Susannah T. Bellows

2.7k total citations
21 papers, 644 citations indexed

About

Susannah T. Bellows is a scholar working on Psychiatry and Mental health, Genetics and Clinical Psychology. According to data from OpenAlex, Susannah T. Bellows has authored 21 papers receiving a total of 644 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Psychiatry and Mental health, 6 papers in Genetics and 4 papers in Clinical Psychology. Recurrent topics in Susannah T. Bellows's work include Epilepsy research and treatment (9 papers), Genomics and Rare Diseases (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Susannah T. Bellows is often cited by papers focused on Epilepsy research and treatment (9 papers), Genomics and Rare Diseases (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Susannah T. Bellows collaborates with scholars based in Australia, United States and United Kingdom. Susannah T. Bellows's co-authors include Samuel F. Berkovic, Ingrid E. Scheffer, Saul A. Mullen, Leanne M. Dibbens, Heather C. Mefford, Marta A. Bayly, Gemma L. Carvill, John C. Mulley, John A. Damiano and Michael S. Hildebrand and has published in prestigious journals such as Neurology, Annals of Neurology and Scientific Reports.

In The Last Decade

Susannah T. Bellows

20 papers receiving 617 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Susannah T. Bellows Australia 13 339 232 211 100 73 21 644
Jiong Qin China 12 119 0.4× 145 0.6× 158 0.7× 74 0.7× 82 1.1× 65 524
Svetlana Gataullina France 13 172 0.5× 135 0.6× 180 0.9× 137 1.4× 108 1.5× 22 527
Laurie E. Seltzer United States 9 143 0.4× 150 0.6× 185 0.9× 132 1.3× 96 1.3× 18 579
Alfredo D’Aniello Italy 15 99 0.3× 82 0.4× 356 1.7× 155 1.6× 208 2.8× 44 647
Kerry D. Conant United States 7 231 0.7× 157 0.7× 106 0.5× 18 0.2× 70 1.0× 8 492
C D Ferrie United Kingdom 8 49 0.1× 109 0.5× 305 1.4× 143 1.4× 216 3.0× 15 477
Marco Emili Italy 15 172 0.5× 185 0.8× 53 0.3× 65 0.7× 52 0.7× 27 520
Lori Christ United States 9 88 0.3× 111 0.5× 119 0.6× 154 1.5× 106 1.5× 25 454
Н. Н. Заваденко Russia 9 54 0.2× 62 0.3× 177 0.8× 37 0.4× 108 1.5× 138 413
Rolando Medina United States 14 147 0.4× 138 0.6× 122 0.6× 89 0.9× 14 0.2× 29 474

Countries citing papers authored by Susannah T. Bellows

Since Specialization
Citations

This map shows the geographic impact of Susannah T. Bellows'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 Susannah T. Bellows with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Susannah T. Bellows more than expected).

Fields of papers citing papers by Susannah T. Bellows

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Susannah T. Bellows. 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 Susannah T. Bellows. The network helps show where Susannah T. Bellows may publish in the future.

Co-authorship network of co-authors of Susannah T. Bellows

This figure shows the co-authorship network connecting the top 25 collaborators of Susannah T. Bellows. A scholar is included among the top collaborators of Susannah T. Bellows 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 Susannah T. Bellows. Susannah T. Bellows 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.
Anderson, Alison, Sarah Barnard, Emma Foster, et al.. (2025). Integrative Deep Learning of Genomic and Clinical Data for Predicting Treatment Response in Newly Diagnosed Epilepsy. Neurology. 105(10). e214315–e214315.
2.
Papadopoulos, Nicole, et al.. (2023). The feasibility and acceptability of AllPlay Dance for autistic children: A pilot randomised controlled trial. Research in autism spectrum disorders. 109. 102271–102271. 1 indexed citations
3.
Bellows, Susannah T., Elizabeth Westrupp, Mark G. Stokes, et al.. (2023). Longitudinal Associations Between COVID-19 Stress and the Mental Health of Children With ADHD. Journal of Attention Disorders. 27(10). 1065–1074. 9 indexed citations
4.
Papadopoulos, Nicole, Emma Sciberras, Harriet Hiscock, et al.. (2022). Sleeping Sound Autism Spectrum Disorder (ASD): a randomised controlled trial of a brief behavioural sleep intervention in primary school‐aged autistic children. Journal of Child Psychology and Psychiatry. 63(11). 1423–1433. 21 indexed citations
5.
Papadopoulos, Nicole, Matthew Fuller‐Tyszkiewicz, Emma Sciberras, et al.. (2022). Randomised Controlled Trial of a Behavioural Sleep Intervention, ‘Sleeping Sound’, for Autistic Children: 12-Month Outcomes and Moderators of Treatment. Journal of Autism and Developmental Disorders. 54(2). 442–457. 8 indexed citations
6.
Bennett, Mark F., Karen Oliver, Brigid M. Regan, et al.. (2020). Familial adult myoclonic epilepsy type 1 SAMD12 TTTCA repeat expansion arose 17,000 years ago and is present in Sri Lankan and Indian families. European Journal of Human Genetics. 28(7). 973–978. 22 indexed citations
7.
Ellis, Colin A., Leonid Churilov, Michael P. Epstein, et al.. (2019). Epilepsy in families: Age at onset is a familial trait, independent of syndrome. Annals of Neurology. 86(1). 91–98. 9 indexed citations
8.
Papadopoulos, Nicole, Emma Sciberras, Harriet Hiscock, et al.. (2019). Sleeping sound with autism spectrum disorder (ASD): study protocol for an efficacy randomised controlled trial of a tailored brief behavioural sleep intervention for ASD. BMJ Open. 9(11). e029767–e029767. 19 indexed citations
9.
Damiano, John A., Susannah T. Bellows, Ingrid E. Scheffer, et al.. (2017). Evaluation of GLUT1 variation in non-acquired focal epilepsy. Epilepsy Research. 133. 54–57. 5 indexed citations
10.
Perucca, Piero, Douglas E. Crompton, Susannah T. Bellows, et al.. (2017). Familial mesial temporal lobe epilepsy and the borderland of déjà vu. Annals of Neurology. 82(2). 166–176. 18 indexed citations
11.
Liu, Yu‐Chi, Susannah T. Bellows, John A. Damiano, et al.. (2016). Evaluation of non‐coding variation in GLUT1 deficiency. Developmental Medicine & Child Neurology. 58(12). 1295–1302. 20 indexed citations
12.
Corbett, Mark, Susannah T. Bellows, Melody Li, et al.. (2016). DominantKCNA2mutation causes episodic ataxia and pharmacoresponsive epilepsy. Neurology. 87(19). 1975–1984. 67 indexed citations
13.
Damiano, John A., Saul A. Mullen, Michael S. Hildebrand, et al.. (2015). Evaluation of multiple putative risk alleles within the 15q13.3 region for genetic generalized epilepsy. Epilepsy Research. 117. 70–73. 5 indexed citations
14.
Hildebrand, Michael S., A. Marie Phillips, Saul A. Mullen, et al.. (2015). Loss of synaptic Zn2+ transporter function increases risk of febrile seizures. Scientific Reports. 5(1). 17816–17816. 29 indexed citations
15.
Hildebrand, Michael S., John A. Damiano, Saul A. Mullen, et al.. (2014). Glucose metabolism transporters and epilepsy: Only GLUT1 has an established role. Epilepsia. 55(2). e18–21. 31 indexed citations
16.
Olson, DaiWai M., et al.. (2013). Interrater Reliability of the Bedside Shivering Assessment Scale. American Journal of Critical Care. 22(1). 70–74. 20 indexed citations
17.
Sadleir, Lynette G., E Chabrol, Eric Leguern, et al.. (2013). Seizure semiology in autosomal dominant epilepsy with auditory features, due to novel LGI1 mutations. Epilepsy Research. 107(3). 311–317. 11 indexed citations
18.
Kim, Young Ok, Susannah T. Bellows, Jacinta M. McMahon, et al.. (2013). Atypical multifocal Dravet syndrome lacks generalized seizures and may show later cognitive decline. Developmental Medicine & Child Neurology. 56(1). 85–90. 13 indexed citations
19.
Mulley, John C., Bree Hodgson, Jacinta M. McMahon, et al.. (2013). Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome. Epilepsia. 54(9). e122–6. 56 indexed citations
20.
Dibbens, Leanne M., Saul A. Mullen, Katherine L. Helbig, et al.. (2009). Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance. Human Molecular Genetics. 18(19). 3626–3631. 168 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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