Craig T. Miller

6.4k total citations
50 papers, 3.2k citations indexed

About

Craig T. Miller is a scholar working on Molecular Biology, Genetics and Nature and Landscape Conservation. According to data from OpenAlex, Craig T. Miller has authored 50 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 24 papers in Genetics and 12 papers in Nature and Landscape Conservation. Recurrent topics in Craig T. Miller's work include Developmental Biology and Gene Regulation (16 papers), dental development and anomalies (13 papers) and Genetic diversity and population structure (13 papers). Craig T. Miller is often cited by papers focused on Developmental Biology and Gene Regulation (16 papers), dental development and anomalies (13 papers) and Genetic diversity and population structure (13 papers). Craig T. Miller collaborates with scholars based in United States, Canada and United Kingdom. Craig T. Miller's co-authors include Charles B. Kimmel, David M. Kingsley, Dolph Schluter, Macie B. Walker, J. Gage Crump, Cecilia B. Moens, Nicholas Ellis, Bonnie Ullmann, John H. Postlethwait and Andrew M. Glazer and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Development.

In The Last Decade

Craig T. Miller

49 papers receiving 3.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Craig T. Miller United States 26 1.9k 1.4k 490 453 342 50 3.2k
Ingo Braasch United States 33 2.2k 1.1× 1.3k 0.9× 505 1.0× 796 1.8× 230 0.7× 68 4.1k
Guadalupe Villarreal United States 15 1.1k 0.6× 1.3k 0.9× 426 0.9× 139 0.3× 292 0.9× 18 2.9k
Matthew P. Harris United States 28 1.7k 0.9× 764 0.5× 179 0.4× 602 1.3× 112 0.3× 66 2.7k
Zbyněk Kozmík Czechia 39 3.7k 1.9× 922 0.6× 117 0.2× 332 0.7× 314 0.9× 114 5.0k
Masakane Yamashita Japan 40 2.3k 1.2× 1.7k 1.2× 358 0.7× 788 1.7× 159 0.5× 156 5.4k
Ann C. Burke United States 18 2.0k 1.0× 709 0.5× 488 1.0× 276 0.6× 72 0.2× 32 3.0k
David W. Stock United States 26 1.6k 0.8× 469 0.3× 365 0.7× 216 0.5× 107 0.3× 37 2.2k
Bruce W. Draper United States 35 3.7k 1.9× 1.8k 1.2× 106 0.2× 799 1.8× 458 1.3× 49 5.4k
S. Randal Voss United States 37 2.0k 1.0× 1.2k 0.8× 323 0.7× 250 0.6× 142 0.4× 112 3.9k
Glenda M. Wright Canada 30 719 0.4× 511 0.4× 463 0.9× 222 0.5× 228 0.7× 100 2.6k

Countries citing papers authored by Craig T. Miller

Since Specialization
Citations

This map shows the geographic impact of Craig T. Miller'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 Craig T. Miller with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Craig T. Miller more than expected).

Fields of papers citing papers by Craig T. Miller

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Craig T. Miller. 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 Craig T. Miller. The network helps show where Craig T. Miller may publish in the future.

Co-authorship network of co-authors of Craig T. Miller

This figure shows the co-authorship network connecting the top 25 collaborators of Craig T. Miller. A scholar is included among the top collaborators of Craig T. Miller 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 Craig T. Miller. Craig T. Miller 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.
2.
Richards, Emilie J., et al.. (2023). Jaw size variation is associated with a novel craniofacial function for galanin receptor 2 in an adaptive radiation of pupfishes. Proceedings of the Royal Society B Biological Sciences. 290(2009). 20231686–20231686. 2 indexed citations
3.
Mack, Katya L., Tyler A. Square, Bin Zhao, Craig T. Miller, & Hunter B. Fraser. (2023). Evolution of Spatial and Temporalcis-Regulatory Divergence in Sticklebacks. Molecular Biology and Evolution. 40(3). 8 indexed citations
4.
Square, Tyler A., et al.. (2021). Evolved Bmp6 enhancer alleles drive spatial shifts in gene expression during tooth development in sticklebacks. Genetics. 219(4). 5 indexed citations
5.
Square, Tyler A., et al.. (2021). Distinct tooth regeneration systems deploy a conserved battery of genes. EvoDevo. 12(1). 4–4. 13 indexed citations
6.
Cleves, Phillip A., et al.. (2018). An intronic enhancer of Bmp6 underlies evolved tooth gain in sticklebacks. PLoS Genetics. 14(6). e1007449–e1007449. 22 indexed citations
7.
Ellis, Nicholas, et al.. (2018). Convergent evolution of gene expression in two high-toothed stickleback populations. PLoS Genetics. 14(6). e1007443–e1007443. 25 indexed citations
8.
Miller, Craig T., et al.. (2017). Sequence-Based Mapping and Genome Editing Reveal Mutations in SticklebackHps5Cause Oculocutaneous Albinism and thecasperPhenotype. G3 Genes Genomes Genetics. 7(9). 3123–3131. 14 indexed citations
9.
Ellis, Nicholas & Craig T. Miller. (2016). Dissection and Flat-mounting of the Threespine Stickleback Branchial Skeleton. Journal of Visualized Experiments. 5 indexed citations
10.
Erickson, Priscilla A., et al.. (2015). A 190 base pair, TGF-β responsive tooth and fin enhancer is required for stickleback Bmp6 expression. Developmental Biology. 401(2). 310–323. 23 indexed citations
11.
Cleves, Phillip A., Nicholas Ellis, Monica T. Jimenez, et al.. (2014). Evolved tooth gain in sticklebacks is associated with acis-regulatory allele ofBmp6. Proceedings of the National Academy of Sciences. 111(38). 13912–13917. 68 indexed citations
12.
Miller, Craig T., Mary E. Swartz, Patricia Khuu, et al.. (2007). mef2ca is required in cranial neural crest to effect Endothelin1 signaling in zebrafish. Developmental Biology. 308(1). 144–157. 78 indexed citations
13.
Walker, Macie B., Craig T. Miller, Jared C. Talbot, David W. Stock, & Charles B. Kimmel. (2006). Zebrafish furin mutants reveal intricacies in regulating Endothelin1 signaling in craniofacial patterning. Developmental Biology. 295(1). 194–205. 94 indexed citations
14.
Walker, Macie B., Craig T. Miller, Mary E. Swartz, Johann K. Eberhart, & Charles B. Kimmel. (2006). phospholipase C, beta 3 is required for Endothelin1 regulation of pharyngeal arch patterning in zebrafish. Developmental Biology. 304(1). 194–207. 53 indexed citations
15.
Miller, Craig T., Lisa Maves, & Charles B. Kimmel. (2004). moz regulates Hox expression and pharyngeal segmental identity in zebrafish. Development. 131(10). 2443–2461. 110 indexed citations
16.
Miller, Craig T., Deborah Yelon, Didier Y. R. Stainier, & Charles B. Kimmel. (2003). Twoendothelin 1effectors,hand2andbapx1,pattern ventral pharyngeal cartilage and the jaw joint. Development. 130(7). 1353–1365. 180 indexed citations
17.
Kimmel, Charles B., Bonnie Ullmann, Macie B. Walker, Craig T. Miller, & J. Gage Crump. (2003). Endothelin 1-mediated regulation of pharyngeal bone development in zebrafish. Development. 130(7). 1339–1351. 110 indexed citations
18.
Miller, Craig T. & Charles B. Kimmel. (2001). Morpholino phenocopies of endothelin 1 (sucker) and other anterior arch class mutations. genesis. 30(3). 186–187. 37 indexed citations
19.
Kimmel, Charles B., et al.. (1998). The Shaping of Pharyngeal Cartilages during Early Development of the Zebrafish. Developmental Biology. 203(2). 245–263. 193 indexed citations
20.
Miller, Craig T., John H. McDonald, & David Francis. (1996). Evolution of promoter sequences: Elements of a canonical promoter for prespore genes of dictyostelium. Journal of Molecular Evolution. 43(3). 185–193. 5 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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