Barbara Beyer

926 total citations
17 papers, 671 citations indexed

About

Barbara Beyer is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Barbara Beyer has authored 17 papers receiving a total of 671 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Cellular and Molecular Neuroscience, 15 papers in Molecular Biology and 3 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Barbara Beyer's work include Neuroscience and Neuropharmacology Research (15 papers), Ion channel regulation and function (9 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Barbara Beyer is often cited by papers focused on Neuroscience and Neuropharmacology Research (15 papers), Ion channel regulation and function (9 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Barbara Beyer collaborates with scholars based in United States, Australia and Belgium. Barbara Beyer's co-authors include Wayne N. Frankel, Verity A. Letts, Wayne N. Frankel, Connie L. Mahaffey, Bruce L. Tempel, H. Steve White, Wen Zhang, Matthew Peterson, Zhongwei Zhang and Rebecca M. Boumil and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Neuroscience and Human Molecular Genetics.

In The Last Decade

Barbara Beyer

17 papers receiving 663 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Barbara Beyer United States 14 391 385 265 178 127 17 671
Sibylle G. Schwab Germany 11 259 0.7× 122 0.3× 336 1.3× 121 0.7× 170 1.3× 14 609
Caroline M. Keeshen United States 6 245 0.6× 188 0.5× 184 0.7× 81 0.5× 166 1.3× 6 450
Carlotta E. Duncan Australia 9 359 0.9× 393 1.0× 91 0.3× 46 0.3× 186 1.5× 10 702
Élise Morice France 10 258 0.7× 264 0.7× 168 0.6× 34 0.2× 115 0.9× 13 575
Lisa M. Sharkey United States 15 532 1.4× 401 1.0× 122 0.5× 144 0.8× 24 0.2× 29 787
My Andersson Sweden 17 311 0.8× 468 1.2× 63 0.2× 90 0.5× 130 1.0× 31 726
Stacey B. B. Dutton United States 9 230 0.6× 295 0.8× 104 0.4× 289 1.6× 52 0.4× 10 512
Sofia Duarte Portugal 13 245 0.6× 136 0.4× 118 0.4× 26 0.1× 64 0.5× 22 450
Lynda El‐Hassar United States 9 173 0.4× 225 0.6× 56 0.2× 54 0.3× 128 1.0× 10 349
Heather McKellar United States 7 291 0.7× 233 0.6× 91 0.3× 36 0.2× 84 0.7× 7 474

Countries citing papers authored by Barbara Beyer

Since Specialization
Citations

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

Fields of papers citing papers by Barbara Beyer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Barbara Beyer

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

All Works

17 of 17 papers shown
1.
Asinof, Samuel K., Connie L. Mahaffey, Barbara Beyer, Wayne N. Frankel, & Rebecca M. Boumil. (2016). Dynamin 1 isoform roles in a mouse model of severe childhood epileptic encephalopathy. Neurobiology of Disease. 95. 1–11. 21 indexed citations
2.
Asinof, Samuel K., Stacey J. Sukoff Rizzo, Barbara Beyer, et al.. (2015). Independent Neuronal Origin of Seizures and Behavioral Comorbidities in an Animal Model of a Severe Childhood Genetic Epileptic Encephalopathy. PLoS Genetics. 11(6). e1005347–e1005347. 26 indexed citations
3.
Zhang, Wen, Matthew Peterson, Barbara Beyer, Wayne N. Frankel, & Zhongwei Zhang. (2014). Loss of MeCP2 From Forebrain Excitatory Neurons Leads to Cortical Hyperexcitation and Seizures. Journal of Neuroscience. 34(7). 2754–2763. 97 indexed citations
4.
Beyer, Barbara, Elena V. Gazina, Lisa Cordeiro, et al.. (2014). Physiological and genetic analysis of multiple sodium channel variants in a model of genetic absence epilepsy. Neurobiology of Disease. 67. 180–190. 17 indexed citations
5.
Frankel, Wayne N., et al.. (2014). Unraveling Genetic Modifiers in the Gria4 Mouse Model of Absence Epilepsy. PLoS Genetics. 10(7). e1004454–e1004454. 16 indexed citations
6.
Letts, Verity A., Barbara Beyer, & Wayne N. Frankel. (2014). Hidden in plain sight: spike‐wave discharges in mouse inbred strains. Genes Brain & Behavior. 13(6). 519–526. 31 indexed citations
7.
Tyler, Anna L., et al.. (2014). A genetic interaction network model of a complex neurological disease. Genes Brain & Behavior. 13(8). 831–840. 12 indexed citations
8.
Koleilat, Issam, et al.. (2013). Overexpression of RCAN1 isoform 4 in mouse neurons leads to a moderate behavioral impairment. Neurological Research. 35(1). 79–89. 9 indexed citations
9.
Papale, Ligia A., Barbara Beyer, Julie Miller Jones, et al.. (2009). Heterozygous mutations of the voltage-gated sodium channel SCN8A are associated with spike-wave discharges and absence epilepsy in mice. Human Molecular Genetics. 18(9). 1633–1641. 85 indexed citations
10.
Frankel, Wayne N., et al.. (2009). Szt2, a novel gene for seizure threshold in mice. Genes Brain & Behavior. 8(5). 568–576. 44 indexed citations
11.
Tokuda, Shinichi, Barbara Beyer, & Wayne N. Frankel. (2008). Genetic complexity of absence seizures in substrains of C3H mice. Genes Brain & Behavior. 8(3). 283–289. 9 indexed citations
12.
Beyer, Barbara, Charlotte Deleuze, Verity A. Letts, et al.. (2008). Absence seizures in C3H/HeJ and knockout mice caused by mutation of the AMPA receptor subunit Gria4. Human Molecular Genetics. 17(12). 1738–1749. 67 indexed citations
13.
Kearney, Jennifer A., Yan Yang, Barbara Beyer, et al.. (2006). Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2. Human Molecular Genetics. 15(6). 1043–1048. 55 indexed citations
14.
Frankel, Wayne N., Barbara Beyer, Christina R. Maxwell, et al.. (2005). Development of a New Genetic Model for Absence Epilepsy: Spike-Wave Seizures in C3H/He and Backcross Mice. Journal of Neuroscience. 25(13). 3452–3458. 28 indexed citations
15.
Letts, Verity A., Connie L. Mahaffey, Barbara Beyer, & Wayne N. Frankel. (2005). A targeted mutation in Cacng4 exacerbates spike-wave seizures in stargazer (Cacng2) mice. Proceedings of the National Academy of Sciences. 102(6). 2123–2128. 28 indexed citations
16.
Letts, Verity A., Myoung‐Goo Kang, Connie L. Mahaffey, et al.. (2003). Phenotypic heterogeneity in the stargazin allelic series. Mammalian Genome. 14(8). 506–513. 21 indexed citations
17.
Frankel, Wayne N., et al.. (2001). Electroconvulsive Thresholds of Inbred Mouse Strains. Genomics. 74(3). 306–312. 105 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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