William Schook

526 total citations
19 papers, 456 citations indexed

About

William Schook is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, William Schook has authored 19 papers receiving a total of 456 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 14 papers in Cell Biology and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in William Schook's work include Cellular transport and secretion (13 papers), Lipid Membrane Structure and Behavior (9 papers) and Ion channel regulation and function (5 papers). William Schook is often cited by papers focused on Cellular transport and secretion (13 papers), Lipid Membrane Structure and Behavior (9 papers) and Ion channel regulation and function (5 papers). William Schook collaborates with scholars based in United States and United Kingdom. William Schook's co-authors include Saul Puszkin, Nathan Moskowitz, Michael P. Lisanti, Lawrence E. Shapiro, Lawrence Shapiro, William T. Norton, W S Bloom, D. Stave Kohtz, Jhumku D. Kohtz and Adam R. Glassman and has published in prestigious journals such as Science, Brain Research and Biochemical and Biophysical Research Communications.

In The Last Decade

William Schook

19 papers receiving 422 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
William Schook United States 14 354 222 112 66 27 19 456
Nathan Moskowitz United States 13 320 0.9× 195 0.9× 101 0.9× 62 0.9× 30 1.1× 21 447
H. Kuzuya Japan 10 309 0.9× 104 0.5× 169 1.5× 75 1.1× 37 1.4× 32 503
M J de Hoop Netherlands 10 443 1.3× 279 1.3× 109 1.0× 82 1.2× 24 0.9× 12 599
Klim King Taiwan 9 443 1.3× 148 0.7× 115 1.0× 36 0.5× 19 0.7× 10 565
Ravi Nadimpalli United States 7 478 1.4× 265 1.2× 155 1.4× 68 1.0× 35 1.3× 7 691
Koh Yano Japan 12 323 0.9× 66 0.3× 117 1.0× 68 1.0× 59 2.2× 18 535
Sara Vanlingen Belgium 16 712 2.0× 229 1.0× 150 1.3× 49 0.7× 25 0.9× 24 872
Lucio A.A. Van Rooijen United States 12 246 0.7× 69 0.3× 124 1.1× 33 0.5× 36 1.3× 23 405
Cynthia M. Van De Walle United States 6 319 0.9× 59 0.3× 116 1.0× 86 1.3× 19 0.7× 7 426
Alan A. Finegold United States 8 343 1.0× 90 0.4× 102 0.9× 94 1.4× 69 2.6× 9 549

Countries citing papers authored by William Schook

Since Specialization
Citations

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

Fields of papers citing papers by William Schook

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of William Schook

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

All Works

19 of 19 papers shown
1.
Hanson, Veneta, William Schook, & Saul Puszkin. (1990). Novel Regulatory Role of Phosphorylated Clathrin Light Chain β in Bovine Brain Coated Vesicles. Journal of Neurochemistry. 54(1). 46–50. 6 indexed citations
2.
Puszkin, Saul, Jhumku D. Kohtz, William Schook, & D. Stave Kohtz. (1989). Clathrin‐Coated Vesicle Subtypes in Mammalian Brain Tissue: Detection of Polypeptide Heterogeneity by Immunoprecipitation with Monoclonal Antibodies. Journal of Neurochemistry. 53(1). 51–63. 18 indexed citations
3.
Schook, William, et al.. (1988). Brain Coated Vesicle Destabilization and Phosphorylation of Coat Proteins. Journal of Neurochemistry. 50(1). 307–315. 17 indexed citations
4.
Schook, William, et al.. (1987). Phosphorylation Characteristics of Brain Clathrin‐Coated Vesicle Endogenous Proteins. Journal of Neurochemistry. 49(2). 434–441. 5 indexed citations
5.
Schook, William, et al.. (1986). Cyclic Nucleotide Phosphodiesterase Activity in Bovine Brain Coated Vesicles. Journal of Neurochemistry. 46(4). 1263–1271. 6 indexed citations
6.
Moskowitz, Nathan, Antonio Andrés, Walter Silva, et al.. (1985). Calcium-dependent binding of calmodulin to phospholipase A2 subunits induces enzymatic activation. Archives of Biochemistry and Biophysics. 241(2). 413–417. 17 indexed citations
7.
Moskowitz, Nathan, William Schook, & Saul Puszkin. (1984). Regulation of endogenous calcium-dependent synaptic membrane phospholipase A2. Brain Research. 290(2). 273–280. 30 indexed citations
8.
Moskowitz, Nathan, et al.. (1983). Phosphorylation of Brain Synaptic and Coated Vesicle Proteins by Endogenous Ca2+/Calmodulin‐ and cAMP‐Dependent Protein Kinases. Journal of Neurochemistry. 40(3). 711–718. 22 indexed citations
9.
Moskowitz, Nathan, Saul Puszkin, & William Schook. (1983). Characterization of Brain Synaptic Vesicle Phospholipase A2 Activity and Its Modulation by Calmodulin, Prostaglandin E2, Prostaglandin F2α, Cyclic AMP, and ATP. Journal of Neurochemistry. 41(6). 1576–1586. 37 indexed citations
10.
Moskowitz, Nathan, Lawrence E. Shapiro, William Schook, & Saul Puszkin. (1983). Phospholipase A 2 modulation by calmodulin, prostaglandins and cyclic nucleotides. Biochemical and Biophysical Research Communications. 115(1). 94–99. 40 indexed citations
11.
Moskowitz, Nathan, et al.. (1983). Preliminary characterization of synaptic vesicle/calmodulin interaction. Brain Research. 263(2). 243–250. 13 indexed citations
12.
Moskowitz, Nathan, William Schook, & Saul Puszkin. (1982). Comparison of calmodulin binding to brain synaptic and coated vesicles. Biochimica et Biophysica Acta (BBA) - Biomembranes. 689(3). 523–530. 13 indexed citations
13.
Moskowitz, Nathan, William Schook, & Saul Puszkin. (1982). Interaction of Brain Synaptic Vesicles Induced by Endogenous Ca 2+ -Dependent Phospholipase A 2. Science. 216(4543). 305–307. 73 indexed citations
14.
Lisanti, Michael P., et al.. (1982). Isolation and Preliminary Characterization of Clathrin-Associated Proteins. European Journal of Biochemistry. 125(2). 463–470. 73 indexed citations
15.
Lisanti, Michael P., et al.. (1982). Brain Clathrin: Studies of Its Ultrastructural Assemblies. European Journal of Biochemistry. 121(3). 617–622. 22 indexed citations
16.
Moskowitz, Nathan, et al.. (1982). Calmodulin Affinity for Brain Coated Vesicle Proteins. Journal of Neurochemistry. 38(6). 1742–1747. 20 indexed citations
17.
Bloom, W S, et al.. (1980). Brain clathrin. Biochimica et Biophysica Acta (BBA) - Biomembranes. 598(3). 447–455. 18 indexed citations
18.
Puszkin, Saul, et al.. (1977). Immunological identification of complex proteins resolved by sodium dodecyl sulfate polyacrylamide disc gel electrophoresis. Biochimica et Biophysica Acta (BBA) - Protein Structure. 494(1). 144–149. 5 indexed citations
19.
Schook, William & William T. Norton. (1976). Neurofilaments account for the lipid in myelin-free axons. Brain Research. 118(3). 517–522. 21 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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