Robert A. Schulz

2.7k total citations
29 papers, 2.1k citations indexed

About

Robert A. Schulz is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Robert A. Schulz has authored 29 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 11 papers in Genetics and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Robert A. Schulz's work include Developmental Biology and Gene Regulation (15 papers), Neurobiology and Insect Physiology Research (7 papers) and Congenital heart defects research (6 papers). Robert A. Schulz is often cited by papers focused on Developmental Biology and Gene Regulation (15 papers), Neurobiology and Insect Physiology Research (7 papers) and Congenital heart defects research (6 papers). Robert A. Schulz collaborates with scholars based in United States, South Korea and Germany. Robert A. Schulz's co-authors include Eric N. Olson, Kathleen Gajewski, Katherine E. Yutzey, Bin Zhao, Michael Perry, Gogineni Ranganayakulu, Brenda Lilly, Bruce M. Paterson, Nancy Fossett and Jeffery D. Molkentin and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Robert A. Schulz

29 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert A. Schulz United States 19 1.8k 508 375 323 209 29 2.1k
Amanda Simcox United States 23 1.5k 0.9× 516 1.0× 201 0.5× 309 1.0× 417 2.0× 39 1.8k
Natalia Azpiazu Spain 12 1.7k 0.9× 516 1.0× 213 0.6× 405 1.3× 289 1.4× 18 2.0k
R. Bodmer United States 11 1.3k 0.7× 401 0.8× 148 0.4× 249 0.8× 211 1.0× 14 1.5k
Xiushan Wu China 23 1.5k 0.9× 249 0.5× 215 0.6× 288 0.9× 174 0.8× 101 2.1k
Carlos V. Cabrera United Kingdom 17 3.0k 1.7× 775 1.5× 387 1.0× 777 2.4× 306 1.5× 21 3.6k
Mar Ruiz‐Gómez Spain 21 1.7k 1.0× 663 1.3× 252 0.7× 305 0.9× 497 2.4× 30 2.1k
Kathleen Gajewski United States 22 1.1k 0.6× 371 0.7× 429 1.1× 178 0.6× 442 2.1× 30 1.6k
James B. Jaynes United States 33 3.3k 1.9× 697 1.4× 258 0.7× 745 2.3× 368 1.8× 53 3.8k
Ralph A.W. Rupp Germany 20 3.0k 1.7× 228 0.4× 206 0.5× 691 2.1× 297 1.4× 40 3.5k
Bernard M. Mechler Germany 27 2.3k 1.3× 256 0.5× 226 0.6× 365 1.1× 730 3.5× 60 2.8k

Countries citing papers authored by Robert A. Schulz

Since Specialization
Citations

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

Fields of papers citing papers by Robert A. Schulz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Robert A. Schulz

This figure shows the co-authorship network connecting the top 25 collaborators of Robert A. Schulz. A scholar is included among the top collaborators of Robert A. Schulz 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 Robert A. Schulz. Robert A. Schulz 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.
Tao, Ye, Audrey E. Christiansen, & Robert A. Schulz. (2007). Second chromosome genes required for heart development in Drosophila melanogaster. genesis. 45(10). 607–617. 8 indexed citations
2.
Tao, Ye & Robert A. Schulz. (2006). Heart development in Drosophila. Seminars in Cell and Developmental Biology. 18(1). 3–15. 71 indexed citations
3.
Gajewski, Kathleen, Jianbo Wang, & Robert A. Schulz. (2005). Calcineurin function is required for myofilament formation and troponin I isoform transition in Drosophila indirect flight muscle. Developmental Biology. 289(1). 17–29. 10 indexed citations
4.
Schulz, Robert A. & Katherine E. Yutzey. (2003). Calcineurin signaling and NFAT activation in cardiovascular and skeletal muscle development. Developmental Biology. 266(1). 1–16. 233 indexed citations
5.
Lo, Patrick C.H., James B. Skeath, Kathleen Gajewski, Robert A. Schulz, & Manfred Frasch. (2002). Homeotic Genes Autonomously Specify the Anteroposterior Subdivision of the Drosophila Dorsal Vessel into Aorta and Heart. Developmental Biology. 251(2). 307–319. 68 indexed citations
6.
7.
Gajewski, Kathleen, Qian Zhang, Cheol Yong Choi, et al.. (2001). Pannier is a Transcriptional Target and Partner of Tinman during Drosophila Cardiogenesis. Developmental Biology. 233(2). 425–436. 58 indexed citations
8.
Hsu, Tien & Robert A. Schulz. (2000). Sequence and functional properties of Ets genes in the model organism Drosophila. Oncogene. 19(55). 6409–6416. 64 indexed citations
9.
Gajewski, Kathleen, Cheol Yong Choi, Yongsok Kim, & Robert A. Schulz. (2000). Genetically distinct cardial cells within theDrosophila heart. genesis. 28(1). 36–43. 66 indexed citations
10.
Gajewski, Kathleen, et al.. (1999). Tinman Regulates the Transcription of the β3 tubulin Gene (βTub60D) in the Dorsal Vessel of Drosophila. Developmental Biology. 216(1). 327–339. 33 indexed citations
11.
Choi, Cheol Yong, Young Mi Lee, Young Ho Kim, et al.. (1999). The Homeodomain Transcription Factor NK-4 Acts as either a Transcriptional Activator or Repressor and Interacts with the p300 Coactivator and the Groucho Corepressor. Journal of Biological Chemistry. 274(44). 31543–31552. 52 indexed citations
12.
Schulz, Robert A., et al.. (1999). Oogenic function of the myogenic factor D-MEF2: Negative regulation of the Decapentaplegic receptor gene thick veins. Proceedings of the National Academy of Sciences. 96(21). 11889–11894. 26 indexed citations
13.
Schulz, Robert A. & Kathleen Gajewski. (1999). Ventral neuroblasts and the Heartless FGF receptor are required for muscle founder cell specification in Drosophila. Oncogene. 18(48). 6818–6823. 7 indexed citations
14.
Lee, Young Mi, Taekyu Park, Robert A. Schulz, & Yongsok Kim. (1997). Twist-mediated Activation of the NK-4 Homeobox Gene in the Visceral Mesoderm of Drosophila Requires Two Distinct Clusters of E-box Regulatory Elements. Journal of Biological Chemistry. 272(28). 17531–17541. 48 indexed citations
15.
Ranganayakulu, Gogineni, et al.. (1995). A Series of Mutations in the D-MEF2 Transcription Factor Reveal Multiple Functions in Larval and Adult Myogenesis in Drosophila. Developmental Biology. 171(1). 169–181. 172 indexed citations
16.
Olson, Eric N., Michael Perry, & Robert A. Schulz. (1995). Regulation of Muscle Differentiation by the MEF2 Family of MADS Box Transcription Factors. Developmental Biology. 172(1). 2–14. 298 indexed citations
17.
Galewsky, Samuel & Robert A. Schulz. (1992). drop out: A third chromosome maternal‐effect locus required for formation of the Drosophila cellular blastoderm. Molecular Reproduction and Development. 32(4). 331–338. 6 indexed citations
18.
19.
Schulz, Robert A., et al.. (1990). cis-Acting sequences required for the germ line expression of the Drosophila gonadal gene. Developmental Biology. 140(2). 455–458. 11 indexed citations
20.
Schulz, Robert A., et al.. (1989). Dorsal expression of the Drosophila z600 gene during early embryogenesis. Developmental Biology. 136(1). 211–221. 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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