Bronwyn E. Grinton

3.4k total citations · 1 hit paper
25 papers, 1.7k citations indexed

About

Bronwyn E. Grinton is a scholar working on Psychiatry and Mental health, Molecular Biology and Genetics. According to data from OpenAlex, Bronwyn E. Grinton has authored 25 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Psychiatry and Mental health, 12 papers in Molecular Biology and 11 papers in Genetics. Recurrent topics in Bronwyn E. Grinton's work include Epilepsy research and treatment (18 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Ion channel regulation and function (8 papers). Bronwyn E. Grinton is often cited by papers focused on Epilepsy research and treatment (18 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Ion channel regulation and function (8 papers). Bronwyn E. Grinton collaborates with scholars based in Australia, United States and United Kingdom. Bronwyn E. Grinton's co-authors include Peter H. Janssen, Paul Taylor, Michelle Sait, Ingrid E. Scheffer, Samuel F. Berkovic, John C. Mulley, Sarah E. Heron, Leanne M. Dibbens, Carla Marini and Karen Oliver and has published in prestigious journals such as Brain, Applied and Environmental Microbiology and Neurology.

In The Last Decade

Bronwyn E. Grinton

25 papers receiving 1.7k citations

Hit Papers

Improved Culturability of Soil Bacteria and Isolation in ... 2002 2026 2010 2018 2002 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bronwyn E. Grinton Australia 16 726 685 455 382 379 25 1.7k
Elizabeth A. Perry United States 16 382 0.5× 273 0.4× 138 0.3× 180 0.5× 91 0.2× 32 1.2k
Baojie Wang China 28 655 0.9× 78 0.1× 234 0.5× 278 0.7× 150 0.4× 176 2.3k
G. R. Wright Canada 13 72 0.1× 291 0.4× 180 0.4× 352 0.9× 188 0.5× 22 947
G.F. Wagner Canada 22 396 0.5× 745 1.1× 299 0.7× 561 1.5× 167 0.4× 40 2.4k
Edit Hermesz Hungary 20 844 1.2× 37 0.1× 237 0.5× 142 0.4× 263 0.7× 53 1.5k
J.R. Dick United Kingdom 24 386 0.5× 127 0.2× 92 0.2× 207 0.5× 111 0.3× 42 2.6k
Laurel Johnstone United States 17 285 0.4× 86 0.1× 259 0.6× 85 0.2× 81 0.2× 28 803
Enrica Capelli Italy 23 318 0.4× 532 0.8× 68 0.1× 202 0.5× 116 0.3× 78 1.5k
Lanlan Zhang China 23 352 0.5× 118 0.2× 104 0.2× 163 0.4× 30 0.1× 114 1.6k
Elżbieta Śliwerska United States 13 329 0.5× 36 0.1× 217 0.5× 235 0.6× 147 0.4× 18 1.0k

Countries citing papers authored by Bronwyn E. Grinton

Since Specialization
Citations

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

Fields of papers citing papers by Bronwyn E. Grinton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bronwyn E. Grinton. 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 Bronwyn E. Grinton. The network helps show where Bronwyn E. Grinton may publish in the future.

Co-authorship network of co-authors of Bronwyn E. Grinton

This figure shows the co-authorship network connecting the top 25 collaborators of Bronwyn E. Grinton. A scholar is included among the top collaborators of Bronwyn E. Grinton 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 Bronwyn E. Grinton. Bronwyn E. Grinton 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.
Oliver, Karen, et al.. (2024). Investigating the effect of polygenic background on epilepsy phenotype in ‘monogenic’ families. EBioMedicine. 109. 105404–105404. 5 indexed citations
2.
Oliver, Karen, Ingrid E. Scheffer, Mark F. Bennett, et al.. (2023). Genes4Epilepsy: An epilepsy gene resource. Epilepsia. 64(5). 1368–1375. 60 indexed citations
3.
Damiano, John A., Bronwyn E. Grinton, Patrick W. Carney, et al.. (2023). Recognition and epileptology of protracted CLN3 disease. Epilepsia. 64(7). 1833–1841. 2 indexed citations
4.
Grinton, Bronwyn E., Liam G. Fearnley, Ingrid E. Scheffer, et al.. (2022). A founder event causing a dominant childhood epilepsy survives 800 years through weak selective pressure. The American Journal of Human Genetics. 109(11). 2080–2087. 3 indexed citations
5.
Myers, Kenneth A., Mark F. Bennett, Bronwyn E. Grinton, et al.. (2021). Contribution of rare genetic variants to drug response in absence epilepsy. Epilepsy Research. 170. 106537–106537. 7 indexed citations
6.
Berecki, Géza, Katherine L. Helbig, Tyson L. Ware, et al.. (2020). Novel Missense CACNA1G Mutations Associated with Infantile-Onset Developmental and Epileptic Encephalopathy. International Journal of Molecular Sciences. 21(17). 6333–6333. 10 indexed citations
7.
Myers, Kenneth A., Margot J. Davey, Michael S. Ching, et al.. (2018). Randomized Controlled Trial of Melatonin for Sleep Disturbance in Dravet Syndrome: The DREAMS Study. Journal of Clinical Sleep Medicine. 14(10). 1697–1704. 20 indexed citations
8.
Puskarjov, Martin, Patricia Seja, Sarah E. Heron, et al.. (2014). A variant of KCC 2 from patients with febrile seizures impairs neuronal Cl extrusion and dendritic spine formation. EMBO Reports. 15(6). 723–729. 131 indexed citations
9.
Tomlinson, Susan E, Hugh Bostock, Bronwyn E. Grinton, et al.. (2012). In vivo loss of slow potassium channel activity in individuals with benign familial neonatal epilepsy in remission. Brain. 135(10). 3144–3152. 17 indexed citations
10.
Vears, Danya F., Meng‐Han Tsai, Lynette G. Sadleir, et al.. (2012). Clinical genetic studies in benign childhood epilepsy with centrotemporal spikes. Epilepsia. 53(2). 319–324. 41 indexed citations
11.
Mulley, John C., Ingrid E. Scheffer, Marta A. Bayly, et al.. (2011). Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypes. Epilepsia. 52(10). e139–e142. 7 indexed citations
12.
Crompton, Douglas E., Ingrid E. Scheffer, I Taylor, et al.. (2010). Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance. Brain. 133(11). 3221–3231. 60 indexed citations
13.
Heron, Sarah E., Ingrid E. Scheffer, Bronwyn E. Grinton, et al.. (2010). Familial neonatal seizures with intellectual disability caused by a microduplication of chromosome 2q24.3. Epilepsia. 51(9). 1865–1869. 24 indexed citations
14.
Herlenius, Eric, Sarah E. Heron, Bronwyn E. Grinton, et al.. (2007). SCN2A Mutations and Benign Familial Neonatal‐Infantile Seizures: The Phenotypic Spectrum. Epilepsia. 48(6). 1138–1142. 78 indexed citations
15.
Scheffer, Ingrid E., Louise A. Harkin, Bronwyn E. Grinton, et al.. (2006). Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations. Brain. 130(1). 100–109. 12 indexed citations
16.
Grinton, Bronwyn E., et al.. (2004). Liquid Serial Dilution Is Inferior to Solid Media for Isolation of Cultures Representative of the Phylum-Level Diversity of Soil Bacteria. Applied and Environmental Microbiology. 70(7). 4363–4366. 105 indexed citations
17.
Berkovic, Samuel F., Sarah E. Heron, Lucio Giordano, et al.. (2004). Benign familial neonatal‐infantile seizures: Characterization of a new sodium channelopathy. Annals of Neurology. 55(4). 550–557. 184 indexed citations
18.
Marini, Carla, Ingrid E. Scheffer, Bronwyn E. Grinton, et al.. (2004). Genetic Architecture of Idiopathic Generalized Epilepsy: Clinical Genetic Analysis of 55 Multiplex Families. Epilepsia. 45(5). 467–478. 92 indexed citations
19.
Mulley, John C., Bree Hodgson, Bronwyn E. Grinton, et al.. (2003). Sodium channel alpha-1 subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms. The American Journal of Human Genetics. 73(5). 11 indexed citations
20.
Sabaz, Mark, et al.. (2003). The health‐related quality of life of childhood epilepsy syndromes. Journal of Paediatrics and Child Health. 39(9). 690–696. 48 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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