Bree Hodgson

2.6k total citations
15 papers, 792 citations indexed

About

Bree Hodgson is a scholar working on Molecular Biology, Psychiatry and Mental health and Genetics. According to data from OpenAlex, Bree Hodgson has authored 15 papers receiving a total of 792 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 8 papers in Psychiatry and Mental health and 6 papers in Genetics. Recurrent topics in Bree Hodgson's work include Epilepsy research and treatment (8 papers), Ion channel regulation and function (5 papers) and Ion Transport and Channel Regulation (4 papers). Bree Hodgson is often cited by papers focused on Epilepsy research and treatment (8 papers), Ion channel regulation and function (5 papers) and Ion Transport and Channel Regulation (4 papers). Bree Hodgson collaborates with scholars based in Australia, United States and United Kingdom. Bree Hodgson's co-authors include Samuel F. Berkovic, Ingrid E. Scheffer, Leanne M. Dibbens, John C. Mulley, Sarah E. Heron, Bronwyn E. Grinton, Louise A. Harkin, Lynette G. Sadleir, Ortrud K. Steinlein and Joanne Tracey Dean and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Annals of Neurology.

In The Last Decade

Bree Hodgson

15 papers receiving 781 citations

Peers

Bree Hodgson

PMH

GENET

CMN

PPCH

Keming Xu China

Isabelle An-Gourfinkel France

Amy McTague United Kingdom

Lata Vadlamudi Australia

Kerstin Hallmann Germany

Goryu Fukuma Japan

R. Anne Howell Australia

Sanjeev Rajakulendran United Kingdom

Maéva Langouët United States

Costin Leu United States

Keming Xu China

Bree Hodgson

274 ×0.6

PMH

355 ×0.9

166 ×0.5

GENET

307 ×1.1

CMN

79 ×0.7

PPCH

Citations per year, relative to Bree Hodgson Bree Hodgson (= 1×) peers Keming Xu

Countries citing papers authored by Bree Hodgson

Since Specialization

Citations

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

Fields of papers citing papers by Bree Hodgson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bree Hodgson

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

All Works

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15 of 15 papers shown

Carroll, Renée, Marie Shaw, Maria Arvio, et al.. (2020). Two novel intragenic variants in the FMR1 gene in patients with suspect clinical diagnosis of Fragile X syndrome and no CGG repeat expansion. European Journal of Medical Genetics. 63(10). 104010–104010. 4 indexed citations

Jasper, Melinda J., et al.. (2018). Combined PGD and PGS by NGS on the same biopsy using a single index. Reproductive BioMedicine Online. 36. e16–e17. 1 indexed citations

Scheffer, Ingrid E., Sarah E. Heron, Brigid M. Regan, et al.. (2014). Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations. Annals of Neurology. 75(5). 782–787. 159 indexed citations

Klein, Karl Martin, Catherine Bromhead, Katherine R. Smith, et al.. (2013). Autosomal dominant vasovagal syncope. Neurology. 80(16). 1485–1493. 17 indexed citations

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

Dibbens, Leanne M., Bree Hodgson, Katherine L. Helbig, et al.. (2012). Rare protein sequence variation in SV2A gene does not affect response to levetiracetam. Epilepsy Research. 101(3). 277–279. 9 indexed citations

Fullston, Tod, Merran Finnis, Anna Hackett, et al.. (2011). Screening and cell-based assessment of mutations in the Aristaless-related homeobox (ARX) gene. Clinical Genetics. 80(6). 510–522. 16 indexed citations

Mulley, John C., Xenia Iona, Bree Hodgson, et al.. (2011). The Role of Seizure-RelatedSEZ6as a Susceptibility Gene in Febrile Seizures. SHILAP Revista de lepidopterología. 2011. 1–4. 19 indexed citations

Dibbens, Leanne M., Christopher A. Reid, Bree Hodgson, et al.. (2009). Augmented currents of an HCN2 variant in patients with febrile seizure syndromes. Annals of Neurology. 67(4). 542–546. 82 indexed citations

10.

Dibbens, Leanne M., Louise A. Harkin, Bree Hodgson, et al.. (2009). The role of neuronal GABAA receptor subunit mutations in idiopathic generalized epilepsies. Neuroscience Letters. 453(3). 162–165. 31 indexed citations

11.

Hodgson, Bree, et al.. (2007). Is Photosensitive Epilepsy Less Common in Males Due to Variation in X Chromosome Photopigment Genes?. Epilepsia. 48(9). 1807–1809. 8 indexed citations

12.

Dibbens, Leanne M., Jenny Ekberg, I Taylor, et al.. (2007). NEDD4‐2 as a potential candidate susceptibility gene for epileptic photosensitivity. Genes Brain & Behavior. 6(8). 750–755. 44 indexed citations

13.

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

14.

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

15.

Wallace, Robyn H., Bree Hodgson, Bronwyn E. Grinton, et al.. (2003). Sodium channel α1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms. Neurology. 61(6). 765–769. 151 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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