Philip J. Norris

12.1k total citations · 2 hit papers
192 papers, 7.2k citations indexed

About

Philip J. Norris is a scholar working on Virology, Immunology and Hematology. According to data from OpenAlex, Philip J. Norris has authored 192 papers receiving a total of 7.2k indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Virology, 51 papers in Immunology and 43 papers in Hematology. Recurrent topics in Philip J. Norris's work include HIV Research and Treatment (55 papers), Blood transfusion and management (38 papers) and Blood groups and transfusion (34 papers). Philip J. Norris is often cited by papers focused on HIV Research and Treatment (55 papers), Blood transfusion and management (38 papers) and Blood groups and transfusion (34 papers). Philip J. Norris collaborates with scholars based in United States, Canada and United Kingdom. Philip J. Norris's co-authors include Michael P. Busch, John W. Heitman, Douglas F. Nixon, Marion C. Lanteri, Sheila M. Keating, Heather C. Inglis, Suchitra Pandey, Mila Lebedeva, Jeffrey M. Milush and Persephone Borrow and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Blood.

In The Last Decade

Philip J. Norris

183 papers receiving 7.1k citations

Hit Papers

Induction of a Striking S... 2009 2026 2014 2020 2009 2010 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
Philip J. Norris United States 44 2.8k 1.9k 1.5k 1.3k 1.2k 192 7.2k
JE Groopman United States 34 1.5k 0.5× 1.6k 0.8× 967 0.6× 755 0.6× 604 0.5× 55 4.5k
Thomas N. Denny United States 42 1.5k 0.5× 1.4k 0.7× 1.2k 0.8× 916 0.7× 1.1k 0.9× 162 5.0k
Arthur J. Ammann United States 39 2.3k 0.8× 812 0.4× 1.1k 0.7× 1.8k 1.5× 947 0.8× 142 5.7k
Ronald T. Mitsuyasu United States 48 3.3k 1.2× 4.2k 2.1× 2.6k 1.8× 2.4k 1.9× 1.8k 1.5× 178 10.3k
Ineke J. M. ten Berge Netherlands 48 3.8k 1.4× 579 0.3× 978 0.7× 2.8k 2.2× 799 0.7× 189 7.7k
Annamari Ranki Finland 47 3.4k 1.2× 1.1k 0.6× 1.2k 0.8× 2.2k 1.7× 1.3k 1.0× 226 8.8k
Tyler J. Curiel United States 52 6.3k 2.2× 857 0.4× 538 0.4× 1.4k 1.2× 3.0k 2.4× 196 11.9k
Savita Pahwa United States 54 5.4k 1.9× 4.7k 2.4× 2.9k 1.9× 3.3k 2.7× 1.3k 1.1× 360 10.9k
W. Conrad Liles United States 52 2.9k 1.0× 136 0.1× 1.2k 0.8× 1.6k 1.3× 2.0k 1.6× 158 9.9k
Sunil K. Ahuja United States 45 3.2k 1.1× 1.9k 1.0× 1.4k 0.9× 1.1k 0.9× 1.0k 0.8× 117 6.8k

Countries citing papers authored by Philip J. Norris

Since Specialization
Citations

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

Fields of papers citing papers by Philip J. Norris

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Philip J. Norris

This figure shows the co-authorship network connecting the top 25 collaborators of Philip J. Norris. A scholar is included among the top collaborators of Philip J. Norris 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 J. Norris. Philip J. Norris 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.
3.
D’Alessandro, Angelo, Gregory R. Keele, Ariel Hay, et al.. (2024). Ferroptosis regulates hemolysis in stored murine and human red blood cells. Blood. 145(7). 765–783. 13 indexed citations
4.
Callegari, Andrea, Gaomai Yang, Mark Kline, et al.. (2021). A bioinspired and chemically defined alternative to dimethyl sulfoxide for the cryopreservation of human hematopoietic stem cells. Bone Marrow Transplantation. 56(11). 2644–2650. 10 indexed citations
5.
Numis, Adam L., et al.. (2021). Comparison of multiplex cytokine assays in a pediatric cohort with epilepsy. Heliyon. 7(3). e06445–e06445. 8 indexed citations
6.
Kelly, Shannon, Evan Jacobs, Mars Stone, et al.. (2020). Influence of sickle cell disease on susceptibility to HIV infection. PLoS ONE. 15(4). e0218880–e0218880. 8 indexed citations
7.
Saris, Anno, Jean‐Louis Kerkhoffs, Philip J. Norris, et al.. (2018). The role of pathogen‐reduced platelet transfusions on HLA alloimmunization in hemato‐oncological patients. Transfusion. 59(2). 470–481. 23 indexed citations
8.
Keating, Sheila M., Jennifer L. Dodge, Philip J. Norris, et al.. (2017). The effect of HIV infection and HCV viremia on inflammatory mediators and hepatic injury—The Women’s Interagency HIV Study. PLoS ONE. 12(9). e0181004–e0181004. 9 indexed citations
9.
Shikuma, Cecilia M., Richard M. Watanabe, Bruce Shiramizu, et al.. (2017). Plasminogen Activator Inhibitor-1 Predicts Negative Alterations in Whole-Body Insulin Sensitivity in Chronic HIV Infection. AIDS Research and Human Retroviruses. 33(7). 723–727. 5 indexed citations
10.
Jackman, Rachael P., Marcus O. Muench, Heather C. Inglis, et al.. (2016). Reduced MHC alloimmunization and partial tolerance protection with pathogen reduction of whole blood. Transfusion. 57(2). 337–348. 12 indexed citations
11.
Baimukanova, Gyulnar, Byron Miyazawa, Daniel Potter, et al.. (2016). The effects of 22°C and 4°C storage of platelets on vascular endothelial integrity and function. Transfusion. 56(S1). S52–64. 30 indexed citations
13.
Toy, Pearl, Peter Bacchetti, Barbara Grimes, et al.. (2014). Recipient clinical risk factors predominate in possible transfusion‐related acute lung injury. Transfusion. 55(5). 947–952. 25 indexed citations
14.
Tandon, Ravi, Glen M. Chew, Persephone Borrow, et al.. (2014). Galectin-9 Is Rapidly Released During Acute HIV-1 Infection and Remains Sustained at High Levels Despite Viral Suppression Even in Elite Controllers. AIDS Research and Human Retroviruses. 30(7). 654–664. 64 indexed citations
15.
Parrinello, Christina M., Alan Landay, Howard N. Hodis, et al.. (2013). Treatment-related changes in serum lipids and inflammation. AIDS. 27(9). 1516–1519. 6 indexed citations
16.
Shikuma, Cecilia M., Jason D. Barbour, Lishomwa C. Ndhlovu, et al.. (2013). Plasma Monocyte Chemoattractant Protein-1 and Tumor Necrosis Factor-α Levels Predict the Presence of Coronary Artery Calcium in HIV-Infected Individuals Independent of Traditional Cardiovascular Risk Factors. AIDS Research and Human Retroviruses. 30(2). 142–146. 21 indexed citations
17.
Eriksson, Emily M., Jeffrey M. Milush, Emily Ho, et al.. (2011). Expansion of CD8+ T cells lacking Sema4D/CD100 during HIV-1 infection identifies a subset of T cells with decreased functional capacity. Blood. 119(3). 745–755. 30 indexed citations
18.
Liu, Jinyan, Brandon F. Keele, Hui Li, et al.. (2010). Low-Dose Mucosal Simian Immunodeficiency Virus Infection Restricts Early Replication Kinetics and Transmitted Virus Variants in Rhesus Monkeys. Journal of Virology. 84(19). 10406–10412. 88 indexed citations
19.
Stacey, Andrea, Philip J. Norris, Qin Li, et al.. (2009). Induction of a Striking Systemic Cytokine Cascade prior to Peak Viremia in Acute Human Immunodeficiency Virus Type 1 Infection, in Contrast to More Modest and Delayed Responses in Acute Hepatitis B and C Virus Infections. Journal of Virology. 83(8). 3719–3733. 555 indexed citations breakdown →
20.
Zavala‐Ruiz, Zarixia, et al.. (2004). A hairpin turn in a class II MHC-bound peptide orients residues outside the binding groove for T cell recognition. Proceedings of the National Academy of Sciences. 101(36). 13279–13284. 55 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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