie Austin United States	25	375 1.4×	776 3.3×	622 2.8×	80 0.4×	58 0.3×	72	2.0k
Nancy D. Leslie United States	18	929 3.4×	523 2.2×	261 1.2×	91 0.5×	107 0.6×	37	1.7k
Richard Ziegler United States	14	664 2.4×	381 1.6×	105 0.5×	55 0.3×	59 0.3×	29	1.2k
Julian Raiman Canada	24	559 2.0×	738 3.1×	228 1.0×	39 0.2×	127 0.7×	58	1.5k
Esther M. Maier Germany	23	974 3.6×	251 1.1×	353 1.6×	61 0.3×	81 0.4×	64	1.7k
Anna Elsa Maria Allegri Italy	18	285 1.0×	108 0.5×	161 0.7×	336 1.8×	26 0.1×	43	830

Countries citing papers authored by Catherine DeVile

Since Specialization

Citations

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

Fields of papers citing papers by Catherine DeVile

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catherine DeVile

This figure shows the co-authorship network connecting the top 25 collaborators of Catherine DeVile. A scholar is included among the top collaborators of Catherine DeVile 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 Catherine DeVile. Catherine DeVile is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

DeVile, Catherine, et al.. (2023). Osteogenesis imperfecta. BJA Education. 23(5). 182–188. 6 indexed citations

Rossor, Thomas, Jane Hassell, Stewart Boyd, et al.. (2020). Diagnostic algorithm for children presenting with epilepsia partialis continua. Epilepsia. 61(10). 2224–2233. 6 indexed citations

Steel, Dora, Marios Kaliakatsos, Catherine DeVile, et al.. (2020). KIF1A‐related disorders in children: A wide spectrum of central and peripheral nervous system involvement. Journal of the Peripheral Nervous System. 25(2). 117–124. 30 indexed citations

Vecchio, Domizia, Sithara Ramdas, Pinki Munot, et al.. (2019). Paediatric myasthenia gravis: Prognostic factors for drug free remission. Neuromuscular Disorders. 30(2). 120–127. 24 indexed citations

Hill, Melissa, Celine Lewis, Catherine DeVile, et al.. (2019). Stakeholder views and attitudes towards prenatal and postnatal transplantation of fetal mesenchymal stem cells to treat Osteogenesis Imperfecta. European Journal of Human Genetics. 27(8). 1244–1253. 16 indexed citations

Scollo, Paolo, Martin P. Snead, Allan J. Richards, Rebecca C. Pollitt, & Catherine DeVile. (2018). Bilateral giant retinal tears in Osteogenesis Imperfecta. BMC Medical Genetics. 19(1). 8–8. 11 indexed citations

Pitt, Matthew, Rahul Phadke, Alexander M. Rossor, et al.. (2018). Clinical spectrum, treatment and outcome of children with suspected diagnosis of chronic inflammatory demyelinating polyradiculoneuropathy. Neuromuscular Disorders. 28(9). 757–765. 14 indexed citations

Chandler, Natalie, Sunayna Best, Jane Hayward, et al.. (2018). Rapid prenatal diagnosis using targeted exome sequencing: a cohort study to assess feasibility and potential impact on prenatal counseling and pregnancy management. Genetics in Medicine. 20(11). 1430–1437. 104 indexed citations

Hill, Melissa, et al.. (2018). Exploring the impact of Osteogenesis Imperfecta on families: A mixed-methods systematic review. Disability and health journal. 12(3). 340–349. 16 indexed citations

10.

Klein, Andrea, Matthew Pitt, John C. McHugh, et al.. (2013). DOK7 congenital myasthenic syndrome in childhood: Early diagnostic clues in 23 children. Neuromuscular Disorders. 23(11). 883–891. 36 indexed citations

11.

Vijayakumar, Kayal, et al.. (2012). Experience of using electromyography of the genioglossus in the investigation of paediatric dysphagia. Developmental Medicine & Child Neurology. 54(12). 1127–1132. 6 indexed citations

12.

Schiffmann, Raphael, Edmond J. FitzGibbon, Chris Harris, et al.. (2008). Randomized, controlled trial of miglustat in Gaucher's disease type 3. Annals of Neurology. 64(5). 514–522. 177 indexed citations

13.

MacLennan, Suzanna C., et al.. (2007). Severe cerebellitis following methadone poisoning. Pediatric Radiology. 38(2). 227–229. 44 indexed citations

14.

DeVile, Catherine, et al.. (2006). Understanding the Information Needs of General Practitioners Managing a Rare Genetic Disorder (Osteogenesis Imperfecta). Public Health Genomics. 9(4). 260–267. 14 indexed citations

15.

Franck, Linda S., et al.. (2005). Fracture and non‐fracture pain in children with osteogenesis imperfecta. Acta Paediatrica. 94(9). 1238–1242. 26 indexed citations

16.

Clayton, Peter T., et al.. (2003). Neonatal epileptic encephalopathy. The Lancet. 361(9369). 1614–1614. 59 indexed citations

17.

Counsell, Serena J., et al.. (2002). Magnetic Resonance Imaging Assessment of Infantile Myofibromatosis. Clinical Radiology. 57(1). 67–70. 13 indexed citations

18.

DeVile, Catherine & R Stanhope. (1997). Hydrocortisone replacement therapy in children and adolescents with hypopituitarism. Clinical Endocrinology. 47(1). 37–41. 32 indexed citations

19.

DeVile, Catherine, et al.. (1995). Lesson of the Week: Occult intracranial tumours masquerading as early onset anorexia nervosa. BMJ. 311(7016). 1359–1360. 33 indexed citations

20.

DeVile, Catherine, et al.. (1993). New Challenges in the Growth Field. Journal of Pediatric Endocrinology and Metabolism. 6(3-4). 295–301. 1 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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