Howard T. Petrie

7.4k total citations
70 papers, 5.8k citations indexed

About

Howard T. Petrie is a scholar working on Immunology, Molecular Biology and Oncology. According to data from OpenAlex, Howard T. Petrie has authored 70 papers receiving a total of 5.8k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Immunology, 23 papers in Molecular Biology and 23 papers in Oncology. Recurrent topics in Howard T. Petrie's work include T-cell and B-cell Immunology (42 papers), Immune Cell Function and Interaction (21 papers) and Immunotherapy and Immune Responses (20 papers). Howard T. Petrie is often cited by papers focused on T-cell and B-cell Immunology (42 papers), Immune Cell Function and Interaction (21 papers) and Immunotherapy and Immune Responses (20 papers). Howard T. Petrie collaborates with scholars based in United States, Australia and Canada. Howard T. Petrie's co-authors include Juan Carlos Zúñiga‐Pflücker, Susan E. Prockop, Douglas Burtrum, Ferenc Livák, Svetlana M. Mazel, Thomas M. Schmitt, David G. Schatz, H. David Kay, Lynell W. Klassen and Ken Shortman and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and The Journal of Experimental Medicine.

In The Last Decade

Howard T. Petrie

69 papers receiving 5.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Howard T. Petrie United States 40 3.8k 1.9k 1.6k 498 296 70 5.8k
Steven D. Gimpel United States 15 2.9k 0.8× 1.5k 0.8× 1.5k 1.0× 524 1.1× 477 1.6× 15 4.9k
Cecilia Melani Italy 37 2.0k 0.5× 1.5k 0.8× 1.6k 1.0× 227 0.5× 443 1.5× 85 4.2k
Kay L. Medina United States 34 2.6k 0.7× 1.9k 1.0× 745 0.5× 848 1.7× 546 1.8× 72 5.1k
Yong-Rui Zou United States 18 2.7k 0.7× 1.7k 0.9× 1.9k 1.2× 731 1.5× 184 0.6× 33 5.0k
Laurence Boumsell France 48 3.4k 0.9× 1.3k 0.7× 886 0.6× 433 0.9× 173 0.6× 152 6.8k
Ulrike Lorenz United States 27 2.2k 0.6× 2.0k 1.0× 942 0.6× 214 0.4× 186 0.6× 44 3.7k
Scott Cooper United States 35 1.9k 0.5× 1.5k 0.8× 1.4k 0.9× 2.4k 4.8× 376 1.3× 97 5.1k
William G. Kerr United States 34 2.4k 0.6× 2.3k 1.2× 1.2k 0.8× 650 1.3× 499 1.7× 109 5.2k
Jeremy B. Swann Australia 25 3.5k 0.9× 1.1k 0.6× 2.3k 1.5× 457 0.9× 230 0.8× 37 5.2k
Linh T. Nguyen Canada 32 2.4k 0.6× 1.3k 0.7× 1.4k 0.9× 262 0.5× 219 0.7× 75 4.3k

Countries citing papers authored by Howard T. Petrie

Since Specialization
Citations

This map shows the geographic impact of Howard T. Petrie'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 Howard T. Petrie with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Howard T. Petrie more than expected).

Fields of papers citing papers by Howard T. Petrie

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Howard T. Petrie. 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 Howard T. Petrie. The network helps show where Howard T. Petrie may publish in the future.

Co-authorship network of co-authors of Howard T. Petrie

This figure shows the co-authorship network connecting the top 25 collaborators of Howard T. Petrie. A scholar is included among the top collaborators of Howard T. Petrie 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 Howard T. Petrie. Howard T. Petrie 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.
Venables, Thomas, et al.. (2019). Dynamic changes in epithelial cell morphology control thymic organ size during atrophy and regeneration. Nature Communications. 10(1). 4402–4402. 49 indexed citations
2.
Griffith, Ann V., Thomas Venables, Jianjun Shi, et al.. (2015). Metabolic Damage and Premature Thymus Aging Caused by Stromal Catalase Deficiency. Cell Reports. 12(7). 1071–1079. 58 indexed citations
3.
Krane, Michael, et al.. (2011). Practical estimation of DPIV uncertainty using pseudo-image pairs. Bulletin of the American Physical Society. 64.
4.
Mohtashami, Mahmood, et al.. (2010). Direct comparison of Dll1- and Dll4-mediated Notch activation levels shows differential lympho-myeloid lineage commitment outcomes (36.27). The Journal of Immunology. 184(Supplement_1). 36.27–36.27. 1 indexed citations
5.
Griffith, Ann V., Mohammad Fallahi, Hiroshi Nakase, et al.. (2009). Spatial Mapping of Thymic Stromal Microenvironments Reveals Unique Features Influencing T Lymphoid Differentiation. Immunity. 31(6). 999–1009. 66 indexed citations
6.
Huang, Jiaxue, Karla P. Garrett, Rosana Pelayo, et al.. (2005). Propensity of Adult Lymphoid Progenitors to Progress to DN2/3 Stage Thymocytes with Notch Receptor Ligation. The Journal of Immunology. 175(8). 4858–4865. 40 indexed citations
7.
Olaru, Alexandru, Howard T. Petrie, & Ferenc Livák. (2005). Beyond the 12/23 Rule of VDJ Recombination Independent of the Rag Proteins. The Journal of Immunology. 174(10). 6220–6226. 7 indexed citations
8.
Misslitz, Ana Clara, Oliver Pabst, Gabriele Hintzen, et al.. (2004). Thymic T Cell Development and Progenitor Localization Depend on CCR7. The Journal of Experimental Medicine. 200(4). 481–491. 166 indexed citations
9.
Prockop, Susan E. & Howard T. Petrie. (2004). Regulation of Thymus Size by Competition for Stromal Niches among Early T Cell Progenitors. The Journal of Immunology. 173(3). 1604–1611. 156 indexed citations
10.
Tabrizifard, Sahba, Alexandru Olaru, Jason Plotkin, et al.. (2004). Analysis of Transcription Factor Expression during Discrete Stages of Postnatal Thymocyte Differentiation. The Journal of Immunology. 173(2). 1094–1102. 49 indexed citations
11.
Schmitt, Thomas M., Maria Ciofani, Howard T. Petrie, & Juan Carlos Zúñiga‐Pflücker. (2004). Maintenance of T Cell Specification and Differentiation Requires Recurrent Notch Receptor–Ligand Interactions. The Journal of Experimental Medicine. 200(4). 469–479. 260 indexed citations
12.
Plotkin, Jason, Susan E. Prockop, Ana Paula Lepique, & Howard T. Petrie. (2003). Critical Role for CXCR4 Signaling in Progenitor Localization and T Cell Differentiation in the Postnatal Thymus. The Journal of Immunology. 171(9). 4521–4527. 179 indexed citations
13.
Prockop, Susan E., et al.. (2002). Stromal Cells Provide the Matrix for Migration of Early Lymphoid Progenitors Through the Thymic Cortex. The Journal of Immunology. 169(8). 4354–4361. 67 indexed citations
14.
Petrie, Howard T., Michelle R. Tourigny, Douglas Burtrum, & Ferenc Livák. (2000). Precursor Thymocyte Proliferation and Differentiation Are Controlled by Signals Unrelated to the Pre-TCR. The Journal of Immunology. 165(6). 3094–3098. 38 indexed citations
15.
Littman, Dan R., et al.. (1999). Role of the Nuclear Hormone Receptor ROR  in Transcriptional Regulation, Thymocyte Survival, and Lymphoid Organogenesis. Cold Spring Harbor Symposia on Quantitative Biology. 64(0). 373–382. 34 indexed citations
16.
Lind, Evan, et al.. (1999). Bcl-2-Induced Changes in E2F Regulatory Complexes Reveal the Potential for Integrated Cell Cycle and Cell Death Functions. The Journal of Immunology. 162(9). 5374–5379. 43 indexed citations
17.
Tourigny, Michelle R., Svetlana M. Mazel, Douglas Burtrum, & Howard T. Petrie. (1997). T Cell Receptor (TCR)-β Gene Recombination: Dissociation from Cell Cycle Regulation and Developmental Progression During T Cell Ontogeny. The Journal of Experimental Medicine. 185(9). 1549–1556. 111 indexed citations
18.
Petrie, Howard T., Ferenc Livák, David G. Schatz, et al.. (1993). Multiple rearrangements in T cell receptor alpha chain genes maximize the production of useful thymocytes.. The Journal of Experimental Medicine. 178(2). 615–622. 190 indexed citations
19.
Hugo, Patrice, Richard L. Boyd, Gary A. Waanders, Howard T. Petrie, & Roland Scollay. (1991). Timing of deletion of autoreactive V β6+ cells and down-modulation of either CD4 orCD8 on phenotypically distinct CD4+8+ subsets of thymocytes expressingintermediate or high levels of T cell receptor. International Immunology. 3(3). 265–272. 33 indexed citations
20.
Wu, Li, et al.. (1990). CD4−CD8− thymocytes that express the T cell receptor may have previously expressed CD8. International Immunology. 2(1). 51–56. 39 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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