Thomas J. Carney

4.3k total citations
58 papers, 2.9k citations indexed

About

Thomas J. Carney is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Thomas J. Carney has authored 58 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 18 papers in Cell Biology and 15 papers in Genetics. Recurrent topics in Thomas J. Carney's work include Zebrafish Biomedical Research Applications (11 papers), Developmental Biology and Gene Regulation (9 papers) and MicroRNA in disease regulation (7 papers). Thomas J. Carney is often cited by papers focused on Zebrafish Biomedical Research Applications (11 papers), Developmental Biology and Gene Regulation (9 papers) and MicroRNA in disease regulation (7 papers). Thomas J. Carney collaborates with scholars based in Singapore, United States and United Kingdom. Thomas J. Carney's co-authors include Robert N. Kelsh, Kirsten Dutton, Matthias Hammerschmidt, Stone Elworthy, Susana S. Lopes, Robert Geisler, Pascal Haffter, Angela Pauliny, Jimann Shin and Andrew J. Latimer and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

Thomas J. Carney

54 papers receiving 2.8k citations

Peers

Thomas J. Carney

GENET

Young‐Ki Bae South Korea

Jimann Shin United States

Tatjana Piotrowski United States

Heinz‐Georg Belting Switzerland

Adam V. Kwiatkowski United States

Kristen M. Kwan United States

Steffen Scholpp United Kingdom

Gaia Gestri United Kingdom

Debra L. Silver United States

Richard I. Dorsky United States

Young‐Ki Bae South Korea

Thomas J. Carney

1.6k ×1.0

835 ×0.8

237 ×0.5

GENET

262 ×0.6

306 ×0.9

Citations per year, relative to Thomas J. Carney Thomas J. Carney (= 1×) peers Young‐Ki Bae

Countries citing papers authored by Thomas J. Carney

Since Specialization

Citations

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

Fields of papers citing papers by Thomas J. Carney

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas J. Carney

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas J. Carney. A scholar is included among the top collaborators of Thomas J. Carney 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 J. Carney. Thomas J. Carney is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Subkhankulova, Tatiana, Л. А. Урошлев, Masataka Nikaido, et al.. (2023). Zebrafish pigment cells develop directly from persistent highly multipotent progenitors. Nature Communications. 14(1). 1258–1258. 26 indexed citations

Benard, Erica L., et al.. (2023). wnt10a is required for zebrafish median fin fold maintenance and adult unpaired fin metamorphosis. Developmental Dynamics. 253(6). 566–592.

Carney, Thomas J., et al.. (2022). Aerobic glycolysis is important for zebrafish larval wound closure and tail regeneration. Wound Repair and Regeneration. 30(6). 665–680. 17 indexed citations

Liu, Ranran, et al.. (2022). Transcriptome Profiling of Osteoblasts in a Medaka (Oryzias latipes) Osteoporosis Model Identifies Mmp13b as Crucial for Osteoclast Activation. Frontiers in Cell and Developmental Biology. 10. 775512–775512. 5 indexed citations

Mahabaleshwar, Harsha, Ser Sue Ng, Weibin Zhang, et al.. (2021). Matriptase activation of Gq drives epithelial disruption and inflammation via RSK and DUOX. eLife. 10. 7 indexed citations

Greaves, Sarah, Harsha Mahabaleshwar, Henry Roehl, et al.. (2021). Tetraspanin Cd9b and Cxcl12a/Cxcr4b have a synergistic effect on the control of collective cell migration. PLoS ONE. 16(11). e0260372–e0260372. 4 indexed citations

Lin, Qifeng, Yuji Matsuoka, Yilong Lian, et al.. (2019). Tracking genome-editing and associated molecular perturbations by SWATH mass spectrometry. Scientific Reports. 9(1). 15240–15240. 6 indexed citations

Carney, Thomas J., et al.. (2019). Fast and Sensitive Quantitative Phase Imaging Using a Frequency Comb. Conference on Lasers and Electro-Optics. 1 indexed citations

Carney, Thomas J. & Christian Mosimann. (2018). Switch and Trace: Recombinase Genetics in Zebrafish. Trends in Genetics. 34(5). 362–378. 43 indexed citations

10.

Roehl, Henry, et al.. (2017). Tetraspanins in zebrafish development. Mechanisms of Development. 145. S64–S65. 1 indexed citations

11.

Ratnayake, Ranjala, Pamela A. Havre, Nam H. Dang, et al.. (2016). Multidimensional Screening Platform for Simultaneously Targeting Oncogenic KRAS and Hypoxia-Inducible Factors Pathways in Colorectal Cancer. ACS Chemical Biology. 11(5). 1322–1331. 27 indexed citations

12.

Poon, Kar Lai, Xingang Wang, Wei Huang Goh, et al.. (2016). Humanizing the zebrafish liver shifts drug metabolic profiles and improves pharmacokinetics of CYP3A4 substrates. Archives of Toxicology. 91(3). 1187–1197. 25 indexed citations

13.

Fischer, Boris, Rebecca J. Richardson, Philipp Knyphausen, et al.. (2014). p53 and TAp63 Promote Keratinocyte Proliferation and Differentiation in Breeding Tubercles of the Zebrafish. PLoS Genetics. 10(1). e1004048–e1004048. 32 indexed citations

14.

Carney, Thomas J. & Philip W. Ingham. (2013). Drugging Hedgehog: signaling the pathway to translation. BMC Biology. 11(1). 37–37. 12 indexed citations

15.

Feitosa, Natália Martins, Jin-Li Zhang, Thomas J. Carney, et al.. (2012). Hemicentin 2 and Fibulin 1 are required for epidermal–dermal junction formation and fin mesenchymal cell migration during zebrafish development. Developmental Biology. 369(2). 235–248. 64 indexed citations

16.

Carney, Thomas J., Natália Martins Feitosa, C. Sonntag, et al.. (2010). Genetic Analysis of Fin Development in Zebrafish Identifies Furin and Hemicentin1 as Potential Novel Fraser Syndrome Disease Genes. PLoS Genetics. 6(4). e1000907–e1000907. 80 indexed citations

17.

Slanchev, Krasimir, Thomas J. Carney, Marc P. Stemmler, et al.. (2009). The Epithelial Cell Adhesion Molecule EpCAM Is Required for Epithelial Morphogenesis and Integrity during Zebrafish Epiboly and Skin Development. PLoS Genetics. 5(7). e1000563–e1000563. 117 indexed citations

18.

Dutton, James R., Anthony Antonellis, Thomas J. Carney, et al.. (2008). An evolutionarily conserved intronic region controls the spatiotemporal expression of the transcription factor Sox10. BMC Developmental Biology. 8(1). 105–105. 88 indexed citations

19.

Blentic, Aida, Panna Tandon, Jennifer Walshe, et al.. (2008). The emergence of ectomesenchyme. Developmental Dynamics. 237(3). 592–601. 59 indexed citations

20.

Takada, Norio, Andrew J. Latimer, Jimann Shin, et al.. (2006). In vivo time-lapse imaging shows dynamic oligodendrocyte progenitor behavior during zebrafish development. Nature Neuroscience. 9(12). 1506–1511. 316 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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