Thomas Kidd

6.1k total citations · 3 hit papers
34 papers, 4.9k citations indexed

About

Thomas Kidd is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Developmental Neuroscience. According to data from OpenAlex, Thomas Kidd has authored 34 papers receiving a total of 4.9k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Cellular and Molecular Neuroscience, 20 papers in Molecular Biology and 15 papers in Developmental Neuroscience. Recurrent topics in Thomas Kidd's work include Axon Guidance and Neuronal Signaling (26 papers), Neurogenesis and neuroplasticity mechanisms (15 papers) and Nerve injury and regeneration (6 papers). Thomas Kidd is often cited by papers focused on Axon Guidance and Neuronal Signaling (26 papers), Neurogenesis and neuroplasticity mechanisms (15 papers) and Nerve injury and regeneration (6 papers). Thomas Kidd collaborates with scholars based in United States, United Kingdom and Canada. Thomas Kidd's co-authors include Corey S. Goodman, K Bland, Katja Brose, Marc Tessier‐Lavigne, William J. Henzel, Kuan Hong Wang, David Arnott, Guy Tear, Kevin J. Mitchell and Richard D. Fetter and has published in prestigious journals such as Science, Cell and Neuron.

In The Last Decade

Thomas Kidd

34 papers receiving 4.9k citations

Hit Papers

Slit Proteins Bind Robo Receptors and Have an Evolutionar... 1998 2026 2007 2016 1999 1999 1998 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas Kidd United States 19 4.2k 2.8k 1.8k 1.6k 141 34 4.9k
Jonathan A. Raper United States 38 5.0k 1.2× 3.1k 1.1× 1.7k 0.9× 2.0k 1.3× 186 1.3× 55 6.3k
Esther T. Stoeckli Switzerland 40 3.7k 0.9× 3.2k 1.2× 1.9k 1.1× 1.8k 1.1× 65 0.5× 101 5.8k
Artur Kania Canada 31 1.9k 0.5× 2.2k 0.8× 811 0.4× 1.1k 0.7× 92 0.7× 74 3.6k
Melitta Schachner Germany 43 3.1k 0.7× 2.6k 0.9× 1.8k 1.0× 1.7k 1.1× 47 0.3× 79 5.6k
Todd McLaughlin United States 21 2.6k 0.6× 1.7k 0.6× 697 0.4× 1.1k 0.7× 53 0.4× 30 3.3k
Domna Karagogeos Greece 34 2.0k 0.5× 2.4k 0.9× 1.2k 0.7× 1.1k 0.7× 46 0.3× 94 4.6k
Greg J. Bashaw United States 31 2.1k 0.5× 2.0k 0.7× 641 0.4× 1.0k 0.7× 54 0.4× 57 3.1k
Britta J. Eickholt Germany 34 1.7k 0.4× 2.2k 0.8× 528 0.3× 892 0.6× 69 0.5× 80 3.6k
Ruben Adler United States 44 3.1k 0.7× 4.8k 1.7× 826 0.5× 984 0.6× 103 0.7× 124 6.4k
Lynda Erskine United Kingdom 29 1.8k 0.4× 1.8k 0.7× 757 0.4× 719 0.5× 54 0.4× 50 2.9k

Countries citing papers authored by Thomas Kidd

Since Specialization
Citations

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

Fields of papers citing papers by Thomas Kidd

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Kidd

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Kidd. A scholar is included among the top collaborators of Thomas Kidd 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 Thomas Kidd. Thomas Kidd 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.
Kidd, Thomas & Timothy A. Evans. (2023). Collection, Fixation, and Antibody Staining ofDrosophilaEmbryos. Cold Spring Harbor Protocols. 2024(9). pdb.prot108116–pdb.prot108116. 2 indexed citations
2.
Mastick, Grant S., Lauren Jones, & Thomas Kidd. (2023). Axons will not be silenced! A balancing act of attractive receptors. Cell Reports. 42(5). 112493–112493. 1 indexed citations
3.
Kidd, Thomas & Timothy A. Evans. (2023). Analysis of Axon Guidance in theDrosophilaEmbryo. Cold Spring Harbor Protocols. 2024(9). pdb.top108109–pdb.top108109. 1 indexed citations
4.
Kidd, Thomas & Timothy A. Evans. (2023). Ventral Nerve Cord Dissection and Microscopy ofDrosophilaEmbryos. Cold Spring Harbor Protocols. 2024(9). pdb.prot108117–pdb.prot108117. 2 indexed citations
5.
Mastick, Grant S., et al.. (2020). Proteolytic cleavage of Slit by the Tolkin protease converts an axon repulsion cue to an axon growth cue in vivo. Development. 147(20). 6 indexed citations
6.
Kidd, Thomas, et al.. (2017). The WAGR syndrome gene PRRG4 is a functional homologue of the commissureless axon guidance gene. PLoS Genetics. 13(8). e1006865–e1006865. 36 indexed citations
7.
Song, Minmin, et al.. (2016). Dscam1 Forms a Complex with Robo1 and the N-Terminal Fragment of Slit to Promote the Growth of Longitudinal Axons. PLoS Biology. 14(9). e1002560–e1002560. 36 indexed citations
8.
Kidd, Thomas, et al.. (2015). Genetic Tools for the Analysis of Drosophila Stomatogastric Nervous System Development. PLoS ONE. 10(6). e0128290–e0128290. 8 indexed citations
9.
Erfurth, Maria‐Luise, Minmin Song, Rachel Bortnick, et al.. (2015). Slit and Receptor Tyrosine Phosphatase 69D Confer Spatial Specificity to Axon Branching via Dscam1. Cell. 162(5). 1140–1154. 57 indexed citations
10.
Clemens, James C., et al.. (2013). Blocking Apoptotic Signaling Rescues Axon Guidance in Netrin Mutants. Cell Reports. 3(3). 595–606. 20 indexed citations
11.
Kidd, Thomas, et al.. (2013). Control of Male and Female Fertility by the Netrin Axon Guidance Genes. PLoS ONE. 8(8). e72524–e72524. 10 indexed citations
12.
Cavalcanti, Francesca, Thomas Kidd, A. Patitucci, et al.. (2009). An Axon Regeneration Signature in a Charcot-Marie-Tooth Disease Type 2 Patient. Journal of Neurogenetics. 23(3). 324–328. 5 indexed citations
13.
Farmer, W. Todd, et al.. (2008). Pioneer longitudinal axons navigate using floor plate and Slit/Robo signals. Development. 135(22). 3643–3653. 56 indexed citations
14.
Andrews, Gracie L., W. Todd Farmer, Steves Morin, et al.. (2008). Dscam guides embryonic axons by Netrin-dependent and -independent functions. Development. 135(23). 3839–3848. 96 indexed citations
15.
Bashaw, Greg J., et al.. (2000). Repulsive Axon Guidance. Cell. 101(7). 703–715. 377 indexed citations
16.
Simpson, J., Thomas Kidd, K Bland, & Corey S. Goodman. (2000). Short-Range and Long-Range Guidance by Slit and Its Robo Receptors. Neuron. 28(3). 753–766. 201 indexed citations
17.
Wang, Kuan Hong, Katja Brose, David Arnott, et al.. (1999). Biochemical Purification of a Mammalian Slit Protein as a Positive Regulator of Sensory Axon Elongation and Branching. Cell. 96(6). 771–784. 400 indexed citations
18.
Nguyen-Ba-Charvet, Kim T., Katja Brose, Thomas Kidd, et al.. (1999). Slit2-Mediated Chemorepulsion and Collapse of Developing Forebrain Axons. Neuron. 22(3). 463–473. 232 indexed citations
19.
Chadwick, Brian P., Thomas Kidd, John Sgouros, David Ish‐Horowicz, & A.-M. Frischauf. (1999). Cloning, mapping and expression of UBL3, a novel ubiquitin-like gene. Gene. 233(1-2). 189–195. 12 indexed citations
20.
Kidd, Thomas, K Bland, & Corey S. Goodman. (1999). Slit Is the Midline Repellent for the Robo Receptor in Drosophila. Cell. 96(6). 785–794. 781 indexed citations breakdown →

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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