Robert M. Weis

2.8k total citations
43 papers, 2.3k citations indexed

About

Robert M. Weis is a scholar working on Molecular Biology, Genetics and Atomic and Molecular Physics, and Optics. According to data from OpenAlex, Robert M. Weis has authored 43 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 14 papers in Genetics and 7 papers in Atomic and Molecular Physics, and Optics. Recurrent topics in Robert M. Weis's work include Lipid Membrane Structure and Behavior (19 papers), Bacterial Genetics and Biotechnology (14 papers) and Protein Structure and Dynamics (10 papers). Robert M. Weis is often cited by papers focused on Lipid Membrane Structure and Behavior (19 papers), Bacterial Genetics and Biotechnology (14 papers) and Protein Structure and Dynamics (10 papers). Robert M. Weis collaborates with scholars based in United States, Netherlands and Germany. Robert M. Weis's co-authors include Harden M. McConnell, Guoyong Li, Lukas K. Tamm, Joydeep Lahiri, Jianghong Rao, George M. Whitesides, Jiayin Li, David G. Long, Lyle Isaacs and Jiayin Li and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Robert M. Weis

43 papers receiving 2.3k 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 M. Weis United States 22 1.8k 633 443 328 224 43 2.3k
Michael C. Wiener United States 33 3.5k 2.0× 823 1.3× 588 1.3× 384 1.2× 306 1.4× 67 4.3k
David P. Millar United States 39 3.0k 1.7× 294 0.5× 462 1.0× 348 1.1× 181 0.8× 115 4.0k
Nam Ki Lee South Korea 26 1.8k 1.1× 247 0.4× 333 0.8× 231 0.7× 268 1.2× 59 3.0k
Gabriele Rummel Switzerland 21 2.6k 1.5× 933 1.5× 216 0.5× 279 0.9× 470 2.1× 24 3.8k
Philippe Ringler Switzerland 27 1.5k 0.9× 478 0.8× 152 0.3× 122 0.4× 168 0.8× 57 2.8k
Dietmar Pörschke Germany 33 2.9k 1.6× 254 0.4× 539 1.2× 302 0.9× 483 2.2× 112 3.6k
Emmanuel Margeat France 29 2.5k 1.4× 829 1.3× 237 0.5× 104 0.3× 339 1.5× 63 3.5k
Pascal Demange France 28 1.7k 1.0× 292 0.5× 396 0.9× 79 0.2× 143 0.6× 84 2.7k
Jean‐Louis Rigaud France 36 3.5k 2.0× 233 0.4× 709 1.6× 271 0.8× 388 1.7× 53 4.3k
Koji Yonekura Japan 31 2.0k 1.1× 543 0.9× 197 0.4× 110 0.3× 188 0.8× 82 3.3k

Countries citing papers authored by Robert M. Weis

Since Specialization
Citations

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

Fields of papers citing papers by Robert M. Weis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Robert M. Weis

This figure shows the co-authorship network connecting the top 25 collaborators of Robert M. Weis. A scholar is included among the top collaborators of Robert M. Weis 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 M. Weis. Robert M. Weis 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.
Weis, Robert M., et al.. (2012). Ligand Affinity and Kinase Activity Are Independent of Bacterial Chemotaxis Receptor Concentration: Insight into Signaling Mechanisms. Biochemistry. 51(35). 6920–6931. 12 indexed citations
2.
Li, Zheng, Kimberly A. Stieglitz, Wei Yang, et al.. (2009). Mobile loop mutations in an archaeal inositol monophosphatase: Modulating three‐metal ion assisted catalysis and lithium inhibition. Protein Science. 19(2). 309–318. 13 indexed citations
3.
Esposito, Edward A., et al.. (2008). Template‐directed Assembly of Signaling Proteins: A Novel Drug Screening and Research Tool. Chemical Biology & Drug Design. 71(3). 278–281. 6 indexed citations
4.
Esposito, Edward A., et al.. (2008). Template-Directed Self-Assembly Enhances RTK Catalytic Domain Function. SLAS DISCOVERY. 13(8). 810–816. 8 indexed citations
5.
Besschetnova, Tatiana Y., et al.. (2008). Receptor density balances signal stimulation and attenuation in membrane-assembled complexes of bacterial chemotaxis signaling proteins. Proceedings of the National Academy of Sciences. 105(34). 12289–12294. 28 indexed citations
6.
Montefusco, David, et al.. (2007). Liposome‐Mediated Assembly of Receptor Signaling Complexes. Methods in enzymology on CD-ROM/Methods in enzymology. 423. 267–298. 11 indexed citations
7.
Zhang, Peijun, Robert M. Weis, Peter J. Peters, & Sriram Subramaniam. (2007). Electron Tomography of Bacterial Chemotaxis Receptor Assemblies. Methods in cell biology. 79. 373–384. 10 indexed citations
8.
Weis, Robert M., et al.. (2006). 12 Reversible methylation of glutamate residues in the receptor proteins of bacterial sensory systems. ˜The œEnzymes. 24. 325–382. 8 indexed citations
9.
Weis, Robert M., et al.. (2006). Competitive and Cooperative Interactions in Receptor Signaling Complexes. Journal of Biological Chemistry. 281(41). 30512–30523. 22 indexed citations
10.
Weis, Robert M., et al.. (2005). Site-specific and synergistic stimulation of methylation on the bacterial chemotaxis receptor Tsr by serine and CheW. BMC Microbiology. 5(1). 12–12. 15 indexed citations
11.
Munzner, Jennifer B., et al.. (2004). Ligand-Specific Activation of Escherichia coli Chemoreceptor Transmethylation. Journal of Bacteriology. 186(22). 7556–7563. 24 indexed citations
12.
Braswell, Emory H., et al.. (2003). Distributed subunit interactions in CheA contribute to dimer stability: a sedimentation equilibrium study. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1696(1). 131–140. 25 indexed citations
13.
Yi, Xianhua, et al.. (2001). Hydrogen Exchange Reveals a Stable and Expandable Core within the Aspartate Receptor Cytoplasmic Domain. Journal of Biological Chemistry. 276(46). 43262–43269. 14 indexed citations
14.
Li, Guoyong & Robert M. Weis. (2000). Covalent Modification Regulates Ligand Binding to Receptor Complexes in the Chemosensory System of Escherichia coli. Cell. 100(3). 357–365. 158 indexed citations
15.
Long, David G., et al.. (1995). Reversible dissociation and unfolding of the Escherichia coli aspartate receptor cytoplasmic fragment. Biochemistry. 34(9). 3056–3065. 16 indexed citations
16.
Li, Jiayin, Ronald V. Swanson, M I Simon, & Robert M. Weis. (1995). Response Regulators CheB and CheY Exhibit Competitive Binding to the Kinase CheA. Biochemistry. 34(45). 14626–14636. 118 indexed citations
17.
Lin, Lung‐Nan, Jiayin Li, John F. Brandts, & Robert M. Weis. (1994). The serine receptor of bacterial chemotaxis exhibits half-site saturation for serine binding. Biochemistry. 33(21). 6564–6570. 66 indexed citations
18.
Long, David G. & Robert M. Weis. (1992). Oligomerization of the cytoplasmic fragment from the aspartate receptor of Escherichia coli. Biochemistry. 31(41). 9904–9911. 39 indexed citations
19.
Weis, Robert M.. (1991). Fluorescence microscopy of phospholipid monolayer phase transitions. Chemistry and Physics of Lipids. 57(2-3). 227–239. 69 indexed citations
20.
Weis, Robert M. & Harden M. McConnell. (1985). Cholesterol stabilizes the crystal-liquid interface in phospholipid monolayers. The Journal of Physical Chemistry. 89(21). 4453–4459. 150 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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