Daniel P. Szeto

4.1k total citations · 1 hit paper
22 papers, 3.4k citations indexed

About

Daniel P. Szeto is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Daniel P. Szeto has authored 22 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 7 papers in Genetics and 5 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Daniel P. Szeto's work include Congenital heart defects research (8 papers), Developmental Biology and Gene Regulation (7 papers) and Growth Hormone and Insulin-like Growth Factors (5 papers). Daniel P. Szeto is often cited by papers focused on Congenital heart defects research (8 papers), Developmental Biology and Gene Regulation (7 papers) and Growth Hormone and Insulin-like Growth Factors (5 papers). Daniel P. Szeto collaborates with scholars based in United States, Italy and United Kingdom. Daniel P. Szeto's co-authors include Michael G. Rosenfeld, Shawn M. O’Connell, Anatoli S. Gleiberman, Mathias Treier, Chrissa Kioussi, Juan Carlos Izpisúa‐Belmonte, Aimee K. Ryan, David Kimelman, David L. Popham and Sydney Kustu and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Daniel P. Szeto

22 papers receiving 3.3k citations

Hit Papers

Pitx2 regulates lung asymmetry, cardiac positioning and p... 1999 2026 2008 2017 1999 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Daniel P. Szeto United States 17 2.6k 1.2k 728 231 218 22 3.4k
E. J. Sanders Canada 30 1.6k 0.6× 699 0.6× 235 0.3× 410 1.8× 157 0.7× 103 2.6k
Rosa Barrio Spain 31 2.0k 0.8× 656 0.5× 229 0.3× 386 1.7× 138 0.6× 100 2.7k
D. A. Melton United States 25 3.9k 1.5× 1.1k 0.9× 255 0.4× 602 2.6× 134 0.6× 31 4.7k
Joshua M. Brickman Denmark 34 3.3k 1.3× 715 0.6× 400 0.5× 222 1.0× 249 1.1× 80 4.0k
Masanori Taira Japan 42 5.0k 1.9× 957 0.8× 204 0.3× 728 3.2× 307 1.4× 133 6.0k
Tadahiro Iimura Japan 31 1.9k 0.7× 389 0.3× 169 0.2× 300 1.3× 194 0.9× 104 2.9k
Thomas D. Sargent United States 40 3.6k 1.4× 909 0.7× 118 0.2× 788 3.4× 266 1.2× 71 4.6k
Paul O. Sheppard United States 22 1.9k 0.7× 401 0.3× 366 0.5× 170 0.7× 158 0.7× 26 3.1k
Ramiro Ramírez‐Solis United Kingdom 23 2.4k 0.9× 1.1k 0.9× 75 0.1× 239 1.0× 138 0.6× 39 3.2k
Paul M. Brickell United Kingdom 28 2.5k 1.0× 841 0.7× 111 0.2× 565 2.4× 126 0.6× 54 3.4k

Countries citing papers authored by Daniel P. Szeto

Since Specialization
Citations

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

Fields of papers citing papers by Daniel P. Szeto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daniel P. Szeto. 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 Daniel P. Szeto. The network helps show where Daniel P. Szeto may publish in the future.

Co-authorship network of co-authors of Daniel P. Szeto

This figure shows the co-authorship network connecting the top 25 collaborators of Daniel P. Szeto. A scholar is included among the top collaborators of Daniel P. Szeto 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 Daniel P. Szeto. Daniel P. Szeto 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.
Gao, Jian, et al.. (2012). In vivo imaging and quantitative analysis of zebrafish embryos by digital holographic microscopy. Biomedical Optics Express. 3(10). 2623–2623. 16 indexed citations
4.
Szeto, Daniel P., et al.. (2010). Zebrafish eve1 regulates the lateral and ventral fates of mesodermal progenitor cells at the onset of gastrulation. Developmental Biology. 349(1). 78–89. 14 indexed citations
5.
Szeto, Daniel P. & David Kimelman. (2006). The regulation of mesodermal progenitor cell commitment to somitogenesis subdivides the zebrafish body musculature into distinct domains. Genes & Development. 20(14). 1923–1932. 44 indexed citations
6.
Cooper, Mark S., Daniel P. Szeto, Jacek Topczewski, et al.. (2004). Visualizing morphogenesis in transgenic zebrafish embryos using BODIPY TR methyl ester dye as a vital counterstain for GFP. Developmental Dynamics. 232(2). 359–368. 111 indexed citations
7.
Szeto, Daniel P. & David Kimelman. (2004). Combinatorial gene regulation by Bmp and Wnt in zebrafish posterior mesoderm formation. Development. 131(15). 3751–3760. 75 indexed citations
8.
Treier, Mathias, Shawn M. O’Connell, Anatoli S. Gleiberman, et al.. (2001). Hedgehog signaling is required for pituitary gland development. Development. 128(3). 377–386. 228 indexed citations
9.
Wang, Zhiyong, David W. Rose, Ola Hermanson, et al.. (2000). Regulation of somatic growth by the p160 coactivator p/CIP. Proceedings of the National Academy of Sciences. 97(25). 13549–13554. 166 indexed citations
10.
Rosenfeld, M G, Paola Briata, Jeremy S. Dasen, et al.. (2000). Multistep signaling and transcriptional requirements for pituitary organogenesis in vivo.. PubMed. 55. 1–13; discussion 13. 57 indexed citations
11.
Lin, Chijen R., Chrissa Kioussi, Paola Briata, et al.. (1999). Pitx2 regulates lung asymmetry, cardiac positioning and pituitary and tooth morphogenesis. Nature. 401(6750). 279–282. 504 indexed citations breakdown →
12.
Szeto, Daniel P., Concepción Rodrı́guez-Esteban, Aimee K. Ryan, et al.. (1999). Role of the Bicoid-related homeodomain factor Pitx1 in specifying hindlimb morphogenesis and pituitary development. Genes & Development. 13(4). 484–494. 339 indexed citations
13.
Dasen, Jeremy S., Shawn M. O’Connell, Sarah E. Flynn, et al.. (1999). Reciprocal Interactions of Pit1 and GATA2 Mediate Signaling Gradient–Induced Determination of Pituitary Cell Types. Cell. 97(5). 587–598. 246 indexed citations
14.
Xu, Lan, Jeremy S. Dasen, Sarah E. Flynn, et al.. (1998). Signal-specific co-activator domain requirements for Pit-1 activation. Nature. 395(6699). 301–306. 246 indexed citations
15.
Treier, Mathias, Anatoli S. Gleiberman, Shawn M. O’Connell, et al.. (1998). Multistep signaling requirements for pituitary organogenesis in vivo. Genes & Development. 12(11). 1691–1704. 375 indexed citations
16.
Miyake, Jon H., Daniel P. Szeto, & William E. Stumph. (1997). Analysis of the structure and expression of the chicken gene encoding a homolog of the human RREB-1 transcription factor. Gene. 202(1-2). 177–186. 7 indexed citations
17.
Szeto, Daniel P., Aimee K. Ryan, Shawn M. O’Connell, & Michael G. Rosenfeld. (1996). P-OTX: a PIT-1-interacting homeodomain factor expressed during anterior pituitary gland development.. Proceedings of the National Academy of Sciences. 93(15). 7706–7710. 227 indexed citations
18.
Roebuck, Kenneth A., et al.. (1990). Octamer and SPH Motifs in the U1 Enhancer Cooperate To Activate U1 RNA Gene Expression. Molecular and Cellular Biology. 10(1). 341–352. 13 indexed citations
19.
Roebuck, Kenneth A., et al.. (1990). Octamer and SPH motifs in the U1 enhancer cooperate to activate U1 RNA gene expression.. Molecular and Cellular Biology. 10(1). 341–352. 38 indexed citations
20.
Popham, David L., Daniel P. Szeto, J Keener, & Sydney Kustu. (1989). Function of a Bacterial Activator Protein That Binds to Transcriptional Enhancers. Science. 243(4891). 629–635. 391 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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