Emma Matthews

5.2k total citations
97 papers, 2.4k citations indexed

About

Emma Matthews is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cellular and Molecular Neuroscience. According to data from OpenAlex, Emma Matthews has authored 97 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 67 papers in Molecular Biology, 44 papers in Cardiology and Cardiovascular Medicine and 39 papers in Cellular and Molecular Neuroscience. Recurrent topics in Emma Matthews's work include Ion channel regulation and function (52 papers), Genetic Neurodegenerative Diseases (32 papers) and Cardiac electrophysiology and arrhythmias (22 papers). Emma Matthews is often cited by papers focused on Ion channel regulation and function (52 papers), Genetic Neurodegenerative Diseases (32 papers) and Cardiac electrophysiology and arrhythmias (22 papers). Emma Matthews collaborates with scholars based in United Kingdom, United States and Italy. Emma Matthews's co-authors include Michael G. Hanna, Doreen Fialho, Adnan Y. Manzur, Richa Sud, Thierry Küntzer, Fatima Jichi, Ruth Brassington, Robert C. Griggs, Martin McKee and Karen Forrest and has published in prestigious journals such as JAMA, SHILAP Revista de lepidopterología and Brain.

In The Last Decade

Emma Matthews

88 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Emma Matthews United Kingdom 24 1.6k 981 957 351 214 97 2.4k
Joohyung Lee Australia 24 717 0.4× 501 0.5× 681 0.7× 146 0.4× 260 1.2× 53 2.0k
Matthew A. Benson United Kingdom 24 1.7k 1.0× 435 0.4× 994 1.0× 407 1.2× 103 0.5× 52 3.0k
Veronica Ramirez United States 18 563 0.4× 229 0.2× 313 0.3× 172 0.5× 156 0.7× 34 2.0k
Grace Yoon Canada 25 1.4k 0.9× 228 0.2× 632 0.7× 364 1.0× 212 1.0× 97 2.1k
Pietro Maffei Italy 29 930 0.6× 200 0.2× 253 0.3× 1.5k 4.2× 197 0.9× 118 3.5k
Valeria Ricotti United Kingdom 23 1.2k 0.7× 239 0.2× 203 0.2× 182 0.5× 97 0.5× 57 1.5k
Lundy Day Canada 10 730 0.5× 153 0.2× 522 0.5× 87 0.2× 491 2.3× 16 2.1k
Mark Corbett Australia 24 1.4k 0.8× 179 0.2× 164 0.2× 715 2.0× 84 0.4× 72 2.5k
Mária Judit Molnár Hungary 24 992 0.6× 65 0.1× 279 0.3× 262 0.7× 377 1.8× 142 1.9k
Mårten Kyllerman Sweden 34 1.2k 0.8× 265 0.3× 350 0.4× 759 2.2× 266 1.2× 88 3.1k

Countries citing papers authored by Emma Matthews

Since Specialization
Citations

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

Fields of papers citing papers by Emma Matthews

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emma Matthews

This figure shows the co-authorship network connecting the top 25 collaborators of Emma Matthews. A scholar is included among the top collaborators of Emma Matthews 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 Emma Matthews. Emma Matthews 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.
Harwood, S., Simon Bailey, Richard B. Reilly, et al.. (2024). Abstracts of the Winter Scientific Meeting 2024, 11‐12 January 2024, QEII Centre, Westminster, London. Anaesthesia. 79(S1). 7–88. 1 indexed citations
2.
Scalco, R., Jasper M. Morrow, Andreea Manole, et al.. (2024). Crossover randomized controlled trial of bumetanide to rescue an attack of exercise induced hand weakness in hypokalaemic periodic paralysis. Neuromuscular Disorders. 35. 33–38.
3.
Matthews, Emma, et al.. (2024). Leigh syndrome with developmental regression and ataxia due to a novel splicing variant in the PMPCB gene. Journal of Human Genetics. 69(6). 283–285. 1 indexed citations
4.
Matthews, Emma, Adrian Dockery, Laura Whelan, et al.. (2024). Novel Splice-Altering Variants in the CHM and CACNA1F Genes Causative of X-Linked Choroideremia and Cone Dystrophy. Genes. 16(1). 25–25.
5.
Matthews, Emma, Jacqueline Palace, Sithara Ramdas, et al.. (2023). Care Recommendations for the Investigation and Management of Children With Skeletal Muscle Channelopathies. Pediatric Neurology. 145. 102–111. 2 indexed citations
6.
Suetterlin, Karen, Roope Männikkö, Emma Matthews, et al.. (2022). Excitability properties of mouse and human skeletal muscle fibres compared by muscle velocity recovery cycles. Neuromuscular Disorders. 32(4). 347–357. 6 indexed citations
7.
Suetterlin, Karen, S. Veronica Tan, Roope Männikkö, et al.. (2021). Ageing contributes to phenotype transition in a mouse model of periodic paralysis. SHILAP Revista de lepidopterología. 4(2). 245–259. 6 indexed citations
8.
Matthews, Emma, Sarah Holmes, & Doreen Fialho. (2021). Skeletal muscle channelopathies: a guide to diagnosis and management. Practical Neurology. 21(3). 196–204. 13 indexed citations
9.
Ribeiro, Ana Freitas, Karen Suetterlin, Iwona Skorupinska, et al.. (2021). The long exercise test as a functional marker of periodic paralysis. Muscle & Nerve. 65(5). 581–585. 3 indexed citations
10.
Vivekanandam, Vinojini, Roope Männikkö, Iwona Skorupinska, et al.. (2021). Andersen–Tawil syndrome: deep phenotyping reveals significant cardiac and neuromuscular morbidity. Brain. 145(6). 2108–2120. 14 indexed citations
11.
Sun, Jian, Sushan Luo, Karen Suetterlin, et al.. (2021). Clinical and genetic spectrum of a Chinese cohort with SCN4A gene mutations. Neuromuscular Disorders. 31(9). 829–838. 4 indexed citations
12.
Gray, Belinda, Richard D. Bagnall, David J. Tester, et al.. (2020). Triadin Knockout Syndrome Is Absent in a Multi-Center Molecular Autopsy Cohort of Sudden Infant Death Syndrome and Sudden Unexplained Death in the Young and Is Extremely Rare in the General Population. Circulation Genomic and Precision Medicine. 13(2). e002731–e002731. 5 indexed citations
13.
Stunnenberg, Bas C., Samantha LoRusso, W. David Arnold, et al.. (2020). Guidelines on clinical presentation and management of nondystrophic myotonias. Muscle & Nerve. 62(4). 430–444. 46 indexed citations
14.
Matthews, Emma, Peter S Blair, Sanjay M. Sisodiya, et al.. (2019). National registry for sudden unexpected deaths of infants and children in England: why do we need one and do families want one?. Archives of Disease in Childhood. 104(10). 989–993. 2 indexed citations
15.
Türkdoğan, Dilşad, Emma Matthews, Kayıhan Uluç, et al.. (2019). Possible role of SCN4A skeletal muscle mutation in apnea during seizure. Epilepsia Open. 4(3). 498–503. 7 indexed citations
16.
Matthews, Emma. (2009). Moralist or Therapist?: Foucault and the Critique of Psychiatry. Project Muse (Johns Hopkins University).
17.
Matthews, Emma, Doreen Fialho, S. Veronica Tan, et al.. (2009). The non-dystrophic myotonias: molecular pathogenesis, diagnosis and treatment. Brain. 133(1). 9–22. 148 indexed citations
18.
Matthews, Emma, Robyn Labrum, Mary G. Sweeney, et al.. (2008). Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis. Neurology. 72(18). 1544–1547. 144 indexed citations
19.
Matthews, Emma. (1999). Disordered Minds: A Response to the Commentaries. Project Muse (Johns Hopkins University). 2 indexed citations
20.
Matthews, Emma. (1998). Choosing Death: Philosophical Observations on Suicide and Euthanasia. Project Muse (Johns Hopkins University). 4 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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