Joseph D. Symonds

3.4k total citations
30 papers, 711 citations indexed

About

Joseph D. Symonds is a scholar working on Psychiatry and Mental health, Genetics and Molecular Biology. According to data from OpenAlex, Joseph D. Symonds has authored 30 papers receiving a total of 711 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Psychiatry and Mental health, 10 papers in Genetics and 8 papers in Molecular Biology. Recurrent topics in Joseph D. Symonds's work include Epilepsy research and treatment (13 papers), Genomics and Rare Diseases (8 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Joseph D. Symonds is often cited by papers focused on Epilepsy research and treatment (13 papers), Genomics and Rare Diseases (8 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Joseph D. Symonds collaborates with scholars based in United Kingdom, United States and Germany. Joseph D. Symonds's co-authors include Sameer M. Zuberi, Andreas Brunklaus, Amy McTague, Dora Steel, Michael R. Johnson, Eduardo Pérez‐Palma, Dennis Lal, Luis Bello‐Espinosa, Ingrid E. Scheffer and Jeffrey Buchhalter and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Epilepsia.

In The Last Decade

Joseph D. Symonds

25 papers receiving 699 citations

Peers

Joseph D. Symonds

PMH

GENET

CMN

PPCH

Xiu‐Yu Shi China

Marilena Vecchi Italy

Amy Schneider Australia

Lata Vadlamudi Australia

Masaharu Ohfu Japan

Amy McTague United Kingdom

Martina Durner United States

Monika Eisermann France

Beth Rosen Sheidley United States

Santiago Galicchio Argentina

Xiu‐Yu Shi China

Joseph D. Symonds

369 ×0.9

PMH

234 ×0.8

GENET

283 ×1.4

219 ×1.5

CMN

143 ×1.0

PPCH

Citations per year, relative to Joseph D. Symonds Joseph D. Symonds (= 1×) peers Xiu‐Yu Shi

Countries citing papers authored by Joseph D. Symonds

Since Specialization

Citations

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

Fields of papers citing papers by Joseph D. Symonds

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Joseph D. Symonds. 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 Joseph D. Symonds. The network helps show where Joseph D. Symonds may publish in the future.

Co-authorship network of co-authors of Joseph D. Symonds

This figure shows the co-authorship network connecting the top 25 collaborators of Joseph D. Symonds. A scholar is included among the top collaborators of Joseph D. Symonds 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 Joseph D. Symonds. Joseph D. Symonds 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

Symonds, Joseph D., et al.. (2026). What is the psychological impact on parents of learning about SUDEP? A mixed methods systematic review. Epilepsy & Behavior. 176. 110915–110915.

Schneider, Amy, Gaëtan Lesca, Joseph D. Symonds, et al.. (2025). SCN1A pathogenic variants do not have a distinctive blood‐derived DNA methylation signature. Epilepsia. 66(4). e66–e72.

Dorris, Liam, et al.. (2025). Trauma, coping, and adjustment when parenting a child with Dravet syndrome. European Journal of Paediatric Neurology. 54. 96–106. 2 indexed citations

Alawi, Malik, et al.. (2025). Novel biallelic NUP107 variants affect the nuclear pore complex and expand the clinical spectrum to include brain malformations. Journal of Medical Genetics. 62(8). 497–501.

Pérez‐Palma, Eduardo, et al.. (2025). SCN9A should not be considered an epilepsy gene; Refuting a gene–disease association. Epilepsia. 66(9). 3516–3527. 1 indexed citations

Hendry, Kirsty, et al.. (2024). Caregiver burden and therapeutic needs in Dravet syndrome - A national UK cross-sectional questionnaire study. European Journal of Paediatric Neurology. 53. 138–143. 3 indexed citations

Makiello, Phoebe, et al.. (2023). Comorbidities and predictors of health‐related quality of life in Dravet syndrome: A 10‐year, prospective follow‐up study. Epilepsia. 64(4). 1012–1020. 16 indexed citations

Makiello, Phoebe, et al.. (2023). Long-term predictors of developmental outcome and disease burden in SCN1A-positive Dravet syndrome. Brain Communications. 6(1). fcae004–fcae004. 11 indexed citations

Hughes-McCormack, Laura Anne, Ewelina Rydzewska, Sally‐Ann Cooper, et al.. (2022). Rates, causes and predictors of all-cause and avoidable mortality in 163 686 children and young people with and without intellectual disabilities: a record linkage national cohort study. BMJ Open. 12(9). e061636–e061636. 8 indexed citations

10.

Brünger, Tobias, Eduardo Pérez‐Palma, Ludovica Montanucci, et al.. (2022). Conserved patterns across ion channels correlate with variant pathogenicity and clinical phenotypes. Brain. 146(3). 923–934. 7 indexed citations

11.

Truesdale, Maria, Craig Melville, Fiona Kate Barlow, et al.. (2021). Respiratory-associated deaths in people with intellectual disabilities: a systematic review and meta-analysis. BMJ Open. 11(7). e043658–e043658. 15 indexed citations

12.

Symonds, Joseph D., Sakthivel Murugan, Vivek Bhargava, et al.. (2020). Infantile spasms: Etiology, lead time and treatment response in a resource limited setting. Epilepsy & Behavior Reports. 14. 100397–100397. 28 indexed citations

13.

Symonds, Joseph D. & Amy McTague. (2019). Epilepsy and developmental disorders: Next generation sequencing in the clinic. European Journal of Paediatric Neurology. 24. 15–23. 97 indexed citations

14.

Myers, Kenneth A., Luis Bello‐Espinosa, Joseph D. Symonds, et al.. (2018). Heart rate variability in epilepsy: A potential biomarker of sudden unexpected death in epilepsy risk. Epilepsia. 59(7). 1372–1380. 112 indexed citations

15.

Symonds, Joseph D. & Sameer M. Zuberi. (2017). Genetics update: Monogenetics, polygene disorders and the quest for modifying genes. Neuropharmacology. 132. 3–19. 13 indexed citations

16.

Symonds, Joseph D. & Sameer M. Zuberi. (2017). WITHDRAWN: Genetics update: Monogenetics, polygene disorders and the quest for modifying genes. Neuropharmacology. 1 indexed citations

17.

Roberts, Stuart, et al.. (2016). Positional plagiocephaly following ventriculoperitoneal shunting in neonates and infancy—how serious is it?. Child s Nervous System. 33(2). 275–280. 4 indexed citations

18.

Wright, Charlotte, et al.. (2016). Does measurement technique explain the mismatch between European head size and WHO charts?. Archives of Disease in Childhood. 102(7). 639–643. 2 indexed citations

19.

Zuberi, Sameer M. & Joseph D. Symonds. (2015). Update on diagnosis and management of childhood epilepsies. Jornal de Pediatria. 91(6). S67–S77. 14 indexed citations

20.

Oliver, Gillian, et al.. (2004). Knowledge management: A New Zealand survey into current practices..

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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