Rosa E. Blanco

1.3k total citations
38 papers, 1.0k citations indexed

About

Rosa E. Blanco is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Developmental Neuroscience. According to data from OpenAlex, Rosa E. Blanco has authored 38 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Cellular and Molecular Neuroscience, 20 papers in Molecular Biology and 13 papers in Developmental Neuroscience. Recurrent topics in Rosa E. Blanco's work include Nerve injury and regeneration (18 papers), Neurogenesis and neuroplasticity mechanisms (13 papers) and Neuroscience and Neuropharmacology Research (10 papers). Rosa E. Blanco is often cited by papers focused on Nerve injury and regeneration (18 papers), Neurogenesis and neuroplasticity mechanisms (13 papers) and Neuroscience and Neuropharmacology Research (10 papers). Rosa E. Blanco collaborates with scholars based in Puerto Rico, Spain and United Kingdom. Rosa E. Blanco's co-authors include Isidró Ferrer, Jonathan M. Blagburn, E. Goutan, Eduard Tolosa, Teresa Ribalta, Eulàlia Martı́, María Jesús Buxó ì Rey, Ileana Soto, Margarita Carmona and Anna M. Planas and has published in prestigious journals such as PLoS ONE, The Journal of Comparative Neurology and Scientific Reports.

In The Last Decade

Rosa E. Blanco

37 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
Rosa E. Blanco Puerto Rico 16 608 498 247 237 170 38 1.0k
Nadhim Bayatti United Kingdom 21 471 0.8× 543 1.1× 304 1.2× 150 0.6× 136 0.8× 30 1.3k
Fredrik Blomstrand Sweden 20 618 1.0× 742 1.5× 185 0.7× 249 1.1× 351 2.1× 29 1.4k
Sylvia A. Rabacchi United States 13 920 1.5× 690 1.4× 416 1.7× 221 0.9× 239 1.4× 16 1.5k
Gabriele Ugolini Italy 14 625 1.0× 502 1.0× 119 0.5× 492 2.1× 115 0.7× 22 1.1k
Yoong Hee Chang United States 16 529 0.9× 513 1.0× 326 1.3× 128 0.5× 128 0.8× 22 1.2k
Marie Simard United States 9 467 0.8× 462 0.9× 138 0.6× 179 0.8× 437 2.6× 11 1.2k
Robert Gardette France 23 706 1.2× 586 1.2× 214 0.9× 115 0.5× 225 1.3× 36 1.2k
Yaisa Andrews‐Zwilling United States 10 572 0.9× 668 1.3× 296 1.2× 482 2.0× 248 1.5× 16 1.4k
Nicola Schiavo Italy 9 442 0.7× 432 0.9× 148 0.6× 119 0.5× 84 0.5× 16 877
Tomoyo Ochiishi Japan 21 589 1.0× 546 1.1× 118 0.5× 206 0.9× 146 0.9× 31 1.2k

Countries citing papers authored by Rosa E. Blanco

Since Specialization
Citations

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

Fields of papers citing papers by Rosa E. Blanco

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rosa E. Blanco. 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 Rosa E. Blanco. The network helps show where Rosa E. Blanco may publish in the future.

Co-authorship network of co-authors of Rosa E. Blanco

This figure shows the co-authorship network connecting the top 25 collaborators of Rosa E. Blanco. A scholar is included among the top collaborators of Rosa E. Blanco 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 Rosa E. Blanco. Rosa E. Blanco 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
2.
Blagburn, Jonathan M., et al.. (2021). Retinoic acid treatment recruits macrophages and increases axonal regeneration after optic nerve injury in the frog Rana pipiens. PLoS ONE. 16(11). e0255196–e0255196. 5 indexed citations
3.
Blanco, Rosa E., et al.. (2019). Increased interactions and engulfment of dendrites by microglia precede Purkinje cell degeneration in a mouse model of Niemann Pick Type-C. Scientific Reports. 9(1). 14722–14722. 38 indexed citations
4.
Blagburn, Jonathan M., et al.. (2016). Optic nerve injury upregulates retinoic acid signaling in the adult frog visual system. Journal of Chemical Neuroanatomy. 77. 80–92. 9 indexed citations
5.
Blagburn, Jonathan M., et al.. (2012). Changes in fibroblast growth factor-2 and FGF receptors in the frog visual system during optic nerve regeneration. Journal of Chemical Neuroanatomy. 46(1-2). 35–44. 7 indexed citations
7.
Soto, Ileana, et al.. (2006). Changes in nNOS and NADPH diaphorase in frog retina and tectum after axotomy and FGF-2 application. Brain Research. 1103(1). 65–75. 7 indexed citations
9.
Soto, Ileana, et al.. (2004). FGF–2 Up–Regulates the Expression of BDNF and TrkB in Retinal Ganglion Cells After Nerve Injury Through the Activation of the ERK/CREB Signaling Pathway. Investigative Ophthalmology & Visual Science. 45(13). 727–727. 1 indexed citations
10.
Soto, Ileana, Bruno Marie, Deborah J. Baro, & Rosa E. Blanco. (2003). FGF‐2 modulates expression and distribution of GAP‐43 in frog retinal ganglion cells after optic nerve injury. Journal of Neuroscience Research. 73(4). 507–517. 20 indexed citations
11.
Soto, Ileana, et al.. (2002). Changes in brain‐derived neurotrophic factor and trkB receptor in the adult Rana pipiens retina and optic tectum after optic nerve injury. The Journal of Comparative Neurology. 454(4). 456–469. 25 indexed citations
12.
Ferrer, Isidró & Rosa E. Blanco. (2000). N-myc and c-myc expression in Alzheimer disease, Huntington disease and Parkinson disease. Molecular Brain Research. 77(2). 270–276. 63 indexed citations
13.
Ferrer, Isidró, Rosa E. Blanco, Blanca Cutillas, & Santiago Ambrosio. (2000). Fas and Fas‐L expression in Huntington's disease and Parkinson's disease. Neuropathology and Applied Neurobiology. 26(5). 424–433. 46 indexed citations
14.
Ferrer, Isidró, María Jesús Buxó ì Rey, Teresa Ribalta, et al.. (1999). BDNF and Full-length and Truncated TrkB Expression in Alzheimer Disease. Implications in Therapeutic Strategies. Journal of Neuropathology & Experimental Neurology. 58(7). 729–739. 332 indexed citations
15.
Blanco, Rosa E., et al.. (1999). Ultrastructural studies of dorsal root axons regenerating through adult frog optic and sciatic nerves. Microscopy Research and Technique. 46(4-5). 310–318. 4 indexed citations
16.
Blagburn, Jonathan M., María A. Sosa, & Rosa E. Blanco. (1996). Specificity of identified central synapses in the embryonic cockroach: Appropriate connections form before the onset of spontaneous afferent activity. The Journal of Comparative Neurology. 373(4). 511–528. 12 indexed citations
17.
Ferrer, Isidró, Rosa E. Blanco, Margarita Carmona, et al.. (1996). CREB-1 and CREB-2 immunoreactivity in the rat brain. Brain Research. 712(1). 159–164. 15 indexed citations
18.
Blanco, Rosa E., Héctor Marrero, Paula M. Orkand, & Richard K. Orkand. (1993). Changes in ultrastructure and voltage‐dependent currents at the glia limitans of the frog optic nerve following retinal ablation. Glia. 8(2). 97–105. 8 indexed citations
19.
Blanco, Rosa E. & Nick Lane. (1990). Changes in intercellular junctions during peripheral nerve regeneration in insects. Journal of Neurocytology. 19(6). 873–882. 1 indexed citations
20.
Blanco, Rosa E.. (1988). Glial cells in peripheral nerves of the cockroach, Periplaneta americana. Tissue and Cell. 20(5). 771–782. 5 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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