Thomas A. Drysdale

1.4k total citations
40 papers, 1.1k citations indexed

About

Thomas A. Drysdale is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Thomas A. Drysdale has authored 40 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 8 papers in Genetics and 4 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Thomas A. Drysdale's work include Congenital heart defects research (15 papers), Developmental Biology and Gene Regulation (10 papers) and Renal and related cancers (4 papers). Thomas A. Drysdale is often cited by papers focused on Congenital heart defects research (15 papers), Developmental Biology and Gene Regulation (10 papers) and Renal and related cancers (4 papers). Thomas A. Drysdale collaborates with scholars based in Canada, United States and Australia. Thomas A. Drysdale's co-authors include Paul A. Krieg, Richard P. Elinson, Kathryn F. Tonissen, Kristin D. Patterson, Richard P. Harvey, Thierry Lints, Steven Deimling, Michael J. Crawford, James R. Hammond and Todd Evans and has published in prestigious journals such as Development, Journal of Virology and Biochemical Journal.

In The Last Decade

Thomas A. Drysdale

40 papers receiving 1.1k 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 A. Drysdale Canada 21 797 239 152 124 106 40 1.1k
Houyan Song China 17 915 1.1× 299 1.3× 134 0.9× 120 1.0× 118 1.1× 59 1.4k
Sang Y. Chun United States 23 912 1.1× 332 1.4× 74 0.5× 80 0.6× 75 0.7× 32 2.2k
Eriko Koshimizu Japan 15 610 0.8× 304 1.3× 91 0.6× 147 1.2× 37 0.3× 51 994
Susumu Sekine Japan 18 844 1.1× 526 2.2× 113 0.7× 100 0.8× 119 1.1× 31 1.6k
Kenshiro Hara Japan 21 945 1.2× 385 1.6× 196 1.3× 108 0.9× 36 0.3× 57 1.7k
David J. Bernard United States 18 938 1.2× 147 0.6× 101 0.7× 357 2.9× 61 0.6× 33 1.8k
Olov Andersson Sweden 22 1.1k 1.4× 329 1.4× 522 3.4× 251 2.0× 62 0.6× 45 1.7k
Leslie F. Jackson United States 13 458 0.6× 139 0.6× 181 1.2× 91 0.7× 172 1.6× 16 1.2k
Sergio P. Acebrón Germany 16 1.3k 1.6× 230 1.0× 115 0.8× 226 1.8× 32 0.3× 22 1.6k
Christian Klausen Canada 29 1.0k 1.3× 297 1.2× 61 0.4× 70 0.6× 173 1.6× 72 2.1k

Countries citing papers authored by Thomas A. Drysdale

Since Specialization
Citations

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

Fields of papers citing papers by Thomas A. Drysdale

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas A. Drysdale

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas A. Drysdale. A scholar is included among the top collaborators of Thomas A. Drysdale 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 A. Drysdale. Thomas A. Drysdale 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.
Coffman, E. J., Heather L. Chandler, Zbyněk Kozmík, et al.. (2025). Shroom3 facilitates optic fissure closure via tissue alignment and reestablishment of apical-basal polarity during epithelial fusion. Developmental Biology. 522. 91–105. 1 indexed citations
2.
Lu, Xiangru, et al.. (2018). Sapropterin Treatment Prevents Congenital Heart Defects Induced by Pregestational Diabetes Mellitus in Mice. Journal of the American Heart Association. 7(21). e009624–e009624. 25 indexed citations
3.
Drysdale, Thomas A.. (2013). Helmet-to-Helmet Contact: Avoiding a Lifetime Penalty by Creating a Duty to Scan Active NFL Players for Chronic Traumatic Encephalopathy. Journal of Legal Medicine. 34(4). 425–452. 2 indexed citations
4.
Deimling, Steven & Thomas A. Drysdale. (2011). Fgf is required to regulate anterior–posterior patterning in the Xenopus lateral plate mesoderm. Mechanisms of Development. 128(7-10). 327–341. 21 indexed citations
5.
Deimling, Steven, et al.. (2011). Retinoic acid is a key regulatory switch determining the difference between lung and thyroid fates in Xenopus laevis. BMC Developmental Biology. 11(1). 75–75. 17 indexed citations
6.
Nascone‐Yoder, Nanette M., et al.. (2010). Direct activation of Shroom3 transcription by Pitx proteins drives epithelial morphogenesis in the developing gut. Development. 137(8). 1339–1349. 45 indexed citations
7.
Kennedy, Karen A., Scott D. Ryan, Feodor D. Price, et al.. (2009). Retinoic acid enhances skeletal muscle progenitor formation and bypasses inhibition by bone morphogenetic protein 4 but not dominant negative β-catenin. BMC Biology. 7(1). 67–67. 63 indexed citations
8.
Chandraratna, Roshantha A.S., Yong Zhao, Steven Deimling, et al.. (2006). Retinoic acid signaling is essential for formation of the heart tube in Xenopus. Developmental Biology. 291(1). 96–109. 34 indexed citations
9.
Marcucci, Katherine T., Stéphanie Cherqui, Andrea Szabó, et al.. (2006). Mice Transgenic for a Human Porcine Endogenous Retrovirus Receptor Are Susceptible to Productive Viral Infection. Journal of Virology. 80(10). 5100–5100. 1 indexed citations
10.
Duan, Li‐Juan, et al.. (2003). Expression of muscle LIM protein during early development in Xenopus laevis. The International Journal of Developmental Biology. 47(4). 299–302. 2 indexed citations
11.
Garriock, Robert J. & Thomas A. Drysdale. (2003). Regulation of heart size in Xenopus laevis. Differentiation. 71(8). 506–515. 5 indexed citations
12.
Duan, Li‐Juan, et al.. (2002). Developmental expression of cardiac myosin-binding protein C in Xenopus. Development Genes and Evolution. 212(1). 47–49. 1 indexed citations
13.
14.
15.
Patterson, Kristin D., Thomas A. Drysdale, & Paul A. Krieg. (2000). Embryonic origins of spleen asymmetry. Development. 127(1). 167–175. 27 indexed citations
16.
Jiang, Yongmei, Thomas A. Drysdale, & Todd Evans. (1999). A Role for GATA-4/5/6 in the Regulation of Nkx2.5 Expression with Implications for Patterning of the Precardiac Field. Developmental Biology. 216(1). 57–71. 53 indexed citations
17.
Drysdale, Thomas A., Kristin D. Patterson, Margaret S. Saha, & Paul A. Krieg. (1997). Retinoic Acid Can Block Differentiation of the Myocardium after Heart Specification. Developmental Biology. 188(2). 205–215. 50 indexed citations
18.
Drysdale, Thomas A. & Michael J. Crawford. (1994). Effects of Localized Application of Retinoic Acid on Xenopus laevis Development. Developmental Biology. 162(2). 394–401. 22 indexed citations
19.
Tonissen, Kathryn F., Thomas A. Drysdale, Thierry Lints, Richard P. Harvey, & Paul A. Krieg. (1994). XNkx-2.5, a Xenopus Gene Related to Nkx-2.5 and tinman: Evidence for a Conserved Role in Cardiac Development. Developmental Biology. 162(1). 325–328. 179 indexed citations
20.
Ringuette, Maurice, Thomas A. Drysdale, & Fina Liu. (1992). Expression and distribution of SPARC in early Xenopus laevis embryos. Development Genes and Evolution. 202(1). 4–9. 8 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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