Mary Philip

8.6k total citations · 4 hit papers
64 papers, 4.9k citations indexed

About

Mary Philip is a scholar working on Oncology, Immunology and Pathology and Forensic Medicine. According to data from OpenAlex, Mary Philip has authored 64 papers receiving a total of 4.9k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Oncology, 22 papers in Immunology and 19 papers in Pathology and Forensic Medicine. Recurrent topics in Mary Philip's work include Immune Cell Function and Interaction (16 papers), Lymphoma Diagnosis and Treatment (16 papers) and Infective Endocarditis Diagnosis and Management (14 papers). Mary Philip is often cited by papers focused on Immune Cell Function and Interaction (16 papers), Lymphoma Diagnosis and Treatment (16 papers) and Infective Endocarditis Diagnosis and Management (14 papers). Mary Philip collaborates with scholars based in United States, France and Italy. Mary Philip's co-authors include Andrea Schietinger, Hans Schreiber, Donald A. Rowley, Peter Lauer, Anjana Rao, W. Nicholas Haining, Nicholas P. Restifo, Christian U. Blank, Axel Kallies and Pamela L. Schwartzberg and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Mary Philip

60 papers receiving 4.8k citations

Hit Papers

Defining ‘T cell exhaustion’ 2016 2026 2019 2022 2019 2017 2021 2016 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mary Philip United States 22 3.0k 2.7k 1.2k 447 352 64 4.9k
Matthew D. Vesely United States 18 2.6k 0.9× 2.4k 0.9× 936 0.8× 400 0.9× 179 0.5× 52 4.1k
Eddy C. Hsueh United States 41 2.5k 0.8× 3.0k 1.1× 1.6k 1.3× 674 1.5× 253 0.7× 95 5.1k
Hagen Kulbe Germany 27 2.6k 0.9× 2.1k 0.8× 1.3k 1.1× 834 1.9× 209 0.6× 67 4.4k
Andrea Schietinger United States 25 3.5k 1.2× 3.1k 1.1× 1.2k 1.0× 336 0.8× 127 0.4× 41 5.1k
Yulia Nefedova United States 29 3.9k 1.3× 2.2k 0.8× 1.9k 1.6× 557 1.2× 158 0.4× 53 5.7k
Lindy G. Durrant United Kingdom 40 2.7k 0.9× 2.0k 0.7× 1.9k 1.5× 338 0.8× 246 0.7× 157 4.7k
Marco Donia Denmark 45 3.8k 1.3× 4.3k 1.6× 2.0k 1.6× 490 1.1× 223 0.6× 195 6.7k
David Avigan United States 42 3.7k 1.3× 2.9k 1.1× 3.0k 2.5× 702 1.6× 329 0.9× 208 7.5k
Giuseppe Masucci Sweden 40 3.2k 1.1× 2.5k 0.9× 908 0.7× 298 0.7× 351 1.0× 125 4.8k
Yanyan Lou United States 33 2.5k 0.9× 3.2k 1.2× 1.4k 1.2× 578 1.3× 211 0.6× 122 5.3k

Countries citing papers authored by Mary Philip

Since Specialization
Citations

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

Fields of papers citing papers by Mary Philip

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mary Philip

This figure shows the co-authorship network connecting the top 25 collaborators of Mary Philip. A scholar is included among the top collaborators of Mary Philip 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 Mary Philip. Mary Philip 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.
Revetta, Frank, et al.. (2024). Vaccination generates functional progenitor tumor-specific CD8 T cells and long-term tumor control. Journal for ImmunoTherapy of Cancer. 12(10). e009129–e009129.
2.
Philip, Mary, Jérôme Hourdain, Noémie Resseguier, et al.. (2024). Atrioventricular conduction disorders in aortic valve infective endocarditis. Archives of cardiovascular diseases. 117(5). 304–312. 1 indexed citations
3.
Murray, Kristen A., et al.. (2023). Tumor-Reactive CD8+ T Cells Enter a TCF1+PD-1− Dysfunctional State. Cancer Immunology Research. 11(12). 1630–1641. 7 indexed citations
4.
Zumbo, Paul, et al.. (2023). Hallmarks of CD8+ T cell dysfunction are established within hours of tumor antigen encounter before cell division. Nature Immunology. 24(9). 1527–1539. 64 indexed citations
5.
Arregle, Florent, Christophe Tribouilloy, Bernard Cosyns, et al.. (2023). Multimodality imaging in marantic endocarditis associated with cancer: a multicentric cohort study. European Heart Journal - Cardiovascular Imaging. 24(12). 1620–1626. 5 indexed citations
6.
Bohbot, Yohann, Rossella Maria Benvenga, Mary Philip, et al.. (2023). Characteristics and prognosis of isolated aortic valve infective endocarditis in patients with bicuspid aortic valves: a propensity matched study. Frontiers in Cardiovascular Medicine. 10. 1304957–1304957. 2 indexed citations
7.
Arregle, Florent, Roch Giorgi, Mary Philip, et al.. (2022). Influence of the healthcare pathway on the outcome of patients with infective endocarditis. European Heart Journal Acute Cardiovascular Care. 11(9). 672–681. 3 indexed citations
8.
Philip, Mary, Julien Mancini, L. Tessonnier, et al.. (2021). 18F-fluorodeoxyglucose positron emission tomography/computed tomography for the diagnosis of native valve infective endocarditis: A prospective study. Archives of cardiovascular diseases. 114(3). 211–220. 11 indexed citations
9.
Philip, Mary & Andrea Schietinger. (2021). CD8+ T cell differentiation and dysfunction in cancer. Nature reviews. Immunology. 22(4). 209–223. 590 indexed citations breakdown →
10.
Lynch, Ryan C., Ryan D. Cassaday, Stephen D. Smith, et al.. (2021). Dose-dense brentuximab vedotin plus ifosfamide, carboplatin, and etoposide for second-line treatment of relapsed or refractory classical Hodgkin lymphoma: a single centre, phase 1/2 study. The Lancet Haematology. 8(8). e562–e571. 33 indexed citations
11.
Bohbot, Yohann, Fanny Peugnet, Andreina Carbone, et al.. (2020). Characteristics and Prognosis of Patients With Left-Sided Native Bivalvular Infective Endocarditis. Canadian Journal of Cardiology. 37(2). 292–299. 14 indexed citations
12.
Carbone, Andreina, Basile Mouhat, Mary Philip, et al.. (2020). Spondylitis: A frequent and severe complication of infective endocarditis. Archives of Cardiovascular Diseases Supplements. 12(1). 82–82.
13.
Li, Zhuoyan, Mary Philip, & P. Brent Ferrell. (2020). Alterations of T-cell-mediated immunity in acute myeloid leukemia. Oncogene. 39(18). 3611–3619. 41 indexed citations
14.
Oyebanji, Oyetola O., et al.. (2018). Utility of Nanomedicine for Cancer Treatment. Journal of Nanomedicine & Nanotechnology. 9(1). 6 indexed citations
15.
Philip, Mary, et al.. (2018). A ten year study of pediatric leprosy cases in a tertiary care centre in south Kerala.. 90(2). 95–99. 2 indexed citations
17.
Graf, Solomon A., Philip A. Stevenson, Leona Holmberg, et al.. (2015). Maintenance rituximab after autologous stem cell transplantation in patients with mantle cell lymphoma. Annals of Oncology. 26(11). 2323–2328. 20 indexed citations
18.
Onishi, Maika, Leona Holmberg, Andrei R. Shustov, et al.. (2013). Brentuximab Vedotin Administered To Platinum-Refractory Transplant Naïve Hodgkin Lymphoma Patients Can Increase The Proportion Achieving FDG-PET Negative Status. Blood. 122(21). 2106–2106. 2 indexed citations
19.
Schietinger, Andrea, Mary Philip, Barbara A. Yoshida, et al.. (2006). A Mutant Chaperone Converts a Wild-Type Protein into a Tumor-Specific Antigen. Science. 314(5797). 304–308. 125 indexed citations
20.
Wu, Terry, Zhihai Qin, Thomas Blankenstein, et al.. (2004). Long-Term Suppression of Tumor Growth by TNF Requires a Stat1- and IFN Regulatory Factor 1-Dependent IFN-γ Pathway but Not IL-12 or IL-18. The Journal of Immunology. 172(5). 3243–3251. 22 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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