Kerrie D. Pierce

1.7k total citations
31 papers, 1.3k citations indexed

About

Kerrie D. Pierce is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Kerrie D. Pierce has authored 31 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 8 papers in Genetics. Recurrent topics in Kerrie D. Pierce's work include Ion channel regulation and function (7 papers), Receptor Mechanisms and Signaling (7 papers) and Neuroscience and Neuropharmacology Research (5 papers). Kerrie D. Pierce is often cited by papers focused on Ion channel regulation and function (7 papers), Receptor Mechanisms and Signaling (7 papers) and Neuroscience and Neuropharmacology Research (5 papers). Kerrie D. Pierce collaborates with scholars based in Australia, United States and Spain. Kerrie D. Pierce's co-authors include Peter R. Schofield, John Shine, Peter H. Barry, Lisa Selbie, Timothy J. Furlong, Sundran Rajendra, Chris French, Philip G. Board, Joseph W. Lynch and J W Lynch and has published in prestigious journals such as Journal of Biological Chemistry, Neuron and Journal of Neuroscience.

In The Last Decade

Kerrie D. Pierce

31 papers receiving 1.2k citations

Peers

Kerrie D. Pierce
Anti Kalda Estonia
Kerrie D. Pierce
Citations per year, relative to Kerrie D. Pierce Kerrie D. Pierce (= 1×) peers Anti Kalda

Countries citing papers authored by Kerrie D. Pierce

Since Specialization
Citations

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

Fields of papers citing papers by Kerrie D. Pierce

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kerrie D. Pierce. 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 Kerrie D. Pierce. The network helps show where Kerrie D. Pierce may publish in the future.

Co-authorship network of co-authors of Kerrie D. Pierce

This figure shows the co-authorship network connecting the top 25 collaborators of Kerrie D. Pierce. A scholar is included among the top collaborators of Kerrie D. Pierce 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 Kerrie D. Pierce. Kerrie D. Pierce 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.
Overs, Bronwyn J., Gloria Roberts, Claudio Toma, et al.. (2022). Epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorder. Translational Psychiatry. 12(1). 310–310. 7 indexed citations
2.
Overs, Bronwyn J., Rhoshel Lenroot, Gloria Roberts, et al.. (2021). Cortical mediation of relationships between dopamine receptor D2 and cognition is absent in youth at risk of bipolar disorder. Psychiatry Research Neuroimaging. 309. 111258–111258. 9 indexed citations
3.
Toma, Claudio, Alex D. Shaw, Richard J. N. Allcock, et al.. (2018). An examination of multiple classes of rare variants in extended families with bipolar disorder. Translational Psychiatry. 8(1). 65–65. 28 indexed citations
4.
Toma, Claudio, Kerrie D. Pierce, Alex D. Shaw, et al.. (2018). Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders. PLoS Genetics. 14(12). e1007535–e1007535. 31 indexed citations
5.
Salminen, Lauren E., Peter R. Schofield, Kerrie D. Pierce, et al.. (2017). Vulnerability of white matter tracts and cognition to the SOD2 polymorphism: A preliminary study of antioxidant defense genes in brain aging. Behavioural Brain Research. 329. 111–119. 12 indexed citations
6.
Salminen, Lauren E., Peter R. Schofield, Kerrie D. Pierce, et al.. (2015). Neuromarkers of the common angiotensinogen polymorphism in healthy older adults: A comprehensive assessment of white matter integrity and cognition. Behavioural Brain Research. 296. 85–93. 10 indexed citations
7.
Salminen, Lauren E., Peter R. Schofield, Kerrie D. Pierce, et al.. (2015). Genetic markers of cholesterol transport and gray matter diffusion: a preliminary study of the CETP I405V polymorphism. Journal of Neural Transmission. 122(11). 1581–1592. 3 indexed citations
8.
Salminen, Lauren E., Peter R. Schofield, Kerrie D. Pierce, et al.. (2014). Impact of the AGTR1 A1166C polymorphism on subcortical hyperintensities and cognition in healthy older adults. AGE. 36(4). 9664–9664. 10 indexed citations
9.
Salminen, Lauren E., Peter R. Schofield, Kerrie D. Pierce, et al.. (2013). Triallelic relationships between the serotonin transporter polymorphism and cognition among healthy older adults. International Journal of Neuroscience. 124(5). 331–338. 2 indexed citations
10.
Wilhelm, Kay, Philip B. Mitchell, Lesley V. Campbell, et al.. (2012). Association between serotonin transporter promoter polymorphisms and psychological distress in a diabetic population. Psychiatry Research. 200(2-3). 343–348. 13 indexed citations
11.
Bryant, Richard A., Kim L. Felmingham, Erin Falconer, et al.. (2010). Preliminary Evidence of the Short Allele of the Serotonin Transporter Gene Predicting Poor Response to Cognitive Behavior Therapy in Posttraumatic Stress Disorder. Biological Psychiatry. 67(12). 1217–1219. 80 indexed citations
12.
Morris, Renée, et al.. (2004). In vivo somatic delivery of plasmid DNA and retrograde transport to obtain cell‐specific gene expression in the central nervous system. Journal of Neurochemistry. 90(6). 1445–1452. 5 indexed citations
13.
Absalom, Nathan L., T. Lewis, Warren Kaplan, Kerrie D. Pierce, & Peter R. Schofield. (2003). Role of Charged Residues in Coupling Ligand Binding and Channel Activation in the Extracellular Domain of the Glycine Receptor. Journal of Biological Chemistry. 278(50). 50151–50157. 66 indexed citations
14.
Keramidas, Angelo, Andrew J. Moorhouse, Kerrie D. Pierce, Peter R. Schofield, & Peter H. Barry. (2002). Cation-selective Mutations in the M2 Domain of the Inhibitory Glycine Receptor Channel Reveal Determinants of Ion-Charge Selectivity. The Journal of General Physiology. 119(5). 393–410. 85 indexed citations
15.
Pierce, Kerrie D., et al.. (2001). A Nonsense Mutation in the α1 Subunit of the Inhibitory Glycine Receptor Associated with Bovine Myoclonus. Molecular and Cellular Neuroscience. 17(2). 354–363. 33 indexed citations
16.
Han, Nian-Lin Reena, et al.. (2001). The Surface Accessibility of the Glycine Receptor M2–M3 Loop Is Increased in the Channel Open State. Journal of Neuroscience. 21(8). 2589–2599. 54 indexed citations
17.
Lynch, Joseph W., Patrice Jacques, Kerrie D. Pierce, & Peter R. Schofield. (1998). Zinc Potentiation of the Glycine Receptor Chloride Channel Is Mediated by Allosteric Pathways. Journal of Neurochemistry. 71(5). 2159–2168. 55 indexed citations
18.
Rajendra, Sundran, Robert J. Vandenberg, Kerrie D. Pierce, et al.. (1995). The unique extracellular disulfide loop of the glycine receptor is a principal ligand binding element.. The EMBO Journal. 14(13). 2987–2998. 79 indexed citations
19.
Rajendra, Sundran, Joseph W. Lynch, Kerrie D. Pierce, et al.. (1995). Mutation of an arginine residue in the human glycine receptor transforms β-alanine and taurine from agonists into competitive antagonists. Neuron. 14(1). 169–175. 132 indexed citations
20.
Pierce, Kerrie D., Timothy J. Furlong, Lisa Selbie, & John Shine. (1992). Molecular cloning and expression of an adenosine A2b receptor from human brain. Biochemical and Biophysical Research Communications. 187(1). 86–93. 166 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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