Amy K. Sater

2.8k total citations
40 papers, 1.5k citations indexed

About

Amy K. Sater is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Amy K. Sater has authored 40 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Amy K. Sater's work include Developmental Biology and Gene Regulation (19 papers), Congenital heart defects research (5 papers) and Neurobiology and Insect Physiology Research (5 papers). Amy K. Sater is often cited by papers focused on Developmental Biology and Gene Regulation (19 papers), Congenital heart defects research (5 papers) and Neurobiology and Insect Physiology Research (5 papers). Amy K. Sater collaborates with scholars based in United States, United Kingdom and Belgium. Amy K. Sater's co-authors include Antone G. Jacobson, Ray Keller, John Shih, Richard A. Steinhardt, Aarti R. Uzgare, J. Akif Uzman, Pierre D. McCrea, Hong Ji, Mousumi Goswami and Christopher M. Spring and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Nature Cell Biology.

In The Last Decade

Amy K. Sater

40 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
Amy K. Sater United States 19 1.2k 315 291 211 83 40 1.5k
R. Bodmer United States 11 1.3k 1.0× 211 0.7× 249 0.9× 401 1.9× 62 0.7× 14 1.5k
Stefan Hoppler United Kingdom 24 2.1k 1.7× 194 0.6× 405 1.4× 218 1.0× 46 0.6× 45 2.4k
Raymond Keller United States 13 1.3k 1.1× 834 2.6× 260 0.9× 239 1.1× 86 1.0× 15 1.9k
Zacharias Kontarakis Germany 16 1.7k 1.4× 587 1.9× 479 1.6× 179 0.8× 51 0.6× 26 2.3k
Adrian W. Moore Japan 20 1.5k 1.2× 416 1.3× 376 1.3× 675 3.2× 76 0.9× 45 2.2k
Anne K. Knecht United States 10 976 0.8× 137 0.4× 379 1.3× 130 0.6× 58 0.7× 12 1.4k
Krzysztof Jagla France 28 1.9k 1.5× 338 1.1× 414 1.4× 580 2.7× 49 0.6× 75 2.4k
Marcos Simões-Costa United States 24 1.6k 1.3× 205 0.7× 412 1.4× 143 0.7× 119 1.4× 46 2.2k
Paul A. Morcos United States 18 1.5k 1.2× 692 2.2× 322 1.1× 150 0.7× 37 0.4× 21 2.3k
Gerd-Jörg Rauch Germany 15 2.6k 2.1× 1.0k 3.2× 436 1.5× 249 1.2× 118 1.4× 16 3.0k

Countries citing papers authored by Amy K. Sater

Since Specialization
Citations

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

Fields of papers citing papers by Amy K. Sater

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Amy K. Sater. 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 Amy K. Sater. The network helps show where Amy K. Sater may publish in the future.

Co-authorship network of co-authors of Amy K. Sater

This figure shows the co-authorship network connecting the top 25 collaborators of Amy K. Sater. A scholar is included among the top collaborators of Amy K. Sater 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 Amy K. Sater. Amy K. Sater 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.
Belkacemi, Louiza, Lu Yang, Amy K. Sater, et al.. (2018). Phosphaplatin Anti-tumor Effect Enhanced by Liposomes Partly via an Up-regulation of PEDF in Breast Cancer. Anticancer Research. 38(2). 623–646. 8 indexed citations
2.
Soibam, Benjamin, et al.. (2016). Data on microRNAs and microRNA-targeted mRNAs in Xenopus ectoderm. Data in Brief. 9. 699–703. 3 indexed citations
3.
Soibam, Benjamin, et al.. (2016). MicroRNAs and ectodermal specification I. Identification of miRs and miR-targeted mRNAs in early anterior neural and epidermal ectoderm. Developmental Biology. 426(2). 200–210. 5 indexed citations
4.
Liu, Chen, Chih‐Hong Lou, Benjamin Soibam, et al.. (2015). Identification of microRNAs and microRNA targets in Xenopus gastrulae: The role of miR-26 in the regulation of Smad1. Developmental Biology. 409(1). 26–38. 8 indexed citations
5.
Mácha, J, Amy K. Sater, Dan E. Wells, et al.. (2012). Deep ancestry of mammalian X chromosome revealed by comparison with the basal tetrapod Xenopus tropicalis. BMC Genomics. 13(1). 315–315. 10 indexed citations
6.
Liu, Chen, et al.. (2012). TAK1 promotes BMP4/Smad1 signaling via inhibition of erk MAPK: A new link in the FGF/BMP regulatory network. Differentiation. 83(4). 210–219. 13 indexed citations
7.
Yergeau, Donald, Clair Kelley, Emin Kuliyev, et al.. (2011). Remobilization of Sleeping Beauty transposons in the germline of Xenopus tropicalis. Mobile DNA. 2(1). 15–15. 6 indexed citations
8.
Pan, Yi, et al.. (2010). Regulation of photoreceptor gene expression by the retinal homeobox (Rx) gene product. Developmental Biology. 339(2). 494–506. 27 indexed citations
9.
Liu, Chen, et al.. (2010). FGFR3 expression in Xenopus laevis. Gene Expression Patterns. 10(2-3). 87–92. 1 indexed citations
10.
Yergeau, Donald, Clair Kelley, Emin Kuliyev, et al.. (2010). Remobilization of Tol2 transposons in Xenopus tropicalis. BMC Developmental Biology. 10(1). 11–11. 12 indexed citations
11.
Klein, Steven L., Daniela S. Gerhard, Lukas Wagner, et al.. (2006). Resources for Genetic and Genomic Studies of Xenopus. Methods in molecular biology. 322. 1–16. 10 indexed citations
12.
Sater, Amy K., Heithem M. El‐Hodiri, Mousumi Goswami, et al.. (2003). Evidence for antagonism of BMP-4 signals by MAP kinase during Xenopus axis determination and neural specification. Differentiation. 71(7). 434–444. 26 indexed citations
13.
Goswami, Mousumi, Aarti R. Uzgare, & Amy K. Sater. (2001). Regulation of MAP Kinase by the BMP-4/TAK1 Pathway in Xenopus Ectoderm. Developmental Biology. 236(2). 259–270. 40 indexed citations
14.
Uzman, J. Akif, Sonali Patil, Aarti R. Uzgare, & Amy K. Sater. (1998). The Role of Intracellular Alkalinization in the Establishment of Anterior Neural Fate inXenopus. Developmental Biology. 193(1). 10–20. 32 indexed citations
15.
Wallingford, John B., Amy K. Sater, J. Akif Uzman, & Michael V. Danilchik. (1997). Inhibition of Morphogenetic Movement duringXenopusGastrulation by Injected Sulfatase: Implications for Anteroposterior and Dorsoventral Axis Formation. Developmental Biology. 187(2). 224–235. 17 indexed citations
16.
17.
Seid, Christopher A., et al.. (1996). A Tissue-Specific Repressor in the Sea Urchin Embryo of Lytechinus pictus Binds the Distal G-String Element in the LpS1-β Promoter. DNA and Cell Biology. 15(6). 511–517. 4 indexed citations
18.
Sater, Amy K., Richard A. Steinhardt, & Ray Keller. (1993). Induction of neuronal differentiation by planar signals in Xenopus embryos. Developmental Dynamics. 197(4). 268–280. 72 indexed citations
19.
Keller, Ray, John Shih, & Amy K. Sater. (1992). The cellular basis of the convergence and extension of the Xenopus neural plate. Developmental Dynamics. 193(3). 199–217. 194 indexed citations
20.
Sater, Amy K. & Antone G. Jacobson. (1990). The restriction of the heart morphogenetic field in Xenopus laevis. Developmental Biology. 140(2). 328–336. 71 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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