Thomas C. Dockendorff

2.0k total citations
21 papers, 1.6k citations indexed

About

Thomas C. Dockendorff is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Thomas C. Dockendorff has authored 21 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 9 papers in Genetics and 5 papers in Plant Science. Recurrent topics in Thomas C. Dockendorff's work include Genetics and Neurodevelopmental Disorders (8 papers), RNA Research and Splicing (5 papers) and Nuclear Structure and Function (4 papers). Thomas C. Dockendorff is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), RNA Research and Splicing (5 papers) and Nuclear Structure and Function (4 papers). Thomas C. Dockendorff collaborates with scholars based in United States, Russia and Austria. Thomas C. Dockendorff's co-authors include Thomas A. Jongens, Charles N. Cole, Sean McBride, Catherine H. Choi, Kathleen K. Siwicki, Lili Wan, Gideon Dreyfuss, Yan Wang, Hanh T. Nguyen and Thomas V. McDonald and has published in prestigious journals such as Neuron, Journal of Neuroscience and The Journal of Cell Biology.

In The Last Decade

Thomas C. Dockendorff

21 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas C. Dockendorff United States 16 1.2k 834 361 209 188 21 1.6k
Steven M. Bray United States 14 683 0.6× 899 1.1× 326 0.9× 50 0.2× 601 3.2× 19 1.6k
Susan E. Swanberg United States 10 661 0.6× 810 1.0× 196 0.5× 86 0.4× 49 0.3× 13 973
Andrew J. Schroeder United States 14 997 0.8× 443 0.5× 64 0.2× 318 1.5× 480 2.6× 19 1.6k
Junhai Han China 20 483 0.4× 195 0.2× 117 0.3× 51 0.2× 506 2.7× 59 1.1k
Omer Durak United States 12 406 0.3× 273 0.3× 129 0.4× 40 0.2× 126 0.7× 14 721
Michael A. Crickmore United States 12 490 0.4× 244 0.3× 53 0.1× 66 0.3× 328 1.7× 15 826
Jianjun Sun United States 16 716 0.6× 254 0.3× 26 0.1× 120 0.6× 273 1.5× 39 1.2k
Chiou‐Fen Chuang United States 19 1.1k 0.9× 92 0.1× 87 0.2× 618 3.0× 288 1.5× 34 1.8k
László Tirián Austria 15 829 0.7× 357 0.4× 19 0.1× 366 1.8× 556 3.0× 22 1.5k
Yves Grau France 20 1.1k 0.9× 330 0.4× 60 0.2× 178 0.9× 970 5.2× 26 1.7k

Countries citing papers authored by Thomas C. Dockendorff

Since Specialization
Citations

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

Fields of papers citing papers by Thomas C. Dockendorff

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas C. Dockendorff

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas C. Dockendorff. A scholar is included among the top collaborators of Thomas C. Dockendorff 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 C. Dockendorff. Thomas C. Dockendorff 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.
Dockendorff, Thomas C., et al.. (2022). The nematode Oscheius tipulae as a genetic model for programmed DNA elimination. Current Biology. 32(23). 5083–5098.e6. 9 indexed citations
2.
Dockendorff, Thomas C. & Mariano Labrador. (2018). The Fragile X Protein and Genome Function. Molecular Neurobiology. 56(1). 711–721. 30 indexed citations
3.
Banerjee, Paromita, Brian P. Schoenfeld, Aaron Bell, et al.. (2010). Short- and Long-Term Memory Are Modulated by Multiple Isoforms of the Fragile X Mental Retardation Protein. Journal of Neuroscience. 30(19). 6782–6792. 44 indexed citations
4.
Bell, Aaron, Sean McBride, & Thomas C. Dockendorff. (2009). Flies as the ointment: Drosophila modeling to enhance drug discovery. Fly. 3(1). 39–49. 22 indexed citations
5.
Banerjee, Paromita, Sarita Hebbar, Catherine Fox, et al.. (2006). Substitution of Critical Isoleucines in the KH Domains of Drosophila Fragile X Protein Results in Partial Loss-of-Function Phenotypes. Genetics. 175(3). 1241–1250. 14 indexed citations
6.
McBride, Sean, Catherine H. Choi, Yan Wang, et al.. (2005). Pharmacological Rescue of Synaptic Plasticity, Courtship Behavior, and Mushroom Body Defects in a Drosophila Model of Fragile X Syndrome. Neuron. 45(5). 753–764. 367 indexed citations
7.
Costa, Alexandre Dias Tavares, Yan Wang, Thomas C. Dockendorff, et al.. (2005). The Drosophila Fragile X Protein Functions as a Negative Regulator in the orb Autoregulatory Pathway. Developmental Cell. 8(3). 331–342. 82 indexed citations
8.
Zarnescu, Daniela C., Peng Jin, Joerg Betschinger, et al.. (2005). Fragile X Protein Functions with Lgl and the PAR Complex in Flies and Mice. Developmental Cell. 8(1). 43–52. 64 indexed citations
9.
Dockendorff, Thomas C., Henry S. Su, Sean McBride, et al.. (2002). Drosophila Lacking dfmr1 Activity Show Defects in Circadian Output and Fail to Maintain Courtship Interest. Neuron. 34(6). 973–984. 238 indexed citations
10.
Wan, Lili, Thomas C. Dockendorff, Thomas A. Jongens, & Gideon Dreyfuss. (2000). Characterization of dFMR1, a Drosophila melanogaster Homolog of the Fragile X Mental Retardation Protein. Molecular and Cellular Biology. 20(22). 8536–8547. 225 indexed citations
11.
Dockendorff, Thomas C., et al.. (2000). Genetic characterization of the 44D-45B region of the Drosophila melanogaster genome based on an F2 lethal screen. Molecular and General Genetics MGG. 263(1). 137–143. 10 indexed citations
12.
Dockendorff, Thomas C., Zhenyu Tang, & Thomas A. Jongens. (1999). Cloning of karyopherin-α3 from Drosophila Through Its Interaction with the Nuclear Localization Sequence of Germ Cell-Less Protein. Biological Chemistry. 380(11). 1263–72. 15 indexed citations
14.
Dockendorff, Thomas C., et al.. (1998). Clonal analysis ofcmp44E, which encodes a conserved putative transmembrane protein, indicates a requirement for cell viability inDrosophila. Developmental Genetics. 23(4). 264–274. 12 indexed citations
15.
Heath, Catherine V., David C. Amberg, Thomas C. Dockendorff, et al.. (1995). Mutation or deletion of the Saccharomyces cerevisiae RAT3/NUP133 gene causes temperature-dependent nuclear accumulation of poly(A)+ RNA and constitutive clustering of nuclear pore complexes.. Molecular Biology of the Cell. 6(4). 401–417. 86 indexed citations
17.
Stacey, Gary, et al.. (1995). Signal exchange in the Bradyrhizobium-soybean symbiosis. Soil Biology and Biochemistry. 27(4-5). 473–483. 33 indexed citations
18.
Dockendorff, Thomas C.. (1994). Identification and Characterization of thenolYZGenes ofBradyrhizobium japonicum. Molecular Plant-Microbe Interactions. 7(2). 173–173. 15 indexed citations
19.
Dockendorff, Thomas C.. (1994). Nol A RepressesnodGene Expression inBradyrhizobium japonic urn. Molecular Plant-Microbe Interactions. 7(5). 596–596. 18 indexed citations
20.
Hooper, S W, Thomas C. Dockendorff, & Gary S. Sayler. (1989). Characteristics and restriction analysis of the 4-chlorobiphenyl catabolic plasmid, pSS50. Applied and Environmental Microbiology. 55(5). 1286–1288. 20 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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