Louis M. Pelus

8.5k total citations
159 papers, 6.3k citations indexed

About

Louis M. Pelus is a scholar working on Hematology, Immunology and Oncology. According to data from OpenAlex, Louis M. Pelus has authored 159 papers receiving a total of 6.3k indexed citations (citations by other indexed papers that have themselves been cited), including 74 papers in Hematology, 65 papers in Immunology and 58 papers in Oncology. Recurrent topics in Louis M. Pelus's work include Hematopoietic Stem Cell Transplantation (53 papers), Acute Myeloid Leukemia Research (27 papers) and Immunotherapy and Immune Responses (27 papers). Louis M. Pelus is often cited by papers focused on Hematopoietic Stem Cell Transplantation (53 papers), Acute Myeloid Leukemia Research (27 papers) and Immunotherapy and Immune Responses (27 papers). Louis M. Pelus collaborates with scholars based in United States, Japan and France. Louis M. Pelus's co-authors include Seiji Fukuda, Jonathan Hoggatt, Hal E. Broxmeyer, Pratibha Singh, Janardhan Sampath, Chang H. Kim, Helen R. Strausser, John R. White, Huimin Bian and Richard S. Bockman and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Louis M. Pelus

153 papers receiving 6.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Louis M. Pelus United States	47	2.5k	2.3k	2.0k	1.8k	780	159	6.3k
Osamu Miura Japan	43	2.7k 1.1×	2.3k 1.0×	1.8k 0.9×	3.4k 1.9×	1.1k 1.4×	243	7.4k
Kenji Oritani Japan	39	2.3k 0.9×	2.4k 1.0×	980 0.5×	1.4k 0.8×	415 0.5×	177	6.3k
Lars Rönnstrand Sweden	54	5.9k 2.4×	2.0k 0.8×	1.9k 1.0×	2.0k 1.1×	1.1k 1.3×	173	10.2k
Norman N. Iscove Canada	43	4.5k 1.8×	3.1k 1.3×	2.4k 1.2×	1.7k 0.9×	1.1k 1.5×	76	9.1k
Giao Hangoc United States	46	3.0k 1.2×	3.0k 1.3×	3.4k 1.7×	3.2k 1.7×	1.4k 1.9×	115	8.6k
J N Ihle United States	33	1.9k 0.8×	2.3k 1.0×	1.5k 0.8×	2.2k 1.2×	597 0.8×	47	5.5k
Motonari Kondo United States	38	2.2k 0.9×	5.7k 2.4×	1.8k 0.9×	1.7k 1.0×	550 0.7×	78	8.4k
Hideki Muramatsu Japan	38	2.5k 1.0×	810 0.3×	1.6k 0.8×	1.0k 0.6×	750 1.0×	274	5.9k
Kazuhito Naka Japan	40	4.0k 1.6×	1.0k 0.4×	1.1k 0.6×	2.0k 1.1×	575 0.7×	92	7.3k
Koichi Nakajima Japan	46	3.6k 1.5×	3.8k 1.6×	907 0.5×	4.0k 2.2×	478 0.6×	95	9.4k

Countries citing papers authored by Louis M. Pelus

Since Specialization

Citations

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

Fields of papers citing papers by Louis M. Pelus

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Louis M. Pelus. 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 Louis M. Pelus. The network helps show where Louis M. Pelus may publish in the future.

Co-authorship network of co-authors of Louis M. Pelus

This figure shows the co-authorship network connecting the top 25 collaborators of Louis M. Pelus. A scholar is included among the top collaborators of Louis M. Pelus 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 Louis M. Pelus. Louis M. Pelus 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

Pelus, Louis M., P. Artur Plett, Carol H. Sampson, et al.. (2023). Further Characterization of Multi-Organ DEARE and Protection by 16,16 Dimethyl Prostaglandin E2 in a Mouse Model of the Hematopoietic Acute Radiation Syndrome. Radiation Research. 199(5). 468–489. 3 indexed citations

Patterson, Andrea M., Liqiong Liu, Christie M. Orschell, & Louis M. Pelus. (2017). Prostaglandin E2 Prevents Apoptosis and Promotes Homeostasis of Hematopoietic Stem Cells after Lethal Irradiation through Alteration of p53 and TNF Signaling. Blood. 130. 3766–3766. 1 indexed citations

Wu, Tong, et al.. (2017). Prostaglandin E2 Promotes Recovery of Thymus in Survivors of the Hematopoietic Acute Radiation Syndrome (H-ARS). Blood. 130. 1008–1008. 1 indexed citations

Hoggatt, Jonathan, Pratibha Singh, Tiffany Tate, et al.. (2017). Rapid Mobilization Reveals a Highly Engraftable Hematopoietic Stem Cell. Cell. 172(1-2). 191–204.e10. 88 indexed citations

Abe, Mariko, Louis M. Pelus, Pratibha Singh, et al.. (2016). Internal Tandem Duplication in FLT3 Attenuates Proliferation and Regulates Resistance to the FLT3 Inhibitor AC220 by Modulating p21Cdkn1a and Pbx1 in Hematopoietic Cells. PMC.

Mantel, Charlie, Heather A. O’Leary, Brahmananda R. Chitteti, et al.. (2015). Enhancing Hematopoietic Stem Cell Transplantation Efficacy by Mitigating Oxygen Shock. PMC.

Mantel, Charlie, Heather A. O’Leary, Brahmananda R. Chitteti, et al.. (2015). Enhancing Hematopoietic Stem Cell Transplantation Efficacy by Mitigating Oxygen Shock. Cell. 161(7). 1553–1565. 238 indexed citations

Hoggatt, Jonathan, Jennifer M. Speth, & Louis M. Pelus. (2013). Sowing the Seeds of a Fruitful Harvest: Hematopoietic Stem Cell Mobilization. PMC. 1 indexed citations

Gang, Eun Ji, Jennifer Pham, Yi Zhao, et al.. (2013). Small-molecule inhibition of CBP/catenin interactions eliminates drug-resistant clones in acute lymphoblastic leukemia. Oncogene. 33(17). 2169–2178. 132 indexed citations

10.

Pelus, Louis M., Jonathan Hoggatt, & Pratibha Singh. (2011). Pulse exposure of haematopoietic grafts to prostaglandin E2 in vitro facilitates engraftment and recovery. PMC. 3 indexed citations

11.

Sampath, Janardhan, Louis M. Pelus, Janardhan Sampath, & Louis M. Pelus. (2007). Alternative Splice Variants of Survivin as Potential Targets in Cancer. Current Drug Discovery Technologies. 4(3). 174–191. 40 indexed citations

12.

Pelus, Louis M. & Seiji Fukuda. (2006). Peripheral blood stem cell mobilization: The CXCR2 ligand GROβ rapidly mobilizes hematopoietic stem cells with enhanced engraftment properties. Experimental Hematology. 34(8). 1010–1020. 105 indexed citations

13.

Fukuda, Seiji, et al.. (2002). Cloning and Characterization of a Proliferation-Associated Cytokine-Inducible Protein, CIP29. Biochemical and Biophysical Research Communications. 292(3). 593–600. 27 indexed citations

14.

Fukuda, Seiji, et al.. (2002). The antiapoptosis protein survivin is associated with cell cycle entry of normal cord blood CD34+ cells and modulates cell cycle and proliferation of mouse hematopoietic progenitor cells. Blood. 100(7). 2463–2471. 117 indexed citations

15.

Wu, Ding Wen, et al.. (2000). SH2-Containing Protein Tyrosine Phosphatase-1 (SHP-1) Association with Jak2 in UT-7/Epo Cells. Blood Cells Molecules and Diseases. 26(1). 15–24. 13 indexed citations

16.

Kim, Chang H., et al.. (1998). CKβ-11/Macrophage Inflammatory Protein-3β/EBI1-Ligand Chemokine Is an Efficacious Chemoattractant for T and B Cells. The Journal of Immunology. 160(5). 2418–2424. 96 indexed citations

17.

Gentile, Patrick S. & Louis M. Pelus. (1988). In vivo modulation of myelopoiesis by prostaglandin E2. IV. Prostaglandin E2 induction of myelopoietic inhibitory activity.. The Journal of Immunology. 141(8). 2714–2720. 12 indexed citations

18.

Broxmeyer, Hal E., D C Bicknell, Steven Gillis, et al.. (1986). Lactoferrin: affinity purification from human milk and polymorphonuclear neutrophils using monoclonal antibody (II 2C) to human lactoferrin, development of an immunoradiometric assay using II 2C, and myelopoietic regulation and receptor-binding characteristics.. PubMed. 11(3). 429–46. 25 indexed citations

19.

Lu, Li, Hal E. Broxmeyer, Louis M. Pelus, Michael Andreeff, & M A Moore. (1981). Detection of luxol-fast-blue positive cells in human promyelocytic leukemia cell line HL-60.. PubMed. 9(9). 887–92. 20 indexed citations

20.

Pelus, Louis M., et al.. (1978). Host-mediated immune suppression in tumor bearing mice. In vitro reversal by indomethacin or removal of adherent cells. Abstr.. The Mouseion at the JAXlibrary (Jackson Laboratory). 37(6). 1451. 3 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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