Mariaestela Ortiz

1.5k total citations
17 papers, 1.1k citations indexed

About

Mariaestela Ortiz is a scholar working on Molecular Biology, Immunology and Hematology. According to data from OpenAlex, Mariaestela Ortiz has authored 17 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 8 papers in Immunology and 5 papers in Hematology. Recurrent topics in Mariaestela Ortiz's work include Acute Myeloid Leukemia Research (4 papers), RNA Interference and Gene Delivery (3 papers) and Immune Cell Function and Interaction (3 papers). Mariaestela Ortiz is often cited by papers focused on Acute Myeloid Leukemia Research (4 papers), RNA Interference and Gene Delivery (3 papers) and Immune Cell Function and Interaction (3 papers). Mariaestela Ortiz collaborates with scholars based in United States, United Kingdom and Japan. Mariaestela Ortiz's co-authors include Jonathan R. Keller, Neal G. Copeland, Nancy A. Jenkins, Pentao Liu, Takuro Nakamura, Rivka A. Rachel, Lino Tessarollo, Peter F. Johnson, Sally E. Spence and N Lohrey and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Mariaestela Ortiz

16 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mariaestela Ortiz United States 13 592 435 185 181 138 17 1.1k
Ko Sasaki Japan 21 602 1.0× 207 0.5× 267 1.4× 290 1.6× 110 0.8× 78 1.3k
Eeshit Dhaval Vaishnav United States 5 571 1.0× 188 0.4× 261 1.4× 135 0.7× 176 1.3× 5 968
Zhiyuan Wu China 22 460 0.8× 100 0.2× 56 0.3× 242 1.3× 69 0.5× 63 1.1k
Natalie Fadle Germany 16 353 0.6× 301 0.7× 94 0.5× 114 0.6× 116 0.8× 38 780
Thomas Stiehl Germany 21 528 0.9× 135 0.3× 404 2.2× 233 1.3× 317 2.3× 49 1.3k
Patrizia Zucchini Italy 22 470 0.8× 307 0.7× 445 2.4× 182 1.0× 453 3.3× 56 1.4k
Richard J. Sharpe United States 12 570 1.0× 238 0.5× 178 1.0× 360 2.0× 29 0.2× 20 1.1k
Mayuko Noda Japan 11 381 0.6× 535 1.2× 45 0.2× 105 0.6× 34 0.2× 12 938
Prem Patel United States 17 604 1.0× 109 0.3× 53 0.3× 428 2.4× 189 1.4× 46 1.2k
Kathleen Roderick United States 9 635 1.1× 626 1.4× 145 0.8× 176 1.0× 75 0.5× 12 1.3k

Countries citing papers authored by Mariaestela Ortiz

Since Specialization
Citations

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

Fields of papers citing papers by Mariaestela Ortiz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mariaestela Ortiz

This figure shows the co-authorship network connecting the top 25 collaborators of Mariaestela Ortiz. A scholar is included among the top collaborators of Mariaestela Ortiz 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 Mariaestela Ortiz. Mariaestela Ortiz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Rahrmann, Eric P., David Shorthouse, Mariaestela Ortiz, et al.. (2022). The NALCN channel regulates metastasis and nonmalignant cell dissemination. Nature Genetics. 54(12). 1827–1838. 38 indexed citations
2.
Mendjan, Sasha, Victoria L. Mascetti, Daniel Ortmann, et al.. (2014). NANOG and CDX2 Pattern Distinct Subtypes of Human Mesoderm during Exit from Pluripotency. Cell stem cell. 15(3). 310–325. 123 indexed citations
3.
Li, Peng, Shannon Burke, Juexuan Wang, et al.. (2010). Reprogramming of T Cells to Natural Killer–Like Cells upon Bcl11b Deletion. Science. 329(5987). 85–89. 267 indexed citations
4.
Su, Qin, Haydn M. Prosser, Lia S. Campos, et al.. (2008). A DNA transposon-based approach to validate oncogenic mutations in the mouse. Proceedings of the National Academy of Sciences. 105(50). 19904–19909. 11 indexed citations
5.
Heath, Victoria L., Hyung C. Suh, Matthew J. Holman, et al.. (2004). C/EBPα deficiency results in hyperproliferation of hematopoietic progenitor cells and disrupts macrophage development in vitro and in vivo. Blood. 104(6). 1639–1647. 88 indexed citations
6.
Ortiz, Mariaestela, Lino Tessarollo, Rivka A. Rachel, et al.. (2004). Deletion of Bcl11a Gene Reveals Roles in Lymphoid, Myeloid, and Leukemic Cell Development.. Blood. 104(11). 385–385. 1 indexed citations
7.
Liu, Pentao, Jonathan R. Keller, Mariaestela Ortiz, et al.. (2003). Bcl11a is essential for normal lymphoid development. Nature Immunology. 4(6). 525–532. 268 indexed citations
8.
Ortiz, Mariaestela, et al.. (2003). Identification of in vitro growth conditions for c-Kit–negative hematopoietic stem cells. Blood. 102(9). 3120–3128. 18 indexed citations
9.
Spence, Sally E., N Lohrey, Mariaestela Ortiz, John Gooya, & Jonathan R. Keller. (2001). Detection of growth factor receptor RNA in individual hematopoietic cells by in situ RT-PCR; comparison with RT-PCR. Journal of Immunological Methods. 257(1-2). 123–136. 2 indexed citations
10.
Ortiz, Mariaestela, John W. Wine, N Lohrey, et al.. (1999). Functional Characterization of a Novel Hematopoietic Stem Cell and Its Place in the c-Kit Maturation Pathway in Bone Marrow Cell Development. Immunity. 10(2). 173–182. 60 indexed citations
11.
Smith, Jeffrey S., Jonathan R. Keller, N Lohrey, et al.. (1999). Redirected infection of directly biotinylated recombinant adenovirus vectors through cell surface receptors and antigens. Proceedings of the National Academy of Sciences. 96(16). 8855–8860. 45 indexed citations
12.
Weiler, Sarah R., John Gooya, Mariaestela Ortiz, et al.. (1999). D3: A Gene Induced During Myeloid Cell Differentiation of Linlo c-Kit+ Sca-1+ Progenitor Cells. Blood. 93(2). 527–536. 12 indexed citations
13.
Weiler, Sarah R., John Gooya, Mariaestela Ortiz, et al.. (1999). D3: A Gene Induced During Myeloid Cell Differentiation of Linlo c-Kit+ Sca-1+ Progenitor Cells. Blood. 93(2). 527–536. 30 indexed citations
14.
Williams, Simon C., Yang Du, Richard C. Schwartz, et al.. (1998). C/EBPε Is a Myeloid-specific Activator of Cytokine, Chemokine, and Macrophage-Colony-stimulating Factor Receptor Genes. Journal of Biological Chemistry. 273(22). 13493–13501. 62 indexed citations
15.
Bankey, Paul E., et al.. (1990). Tumor necrosis factor production by Kupffer cells requires protein kinase C activation. Journal of Surgical Research. 49(3). 256–261. 35 indexed citations
16.
Bankey, Paul E., et al.. (1990). Hepatic Acute Phase Protein Synthesis is Indirectly Regulated by Tumor Necrosis Factor. The Journal of Trauma: Injury, Infection, and Critical Care. 30(10). 1181–1188. 16 indexed citations
17.
Ortiz, Mariaestela, et al.. (1982). Heat transfer coefficients for the upstream face of a perforated plate positioned normal to an oncoming flow. International Journal of Heat and Mass Transfer. 25(1). 127–135. 49 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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