Gail Eglon

529 total citations
10 papers, 302 citations indexed

About

Gail Eglon is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Gail Eglon has authored 10 papers receiving a total of 302 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Cellular and Molecular Neuroscience, 5 papers in Molecular Biology and 3 papers in Neurology. Recurrent topics in Gail Eglon's work include Genetic Neurodegenerative Diseases (6 papers), Mitochondrial Function and Pathology (4 papers) and Hereditary Neurological Disorders (4 papers). Gail Eglon is often cited by papers focused on Genetic Neurodegenerative Diseases (6 papers), Mitochondrial Function and Pathology (4 papers) and Hereditary Neurological Disorders (4 papers). Gail Eglon collaborates with scholars based in United Kingdom, Germany and Hungary. Gail Eglon's co-authors include Patrick F. Chinnery, Rita Horváth, Angela Pyle, Helen Griffin, Gerald Pfeffer, Konstantinos Douroudis, Jennifer Duff, Patrick Yu‐Wai‐Man, David Bargiela and Brook Galna and has published in prestigious journals such as Brain, Neurology and Movement Disorders.

In The Last Decade

Gail Eglon

10 papers receiving 297 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gail Eglon United Kingdom	8	190	172	82	72	56	10	302
M Milani Italy	12	236 1.2×	108 0.6×	107 1.3×	109 1.5×	29 0.5×	18	380
Anne Kjersti Erichsen Norway	8	222 1.2×	113 0.7×	103 1.3×	58 0.8×	25 0.4×	12	297
Viorica Chelban United Kingdom	13	162 0.9×	128 0.7×	85 1.0×	185 2.6×	45 0.8×	27	381
Maartje Pennings Netherlands	10	112 0.6×	134 0.8×	44 0.5×	48 0.7×	76 1.4×	21	272
Elisabetta Indelicato Austria	12	221 1.2×	202 1.2×	31 0.4×	161 2.2×	71 1.3×	40	397
Meyke Schouten Netherlands	10	124 0.7×	221 1.3×	49 0.6×	60 0.8×	126 2.3×	19	420
Milena Janković Serbia	12	91 0.5×	106 0.6×	40 0.5×	152 2.1×	29 0.5×	37	337
Miriam Rodrigues New Zealand	9	187 1.0×	165 1.0×	30 0.4×	71 1.0×	55 1.0×	24	295
Raoul van de Graaf Netherlands	6	129 0.7×	240 1.4×	46 0.6×	80 1.1×	81 1.4×	9	362
Wotu Tian China	10	68 0.4×	105 0.6×	47 0.6×	68 0.9×	73 1.3×	39	280

Countries citing papers authored by Gail Eglon

Since Specialization

Citations

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

Fields of papers citing papers by Gail Eglon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gail Eglon

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

All Works

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10 of 10 papers shown

Willis, Derek, et al.. (2024). Myotonic dystrophy type 1: palliative care guidelines. BMJ Supportive & Palliative Care. 14(e2). e2163–e2166. 2 indexed citations

Wood, Libby, Chiara Marini‐Bettolo, Michela Guglieri, et al.. (2017). Respiratory involvement in ambulant and non-ambulant patients with facioscapulohumeral muscular dystrophy. Journal of Neurology. 264(6). 1271–1280. 29 indexed citations

Griffin, Helen, Konstantinos Douroudis, Stephanie Kleinle, et al.. (2015). Whole exome sequencing and the clinician: we need clinical skills and functional validation in variant filtering. Journal of Neurology. 262(7). 1673–1677. 14 indexed citations

Pfeffer, Gerald, Angela Pyle, Helen Griffin, et al.. (2015). SPG7 mutations are a common cause of undiagnosed ataxia. Neurology. 84(11). 1174–1176. 69 indexed citations

Keogh, Michael J., Angela Pyle, Helen Griffin, et al.. (2015). Clinical heterogeneity of primary familial brain calcification due to a novel mutation in PDGFB. Neurology. 84(17). 1818–1820. 13 indexed citations

Pyle, Angela, Venkateswaran Ramesh, Marina Bartsakoulia, et al.. (2014). Behr's Syndrome is Typically Associated with Disturbed Mitochondrial Translation and Mutations in the C12orf65 Gene. Journal of Neuromuscular Diseases. 1(1). 55–63. 14 indexed citations

Pyle, Angela, David Bargiela, Helen Griffin, et al.. (2014). Exome sequencing in undiagnosed inherited and sporadic ataxias. Brain. 138(2). 276–283. 94 indexed citations

Bargiela, David, Gail Eglon, Rita Horváth, & Patrick F. Chinnery. (2013). An under-recognised cause of spastic paraparesis in middle-aged women. Practical Neurology. 14(3). 182–184. 4 indexed citations

Rochester, Lynn, Brook Galna, Sue Lord, et al.. (2013). Gait impairment precedes clinical symptoms in spinocerebellar ataxia type 6. Movement Disorders. 29(2). 252–255. 44 indexed citations

10.

Pyle, Angela, Helen Griffin, Patrick Yu‐Wai‐Man, et al.. (2012). Prominent Sensorimotor Neuropathy Due to SACS Mutations Revealed by Whole-Exome Sequencing. Archives of Neurology. 69(10). 1351–4. 19 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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