Christie M. Orschell

4.7k total citations · 2 hit papers
70 papers, 3.8k citations indexed

About

Christie M. Orschell is a scholar working on Radiology, Nuclear Medicine and Imaging, Hematology and Oncology. According to data from OpenAlex, Christie M. Orschell has authored 70 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Radiology, Nuclear Medicine and Imaging, 29 papers in Hematology and 17 papers in Oncology. Recurrent topics in Christie M. Orschell's work include Effects of Radiation Exposure (36 papers), Hematopoietic Stem Cell Transplantation (25 papers) and Radiation Therapy and Dosimetry (6 papers). Christie M. Orschell is often cited by papers focused on Effects of Radiation Exposure (36 papers), Hematopoietic Stem Cell Transplantation (25 papers) and Radiation Therapy and Dosimetry (6 papers). Christie M. Orschell collaborates with scholars based in United States, France and United Kingdom. Christie M. Orschell's co-authors include Keith L. March, Jalees Rehman, Jingling Li, P. Artur Plett, Edward F. Srour, Hal E. Broxmeyer, Xiaxin Li, Hui Lin Chua, Carol H. Sampson and Scott Cooper and has published in prestigious journals such as Journal of Biological Chemistry, Circulation and Journal of Clinical Investigation.

In The Last Decade

Christie M. Orschell

65 papers receiving 3.7k citations

Hit Papers

Peripheral Blood “Endothe... 2003 2026 2010 2018 2003 2005 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christie M. Orschell United States 24 1.7k 891 805 795 787 70 3.8k
Ronald van Os Netherlands 35 1.5k 0.9× 833 0.9× 999 1.2× 676 0.9× 311 0.4× 68 3.7k
Johan Lennartsson Sweden 31 1.8k 1.1× 715 0.8× 388 0.5× 880 1.1× 239 0.3× 76 3.5k
Barbara Schmalfeldt Germany 33 1.2k 0.7× 1.5k 1.7× 327 0.4× 728 0.9× 431 0.5× 130 4.2k
Yusuke Shiozawa United States 40 1.8k 1.1× 2.4k 2.7× 825 1.0× 818 1.0× 343 0.4× 103 4.9k
Antonio Pinto Italy 40 1.3k 0.8× 2.2k 2.5× 757 0.9× 1.6k 2.0× 449 0.6× 239 5.6k
Wolfgang Oster Germany 28 674 0.4× 760 0.9× 666 0.8× 791 1.0× 489 0.6× 101 3.0k
Bertrand Knebelmann France 46 3.0k 1.8× 519 0.6× 729 0.9× 593 0.7× 213 0.3× 123 6.2k
Kewal Asosingh United States 43 1.9k 1.1× 1.1k 1.2× 1.1k 1.3× 617 0.8× 222 0.3× 118 4.4k
Yukihiko Sonoda Japan 32 1.6k 1.0× 596 0.7× 1.2k 1.5× 275 0.3× 492 0.6× 224 4.6k
Leslie V. Parise United States 40 2.1k 1.2× 496 0.6× 1.6k 2.0× 558 0.7× 194 0.2× 95 4.8k

Countries citing papers authored by Christie M. Orschell

Since Specialization
Citations

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

Fields of papers citing papers by Christie M. Orschell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christie M. Orschell

This figure shows the co-authorship network connecting the top 25 collaborators of Christie M. Orschell. A scholar is included among the top collaborators of Christie M. Orschell 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 Christie M. Orschell. Christie M. Orschell 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.
Plett, P. Artur, Hui Lin Chua, Carol H. Sampson, et al.. (2024). Effect of Age at Time of Irradiation, Sex, Genetic Diversity, and Granulopoietic Cytokine Radiomitigation on Lifespan and Lymphoma Development in Murine H-ARS Survivors. Radiation Research. 202(3). 580–598. 1 indexed citations
2.
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
3.
Orschell, Christie M., Tong Wu, & Andrea M. Patterson. (2022). Impact of Age, Sex, and Genetic Diversity in Murine Models of the Hematopoietic Acute Radiation Syndrome (H-ARS) and the Delayed Effects of Acute Radiation Exposure (DEARE). Current Stem Cell Reports. 8(3). 139–149. 13 indexed citations
4.
Gao, Feng, Jayashree Narayanan, Elizabeth R. Jacobs, et al.. (2021). Polypharmacy to Mitigate Acute and Delayed Radiation Syndromes. Frontiers in Pharmacology. 12. 634477–634477. 16 indexed citations
5.
Broxmeyer, Hal E., Yan Liu, Reuben Kapur, et al.. (2020). Fate of Hematopoiesis During Aging. What Do We Really Know, and What are its Implications?. Publisher. 1 indexed citations
6.
Broxmeyer, Hal E., Yan Liu, Reuben Kapur, et al.. (2020). Fate of Hematopoiesis During Aging. What Do We Really Know, and What are its Implications?. Stem Cell Reviews and Reports. 16(6). 1020–1048. 20 indexed citations
7.
Patterson, Andrea M., Liqiong Liu, Carol H. Sampson, et al.. (2020). A Single Radioprotective Dose of Prostaglandin E2 Blocks Irradiation-Induced Apoptotic Signaling and Early Cycling of Hematopoietic Stem Cells. Stem Cell Reports. 15(2). 358–373. 29 indexed citations
8.
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
9.
10.
Mi, Deming, et al.. (2015). Relationships Between Renal Parameters and Serum and Urine Markers of Inflammation in Those With and Without HIV Infection. AIDS Research and Human Retroviruses. 31(4). 375–383. 8 indexed citations
11.
Plett, P. Artur, Carol H. Sampson, Hui Lin Chua, et al.. (2015). The H-ARS Dose Response Relationship (DRR). Health Physics. 109(5). 391–398. 33 indexed citations
12.
Garrett, Joy, Christie M. Orschell, Marc S. Mendonca, Robert M. Bigsby, & Joseph R. Dynlacht. (2014). Subcutaneous Wounding Postirradiation Reduces Radiation Lethality in Mice. Radiation Research. 181(6). 578–583. 14 indexed citations
13.
Chua, Hui Lin, P. Artur Plett, Carol H. Sampson, et al.. (2013). Survival Efficacy of the PEGylated G-CSFs Maxy-G34 and Neulasta in a Mouse Model of Lethal H-ARS, and Residual Bone Marrow Damage in Treated Survivors. Health Physics. 106(1). 21–38. 47 indexed citations
14.
Mendonca, Marc S., Paul Todd, Christie M. Orschell, et al.. (2012). High-energy proton irradiation of C57Bl6 mice under hindlimb unloading. cosp. 39. 1225. 1 indexed citations
15.
Chua, Hui Lin, P. Artur Plett, Carol H. Sampson, et al.. (2012). Long-Term Hematopoietic Stem Cell Damage in a Murine Model of the Hematopoietic Syndrome of the Acute Radiation Syndrome. Health Physics. 103(4). 356–366. 70 indexed citations
16.
Shakhov, Alexander N., Vijay K. Singh, Peter Krasnov, et al.. (2012). Prevention and Mitigation of Acute Radiation Syndrome in Mice by Synthetic Lipopeptide Agonists of Toll-Like Receptor 2 (TLR2). PLoS ONE. 7(3). e33044–e33044. 66 indexed citations
17.
Plett, P. Artur, Carol H. Sampson, Hui Lin Chua, et al.. (2012). Establishing a Murine Model of the Hematopoietic Syndrome of the Acute Radiation Syndrome. Health Physics. 103(4). 343–355. 126 indexed citations
18.
Orschell, Christie M., Jovencio Borneo, Veerendra Munugalavadla, et al.. (2008). Deficiency of Src family kinases compromises the repopulating ability of hematopoietic stem cells. Experimental Hematology. 36(5). 655–666. 13 indexed citations
19.
Borneo, Jovencio, Veerendra Munugalavadla, Emily Sims, et al.. (2007). Src family kinase–mediated negative regulation of hematopoietic stem cell mobilization involves both intrinsic and microenvironmental factors. Experimental Hematology. 35(7). 1026–1037. 9 indexed citations
20.
Mitra, Ranjana, Anjaiah Srirangam, John W. Hawes, et al.. (2004). Calpain inhibition down-regulates Akt and induces death of non-cycling breast cancer cells. Cancer Research. 64. 1117–1117. 1 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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