James H. Eubanks

5.4k total citations
108 papers, 4.3k citations indexed

About

James H. Eubanks is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, James H. Eubanks has authored 108 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Molecular Biology, 47 papers in Cellular and Molecular Neuroscience and 43 papers in Genetics. Recurrent topics in James H. Eubanks's work include Neuroscience and Neuropharmacology Research (37 papers), Genetics and Neurodevelopmental Disorders (37 papers) and Autism Spectrum Disorder Research (24 papers). James H. Eubanks is often cited by papers focused on Neuroscience and Neuropharmacology Research (37 papers), Genetics and Neurodevelopmental Disorders (37 papers) and Autism Spectrum Disorder Research (24 papers). James H. Eubanks collaborates with scholars based in Canada, United States and China. James H. Eubanks's co-authors include Liang Zhang, Denis G.M. Jugloff, Benjamin Jung, Reiko Maki Fitzsimonds, Yukiko Asaka, Bing Ren, Emma Dempster, Wei Xie, Ah Young Lee and M. Christopher Wallace and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Neuroscience.

In The Last Decade

James H. Eubanks

108 papers receiving 4.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
James H. Eubanks Canada 37 2.5k 1.7k 1.2k 1.0k 290 108 4.3k
Zhi‐Qi Xiong China 33 1.8k 0.7× 1.0k 0.6× 1.6k 1.3× 527 0.5× 338 1.2× 94 4.0k
Maria Karayiorgou United States 34 2.9k 1.1× 1.6k 0.9× 1.5k 1.3× 981 0.9× 90 0.3× 63 5.5k
Maria Vincenza Catania Italy 41 1.9k 0.7× 814 0.5× 2.3k 1.9× 778 0.8× 522 1.8× 77 3.7k
Elisabetta Ciani Italy 37 1.7k 0.7× 1.5k 0.9× 808 0.7× 417 0.4× 303 1.0× 99 4.0k
Maria Passafaro Italy 36 2.8k 1.1× 678 0.4× 2.8k 2.3× 586 0.6× 364 1.3× 82 4.8k
Farahnaz Sananbenesi Germany 26 3.1k 1.2× 1.1k 0.6× 1.3k 1.1× 653 0.6× 561 1.9× 37 5.4k
Peter W. Vanderklish United States 35 2.3k 0.9× 802 0.5× 1.9k 1.6× 687 0.7× 429 1.5× 61 4.1k
Anne E. Anderson United States 33 2.8k 1.1× 612 0.4× 2.5k 2.1× 668 0.6× 277 1.0× 73 4.7k
Jinsoo Seo South Korea 29 3.0k 1.2× 834 0.5× 1.5k 1.3× 888 0.9× 728 2.5× 71 5.3k
Juan I. Young United States 32 2.3k 0.9× 1.7k 1.0× 347 0.3× 803 0.8× 178 0.6× 76 3.8k

Countries citing papers authored by James H. Eubanks

Since Specialization
Citations

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

Fields of papers citing papers by James H. Eubanks

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by James H. Eubanks. 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 James H. Eubanks. The network helps show where James H. Eubanks may publish in the future.

Co-authorship network of co-authors of James H. Eubanks

This figure shows the co-authorship network connecting the top 25 collaborators of James H. Eubanks. A scholar is included among the top collaborators of James H. Eubanks 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 James H. Eubanks. James H. Eubanks 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.
Arsenault, Jason, Shervin Gholizadeh, Tian Fook Kong, et al.. (2020). Interregulation between fragile X mental retardation protein and methyl CpG binding protein 2 in the mouse posterior cerebral cortex. Human Molecular Genetics. 29(23). 3744–3756. 9 indexed citations
2.
Song, Hongmei, Justin Z. Wang, Chiping Wu, et al.. (2018). Contributions of the Hippocampal CA3 Circuitry to Acute Seizures and Hyperexcitability Responses in Mouse Models of Brain Ischemia. Frontiers in Cellular Neuroscience. 12. 278–278. 11 indexed citations
3.
Galaverna, Renan, et al.. (2017). Telescoped continuous flow generation of a library of highly substituted 3-thio-1,2,4-triazoles. Reaction Chemistry & Engineering. 2(6). 896–907. 12 indexed citations
4.
Sheikh, Taimoor I., Juan Ausió, Josh Silver, et al.. (2016). From Function to Phenotype: Impaired DNA Binding and Clustering Correlates with Clinical Severity in Males with Missense Mutations in MECP2. Scientific Reports. 6(1). 38590–38590. 19 indexed citations
5.
Wither, Robert G., et al.. (2016). Prediction of antiepileptic drug treatment outcomes using machine learning. Journal of Neural Engineering. 14(1). 16002–16002. 22 indexed citations
6.
Li, Ran, et al.. (2015). Effects of neonatal hypoxic-ischemic episodes on late seizure outcomes in C57 black mice. Epilepsy Research. 111. 142–149. 9 indexed citations
7.
Wither, Robert G., et al.. (2012). Daily Rhythmic Behaviors and Thermoregulatory Patterns Are Disrupted in Adult Female MeCP2-Deficient Mice. PLoS ONE. 7(4). e35396–e35396. 37 indexed citations
8.
Kernohan, Kristin D., Yan Jiang, Deanna C. Tremblay, et al.. (2010). ATRX Partners with Cohesin and MeCP2 and Contributes to Developmental Silencing of Imprinted Genes in the Brain. Developmental Cell. 18(2). 191–202. 136 indexed citations
9.
Popescu, Andreea C., et al.. (2010). Aminoglycoside‐mediated partial suppression of MECP2 nonsense mutations responsible for Rett syndrome in vitro. Journal of Neuroscience Research. 88(11). 2316–2324. 37 indexed citations
10.
Thambirajah, Anita A., James H. Eubanks, & Juan Ausió. (2009). MeCP2 post‐translational regulation through PEST domains: two novel hypotheses. BioEssays. 31(5). 561–569. 23 indexed citations
11.
Jugloff, Denis G.M., Katleen Vandamme, Richard F. Logan, et al.. (2008). Targeted delivery of an Mecp2 transgene to forebrain neurons improves the behavior of female Mecp2-deficient mice. Human Molecular Genetics. 17(10). 1386–1396. 77 indexed citations
12.
Zhang, Liang, Ji-Wei He, Denis G.M. Jugloff, & James H. Eubanks. (2007). The MeCP2‐null mouse hippocampus displays altered basal inhibitory rhythms and is prone to hyperexcitability. Hippocampus. 18(3). 294–309. 120 indexed citations
13.
Jugloff, Denis G.M., Richard Logan, & James H. Eubanks. (2006). Breeding and maintenance of an Mecp2-deficient mouse model of Rett syndrome. Journal of Neuroscience Methods. 154(1-2). 89–95. 26 indexed citations
14.
Francis, Joseph, et al.. (2002). Kindling induces the mRNA expression of methyl DNA-binding factors in the adult rat hippocampus. Neuroscience. 113(1). 79–87. 13 indexed citations
15.
Jung, Benjamin, et al.. (2001). Somatostatin type 2 receptor expression in the rat hippocampus following cerebral ischemia. Neuroreport. 12(10). 2105–2109. 1 indexed citations
16.
Wei, Kuiru, James H. Eubanks, Joseph Francis, Zhengping Jia, & O. Carter Snead. (2001). Cloning and tissue distribution of a novel isoform of the rat GABABR1 receptor subunit. Neuroreport. 12(4). 833–837. 20 indexed citations
17.
Francis, Joseph, James H. Eubanks, & W. McIntyre Burnham. (2000). Diazepam-potentiated [3H]phenytoin binding is associated with peripheral-type benzodiazepine receptors and not with voltage-dependent sodium channels. Brain Research. 876(1-2). 131–140. 1 indexed citations
18.
19.
Bolino, Alessandra, Marco Seri, Francesco Caroli, et al.. (1998). Exclusion of the SCN2B gene as candidate for CMT4B. European Journal of Human Genetics. 6(6). 629–634. 1 indexed citations
20.
Puranam, Ram S., et al.. (1993). Chromosomal localization of gene for human glutamate receptor subunit-7. Somatic Cell and Molecular Genetics. 19(6). 581–588. 12 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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