Wendy S. Pratt

2.2k total citations
32 papers, 1.7k citations indexed

About

Wendy S. Pratt is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Wendy S. Pratt has authored 32 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 14 papers in Cellular and Molecular Neuroscience and 6 papers in Genetics. Recurrent topics in Wendy S. Pratt's work include Ion channel regulation and function (19 papers), Neuroscience and Neuropharmacology Research (12 papers) and Glycosylation and Glycoproteins Research (7 papers). Wendy S. Pratt is often cited by papers focused on Ion channel regulation and function (19 papers), Neuroscience and Neuropharmacology Research (12 papers) and Glycosylation and Glycoproteins Research (7 papers). Wendy S. Pratt collaborates with scholars based in United Kingdom, United States and France. Wendy S. Pratt's co-authors include Annette Dolphin, Dallas M. Swallow, Anthony Davies, Ivan Kadurin, James R. Gum, Laurent Ferron, Manuela Nieto‐Rostro, Leon Douglas, Jean‐Pierre Aubert and Shehrazade Dahimène and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Neuroscience.

In The Last Decade

Wendy S. Pratt

31 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Wendy S. Pratt United Kingdom 23 1.4k 670 215 201 197 32 1.7k
A. D. Strosberg France 28 1.3k 0.9× 587 0.9× 365 1.7× 146 0.7× 289 1.5× 66 2.4k
Ulla E. Petäjä‐Repo Finland 24 1.7k 1.2× 883 1.3× 216 1.0× 53 0.3× 459 2.3× 50 2.4k
Kenji Kangawa Japan 11 1.2k 0.8× 453 0.7× 142 0.7× 503 2.5× 138 0.7× 13 1.5k
K. Naito Japan 6 980 0.7× 446 0.7× 186 0.9× 114 0.6× 106 0.5× 14 1.5k
Elaine V. Hill United Kingdom 16 1.2k 0.8× 203 0.3× 126 0.6× 142 0.7× 102 0.5× 21 1.8k
Friederike Zunke Germany 22 778 0.6× 365 0.5× 898 4.2× 129 0.6× 559 2.8× 52 2.3k
Thierry Coppola France 27 1.7k 1.2× 950 1.4× 300 1.4× 198 1.0× 765 3.9× 46 2.7k
Sonia Terrillon United States 12 1.2k 0.8× 684 1.0× 67 0.3× 51 0.3× 110 0.6× 17 1.6k
Fabrice Vandeput United States 16 1.3k 0.9× 274 0.4× 74 0.3× 198 1.0× 63 0.3× 21 1.9k
Lisa Kockeritz Canada 9 1.4k 1.0× 563 0.8× 189 0.9× 104 0.5× 158 0.8× 10 2.2k

Countries citing papers authored by Wendy S. Pratt

Since Specialization
Citations

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

Fields of papers citing papers by Wendy S. Pratt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wendy S. Pratt. 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 Wendy S. Pratt. The network helps show where Wendy S. Pratt may publish in the future.

Co-authorship network of co-authors of Wendy S. Pratt

This figure shows the co-authorship network connecting the top 25 collaborators of Wendy S. Pratt. A scholar is included among the top collaborators of Wendy S. Pratt 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 Wendy S. Pratt. Wendy S. Pratt 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.
Dahimène, Shehrazade, Karen Page, Manuela Nieto‐Rostro, Wendy S. Pratt, & Annette Dolphin. (2023). The Interplay Between Splicing of Two Exon Combinations Differentially Affects Membrane Targeting and Function of Human CaV2.2. Function. 5(1). zqad060–zqad060. 2 indexed citations
2.
Giacalone, E., et al.. (2023). T-type Ca2+ and persistent Na+ currents synergistically elevate ventral, not dorsal, entorhinal cortical stellate cell excitability. Cell Reports. 42(7). 112699–112699. 1 indexed citations
3.
Dahimène, Shehrazade, Davor Lessel, Kjara S Pilch, et al.. (2022). Biallelic CACNA2D1 loss-of-function variants cause early-onset developmental epileptic encephalopathy. Brain. 145(8). 2721–2729. 29 indexed citations
4.
Dahimène, Shehrazade, Karen M. Page, Laurent Ferron, et al.. (2019). Disruption of the Key Ca2+ Binding Site in the Selectivity Filter of Neuronal Voltage-Gated Calcium Channels Inhibits Channel Trafficking. Cell Reports. 29(1). 22–33.e5. 16 indexed citations
5.
Nieto‐Rostro, Manuela, et al.. (2018). Ablation of α 2 δ-1 inhibits cell-surface trafficking of endogenous N-type calcium channels in the pain pathway in vivo. Proceedings of the National Academy of Sciences. 115(51). E12043–E12052. 52 indexed citations
6.
Dahimène, Shehrazade, et al.. (2016). A CaV2.1 N-terminal fragment relieves the dominant-negative inhibition by an Episodic ataxia 2 mutant. Neurobiology of Disease. 93. 243–256. 8 indexed citations
7.
Kadurin, Ivan, Laurent Ferron, Simon Rothwell, et al.. (2016). Proteolytic maturation of α2δ represents a checkpoint for activation and neuronal trafficking of latent calcium channels. eLife. 5. 42 indexed citations
8.
Pratt, Wendy S., Elliott Rees, Shehrazade Dahimène, et al.. (2015). Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders. Progress in Neurobiology. 134. 36–54. 157 indexed citations
9.
Lana, Beatrice, Bettina Schlick, Stuart Martin, et al.. (2013). Differential upregulation in DRG neurons of an α2δ-1 splice variant with a lower affinity for gabapentin after peripheral sensory nerve injury. Pain. 155(3). 522–533. 36 indexed citations
10.
Kadurin, Ivan, Anita Alvarez‐Laviada, Josephine Ng, et al.. (2012). Calcium Currents Are Enhanced by α2δ-1 Lacking Its Membrane Anchor. Journal of Biological Chemistry. 287(40). 33554–33566. 31 indexed citations
11.
Page, Karen M., Fay Heblich, Wojciech Margas, et al.. (2009). N Terminus Is Key to the Dominant Negative Suppression of CaV2 Calcium Channels. Journal of Biological Chemistry. 285(2). 835–844. 42 indexed citations
12.
Page, Karen M., et al.. (2008). Determinants of the voltage dependence of G protein modulation within calcium channel β subunits. Pflügers Archiv - European Journal of Physiology. 457(4). 743–756. 16 indexed citations
13.
Richards, Mark W., Jérôme Leroy, Wendy S. Pratt, & Annette Dolphin. (2007). The HOOK-Domain Between the SH3- and the GK-Domains of CaVβ Subunits Contains Key Determinants Controlling Calcium Channel Inactivation. Channels. 1(2). 92–101. 30 indexed citations
14.
Davies, Anthony, Leon Douglas, Jan Hendrich, et al.. (2006). The Calcium Channel α2δ-2 Subunit Partitions with CaV2.1 into Lipid Rafts in Cerebellum: Implications for Localization and Function. Journal of Neuroscience. 26(34). 8748–8757. 121 indexed citations
16.
Pratt, Wendy S., Suzanne Crawley, Jim Hicks, et al.. (2000). Multiple Transcripts of MUC3: Evidence for Two Genes, MUC3A and MUC3B. Biochemical and Biophysical Research Communications. 275(3). 916–923. 81 indexed citations
17.
Vinall, Lynne E., Alexander S. Hill, Pascal Pigny, et al.. (1998). Variable number tandem repeat polymorphism of the mucin genes located in the complex on 11p15.5. Human Genetics. 102(3). 357–366. 79 indexed citations
18.
Pratt, Wendy S., et al.. (1998). A microsatellite within the MUC1 locus at 1q21 is altered in the neoplastic cells of breast cancer patients. Cancer Genetics and Cytogenetics. 100(1). 63–67. 10 indexed citations
19.
Pigny, Pascal, Veronique Guyonnet‐Dupérat, Alexander S. Hill, et al.. (1996). Human Mucin Genes Assigned to 11p15.5: Identification and Organization of a Cluster of Genes. Genomics. 38(3). 340–352. 193 indexed citations
20.
Pratt, Wendy S., et al.. (1996). Two additional polymorphisms within the hypervariable MUC1 gene: association of alleles either side of the VNTR region. Annals of Human Genetics. 60(1). 21–28. 26 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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