David E. Krantz

5.5k total citations
81 papers, 3.9k citations indexed

About

David E. Krantz is a scholar working on Cellular and Molecular Neuroscience, Cell Biology and Molecular Biology. According to data from OpenAlex, David E. Krantz has authored 81 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Cellular and Molecular Neuroscience, 26 papers in Cell Biology and 25 papers in Molecular Biology. Recurrent topics in David E. Krantz's work include Neurobiology and Insect Physiology Research (32 papers), Cellular transport and secretion (22 papers) and Transcranial Magnetic Stimulation Studies (17 papers). David E. Krantz is often cited by papers focused on Neurobiology and Insect Physiology Research (32 papers), Cellular transport and secretion (22 papers) and Transcranial Magnetic Stimulation Studies (17 papers). David E. Krantz collaborates with scholars based in United States, France and Canada. David E. Krantz's co-authors include Robert H. Edwards, S Lawrence Zipursky, Kristin E. Larsen, David Sulzer, Rosemary Reinke, Yongjian Liu, Elizabeth S. Brooks, Hakeem O. Lawal, Aaron DiAntonio and Anne F. Simon and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

David E. Krantz

80 papers receiving 3.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David E. Krantz United States 34 2.2k 1.5k 841 768 434 81 3.9k
Esther Asan Germany 34 2.2k 1.0× 1.5k 1.0× 509 0.6× 395 0.5× 318 0.7× 73 3.9k
Sean T. Sweeney United Kingdom 29 2.3k 1.1× 2.0k 1.3× 1.3k 1.5× 244 0.3× 122 0.3× 78 4.3k
Paul M. Salvaterra United States 38 3.6k 1.7× 3.5k 2.3× 600 0.7× 277 0.4× 306 0.7× 72 6.5k
Wayne S. Sossin Canada 41 3.1k 1.4× 4.0k 2.6× 1.4k 1.7× 204 0.3× 263 0.6× 129 6.2k
Akinori Nishi Japan 43 3.4k 1.6× 4.0k 2.6× 886 1.1× 545 0.7× 238 0.5× 121 6.8k
Charles A. Greer United States 51 4.8k 2.2× 1.6k 1.1× 351 0.4× 155 0.2× 922 2.1× 157 7.9k
Bruce L. Tempel United States 36 3.8k 1.8× 4.6k 3.0× 318 0.4× 181 0.2× 232 0.5× 64 6.5k
J. Troy Littleton United States 46 4.2k 1.9× 4.9k 3.2× 3.9k 4.6× 421 0.5× 228 0.5× 120 7.4k
Milton P. Charlton Canada 40 4.0k 1.9× 3.9k 2.5× 1.6k 1.9× 475 0.6× 253 0.6× 93 5.9k
Pascal Steullet Switzerland 33 1.7k 0.8× 996 0.6× 258 0.3× 90 0.1× 465 1.1× 64 4.0k

Countries citing papers authored by David E. Krantz

Since Specialization
Citations

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

Fields of papers citing papers by David E. Krantz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David E. Krantz. 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 David E. Krantz. The network helps show where David E. Krantz may publish in the future.

Co-authorship network of co-authors of David E. Krantz

This figure shows the co-authorship network connecting the top 25 collaborators of David E. Krantz. A scholar is included among the top collaborators of David E. Krantz 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 David E. Krantz. David E. Krantz 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.
Sanfilippo, Piero, et al.. (2024). Constitutive and Conditional Epitope Tagging of Endogenous G-Protein–Coupled Receptors in Drosophila. Journal of Neuroscience. 44(33). e2377232024–e2377232024. 7 indexed citations
2.
Corlier, Juliana, Andrew Wilson, Scott A. Wilke, et al.. (2023). Pretreatment pupillary reactivity is associated with outcome of Repetitive Transcranial Magnetic Stimulation (rTMS) treatment of Major Depressive Disorder (MDD). Journal of Affective Disorders. 339. 412–417. 6 indexed citations
3.
Krantz, David E., et al.. (2023). Transcriptional changes in specific subsets of Drosophila neurons following inhibition of the serotonin transporter. Translational Psychiatry. 13(1). 226–226. 4 indexed citations
4.
Wilson, Andrew, Nicholas Jackson, David E. Krantz, et al.. (2023). A comparison of self- and observer-rated scales for detecting clinical improvement during repetitive transcranial stimulation (rTMS) treatment of depression. Psychiatry Research. 330. 115608–115608. 7 indexed citations
6.
Tadayonnejad, Reza, Andrew Wilson, Juliana Corlier, et al.. (2022). Use of right orbitofrontal repetitive transcranial magnetic stimulation (rTMS) augmentation for treatment-refractory obsessive-compulsive disorder with comorbid major depressive disorder. Psychiatry Research. 317. 114856–114856. 11 indexed citations
7.
Rosenberg, Benjamin M., Andrew F. Leuchter, David E. Krantz, et al.. (2022). Treatment of Spider Phobia Using Repeated Exposures and Adjunctive Repetitive Transcranial Magnetic Stimulation: A Proof-of-Concept Study. Frontiers in Psychiatry. 13. 823158–823158. 8 indexed citations
8.
Lee, Jonathan, Juliana Corlier, Andrew Wilson, et al.. (2021). Subthreshold stimulation intensity is associated with greater clinical efficacy of intermittent theta-burst stimulation priming for Major Depressive Disorder. Brain stimulation. 14(4). 1015–1021. 20 indexed citations
9.
Corlier, Juliana, Reza Tadayonnejad, Andrew Wilson, et al.. (2021). Repetitive transcranial magnetic stimulation treatment of major depressive disorder and comorbid chronic pain: response rates and neurophysiologic biomarkers. Psychological Medicine. 53(3). 823–832. 23 indexed citations
10.
Tadayonnejad, Reza, Andrew Wilson, Juliana Corlier, et al.. (2020). Sequential multi-locus transcranial magnetic stimulation for treatment of obsessive-compulsive disorder with comorbid major depression: A case series. Brain stimulation. 13(6). 1600–1602. 8 indexed citations
11.
Lee, Jonathan, Andrew Wilson, Juliana Corlier, et al.. (2020). Strategies for augmentation of high-frequency left-sided repetitive transcranial magnetic stimulation treatment of major depressive disorder. Journal of Affective Disorders. 277. 964–969. 15 indexed citations
12.
Corlier, Juliana, Andrew Wilson, Aimee M. Hunter, et al.. (2019). Changes in Functional Connectivity Predict Outcome of Repetitive Transcranial Magnetic Stimulation Treatment of Major Depressive Disorder. Cerebral Cortex. 29(12). 4958–4967. 48 indexed citations
13.
Grygoruk, Anna, Audrey Chen, Hakeem O. Lawal, et al.. (2014). The Redistribution ofDrosophilaVesicular Monoamine Transporter Mutants from Synaptic Vesicles to Large Dense-Core Vesicles Impairs Amine-Dependent Behaviors. Journal of Neuroscience. 34(20). 6924–6937. 23 indexed citations
14.
Leuchter, Andrew F., Aimee M. Hunter, David E. Krantz, & Ian A. Cook. (2014). Intermediate phenotypes and biomarkers of treatment outcome in major depressive disorder. Dialogues in Clinical Neuroscience. 16(4). 525–537. 28 indexed citations
15.
Chen, Audrey, Fanny Ng, Tim Lebestky, et al.. (2012). Dispensable, Redundant, Complementary, and Cooperative Roles of Dopamine, Octopamine, and Serotonin in Drosophila melanogaster. Genetics. 193(1). 159–176. 43 indexed citations
16.
Brooks, Elizabeth S., Christina Greer, Rafael Romero‐Calderón, et al.. (2011). A Putative Vesicular Transporter Expressed in Drosophila Mushroom Bodies that Mediates Sexual Behavior May Define a Neurotransmitter System. Neuron. 72(2). 316–329. 18 indexed citations
17.
Mosharov, Eugene V., Kristin E. Larsen, Ellen Kanter, et al.. (2009). Interplay between Cytosolic Dopamine, Calcium, and α-Synuclein Causes Selective Death of Substantia Nigra Neurons. Neuron. 62(2). 218–229. 420 indexed citations
18.
Hao, Fei, Anna Grygoruk, Elizabeth S. Brooks, Audrey Chen, & David E. Krantz. (2008). Trafficking of Vesicular Neurotransmitter Transporters. Traffic. 9(9). 1425–1436. 51 indexed citations
19.
Sang, Tzu‐Kang, Hui-Yun Chang, George Lawless, et al.. (2007). A Drosophila Model of Mutant Human Parkin-Induced Toxicity Demonstrates Selective Loss of Dopaminergic Neurons and Dependence on Cellular Dopamine. Journal of Neuroscience. 27(5). 981–992. 99 indexed citations
20.
Grygoruk, Anna, Elizabeth S. Brooks, Larry C. Ackerson, et al.. (2005). Overexpression of the Drosophila vesicular monoamine transporter increases motor activity and courtship but decreases the behavioral response to cocaine. Molecular Psychiatry. 11(1). 99–113. 89 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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