Robert W. Mercer

2.3k total citations · 1 hit paper
32 papers, 1.9k citations indexed

About

Robert W. Mercer is a scholar working on Molecular Biology, Physiology and Plant Science. According to data from OpenAlex, Robert W. Mercer has authored 32 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 5 papers in Physiology and 5 papers in Plant Science. Recurrent topics in Robert W. Mercer's work include Ion Transport and Channel Regulation (15 papers), Ion channel regulation and function (6 papers) and Pluripotent Stem Cells Research (4 papers). Robert W. Mercer is often cited by papers focused on Ion Transport and Channel Regulation (15 papers), Ion channel regulation and function (6 papers) and Pluripotent Stem Cells Research (4 papers). Robert W. Mercer collaborates with scholars based in United States, Italy and United Kingdom. Robert W. Mercer's co-authors include Gustavo Blanco, Gladis Sánchez, Joseph C. Koster, Roger J. Melton, Qun Sha, Colin G. Nichols, James E. Huettner, Jason C. Mills, Mijeong Kim and Jason M. Doherty and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Medicine.

In The Last Decade

Robert W. Mercer

32 papers receiving 1.9k citations

Hit Papers

Isozymes of the Na-K-ATPase: heterogeneity in structure, ... 1998 2026 2007 2016 1998 250 500 750 1000

Peers

Robert W. Mercer
Carl A. Hansen United States
Gustavo Blanco United States
Pei‐San Tsai United States
Pascal Béguin Switzerland
Inès Royaux United States
K. Geering Switzerland
Carl A. Hansen United States
Robert W. Mercer
Citations per year, relative to Robert W. Mercer Robert W. Mercer (= 1×) peers Carl A. Hansen

Countries citing papers authored by Robert W. Mercer

Since Specialization
Citations

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

Fields of papers citing papers by Robert W. Mercer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Robert W. Mercer

This figure shows the co-authorship network connecting the top 25 collaborators of Robert W. Mercer. A scholar is included among the top collaborators of Robert W. Mercer 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 W. Mercer. Robert W. Mercer 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.
Kim, Mijeong, et al.. (2009). Regulation of mouse embryonic stem cell neural differentiation by retinoic acid. Developmental Biology. 328(2). 456–471. 76 indexed citations
2.
Sha, Qun, et al.. (2008). Human FXYD2 G41R mutation responsible for renal hypomagnesemia behaves as an inward-rectifying cation channel. American Journal of Physiology-Renal Physiology. 295(1). F91–F99. 21 indexed citations
3.
Haipek, Carrie A., et al.. (2005). Akt-Dependent Cell Size Regulation by the Adhesion Molecule on Glia Occurs Independently of Phosphatidylinositol 3-Kinase and Rheb Signaling. Molecular and Cellular Biology. 25(8). 3151–3162. 29 indexed citations
4.
Mercer, Robert W., et al.. (2005). Cytoplasmic targeting signals mediate delivery of phospholemman to the plasma membrane. American Journal of Physiology-Cell Physiology. 290(5). C1275–C1286. 23 indexed citations
5.
Krajnak, Kristine, Robert W. Mercer, Brent A. Baker, Kenneth B. Geronilla, & Gerald R. Miller. (2004). A Novel Stereological Method used to Quantify Muscle Damage Induced by Injurious Stretch-Shortening Cycles. Medicine & Science in Sports & Exercise. 36(Supplement). S271–S271. 1 indexed citations
6.
Sha, Qun, et al.. (2001). Heterologous expression of the Na+,K+‐ATPase γ subunit in Xenopus oocytes induces an endogenous, voltage‐gated large diameter pore. The Journal of Physiology. 535(2). 407–417. 23 indexed citations
7.
Blanco, Gustavo, et al.. (2000). Expression, activity and distribution of Na,K-ATPase subunits during in vitro neuronal induction. Brain Research. 875(1-2). 1–13. 19 indexed citations
8.
Mercer, Robert W., et al.. (2000). Embryonic Stem Cells: A Model to Study Na,K-ATPase Isoform Expression during Development. Molecular Genetics and Metabolism. 71(1-2). 387–390. 1 indexed citations
9.
Blanco, Gustavo, Gladis Sánchez, & Robert W. Mercer. (1998). Differential Regulation of Na,K-ATPase Isozymes by Protein Kinases and Arachidonic Acid. Archives of Biochemistry and Biophysics. 359(2). 139–150. 65 indexed citations
10.
Thomas, James L., Gustavo Blanco, Robert W. Mercer, et al.. (1998). Site-directed mutagenesis identifies amino acid residues associated with the dehydrogenase and isomerase activities of human type I (placental) 3β-hydroxysteroid dehydrogenase/Isomerase. The Journal of Steroid Biochemistry and Molecular Biology. 66(5-6). 327–334. 34 indexed citations
11.
Allen, Jeffrey C., et al.. (1997). αIT Can Support Na+, K+ ‐ATPase: Na+ Pump Functions in Expression Systems. Annals of the New York Academy of Sciences. 834(1). 457–458. 3 indexed citations
12.
Blanco, Gustavo, et al.. (1997). Studies of Na, K‐ATPase Structure and Function Using Baculovirus. Annals of the New York Academy of Sciences. 834(1). 88–96. 5 indexed citations
13.
Koster, Joseph C., et al.. (1997). Characterization of Na,K‐ATPase α/α Oligomerization. Annals of the New York Academy of Sciences. 834(1). 135–138. 3 indexed citations
14.
Blanco, Gustavo & Robert W. Mercer. (1997). Regulation of the α2β1 and α3β1 Isozymes of the Na,K‐ATPase by Ca2+, PKA, and PKCa. Annals of the New York Academy of Sciences. 834(1). 572–575. 7 indexed citations
15.
Grindstaff, Kent K., Gustavo Blanco, & Robert W. Mercer. (1996). Translational Regulation of Na,K-ATPase α1 and β1 Polypeptide Expression in Epithelial Cells. Journal of Biological Chemistry. 271(38). 23211–23221. 12 indexed citations
16.
Koster, Joseph C., et al.. (1996). Substitutions of Glutamate 781 in the Na,K-ATPase α Subunit Demonstrate Reduced Cation Selectivity and an Increased Affinity for ATP. Journal of Biological Chemistry. 271(5). 2413–2421. 53 indexed citations
17.
Koster, Joseph C., et al.. (1995). Kinetic Properties of the .alpha.2.beta.1 and .alpha.2.beta.2 Isoenzymes of the Na,K-ATPase. Biochemistry. 34(1). 319–325. 72 indexed citations
18.
Koster, Joseph C., Gustavo Blanco, & Robert W. Mercer. (1995). A Cytoplasmic Region of the Na,K-ATPase α-Subunit Is Necessary for Specific α/α Association. Journal of Biological Chemistry. 270(24). 14332–14339. 40 indexed citations
19.
Mercer, Robert W.. (1993). Structure of the Na,K-ATPase.. PubMed. 137C. 139–68. 66 indexed citations
20.
Mercer, Robert W., Jay W. Schneider, Adam Savitz, et al.. (1986). Rat-Brain Na,K-ATPase β-Chain Gene: Primary Structure, Tissue-Specific Expression, and Amplification in Ouabain-Resistant HeLa C + Cells. Molecular and Cellular Biology. 6(11). 3884–3890. 29 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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