Elise Brimble

712 total citations
25 papers, 340 citations indexed

About

Elise Brimble is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Elise Brimble has authored 25 papers receiving a total of 340 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 10 papers in Genetics and 5 papers in Cell Biology. Recurrent topics in Elise Brimble's work include Genetics and Neurodevelopmental Disorders (7 papers), Genomics and Rare Diseases (5 papers) and Endoplasmic Reticulum Stress and Disease (5 papers). Elise Brimble is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Genomics and Rare Diseases (5 papers) and Endoplasmic Reticulum Stress and Disease (5 papers). Elise Brimble collaborates with scholars based in United States, Canada and Italy. Elise Brimble's co-authors include Jeffrey G. Dickhout, Rachel E. Carlisle, Alistair J. Ingram, Kjetil Ask, Richard C. Austin, Maura Ruzhnikov, Šárka Lhoták, Stephen Colgan, Sudesh K. Sood and Limin Liu and has published in prestigious journals such as Nature Communications, Journal of Clinical Oncology and Blood.

In The Last Decade

Elise Brimble

20 papers receiving 339 citations

Peers

Elise Brimble

EPIDE

GENET

NEPHR

Beatrice Paola Festa Switzerland

Zhuohua Zhang China

Haofeng Huang China

Hirotake Sawada Japan

Ines Martin Padura Italy

Sandra M. Soares United States

Boris Pantic Italy

Hongbin Luo China

Anna Hammer Germany

Beatrice Paola Festa Switzerland

Elise Brimble

153 ×1.0

59 ×0.5

81 ×1.2

EPIDE

36 ×0.7

GENET

25 ×0.6

NEPHR

Citations per year, relative to Elise Brimble Elise Brimble (= 1×) peers Beatrice Paola Festa

Countries citing papers authored by Elise Brimble

Since Specialization

Citations

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

Fields of papers citing papers by Elise Brimble

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elise Brimble

This figure shows the co-authorship network connecting the top 25 collaborators of Elise Brimble. A scholar is included among the top collaborators of Elise Brimble 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 Elise Brimble. Elise Brimble 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

Kaufman, Michael C., Shridhar Parthasarathy, Julie Xian, et al.. (2025). Deciphering the Natural History of SCN8A -Related Disorders. Neurology. 104(9). e213533–e213533. 1 indexed citations

Li, Liwen, Seon‐Ung Hwang, HJ Lee, et al.. (2025). The patient-specific mouse model with Foxg1 frameshift mutation provides insights into the pathophysiology of FOXG1 syndrome. Nature Communications. 16(1). 4760–4760. 2 indexed citations

Schmidt, James J., Jeanselle Dea, Elise Brimble, et al.. (2025). Autism gene variants disrupt enteric neuron migration and cause gastrointestinal dysmotility. Nature Communications. 16(1). 2238–2238. 4 indexed citations

Brimble, Elise, Pamela Ventola, Christopher E. Hart, et al.. (2025). Longitudinal characterization of clinical, developmental, and behavioral phenotypes in 101 children and adults with FOXG1 syndrome. Journal of Neurodevelopmental Disorders. 17(1). 64–64.

McKee, Jillian L., Julie Xian, Abiola Harrison, et al.. (2025). Clinical signatures of SYNGAP1-related disorders through data integration. Genetics in Medicine. 27(6). 101419–101419.

Brimble, Elise, et al.. (2024). Comprehensive phenotypes of patients with SYNGAP1‐related disorder reveals high rates of epilepsy and autism. Epilepsia. 65(5). 1428–1438. 7 indexed citations

Brimble, Elise, et al.. (2024). Validation and clinical discovery demonstration of breast cancer data from a real-world data extraction platform. JAMIA Open. 7(2).

Brimble, Elise, Orrin Devinsky, Maura Ruzhnikov, et al.. (2023). Expanding genotype–phenotype correlations in FOXG1 syndrome: results from a patient registry. Orphanet Journal of Rare Diseases. 18(1). 149–149. 7 indexed citations

Martin, Richard L., et al.. (2023). Real-World Patterns of MRD Testing and Impact on Treatment for Chronic Lymphocytic Leukemia Patients. Blood. 142(Supplement 1). 6527–6527.

10.

Brown, Tanya L., et al.. (2023). Characterizing a rare neurogenetic disease, SLC13A5 citrate transporter disorder, utilizing clinical data in a cloud-based medical record collection system. Frontiers in Genetics. 14. 1109547–1109547. 9 indexed citations

11.

Xian, Julie, Jillian L. McKee, Elise Brimble, et al.. (2023). Delineating clinical and developmental outcomes in STXBP1-related disorders. Brain. 146(12). 5182–5197. 13 indexed citations

12.

Javle, Milind, Mitesh J. Borad, Nilofer S. Azad, et al.. (2023). A novel patient-centric longitudinal data registry platform to generate insights into real-world cholangiocarcinoma (CCA) clinical practice.. Journal of Clinical Oncology. 41(16_suppl). 4084–4084.

13.

Carlisle, Rachel E., et al.. (2021). Inhibition of histone deacetylation with vorinostat does not prevent tunicamycin-mediated acute kidney injury. PLoS ONE. 16(11). e0260519–e0260519. 3 indexed citations

14.

Ng, Bobby G., Hassan Dastsooz, Parham Habibzadeh, et al.. (2020). Expanding the molecular and clinical phenotypes of FUT8‐CDG. Journal of Inherited Metabolic Disease. 43(4). 871–879. 27 indexed citations

15.

Reuter, Chloe M., Elise Brimble, Annika M. Dries, et al.. (2018). A New Approach to Rare Diseases of Children: The Undiagnosed Diseases Network. The Journal of Pediatrics. 196. 291–297.e2. 11 indexed citations

16.

Carlisle, Rachel E., Chao Lü, Elise Brimble, et al.. (2016). Endoplasmic reticulum stress inhibition limits the progression of chronic kidney disease in the Dahl salt-sensitive rat. American Journal of Physiology-Renal Physiology. 312(1). F230–F244. 30 indexed citations

17.

Khattak, Shahryar, Elise Brimble, Kirill Zaslavsky, et al.. (2015). Human induced pluripotent stem cell derived neurons as a model for Williams-Beuren syndrome. Molecular Brain. 8(1). 77–77. 33 indexed citations

18.

Carlisle, Rachel E., et al.. (2014). 4-Phenylbutyrate Inhibits Tunicamycin-Induced Acute Kidney Injury via CHOP/GADD153 Repression. PLoS ONE. 9(1). e84663–e84663. 81 indexed citations

19.

Brimble, Elise, et al.. (2013). The HDAC inhibitor, vorinastat, prevents TGF‐β1 induced EMT and apoptosis in human renal proximal tubular cells. The FASEB Journal. 27(S1). 1 indexed citations

20.

Carlisle, Rachel E., Elise Brimble, Limin Liu, et al.. (2012). TDAG51 mediates epithelial-to-mesenchymal transition in human proximal tubular epithelium. American Journal of Physiology-Renal Physiology. 303(3). F467–F481. 42 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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