David M. Standiford

693 total citations
12 papers, 557 citations indexed

About

David M. Standiford is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, David M. Standiford has authored 12 papers receiving a total of 557 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 3 papers in Genetics and 3 papers in Plant Science. Recurrent topics in David M. Standiford's work include RNA Research and Splicing (5 papers), Protist diversity and phylogeny (4 papers) and RNA and protein synthesis mechanisms (4 papers). David M. Standiford is often cited by papers focused on RNA Research and Splicing (5 papers), Protist diversity and phylogeny (4 papers) and RNA and protein synthesis mechanisms (4 papers). David M. Standiford collaborates with scholars based in United States, Netherlands and Switzerland. David M. Standiford's co-authors include Charles P. Emerson, Weitao Sun, Gurtej K. Dhoot, Xingbin Ai, Mary B. Davis, Joel D. Richter, Clara Franzini‐Armstrong, Wei Sun and Erzsébet Polyák and has published in prestigious journals such as Science, The Journal of Cell Biology and Journal of Molecular Biology.

In The Last Decade

David M. Standiford

12 papers receiving 537 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David M. Standiford United States 9 427 274 106 48 47 12 557
Keith A. Mintzer United States 9 768 1.8× 394 1.4× 168 1.6× 36 0.8× 55 1.2× 9 1.0k
Merrill B. Hille United States 17 659 1.5× 205 0.7× 125 1.2× 24 0.5× 21 0.4× 34 921
Alasdair J. Street United Kingdom 12 639 1.5× 174 0.6× 91 0.9× 85 1.8× 16 0.3× 14 925
Michael A. Pickart United States 10 312 0.7× 159 0.6× 89 0.8× 12 0.3× 13 0.3× 18 471
Michiko Muraki Japan 9 584 1.4× 72 0.3× 74 0.7× 30 0.6× 18 0.4× 9 684
Alexander Hirschi United States 9 602 1.4× 151 0.6× 78 0.7× 29 0.6× 6 0.1× 12 797
Isabella Ponzanelli Italy 13 642 1.5× 172 0.6× 71 0.7× 39 0.8× 13 0.3× 21 886
Wenhao Jin United States 11 865 2.0× 144 0.5× 33 0.3× 22 0.5× 40 0.9× 14 1.1k
Kazuhide Tsuneizumi Japan 10 652 1.5× 140 0.5× 95 0.9× 45 0.9× 10 0.2× 19 772
Carla S. Lopes Portugal 14 548 1.3× 353 1.3× 69 0.7× 122 2.5× 9 0.2× 20 718

Countries citing papers authored by David M. Standiford

Since Specialization
Citations

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

Fields of papers citing papers by David M. Standiford

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David M. Standiford. 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 David M. Standiford. The network helps show where David M. Standiford may publish in the future.

Co-authorship network of co-authors of David M. Standiford

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

All Works

12 of 12 papers shown
1.
Polyák, Erzsébet, et al.. (2003). Contribution of Myosin Rod Protein to the Structural Organization of Adult and Embryonic Muscles in Drosophila. Journal of Molecular Biology. 331(5). 1077–1091. 8 indexed citations
2.
Davis, Mary B., Weitao Sun, & David M. Standiford. (2002). Lineage-specific expression of polypyrimidine tract binding protein (PTB) in Drosophila embryos. Mechanisms of Development. 111(1-2). 143–147. 18 indexed citations
3.
Dhoot, Gurtej K., et al.. (2001). Regulation of Wnt Signaling and Embryo Patterning by an Extracellular Sulfatase. Science. 293(5535). 1663–1666. 383 indexed citations
4.
Standiford, David M., Wei Sun, Mary B. Davis, & Charles P. Emerson. (2001). Positive and Negative Intronic Regulatory Elements Control Muscle-Specific Alternative Exon Splicing of Drosophila Myosin Heavy Chain Transcripts. Genetics. 157(1). 259–271. 14 indexed citations
5.
Davis, Mary B., et al.. (1998). Transposable Element Insertions Respecify Alternative Exon Splicing in Three Drosophila Myosin Heavy Chain Mutants. Genetics. 150(3). 1105–1114. 13 indexed citations
6.
Standiford, David M., et al.. (1997). Myosin rod protein: a novel thick filament component of Drosophila muscle. Journal of Molecular Biology. 265(1). 40–55. 24 indexed citations
7.
Standiford, David M., Mary B. Davis, Weitao Sun, & Charles P. Emerson. (1997). Splice-Junction Elements and Intronic Sequences Regulate Alternative Splicing of the Drosophila Myosin Heavy Chain Gene Transcript. Genetics. 147(2). 725–741. 13 indexed citations
8.
Standiford, David M. & Joel D. Richter. (1992). Analysis of a developmentally regulated nuclear localization signal in Xenopus.. The Journal of Cell Biology. 118(5). 991–1002. 34 indexed citations
9.
Standiford, David M.. (1989). Development of the large nucleolus in the oocytes of the copepod Acanthocyclops vernalis: an electron microscope study. Biology of the Cell. 65(2). 127–132. 1 indexed citations
10.
Standiford, David M., et al.. (1989). Development of the large nucleolus in the oocytes of the copepod Acanthocyclops vernalis: an electron microscope study. Biology of the Cell. 65(2). 127–132. 2 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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