Adriano Senatore

1.1k total citations
34 papers, 745 citations indexed

About

Adriano Senatore is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Paleontology. According to data from OpenAlex, Adriano Senatore has authored 34 papers receiving a total of 745 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 20 papers in Cellular and Molecular Neuroscience and 5 papers in Paleontology. Recurrent topics in Adriano Senatore's work include Ion channel regulation and function (18 papers), Neurobiology and Insect Physiology Research (12 papers) and Marine Invertebrate Physiology and Ecology (5 papers). Adriano Senatore is often cited by papers focused on Ion channel regulation and function (18 papers), Neurobiology and Insect Physiology Research (12 papers) and Marine Invertebrate Physiology and Ecology (5 papers). Adriano Senatore collaborates with scholars based in Canada, United States and United Kingdom. Adriano Senatore's co-authors include J. David Spafford, Carolyn L. Smith, Manfred Schmidt, Charles D. Derby, Thomas S. Reese, Adrienne N. Boone, Phuong Le, Paul S. Katz, Boris S. Zhorov and John S. Greenwood and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Neuroscience and PLoS ONE.

In The Last Decade

Adriano Senatore

31 papers receiving 737 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Adriano Senatore Canada 18 393 381 138 113 73 34 745
Barbara‐Anne Battelle United States 19 690 1.8× 677 1.8× 119 0.9× 80 0.7× 60 0.8× 40 1.1k
B.‐A. Battelle United States 18 687 1.7× 312 0.8× 178 1.3× 84 0.7× 100 1.4× 30 858
Atsuo Nishino Japan 16 238 0.6× 445 1.2× 43 0.3× 76 0.7× 43 0.6× 34 702
Ricardo M. Zayas United States 17 125 0.3× 894 2.3× 86 0.6× 173 1.5× 40 0.5× 31 1.1k
Jane A. Davies United Kingdom 14 368 0.9× 519 1.4× 52 0.4× 56 0.5× 47 0.6× 21 795
Blanca E. Galindo Mexico 11 188 0.5× 258 0.7× 56 0.4× 30 0.3× 91 1.2× 14 741
Jillian Henss United States 5 83 0.2× 370 1.0× 175 1.3× 45 0.4× 267 3.7× 6 796
Constance M. Smith United States 15 187 0.5× 494 1.3× 178 1.3× 32 0.3× 400 5.5× 24 1.3k
Elena E. Voronezhskaya Russia 21 712 1.8× 271 0.7× 345 2.5× 95 0.8× 587 8.0× 70 1.4k
Leonid P. Nezlin Russia 20 485 1.2× 191 0.5× 424 3.1× 91 0.8× 339 4.6× 41 1.2k

Countries citing papers authored by Adriano Senatore

Since Specialization
Citations

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

Fields of papers citing papers by Adriano Senatore

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Adriano Senatore

This figure shows the co-authorship network connecting the top 25 collaborators of Adriano Senatore. A scholar is included among the top collaborators of Adriano Senatore 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 Adriano Senatore. Adriano Senatore 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.
Erclik, Ted, et al.. (2024). Mint/X11 PDZ domains from non-bilaterian animals recognize and bind CaV2 calcium channel C-termini in vitro. Scientific Reports. 14(1). 21615–21615.
2.
Yáñez-Guerra, Luis Alfonso, et al.. (2023). Function and phylogeny support the independent evolution of an ASIC-like Deg/ENaC channel in the Placozoa. Communications Biology. 6(1). 951–951. 13 indexed citations
3.
Boulet, Aren, Nicholas J. Lowe, Jiashu Liu, et al.. (2021). Homeostatic control of nuclear-encoded mitochondrial gene expression by the histone variant H2A.Z is essential for neuronal survival. Cell Reports. 36(11). 109704–109704. 9 indexed citations
4.
Piekut, Thomas, Sarah E. Walker, Carolyn L. Smith, et al.. (2020). Early Metazoan Origin and Multiple Losses of a Novel Clade of RIM Presynaptic Calcium Channel Scaffolding Protein Homologs. Genome Biology and Evolution. 12(8). 1217–1239. 9 indexed citations
5.
Walker, Sarah E., Adriano Senatore, Robert L. Carlone, & Gaynor E. Spencer. (2020). Context-Dependent Role of miR-124 in Retinoic Acid-Induced Growth Cone Attraction of Regenerating Motorneurons. Cellular and Molecular Neurobiology. 42(3). 847–869. 5 indexed citations
6.
Pawar, Shrikant, et al.. (2020). Comparison of transcriptomes from two chemosensory organs in four decapod crustaceans reveals hundreds of candidate chemoreceptor proteins. PLoS ONE. 15(3). e0230266–e0230266. 45 indexed citations
7.
Piekut, Thomas, et al.. (2020). Conserved biophysical features of the CaV2 presynaptic Ca2+ channel homologue from the early-diverging animal Trichoplax adhaerens. Journal of Biological Chemistry. 295(52). 18553–18578. 8 indexed citations
8.
9.
Smith, Carolyn L., Phuong Le, Liana Artinian, et al.. (2017). Evolutionary insights into T-type Ca2+ channel structure, function, and ion selectivity from the Trichoplax adhaerens homologue. The Journal of General Physiology. 149(4). 483–510. 23 indexed citations
10.
11.
Senatore, Adriano, et al.. (2015). Identification of genes related to learning and memory in the brain transcriptome of the mollusc,Hermissenda crassicornis. Learning & Memory. 22(12). 617–621. 13 indexed citations
12.
Senatore, Adriano, et al.. (2014). Cav3 T-type channels: regulators for gating, membrane expression, and cation selectivity. Pflügers Archiv - European Journal of Physiology. 466(4). 645–660. 21 indexed citations
13.
Boone, Adrienne N., Adriano Senatore, Joshua Piticaru, et al.. (2014). Gene Splicing of an Invertebrate Beta Subunit (LCavβ) in the N-Terminal and HOOK Domains and Its Regulation of LCav1 and LCav2 Calcium Channels. PLoS ONE. 9(4). e92941–e92941. 12 indexed citations
14.
Senatore, Adriano, et al.. (2014). T-type Channels Become Highly Permeable to Sodium Ions Using an Alternative Extracellular Turret Region (S5-P) Outside the Selectivity Filter. Journal of Biological Chemistry. 289(17). 11952–11969. 24 indexed citations
15.
Boone, Adrienne N., et al.. (2013). The Calmodulin-Binding, Short Linear Motif, NSCaTE Is Conserved in L-Type Channel Ancestors of Vertebrate Cav1.2 and Cav1.3 Channels. PLoS ONE. 8(4). e61765–e61765. 36 indexed citations
16.
17.
Senatore, Adriano, et al.. (2011). Mapping of dihydropyridine binding residues in a less sensitive invertebrate L-type calcium channel (LCav1). Channels. 5(2). 173–187. 22 indexed citations
18.
Senatore, Adriano, Adrienne N. Boone, & J. David Spafford. (2011). Optimized Transfection Strategy for Expression and Electrophysiological Recording of Recombinant Voltage-Gated Ion Channels in HEK-293T Cells. Journal of Visualized Experiments. 8 indexed citations
19.
Senatore, Adriano, Adrienne N. Boone, & J. David Spafford. (2011). Optimized Transfection Strategy for Expression and Electrophysiological Recording of Recombinant Voltage-Gated Ion Channels in HEK-293T Cells. Journal of Visualized Experiments. 19 indexed citations
20.
Zhang, Yalan, et al.. (2008). PKC-Induced Intracellular Trafficking of CaV2 Precedes Its Rapid Recruitment to the Plasma Membrane. Journal of Neuroscience. 28(10). 2601–2612. 29 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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