Odette M. Smith

5.7k total citations
42 papers, 1.7k citations indexed

About

Odette M. Smith is a scholar working on Immunology, Hematology and Molecular Biology. According to data from OpenAlex, Odette M. Smith has authored 42 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Immunology, 21 papers in Hematology and 10 papers in Molecular Biology. Recurrent topics in Odette M. Smith's work include Hematopoietic Stem Cell Transplantation (21 papers), Immune Cell Function and Interaction (18 papers) and T-cell and B-cell Immunology (13 papers). Odette M. Smith is often cited by papers focused on Hematopoietic Stem Cell Transplantation (21 papers), Immune Cell Function and Interaction (18 papers) and T-cell and B-cell Immunology (13 papers). Odette M. Smith collaborates with scholars based in United States, Australia and Germany. Odette M. Smith's co-authors include Marcel R.M. van den Brink, Amanda M. Holland, Jarrod A. Dudakov, Richard L. Boyd, David Suh, Alan M. Hanash, Gabrielle L. Goldberg, Jennifer J. Tsai, Natalie V. Singer and Mallory L. West and has published in prestigious journals such as Science, Journal of Clinical Investigation and The Journal of Experimental Medicine.

In The Last Decade

Odette M. Smith

41 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Odette M. Smith United States 18 1.0k 655 390 380 107 42 1.7k
Amanda M. Holland United States 14 764 0.7× 434 0.7× 328 0.8× 283 0.7× 79 0.7× 25 1.3k
Catherine M. Sawai United States 13 768 0.7× 398 0.6× 632 1.6× 266 0.7× 138 1.3× 19 1.6k
Dapeng Wang United States 19 571 0.6× 241 0.4× 494 1.3× 288 0.8× 220 2.1× 44 1.4k
Alexandra Schnell United States 12 713 0.7× 253 0.4× 329 0.8× 208 0.5× 80 0.7× 16 1.2k
Divino Deoliveira United States 10 774 0.8× 226 0.3× 341 0.9× 257 0.7× 52 0.5× 19 1.3k
Jens Volkmer United States 8 862 0.8× 162 0.2× 381 1.0× 355 0.9× 71 0.7× 9 1.4k
Jorg van Loosdregt Netherlands 23 1.2k 1.2× 300 0.5× 800 2.1× 382 1.0× 50 0.5× 46 2.2k
Tatsuo Kina Japan 18 1.1k 1.1× 632 1.0× 648 1.7× 245 0.6× 219 2.0× 45 2.0k
A. Ythier France 18 565 0.5× 244 0.4× 308 0.8× 233 0.6× 68 0.6× 38 1.3k
Vasiliki Koliaraki Greece 20 406 0.4× 282 0.4× 414 1.1× 435 1.1× 276 2.6× 38 1.3k

Countries citing papers authored by Odette M. Smith

Since Specialization
Citations

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

Fields of papers citing papers by Odette M. Smith

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Odette M. Smith

This figure shows the co-authorship network connecting the top 25 collaborators of Odette M. Smith. A scholar is included among the top collaborators of Odette M. Smith 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 Odette M. Smith. Odette M. Smith 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.
Staffas, Anna, Marina Burgos da Silva, Ann E. Slingerland, et al.. (2018). Nutritional Support From the Intestinal Microbiota Improves Hematopoietic Reconstitution after Bone Marrow Transplantation in Mice. Biology of Blood and Marrow Transplantation. 24(3). S75–S75. 3 indexed citations
2.
Dudakov, Jarrod A., Anna Mertelsmann, Margaret O'Connor, et al.. (2017). Loss of thymic innate lymphoid cells leads to impaired thymopoiesis in experimental graft-versus-host disease. Blood. 130(7). 933–942. 55 indexed citations
3.
Shono, Yusuke, Andrea Z. Tuckett, Hsiou‐Chi Liou, et al.. (2016). Characterization of a c-Rel Inhibitor That Mediates Anticancer Properties in Hematologic Malignancies by Blocking NF-κB–Controlled Oxidative Stress Responses. Cancer Research. 76(2). 377–389. 33 indexed citations
4.
Shono, Yusuke, Andrea Z. Tuckett, Samedy Ouk, et al.. (2014). A Small-Molecule c-Rel Inhibitor Reduces Alloactivation of T Cells without Compromising Antitumor Activity. Cancer Discovery. 4(5). 578–591. 42 indexed citations
5.
Tsai, Jennifer J., Jarrod A. Dudakov, Koichi Takahashi, et al.. (2013). Nrf2 regulates haematopoietic stem cell function. Nature Cell Biology. 15(3). 309–316. 167 indexed citations
6.
Velardi, Enrico, Jennifer J. Tsai, Amanda M. Holland, et al.. (2013). Sex Steroid Blockade Enhances Thymopoiesis By Modulating Notch Signaling. Blood. 122(21). 291–291. 1 indexed citations
7.
8.
Dudakov, Jarrod A., Alan M. Hanash, Lauren Young, et al.. (2013). Intrathymic Innate Lymphoid Cells: Long-Lived Mediators Of Immune Regeneration. Blood. 122(21). 289–289. 2 indexed citations
9.
Dudakov, Jarrod A., Alan M. Hanash, Robert R. Jenq, et al.. (2012). Interleukin-22 Drives Endogenous Thymic Regeneration in Mice. Science. 336(6077). 91–95. 286 indexed citations
10.
Holland, Amanda M., Johannes L. Zakrzewski, Jennifer J. Tsai, et al.. (2012). Extrathymic development of murine T cells after bone marrow transplantation. Journal of Clinical Investigation. 122(12). 4716–4726. 15 indexed citations
11.
Dudakov, Jarrod A., Alan M. Hanash, Robert R. Jenq, et al.. (2012). Interleukin-22 drives endogenous thymic regeneration in mice (44.6). The Journal of Immunology. 188(1_Supplement). 44.6–44.6. 10 indexed citations
12.
Ghosh, Arnab, Yildirim Dogan, Amanda M. Holland, et al.. (2011). Over-Expression of TRAIL on Donor T Cells Enhances GVT and Suppresses Gvhd Via Elimination of Alloreactive T Cells and Host APC. Blood. 118(21). 817–817.
13.
Penack, Olaf, Erik Henke, David Suh, et al.. (2010). Inhibition of Neovascularization to Simultaneously Ameliorate Graft-vs-Host Disease and Decrease Tumor Growth. JNCI Journal of the National Cancer Institute. 102(12). 894–908. 48 indexed citations
14.
Penack, Olaf, Odette M. Smith, Amy Cunningham‐Bussel, et al.. (2009). NOD2 regulates hematopoietic cell function during graft-versus-host disease. The Journal of Experimental Medicine. 206(10). 2101–2110. 84 indexed citations
15.
Goldberg, Gabrielle L., Christopher King, David Suh, et al.. (2009). Luteinizing Hormone-Releasing Hormone Enhances T Cell Recovery following Allogeneic Bone Marrow Transplantation. The Journal of Immunology. 182(9). 5846–5854. 64 indexed citations
16.
Zakrzewski, Johannes L., David Suh, John C. Markley, et al.. (2008). Tumor immunotherapy across MHC barriers using allogeneic T-cell precursors. Nature Biotechnology. 26(4). 453–461. 89 indexed citations
17.
18.
Lu, Sydney X., Neel Patel, Suzanne McGoldrick, et al.. (2008). Rapidly proliferating CD44hi peripheral T cells undergo apoptosis and delay posttransplantation T-cell reconstitution after allogeneic bone marrow transplantation. Blood. 112(12). 4755–4764. 13 indexed citations
19.
Zakrzewski, Johannes L., Gabrielle L. Goldberg, Odette M. Smith, & Marcel R.M. van den Brink. (2007). Enhancing T cell reconstitution after hematopoietic stem cell transplantation: A brief update of the latest trends. Blood Cells Molecules and Diseases. 40(1). 44–47. 15 indexed citations
20.
Alpdoğan, Önder, Vanessa M. Hubbard, Stephanie J. Muriglan, et al.. (2004). Keratinocyte Growth Factor (KGF) Is Required for Post-Natal Thymic Regeneration.. Blood. 104(11). 1231–1231. 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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