William R. Randall

2.2k total citations
44 papers, 1.8k citations indexed

About

William R. Randall is a scholar working on Molecular Biology, Pharmacology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, William R. Randall has authored 44 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 13 papers in Pharmacology and 8 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in William R. Randall's work include Cholinesterase and Neurodegenerative Diseases (13 papers), Muscle Physiology and Disorders (11 papers) and Signaling Pathways in Disease (9 papers). William R. Randall is often cited by papers focused on Cholinesterase and Neurodegenerative Diseases (13 papers), Muscle Physiology and Disorders (11 papers) and Signaling Pathways in Disease (9 papers). William R. Randall collaborates with scholars based in United States, United Kingdom and Brazil. William R. Randall's co-authors include Martin F. Schneider, Yewei Liu, Edson X. Albuquerque, Edna F. R. Pereira, William P. Fawcett, Zoltán Cseresnyés, Tiansheng Shen, Luis E.F. Almeida, Karl Wah Keung Tsim and Gary T. Patterson and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Neuroscience.

In The Last Decade

William R. Randall

44 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
William R. Randall United States	24	1.1k	347	334	327	274	44	1.8k
Bernard Schmidt Germany	25	754 0.7×	462 1.3×	687 2.1×	337 1.0×	68 0.2×	77	1.7k
Igor Rebrin United States	26	1.4k 1.2×	137 0.4×	251 0.8×	549 1.7×	62 0.2×	44	2.3k
Vijaya B. Kumar United States	27	1.2k 1.0×	204 0.6×	461 1.4×	1.1k 3.2×	545 2.0×	46	2.9k
A.P. Carvalho Portugal	27	1.1k 0.9×	133 0.4×	845 2.5×	289 0.9×	134 0.5×	61	2.1k
Н. Г. Колосова Russia	32	1.7k 1.5×	221 0.6×	397 1.2×	1.2k 3.7×	87 0.3×	216	3.2k
Naoya Sawamura Japan	25	1.4k 1.2×	221 0.6×	472 1.4×	1.2k 3.6×	59 0.2×	48	2.4k
Alexander J. Stokes United States	23	854 0.8×	275 0.8×	380 1.1×	256 0.8×	548 2.0×	43	2.9k
Zipora Pittel Israel	20	763 0.7×	456 1.3×	590 1.8×	409 1.3×	89 0.3×	37	1.4k
Peter F. T. Vaughan United Kingdom	27	1.3k 1.2×	158 0.5×	902 2.7×	422 1.3×	113 0.4×	89	2.0k
Thimmasettappa Thippeswamy United States	24	488 0.4×	141 0.4×	797 2.4×	422 1.3×	197 0.7×	71	1.6k

Countries citing papers authored by William R. Randall

Since Specialization

Citations

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

Fields of papers citing papers by William R. Randall

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by William R. Randall. 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 William R. Randall. The network helps show where William R. Randall may publish in the future.

Co-authorship network of co-authors of William R. Randall

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

All Works

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20 of 20 papers shown

Alkondon, Manickavasagom, et al.. (2014). Functional G-protein-coupled receptor 35 is expressed by neurons in the CA1 field of the hippocampus. Biochemical Pharmacology. 93(4). 506–518. 31 indexed citations

Shen, Tiansheng, Yewei Liu, Minerva Contreras, et al.. (2010). DNA binding sites target nuclear NFATc1 to heterochromatin regions in adult skeletal muscle fibers. Histochemistry and Cell Biology. 134(4). 387–402. 17 indexed citations

Zhang, Yinghua, et al.. (2010). Characterization and expression of a heart-selective alternatively spliced variant of αII-spectrin, cardi+, during development in the rat. Journal of Molecular and Cellular Cardiology. 48(6). 1050–1059. 14 indexed citations

Liu, Yewei, Minerva Contreras, Tiansheng Shen, William R. Randall, & Martin F. Schneider. (2009). α‐Adrenergic signalling activates protein kinase D and causes nuclear efflux of the transcriptional repressor HDAC5 in cultured adult mouse soleus skeletal muscle fibres. The Journal of Physiology. 587(5). 1101–1115. 18 indexed citations

Goldblum, Rebecca R., et al.. (2009). Novel Functions of Protein Kinase D in Cardiac Excitation-Contraction Coupling. Biophysical Journal. 96(3). 622a–623a. 2 indexed citations

Bowman, Amber L., Dawn H. Catino, John Strong, et al.. (2008). The Rho-Guanine Nucleotide Exchange Factor Domain of Obscurin Regulates Assembly of Titin at the Z-Disk through Interactions with Ran Binding Protein 9. Molecular Biology of the Cell. 19(9). 3782–3792. 51 indexed citations

Ursitti, Jeanine A., Brian G. Petrich, Wendy G. Resneck, et al.. (2007). Role of an alternatively spliced form of αII-spectrin in localization of connexin 43 in cardiomyocytes and regulation by stress-activated protein kinase. Journal of Molecular and Cellular Cardiology. 42(3). 572–581. 29 indexed citations

Albuquerque, Edson X., Edna F. R. Pereira, Yasco Aracava, et al.. (2006). Effective countermeasure against poisoning by organophosphorus insecticides and nerve agents. Proceedings of the National Academy of Sciences. 103(35). 13220–13225. 124 indexed citations

Shen, Tiansheng, Zoltán Cseresnyés, Yewei Liu, William R. Randall, & Martin F. Schneider. (2006). Regulation of the nuclear export of the transcription factor NFATc1 by protein kinases after slow fibre type electrical stimulation of adult mouse skeletal muscle fibres. The Journal of Physiology. 579(2). 535–551. 35 indexed citations

10.

Shen, Tiansheng, Yewei Liu, William R. Randall, & Martin F. Schneider. (2006). Parallel mechanisms for resting nucleo-cytoplasmic shuttling and activity dependent translocation provide dual control of transcriptional regulators HDAC and NFAT in skeletal muscle fiber type plasticity. Journal of Muscle Research and Cell Motility. 27(5-7). 405–411. 30 indexed citations

11.

Shen, Tiansheng, Yewei Liu, Zoltán Cseresnyés, et al.. (2006). Activity- and Calcineurin-independent Nuclear Shuttling of NFATc1, but Not NFATc3, in Adult Skeletal Muscle Fibers. Molecular Biology of the Cell. 17(4). 1570–1582. 38 indexed citations

12.

Cohen, Tatiana V. & William R. Randall. (2006). The regulation of acetylcholinesterase by cis‐elements within intron I in cultured contracting myotubes. Journal of Neurochemistry. 98(3). 723–734. 6 indexed citations

13.

Liu, Yewei, Tiansheng Shen, William R. Randall, & Martin F. Schneider. (2005). Signaling pathways in activity-dependent fiber type plasticity in adult skeletal muscle. Journal of Muscle Research and Cell Motility. 26(1). 13–21. 73 indexed citations

14.

Cohen, Tatiana V. & William R. Randall. (2004). NFATc1 activates the acetylcholinesterase promoter in rat muscle. Journal of Neurochemistry. 90(5). 1059–1067. 11 indexed citations

15.

Pereira, Edna F. R., Ping Yü, Emerson Z. Arruda, et al.. (2004). Targeted Deletion of the Kynurenine Aminotransferase II Gene Reveals a Critical Role of Endogenous Kynurenic Acid in the Regulation of Synaptic Transmission viaα7 Nicotinic Receptors in the Hippocampus. Journal of Neuroscience. 24(19). 4635–4648. 114 indexed citations

16.

Salpeter, E. E., et al.. (2002). Transients in acetylcholine receptor site density and degradation during reinnervation of mouse sternomastoid muscle. Journal of Neurochemistry. 84(1). 180–188. 10 indexed citations

17.

Almeida, Luis E.F., Edna F. R. Pereira, Manickavasagom Alkondon, et al.. (2000). The opioid antagonist naltrexone inhibits activity and alters expression of α7 and α4β2 nicotinic receptors in hippocampal neurons: implications for smoking cessation programs. Neuropharmacology. 39(13). 2740–2755. 39 indexed citations

18.

Alkondon, Manickavasagom, Edna F. R. Pereira, Luis E.F. Almeida, William R. Randall, & Edson X. Albuquerque. (2000). Nicotine at concentrations found in cigarette smokers activates and desensitizes nicotinic acetylcholine receptors in CA1 interneurons of rat hippocampus. Neuropharmacology. 39(13). 2726–2739. 119 indexed citations

19.

Rimer, Mendell & William R. Randall. (1999). Denervation of Chicken Skeletal Muscle Causes an Increase in Acetylcholinesterase mRNA Synthesis. Biochemical and Biophysical Research Communications. 260(1). 251–255. 8 indexed citations

20.

Tsim, Karl Wah Keung, William R. Randall, & Eric A. Barnard. (1988). Identification of a 17 S asymmetric butyrylcholinesterase in chick muscle by monoclonal antibodies. Neuroscience Letters. 86(2). 245–249. 4 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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