Nicholas W. Plummer

3.6k total citations
41 papers, 2.7k citations indexed

About

Nicholas W. Plummer is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Nicholas W. Plummer has authored 41 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 17 papers in Cellular and Molecular Neuroscience and 6 papers in Neurology. Recurrent topics in Nicholas W. Plummer's work include Receptor Mechanisms and Signaling (9 papers), Neuroscience and Neuropharmacology Research (8 papers) and Ion channel regulation and function (8 papers). Nicholas W. Plummer is often cited by papers focused on Receptor Mechanisms and Signaling (9 papers), Neuroscience and Neuropharmacology Research (8 papers) and Ion channel regulation and function (8 papers). Nicholas W. Plummer collaborates with scholars based in United States, Canada and Brazil. Nicholas W. Plummer's co-authors include Miriam H. Meisler, Patricia Jensen, Douglas A. Marchuk, Sabrina D. Robertson, M.R. Smith, Alan L. Goldin, Jacqueline de Marchena, Daniel L. Burgess, Julie Miller Jones and David C. Kohrman and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Genetics.

In The Last Decade

Nicholas W. Plummer

39 papers receiving 2.6k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Nicholas W. Plummer 1.4k 1.1k 562 305 272 41 2.7k
Claudia A. Sailer 1.4k 1.0× 1.2k 1.1× 203 0.4× 183 0.6× 379 1.4× 17 2.1k
Osvaldo D. Uchitel 2.5k 1.8× 2.2k 1.9× 805 1.4× 310 1.0× 118 0.4× 112 3.7k
John E. McRory 2.5k 1.8× 2.5k 2.2× 192 0.3× 219 0.7× 342 1.3× 40 4.0k
Harriet Baker 926 0.7× 1.2k 1.1× 371 0.7× 172 0.6× 197 0.7× 48 2.2k
Geoffrey G. Murphy 1.9k 1.4× 2.0k 1.8× 465 0.8× 767 2.5× 168 0.6× 84 3.9k
Herman Moreno 2.0k 1.4× 1.6k 1.4× 165 0.3× 520 1.7× 325 1.2× 44 3.5k
Dane M. Chetkovich 2.1k 1.5× 2.7k 2.4× 255 0.5× 651 2.1× 168 0.6× 59 3.9k
Filippo Tempia 1.3k 0.9× 1.4k 1.3× 102 0.2× 527 1.7× 153 0.6× 75 2.5k
Amber L. Southwell 2.3k 1.6× 2.0k 1.8× 687 1.2× 99 0.3× 74 0.3× 48 3.2k
Pratap Meera 3.2k 2.3× 2.1k 1.9× 515 0.9× 176 0.6× 1.1k 4.2× 45 4.1k

Countries citing papers authored by Nicholas W. Plummer

Since Specialization
Citations

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

Fields of papers citing papers by Nicholas W. Plummer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nicholas W. Plummer. 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 Nicholas W. Plummer. The network helps show where Nicholas W. Plummer may publish in the future.

Co-authorship network of co-authors of Nicholas W. Plummer

This figure shows the co-authorship network connecting the top 25 collaborators of Nicholas W. Plummer. A scholar is included among the top collaborators of Nicholas W. Plummer 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 Nicholas W. Plummer. Nicholas W. Plummer 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.
Wilson, Leslie R., Nicholas W. Plummer, Irina Y. Evsyukova, et al.. (2023). Partial or Complete Loss of Norepinephrine Differentially Alters Contextual Fear and Catecholamine Release Dynamics in Hippocampal CA1. SHILAP Revista de lepidopterología. 4(1). 51–60. 3 indexed citations
2.
Sciolino, Natale R., Christopher M. Mazzone, Leslie R. Wilson, et al.. (2022). Natural locus coeruleus dynamics during feeding. Science Advances. 8(33). eabn9134–eabn9134. 26 indexed citations
3.
Waterhouse, Barry D., et al.. (2022). Probing the structure and function of locus coeruleus projections to CNS motor centers. Frontiers in Neural Circuits. 16. 895481–895481. 19 indexed citations
4.
Sciolino, Natale R., Nicholas W. Plummer, Daniel J. Lustberg, et al.. (2020). Elimination of galanin synthesis in noradrenergic neurons reduces galanin in select brain areas and promotes active coping behaviors. Brain Structure and Function. 225(2). 785–803. 28 indexed citations
5.
Plummer, Nicholas W., et al.. (2019). DEFiNE: A Method for Enhancement and Quantification of Fluorescently Labeled Axons. Frontiers in Neuroanatomy. 12. 117–117. 8 indexed citations
6.
Das, Manasmita, Esteban A. Oyarzabal, Qing Cheng, et al.. (2018). Genetic identification of a population of noradrenergic neurons implicated in attenuation of stress-related responses. Molecular Psychiatry. 24(5). 710–725. 23 indexed citations
7.
Sciolino, Natale R., Nicholas W. Plummer, Yuwei Chen, et al.. (2016). Recombinase-Dependent Mouse Lines for Chemogenetic Activation of Genetically Defined Cell Types. Cell Reports. 15(11). 2563–2573. 83 indexed citations
8.
Robertson, Sabrina D., Nicholas W. Plummer, & Patricia Jensen. (2015). Uncovering diversity in the development of central noradrenergic neurons and their efferents. Brain Research. 1641(Pt B). 234–244. 22 indexed citations
9.
Nagy, Gergő Attila, Gergő Botond, Zsolt Borhegyi, et al.. (2012). DAG‐sensitive and Ca2+ permeable TRPC6 channels are expressed in dentate granule cells and interneurons in the hippocampal formation. Hippocampus. 23(3). 221–232. 26 indexed citations
10.
Plummer, Nicholas W., Teresa L. Squire, Sudha Srinivasan, et al.. (2006). Neuronal expression of the Ccm2 gene in a new mouse model of cerebral cavernous malformations. Mammalian Genome. 17(2). 119–128. 50 indexed citations
11.
Meisler, Miriam H., Nicholas W. Plummer, Daniel L. Burgess, David A. Buchner, & Leslie K. Sprunger. (2004). Allelic mutations of the sodium channel SCN8A reveal multiple cellular and physiological functions. Genetica. 122(1). 37–45. 54 indexed citations
12.
Plummer, Nicholas W., Carol J. Gallione, Sudha Srinivasan, et al.. (2004). Loss of p53 Sensitizes Mice with a Mutation in Ccm1 (KRIT1) to Development of Cerebral Vascular Malformations. American Journal Of Pathology. 165(5). 1509–1518. 89 indexed citations
13.
Liquori, Christina L., Michel J. Berg, Adrian M. Siegel, et al.. (2003). Mutations in a Gene Encoding a Novel Protein Containing a Phosphotyrosine-Binding Domain Cause Type 2 Cerebral Cavernous Malformations. The American Journal of Human Genetics. 73(6). 1459–1464. 261 indexed citations
14.
Kearney, Jennifer A., Nicholas W. Plummer, M.R. Smith, et al.. (2001). A gain-of-function mutation in the sodium channel gene Scn2a results in seizures and behavioral abnormalities. Neuroscience. 102(2). 307–317. 183 indexed citations
15.
Plummer, Nicholas W. & Miriam H. Meisler. (1999). Evolution and Diversity of Mammalian Sodium Channel Genes. Genomics. 57(2). 323–331. 161 indexed citations
16.
Plummer, Nicholas W.. (1998). Neuronal sodium channel SCN8A: Genomic organization, alternative splicing, and role in neurological disease.. Deep Blue (University of Michigan). 1 indexed citations
17.
Plummer, Nicholas W., James R. Galt, Julie Miller Jones, et al.. (1998). Exon Organization, Coding Sequence, Physical Mapping, and Polymorphic Intragenic Markers for the Human Neuronal Sodium Channel GeneSCN8A. Genomics. 54(2). 287–296. 80 indexed citations
18.
Plummer, Nicholas W., Michael W. McBurney, & Miriam H. Meisler. (1997). Alternative Splicing of the Sodium Channel SCN8A Predicts a Truncated Two-domain Protein in Fetal Brain and Non-neuronal Cells. Journal of Biological Chemistry. 272(38). 24008–24015. 124 indexed citations
19.
Kohrman, David C., Nicholas W. Plummer, Timothy G. Schuster, et al.. (1995). Insertional mutation of the motor endplate disease (med) locus on mouse chromosome 15. Genomics. 26(2). 171–177. 43 indexed citations
20.
Burgess, Daniel L., David C. Kohrman, James R. Galt, et al.. (1995). Mutation of a new sodium channel gene, Scn8a, in the mouse mutant ‘motor endplate disease’. Nature Genetics. 10(4). 461–465. 255 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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