William D. Swaim

4.2k total citations
61 papers, 3.4k citations indexed

About

William D. Swaim is a scholar working on Molecular Biology, Physiology and Immunology. According to data from OpenAlex, William D. Swaim has authored 61 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 18 papers in Physiology and 17 papers in Immunology. Recurrent topics in William D. Swaim's work include Salivary Gland Disorders and Functions (12 papers), Ion Channels and Receptors (11 papers) and Monoclonal and Polyclonal Antibodies Research (6 papers). William D. Swaim is often cited by papers focused on Salivary Gland Disorders and Functions (12 papers), Ion Channels and Receptors (11 papers) and Monoclonal and Polyclonal Antibodies Research (6 papers). William D. Swaim collaborates with scholars based in United States, Japan and United Kingdom. William D. Swaim's co-authors include Indu S. Ambudkar, Xibao Liu, Kwong Tai Cheng, Brij B. Singh, Reuben P. Siraganian, Hwei Ling Ong, Bidhan C. Bandyopadhyay, Sharon M. Wahl, Changyu Zheng and Kenji Minoguchi and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

William D. Swaim

61 papers receiving 3.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
William D. Swaim United States	33	1.3k	915	773	569	369	61	3.4k
Chaker N. Adra United States	32	1.6k 1.2×	599 0.7×	201 0.3×	649 1.1×	247 0.7×	57	3.5k
Dennis Brown United States	22	2.1k 1.5×	414 0.5×	269 0.3×	355 0.6×	585 1.6×	34	3.9k
Troy Stevens United States	51	3.2k 2.4×	1.4k 1.6×	716 0.9×	593 1.0×	718 1.9×	158	6.6k
Keiko Uchida Japan	35	1.8k 1.3×	360 0.4×	203 0.3×	451 0.8×	270 0.7×	233	4.9k
Austin K. Mircheff United States	37	1.4k 1.0×	1.1k 1.2×	184 0.2×	236 0.4×	599 1.6×	125	4.4k
Tetsuji Yamashita Japan	28	681 0.5×	556 0.6×	383 0.5×	648 1.1×	136 0.4×	79	2.5k
Yoichi Matsubara Japan	43	4.0k 3.0×	515 0.6×	250 0.3×	849 1.5×	407 1.1×	229	6.6k
Junji Nishimura Japan	36	2.7k 2.0×	1.5k 1.6×	141 0.2×	523 0.9×	375 1.0×	276	5.6k
Thomas Boettger Germany	45	5.4k 4.0×	839 0.9×	233 0.3×	613 1.1×	321 0.9×	98	8.1k
Gillian L. Busch Germany	17	1.6k 1.2×	573 0.6×	134 0.2×	218 0.4×	467 1.3×	24	2.6k

Countries citing papers authored by William D. Swaim

Since Specialization

Citations

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

Fields of papers citing papers by William D. Swaim

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of William D. Swaim

This figure shows the co-authorship network connecting the top 25 collaborators of William D. Swaim. A scholar is included among the top collaborators of William D. Swaim 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 D. Swaim. William D. Swaim 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

Tanaka, Tsutomu, Maria C. Guimaro, Hiroyuki Nakamura, et al.. (2023). Association of G protein‐coupled receptor 78 with salivary dysfunction in male Sjögren's patients. Oral Diseases. 30(3). 1173–1182. 3 indexed citations

Nakamura, Hiroyuki, Tsutomu Tanaka, Thomas Pranzatelli, et al.. (2021). Lysosome-associated membrane protein 3 misexpression in salivary glands induces a Sjögren's syndrome-like phenotype in mice. Annals of the Rheumatic Diseases. 80(8). 1031–1039. 26 indexed citations

Yin, Hongen, Zhennan Lai, Maria C. Guimaro, et al.. (2020). Inhibition of bone morphogenetic protein 6 receptors ameliorates Sjögren’s syndrome in mice. Scientific Reports. 10(1). 2967–2967. 17 indexed citations

Weller, Melodie L., Michael A. Smith, Elisa Astorri, et al.. (2016). Hepatitis Delta Virus Detected in Salivary Glands of Sjögren’s Syndrome Patients and Recapitulates a Sjögren’s Syndrome-Like Phenotype in Vivo. SHILAP Revista de lepidopterología. 1(1). 12–12. 39 indexed citations

Katayama, Kazuhiro, Khyati Kapoor, Shinobu Ohnuma, et al.. (2015). Revealing the fate of cell surface human P-glycoprotein (ABCB1): The lysosomal degradation pathway. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1853(10). 2361–2370. 31 indexed citations

Cowen, Edward W., Jeremy J. Rose, William D. Swaim, et al.. (2014). Comparative analysis of FoxP3+ regulatory T cells in the target tissues and blood in chronic graft versus host disease. Leukemia. 28(10). 2016–2027. 30 indexed citations

Liu, Xibao, Ana P. Cotrim, Changyu Zheng, et al.. (2013). Loss of TRPM2 function protects against irradiation-induced salivary gland dysfunction. Nature Communications. 4(1). 1515–1515. 58 indexed citations

Cheng, Kwong Tai, Xibao Liu, Hwei Ling Ong, William D. Swaim, & Indu S. Ambudkar. (2011). Local Ca2+ Entry Via Orai1 Regulates Plasma Membrane Recruitment of TRPC1 and Controls Cytosolic Ca2+ Signals Required for Specific Cell Functions. PLoS Biology. 9(3). e1001025–e1001025. 208 indexed citations

Hall, Bradford E., Changyu Zheng, William D. Swaim, et al.. (2010). Conditional overexpression of TGF-β1 disrupts mouse salivary gland development and function. Laboratory Investigation. 90(4). 543–555. 76 indexed citations

10.

Landek‐Salgado, Melissa A., Hongen Yin, William D. Swaim, et al.. (2009). Interleukin‐12 induces salivary gland dysfunction in transgenic mice, providing a new model of Sjögren's syndrome. Arthritis & Rheumatism. 60(12). 3633–3641. 48 indexed citations

11.

Voutetakis, Antonis, Changyu Zheng, Ana P. Cotrim, et al.. (2009). AAV5-mediated gene transfer to the parotid glands of non-human primates. Gene Therapy. 17(1). 50–60. 12 indexed citations

12.

Zhang, Guofeng, Hiroki Hirai, Tao Cai, et al.. (2007). RESP18, a homolog of the luminal domain IA-2, is found in dense core vesicles in pancreatic islet cells and is induced by high glucose. Journal of Endocrinology. 195(2). 313–321. 21 indexed citations

13.

Wellner, Robert B., Robert S. Redman, William D. Swaim, & Bruce J. Baum. (2005). Further evidence for AQP8 expression in the myoepithelium of rat submandibular and parotid glands. Pflügers Archiv - European Journal of Physiology. 451(5). 642–645. 25 indexed citations

14.

Bandyopadhyay, Bidhan C., William D. Swaim, Xibao Liu, et al.. (2004). Apical Localization of a Functional TRPC3/TRPC6-Ca2+-Signaling Complex in Polarized Epithelial Cells. Journal of Biological Chemistry. 280(13). 12908–12916. 89 indexed citations

15.

Swaim, William D., et al.. (2003). Immunohistochemical Localization of μ-Opioid Receptors in Human Dental Pulp. Journal of Endodontics. 29(2). 108–110. 29 indexed citations

16.

Singh, Brij B., et al.. (2003). Caveolin-1 Contributes to Assembly of Store-operated Ca2+ Influx Channels by Regulating Plasma Membrane Localization of TRPC1. Journal of Biological Chemistry. 278(29). 27208–27215. 183 indexed citations

17.

Hoque, A.T.M. Shamsul, Seiichi Yamano, Xibao Liu, et al.. (2002). Expression of the aquaporin 8 water channel in a rat salivary epithelial cell line†. Journal of Cellular Physiology. 191(3). 336–341. 13 indexed citations

18.

Hoque, A.T.M. Shamsul, Xibao Liu, Hideaki Kagami, et al.. (2000). Construction and function of a recombinant adenovirus encoding a human aquaporin 1-green fluorescent protein fusion product. Cancer Gene Therapy. 7(3). 476–485. 14 indexed citations

19.

Swieter, Mark, Elsa H. Berenstein, William D. Swaim, & Reuben P. Siraganian. (1995). Aggregation of IgE Receptors in Rat Basophilic Leukemia 2H3 Cells Induces Tyrosine Phosphorylation of the Cytosolic Protein-tyrosine Phosphatase HePTP. Journal of Biological Chemistry. 270(37). 21902–21906. 24 indexed citations

20.

Hamawy, Majed M., William D. Swaim, Kenji Minoguchi, et al.. (1994). The aggregation of the high affinity IgE receptor induces tyrosine phosphorylation of paxillin, a focal adhesion protein.. The Journal of Immunology. 153(10). 4655–4662. 34 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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