William L. Pak

7.2k total citations · 1 hit paper
98 papers, 5.7k citations indexed

About

William L. Pak is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Endocrine and Autonomic Systems. According to data from OpenAlex, William L. Pak has authored 98 papers receiving a total of 5.7k indexed citations (citations by other indexed papers that have themselves been cited), including 80 papers in Cellular and Molecular Neuroscience, 68 papers in Molecular Biology and 17 papers in Endocrine and Autonomic Systems. Recurrent topics in William L. Pak's work include Neurobiology and Insect Physiology Research (68 papers), Retinal Development and Disorders (38 papers) and Photoreceptor and optogenetics research (32 papers). William L. Pak is often cited by papers focused on Neurobiology and Insect Physiology Research (68 papers), Retinal Development and Disorders (38 papers) and Photoreceptor and optogenetics research (32 papers). William L. Pak collaborates with scholars based in United States, South Korea and Bulgaria. William L. Pak's co-authors include Randall D. Shortridge, Joseph E. O’Tousa, Stephan Schneuwly, Martin G. Burg, Joseph Grossfield, Baruch Minke, Paulo A. Ferreira, Brian T. Bloomquist, Hung‐Tat Leung and Meredithe Applebury and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

William L. Pak

97 papers receiving 5.5k citations

Hit Papers

Isolation of a putative phospholipase c gene of drosophil... 1988 2026 2000 2013 1988 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
William L. Pak United States 45 4.0k 3.3k 876 657 575 98 5.7k
Baruch Minke Israel 42 4.0k 1.0× 2.8k 0.8× 937 1.1× 383 0.6× 2.0k 3.5× 125 5.9k
Paul M. Salvaterra United States 38 3.6k 0.9× 3.5k 1.1× 432 0.5× 600 0.9× 146 0.3× 72 6.5k
Chun‐Fang Wu United States 39 3.1k 0.8× 2.2k 0.7× 229 0.3× 718 1.1× 203 0.4× 96 4.6k
Robert W. Hardy United States 25 1.5k 0.4× 2.4k 0.7× 273 0.3× 625 1.0× 216 0.4× 31 3.7k
Stephan Schneuwly Germany 32 1.9k 0.5× 2.3k 0.7× 609 0.7× 466 0.7× 118 0.2× 52 4.0k
Barry Ganetzky United States 58 5.2k 1.3× 7.8k 2.4× 448 0.5× 1.8k 2.8× 282 0.5× 137 11.3k
Thomas Préat France 41 4.0k 1.0× 1.9k 0.6× 573 0.7× 662 1.0× 197 0.3× 96 6.0k
Benjamin H. White United States 33 3.2k 0.8× 1.6k 0.5× 717 0.8× 360 0.5× 125 0.2× 56 4.4k
Sean T. Sweeney United Kingdom 29 2.3k 0.6× 2.0k 0.6× 279 0.3× 1.3k 2.0× 179 0.3× 78 4.3k
Toshihiro Kitamoto United States 31 3.2k 0.8× 1.1k 0.3× 628 0.7× 275 0.4× 182 0.3× 74 4.0k

Countries citing papers authored by William L. Pak

Since Specialization
Citations

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

Fields of papers citing papers by William L. Pak

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of William L. Pak

This figure shows the co-authorship network connecting the top 25 collaborators of William L. Pak. A scholar is included among the top collaborators of William L. Pak 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 L. Pak. William L. Pak 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.
Mahapatra, Cecon T., Elvin Woodruff, Jeffrey Rohrbough, et al.. (2010). The nonsense-mediated decay pathway maintains synapse architecture and synaptic vesicle cycle efficacy. Journal of Cell Science. 123(19). 3303–3315. 43 indexed citations
2.
Pak, William L.. (2010). WhyDrosophilato Study Phototransduction?. Journal of Neurogenetics. 24(2). 55–66. 21 indexed citations
3.
Lu, Haiqin, Hung‐Tat Leung, Ning Wang, William L. Pak, & Bih‐Hwa Shieh. (2009). Role of Ca2+/Calmodulin-dependent Protein Kinase II in Drosophila Photoreceptors. Journal of Biological Chemistry. 284(17). 11100–11109. 16 indexed citations
4.
Geng, Chaoxian, et al.. (2004). Complete RNAi rescue of neuronal degeneration in a constitutively active Drosophila TRP channel mutant. Biochimica et Biophysica Acta (BBA) - General Subjects. 1674(1). 91–97. 4 indexed citations
5.
Geng, Chaoxian & William L. Pak. (2002). Photoreceptor Degeneration and Ca2+ Influx Through Light-Activated Channels of Drosophila. Advances in experimental medicine and biology. 514. 585–599. 5 indexed citations
6.
Leung, Hung‐Tat, Zhan Yin, Eugene Semenov, et al.. (2002). The Target of Drosophila Photoreceptor Synaptic Transmission Is a Histamine-gated Chloride Channel Encoded byort (hclA). Journal of Biological Chemistry. 277(44). 42113–42120. 104 indexed citations
7.
Semenov, Eugene & William L. Pak. (1999). Diversification of Drosophila Chloride Channel Gene by Multiple Posttranscriptional mRNA Modifications. Journal of Neurochemistry. 72(1). 66–72. 71 indexed citations
8.
Burg, Martin G., et al.. (1996). Drosophila Rosa Gene, Which When Mutant Causes Aberrant Photoreceptor Oscillation, Encodes A Novel Neurotransmitter Transporter Homologue. Journal of Neurogenetics. 11(1-2). 59–79. 15 indexed citations
9.
Buchner, Sigrid, Franziska F. Wiebel, Ronni Wolf, et al.. (1996). Genetic depletion of histamine from the nervous system of Drosophila eliminates specific visual and mechanosensory behavior. Journal of Comparative Physiology A. 179(6). 763–73. 70 indexed citations
10.
Matsumoto, Hiroyuki, Biji T. Kurien, Yuichiro Takagi, et al.. (1994). Phosrestin I undergoes the earliest light-induced phosphorylation by a calcium/calmodulin-dependent protein kinase in drosophila photoreceptors. Neuron. 12(5). 997–1010. 96 indexed citations
11.
Bowman, Valorie D., et al.. (1992). Degeneration of photoreceptors in rhodopsin mutants of Drosophila. Journal of Neurobiology. 23(6). 605–626. 81 indexed citations
12.
Pak, William L.. (1986). Genes encoding visual pigments. Photobiochemistry and photobiophysics.. 13(3-4). 229–244. 4 indexed citations
13.
Johnson, Edwin C. & William L. Pak. (1986). Electrophysiological study of Drosophila rhodopsin mutants.. The Journal of General Physiology. 88(5). 651–673. 76 indexed citations
14.
Lo, Megan & William L. Pak. (1981). Light-induced pigment granule migration in the retinular cells of Drosophila melanogaster. Comparison of wild type with ERG-defective mutants.. The Journal of General Physiology. 77(2). 155–175. 44 indexed citations
15.
Stephenson, Robert S. & William L. Pak. (1980). Heterogenic components of a fast electrical potential in Drosophila compound eye and their relation to visual pigment photoconversion.. The Journal of General Physiology. 75(4). 353–379. 19 indexed citations
16.
Pak, William L., et al.. (1978). Ionic mechanism for the generation of horizontal cell potentials in isolated axolotl retina.. The Journal of General Physiology. 71(1). 69–92. 16 indexed citations
17.
Wu, Chunfu & William L. Pak. (1978). Light-induced voltage noise in the photoreceptor of Drosophila melanogaster.. The Journal of General Physiology. 71(3). 249–268. 46 indexed citations
18.
Pak, William L., et al.. (1974). Fast Electrical Potential from a Long-Lived, Long-Wavelength Photoproduct of Fly Visual Pigment. The Journal of General Physiology. 63(6). 740–756. 73 indexed citations
19.
Pinto, Lawrence H. & William L. Pak. (1974). Light-Induced Changes in Photoreceptor Membrane Resistance and Potential in Gecko Retinas. The Journal of General Physiology. 64(1). 26–48. 26 indexed citations
20.
Pak, William L. & Thomas G. Ebrey. (1966). Early Receptor Potentials of Rods and Cones in Rodents. The Journal of General Physiology. 49(6). 1199–1208. 24 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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