R Espinosa

1.2k total citations
15 papers, 1.0k citations indexed

About

R Espinosa is a scholar working on Molecular Biology, Surgery and Hematology. According to data from OpenAlex, R Espinosa has authored 15 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Surgery and 4 papers in Hematology. Recurrent topics in R Espinosa's work include Pancreatic function and diabetes (4 papers), Acute Myeloid Leukemia Research (3 papers) and Chronic Myeloid Leukemia Treatments (3 papers). R Espinosa is often cited by papers focused on Pancreatic function and diabetes (4 papers), Acute Myeloid Leukemia Research (3 papers) and Chronic Myeloid Leukemia Treatments (3 papers). R Espinosa collaborates with scholars based in United States, Finland and Japan. R Espinosa's co-authors include Michelle M. Le Beau, Timothy W. McKeithan, Beverly W. Baron, Norah R. McCabe, Giuseppina Nucifora, Richard Baer, J. Lesley Brown, Michael J. Siciliano, Wendy Stock and C A Westbrook and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Neuroscience and Diabetologia.

In The Last Decade

R Espinosa

15 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
R Espinosa United States 12 578 242 208 192 172 15 1.0k
Anthony A. Fernald United States 18 707 1.2× 468 1.9× 145 0.7× 87 0.5× 174 1.0× 36 1.1k
Stephanie Lerach United States 9 901 1.6× 257 1.1× 310 1.5× 348 1.8× 203 1.2× 13 1.5k
Patricia Thompson United States 12 571 1.0× 360 1.5× 133 0.6× 100 0.5× 177 1.0× 22 1.1k
Carin Lassen Sweden 21 642 1.1× 570 2.4× 180 0.9× 101 0.5× 297 1.7× 35 1.3k
Alessandro Pastore Germany 16 384 0.7× 259 1.1× 182 0.9× 195 1.0× 179 1.0× 33 885
Nicola Hawe United States 7 642 1.1× 137 0.6× 280 1.3× 231 1.2× 145 0.8× 8 1.2k
Inga Nagel Germany 20 359 0.6× 140 0.6× 335 1.6× 546 2.8× 322 1.9× 51 1.1k
Malwina Suszyńska United States 20 567 1.0× 229 0.9× 152 0.7× 59 0.3× 192 1.1× 42 1.1k
R Berthier France 15 763 1.3× 590 2.4× 173 0.8× 59 0.3× 219 1.3× 41 1.5k
Helen Parker United Kingdom 23 492 0.9× 296 1.2× 131 0.6× 325 1.7× 404 2.3× 48 1.3k

Countries citing papers authored by R Espinosa

Since Specialization
Citations

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

Fields of papers citing papers by R Espinosa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R Espinosa

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

All Works

15 of 15 papers shown
1.
Sato, Yuko, Hirofumi Kobayashi, Yasushi Suto, et al.. (2001). Chromosomal instability in chromosome band 12p13: multiple breaks leading to complex rearrangements including cytogenetically undetectable sub-clones. Leukemia. 15(8). 1193–1202. 24 indexed citations
2.
Cook, Paul A., et al.. (1998). Microarterial anatomy of the lesser toe proximal interphalangeal joints. The Journal Of Hand Surgery. 23(2). 256–260. 10 indexed citations
3.
Levi‐Setti, R., J. M. Chabala, Konstantin L. Gavrilov, R Espinosa, & Michelle M. Le Beau. (1996). Advances in high resolution SIMS studies of BrdU-labelled human metaphase chromosomes.. PubMed. 42(3). 301–24. 10 indexed citations
4.
Martínez-Climent, José A., Michael J. Thirman, R Espinosa, Michelle M. Le Beau, & J D Rowley. (1995). Detection of 11q23/MLL rearrangements in infant leukemias with fluorescence in situ hybridization and molecular analysis.. PubMed. 9(8). 1299–304. 36 indexed citations
5.
Economides, Aris N., et al.. (1995). Identification of mammalian noggin and its expression in the adult nervous system. Journal of Neuroscience. 15(9). 6077–6084. 120 indexed citations
6.
Olopade, Olufunmilayo I., Helen M. Pomykala, Fitsum Hagos, et al.. (1995). Construction of a 2.8-megabase yeast artificial chromosome contig and cloning of the human methylthioadenosine phosphorylase gene from the tumor suppressor region on 9p21.. Proceedings of the National Academy of Sciences. 92(14). 6489–6493. 77 indexed citations
7.
Lehto, Markku, K. Xiang, Markus Stoffel, et al.. (1993). Human hexokinase II: localization of the polymorphic gene to chromosome 2. Diabetologia. 36(12). 1299–1302. 26 indexed citations
8.
Stoffel, Markus, R Espinosa, Susanne R. Keller, et al.. (1993). Human insulin receptor substrate-1 gene (IRS1): chromosomal localization to 2q35-q36.1 and identification of a simple tandem repeat DNA polymorphism. Diabetologia. 36(4). 335–337. 8 indexed citations
9.
Beau, Michelle M. Le, R Espinosa, W.L. Neuman, et al.. (1993). Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases.. Proceedings of the National Academy of Sciences. 90(12). 5484–5488. 210 indexed citations
10.
Baron, Beverly W., Giuseppina Nucifora, Norah R. McCabe, et al.. (1993). Identification of the gene associated with the recurring chromosomal translocations t(3;14)(q27;q32) and t(3;22)(q27;q11) in B-cell lymphomas.. Proceedings of the National Academy of Sciences. 90(11). 5262–5266. 240 indexed citations
11.
Brown, J. Lesley, R Espinosa, Michelle M. Le Beau, Michael J. Siciliano, & Richard Baer. (1992). HEN1 and HEN2: a subgroup of basic helix-loop-helix genes that are coexpressed in a human neuroblastoma.. Proceedings of the National Academy of Sciences. 89(18). 8492–8496. 53 indexed citations
12.
McKeithan, Timothy W., et al.. (1992). Molecular cloning of the breakpoints of a complex Philadelphia chromosome translocation: identification of a repeated region on chromosome 17.. Proceedings of the National Academy of Sciences. 89(11). 4923–4927. 11 indexed citations
13.
Ohagi, Shinya, J LaMendola, Michelle M. LeBeau, et al.. (1992). Identification and analysis of the gene encoding human PC2, a prohormone convertase expressed in neuroendocrine tissues.. Proceedings of the National Academy of Sciences. 89(11). 4977–4981. 56 indexed citations
14.
Espinosa, R, et al.. (1991). Localization of the gene encoding insulin-degrading enzyme to human chromosome 10, bands q23→q25. Cytogenetic and Genome Research. 57(4). 184–186. 11 indexed citations
15.
Xia, Ying, J. Lesley Brown, Michael J. Siciliano, et al.. (1991). TAL2, a helix-loop-helix gene activated by the (7;9)(q34;q32) translocation in human T-cell leukemia.. Proceedings of the National Academy of Sciences. 88(24). 11416–11420. 147 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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