Philip Willson

4.2k total citations
81 papers, 3.3k citations indexed

About

Philip Willson is a scholar working on Immunology, Infectious Diseases and Microbiology. According to data from OpenAlex, Philip Willson has authored 81 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Immunology, 20 papers in Infectious Diseases and 20 papers in Microbiology. Recurrent topics in Philip Willson's work include Immune Response and Inflammation (14 papers), Viral gastroenteritis research and epidemiology (13 papers) and Streptococcal Infections and Treatments (12 papers). Philip Willson is often cited by papers focused on Immune Response and Inflammation (14 papers), Viral gastroenteritis research and epidemiology (13 papers) and Streptococcal Infections and Treatments (12 papers). Philip Willson collaborates with scholars based in Canada, United States and Germany. Philip Willson's co-authors include Andrew Potter, Susantha Gomis, Lorne A. Babiuk, Brenda Allan, Marcelo Gottschalk, José Perez‐Casal, Sonia Lacouture, John C. S. Harding, Shichun Lun and Lori E. Hassard and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Virology and Scientific Reports.

In The Last Decade

Philip Willson

81 papers receiving 3.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Philip Willson Canada 34 1.1k 867 753 708 638 81 3.3k
Paul C. Bartlett United States 40 800 0.7× 367 0.4× 896 1.2× 386 0.5× 312 0.5× 159 4.5k
M. M. Chengappa United States 33 1.4k 1.2× 477 0.6× 464 0.6× 1.2k 1.6× 1.3k 2.0× 102 3.9k
Peter Ahrens Denmark 43 1.1k 1.0× 610 0.7× 992 1.3× 1.4k 1.9× 304 0.5× 163 5.7k
Hugh G.G. Townsend Canada 38 942 0.8× 490 0.6× 1.0k 1.4× 569 0.8× 212 0.3× 138 4.5k
Greg Keefe Canada 38 448 0.4× 502 0.6× 484 0.6× 461 0.7× 178 0.3× 97 4.4k
R. Ducatelle Belgium 27 544 0.5× 605 0.7× 316 0.4× 668 0.9× 148 0.2× 100 2.3k
R.C. Bicalho United States 49 558 0.5× 1.1k 1.3× 654 0.9× 680 1.0× 239 0.4× 159 6.6k
Daisy Vanrompay Belgium 41 929 0.8× 369 0.4× 675 0.9× 3.0k 4.3× 324 0.5× 191 5.1k
John F. Timoney United States 39 1.3k 1.1× 361 0.4× 476 0.6× 1.5k 2.1× 2.1k 3.3× 180 4.9k
In‐Soo Choi South Korea 34 1.5k 1.4× 799 0.9× 460 0.6× 206 0.3× 138 0.2× 193 3.7k

Countries citing papers authored by Philip Willson

Since Specialization
Citations

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

Fields of papers citing papers by Philip Willson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Philip Willson

This figure shows the co-authorship network connecting the top 25 collaborators of Philip Willson. A scholar is included among the top collaborators of Philip Willson 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 Philip Willson. Philip Willson 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.
Ahmed, Khawaja Ashfaque, Kalhari Goonewardene, Shelly Popowich, et al.. (2020). CpG‐ODN Induces a Dose‐Dependent Enrichment of Immunological Niches in the Spleen and Lungs of Neonatal Chicks That Correlates with the Protective Immunity against Escherichia coli. Journal of Immunology Research. 2020(1). 2704728–2704728. 10 indexed citations
2.
Gupta, Ashish, Khawaja Ashfaque Ahmed, Lisanework E. Ayalew, et al.. (2017). Immunogenicity and protective efficacy of virus-like particles and recombinant fiber proteins in broiler-breeder vaccination against fowl adenovirus (FAdV)-8b. Vaccine. 35(20). 2716–2722. 37 indexed citations
3.
Gupta, Ashish, Shelly Popowich, Davor Ojkić, et al.. (2017). Inactivated and live bivalent fowl adenovirus (FAdV8b + FAdV11) breeder vaccines provide broad-spectrum protection in chicks against inclusion body hepatitis (IBH). Vaccine. 36(5). 744–750. 16 indexed citations
4.
Ahmed, Khawaja Ashfaque, Davor Ojkić, Kalhari Goonewardene, et al.. (2017). Modified live infectious bursal disease virus (IBDV) vaccine delays infection of neonatal broiler chickens with variant IBDV compared to turkey herpesvirus (HVT)-IBDV vectored vaccine. Vaccine. 35(6). 882–888. 23 indexed citations
5.
Popowich, Shelly, et al.. (2016). A 5-year study of the incidence and economic impact of variant infectious bursal disease viruses on broiler production in Saskatchewan, Canada.. PubMed. 80(4). 255–261. 34 indexed citations
6.
Pahwa, Punam, Chandima Karunanayake, Philip Willson, et al.. (2012). Prevalence of Chronic Bronchitis in Farm and Nonfarm Rural Residents in Saskatchewan. Journal of Occupational and Environmental Medicine. 54(12). 1481–1490. 11 indexed citations
7.
Willson, Philip, et al.. (2010). Fractionation of Swine Barn Dust and Assessment of Its Impact on the Respiratory Tract Following Repeated Airway Exposure. Journal of Toxicology and Environmental Health. 73(16). 1090–1101. 14 indexed citations
8.
Gomis, Susantha, Arshud Dar, Philip Willson, et al.. (2008). Oligodeoxynucleotides containing CpG motifs (CpG-ODN) predominantly induce Th1-type immune response in neonatal chicks. Developmental & Comparative Immunology. 32(9). 1041–1049. 56 indexed citations
9.
Willson, Philip, B. H. J. Juurlink, Ambikaipakan Senthilselvan, et al.. (2008). In VitroProduction of Tumor Necrosis Factor-Alpha by Human Monocytes Stimulated with Lipopolysaccharide is Positively Correlated with Increased Blood Monocytes After Exposure to a Swine Barn. Journal of Toxicology and Environmental Health. 71(21). 1401–1406. 6 indexed citations
10.
Gomis, Susantha, Lorne A. Babiuk, Brenda Allan, et al.. (2007). Protection of Chickens Against a Lethal Challenge of Escherichia coli by a Vaccine Containing CpG Oligodeoxynucleotides as an Adjuvant. Avian Diseases. 51(1). 78–83. 32 indexed citations
11.
Biswas, Debabrata, Brenda Allan, S. K. ATTAH‐POKU, et al.. (2007). Serological assessment of synthetic peptides of Campylobacter jejuni NCTC11168 FlaA protein using antibodies against multiple serotypes. Medical Microbiology and Immunology. 197(1). 45–53. 6 indexed citations
12.
Kirychuk, Shelley, J A Dosman, Stephen J. Reynolds, et al.. (2006). Total Dust and Endotoxin in Poultry Operations: Comparison Between Cage and Floor Housing and Respiratory Effects in Workers. Journal of Occupational and Environmental Medicine. 48(7). 741–748. 72 indexed citations
13.
Baca‐Estrada, Maria E., Marco Antonio Vega‐López, Philip Willson, et al.. (2005). Mucosal delivery of bacterial antigens and CpG oligonucleotides formulated in biphasic lipid vesicles in pigs. The AAPS Journal. 7(3). E566–E571. 21 indexed citations
14.
Gomis, Susantha, Lorne A. Babiuk, Brenda Allan, et al.. (2004). Protection of Neonatal Chicks Against a Lethal Challenge of Escherichia coli Using DNA Containing Cytosine-Phosphodiester-Guanine Motifs. Avian Diseases. 48(4). 813–822. 70 indexed citations
15.
Carrillo, Catherine D., Eduardo N. Taboada, John H. E. Nash, et al.. (2004). Genome-wide Expression Analyses of Campylobacter jejuni NCTC11168 Reveals Coordinate Regulation of Motility and Virulence by flhA. Journal of Biological Chemistry. 279(19). 20327–20338. 156 indexed citations
16.
Lun, Shichun, José Perez‐Casal, Wayne Connor, & Philip Willson. (2003). Role of suilysin in pathogenesis of Streptococcus suis capsular serotype 2. Microbial Pathogenesis. 34(1). 27–37. 92 indexed citations
17.
Perez‐Casal, José, et al.. (2002). Changes in the leucocyte subpopulations of the palatine tonsillar crypt epithelium of pigs in response to Streptococcus suis type 2 infection. Veterinary Immunology and Immunopathology. 87(1-2). 51–63. 18 indexed citations
18.
Cooper, Barry, et al.. (1989). CATALYSTS IN AUTOMOBILES : A HISTORY. Automotive engineering. 97(6). 2 indexed citations
19.
Willson, Philip, et al.. (1987). Detection of Actinobacillus pleuropneumoniae Infection in Pigs.. PubMed. 28(3). 111–6. 30 indexed citations
20.
Raybould, T. J. G., et al.. (1985). A porcine-murine hybridoma that secretes porcine monoclonal antibody of defined specificity. American Journal of Veterinary Research. 46(8). 1768–1769. 13 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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