Anna La Torre

2.1k total citations
37 papers, 1.2k citations indexed

About

Anna La Torre is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, Anna La Torre has authored 37 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 16 papers in Cellular and Molecular Neuroscience and 7 papers in Cell Biology. Recurrent topics in Anna La Torre's work include Retinal Development and Disorders (17 papers), Axon Guidance and Neuronal Signaling (7 papers) and Neurogenesis and neuroplasticity mechanisms (6 papers). Anna La Torre is often cited by papers focused on Retinal Development and Disorders (17 papers), Axon Guidance and Neuronal Signaling (7 papers) and Neurogenesis and neuroplasticity mechanisms (6 papers). Anna La Torre collaborates with scholars based in United States, Spain and Italy. Anna La Torre's co-authors include Thomas A. Reh, Sean Georgi, Sergi Simó, Eduardo Soriano, Jesús M. Ureña, José Antonio del Rı́o, Lluı́s Pujadas, Matthew S. Wilken, Akina Hoshino and Marta Pascual and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Neuroscience and Development.

In The Last Decade

Anna La Torre

36 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anna La Torre United States 17 905 422 214 174 168 37 1.2k
David M. Feliciano United States 19 775 0.9× 158 0.4× 213 1.0× 111 0.6× 209 1.2× 37 1.3k
Stéphane Belin France 15 904 1.0× 924 2.2× 550 2.6× 102 0.6× 104 0.6× 26 1.6k
Sandrine Joly Canada 21 836 0.9× 599 1.4× 313 1.5× 113 0.6× 46 0.3× 50 1.4k
Stacy L. Donovan United States 15 961 1.1× 306 0.7× 162 0.8× 199 1.1× 127 0.8× 19 1.6k
Suzanne Claxton United Kingdom 11 535 0.6× 174 0.4× 75 0.4× 189 1.1× 67 0.4× 15 827
Matthew Swire United Kingdom 11 358 0.4× 266 0.6× 420 2.0× 94 0.5× 127 0.8× 13 1.1k
Harald J. Junge United States 16 1.2k 1.3× 545 1.3× 56 0.3× 638 3.7× 63 0.4× 23 1.6k
Norbert Kinkl Germany 16 957 1.1× 385 0.9× 53 0.2× 266 1.5× 47 0.3× 21 1.4k
Arpad Palfi Ireland 23 1.5k 1.7× 424 1.0× 52 0.2× 103 0.6× 178 1.1× 49 1.8k
Hidemasa Kato Japan 17 699 0.8× 318 0.8× 236 1.1× 122 0.7× 79 0.5× 34 1.1k

Countries citing papers authored by Anna La Torre

Since Specialization
Citations

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

Fields of papers citing papers by Anna La Torre

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anna La Torre. 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 Anna La Torre. The network helps show where Anna La Torre may publish in the future.

Co-authorship network of co-authors of Anna La Torre

This figure shows the co-authorship network connecting the top 25 collaborators of Anna La Torre. A scholar is included among the top collaborators of Anna La Torre 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 Anna La Torre. Anna La Torre 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.
2.
Simó, Sergi, et al.. (2023). Expression patterns of CYP26A1, FGF8, CDKN1A, and NPVF in the developing rhesus monkey retina. Differentiation. 135. 100743–100743. 2 indexed citations
3.
Zhao, Mengya, Kenichi Toma, Benyam Kinde, et al.. (2023). Osteopontin drives retinal ganglion cell resiliency in glaucomatous optic neuropathy. Cell Reports. 42(9). 113038–113038. 14 indexed citations
4.
Rogers, Jeffrey, J. Timothy Stout, Sara M. Thomasy, et al.. (2022). Retinal organoids derived from rhesus macaque iPSCs undergo accelerated differentiation compared to human stem cells. Cell Proliferation. 55(4). e13198–e13198. 7 indexed citations
5.
Hino, Keiko, et al.. (2022). The E3 Ubiquitin Ligase CRL5 Regulates Dentate Gyrus Morphogenesis, Adult Neurogenesis, and Animal Behavior. Frontiers in Neuroscience. 16. 908719–908719. 5 indexed citations
6.
Han, Jisoo S., et al.. (2022). Oscillatory Behaviors of microRNA Networks: Emerging Roles in Retinal Development. Frontiers in Cell and Developmental Biology. 10. 831750–831750. 6 indexed citations
7.
Moshiri, Ala, et al.. (2021). MicroRNA Signatures of the Developing Primate Fovea. Frontiers in Cell and Developmental Biology. 9. 654385–654385. 6 indexed citations
8.
Pereiro, Xandra, et al.. (2020). Effects of Adult Müller Cells and Their Conditioned Media on the Survival of Stem Cell-Derived Retinal Ganglion Cells. Cells. 9(8). 1759–1759. 11 indexed citations
9.
Patel, Amit K., Risa Broyer, Anna La Torre, et al.. (2020). Inhibition of GCK-IV kinases dissociates cell death and axon regeneration in CNS neurons. Proceedings of the National Academy of Sciences. 117(52). 33597–33607. 21 indexed citations
10.
Zhang, Pengfei, et al.. (2019). A Novel Reporter Mouse Uncovers Endogenous Brn3b Expression. International Journal of Molecular Sciences. 20(12). 2903–2903. 6 indexed citations
11.
Chao, Jennifer R., Deepak A. Lamba, Todd R. Klesert, et al.. (2017). Transplantation of Human Embryonic Stem Cell-Derived Retinal Cells into the Subretinal Space of a Non-Human PrimateChao et al.. eScholarship (California Digital Library). 63 indexed citations
12.
Hoshino, Akina, Rinki Ratnapriya, Matthew J. Brooks, et al.. (2017). Molecular Anatomy of the Developing Human Retina. Developmental Cell. 43(6). 763–779.e4. 169 indexed citations
13.
Torre, Anna La & Maura Lusignani. (2013). [Florence Nightingale and the Risorgimento: her way of thinking through her correspondence, 1837- 1872].. PubMed. 65(1). 4–10.
14.
Torre, Anna La, M. Masdeu, Tiziana Cotrufo, et al.. (2013). A role for the tyrosine kinase ACK1 in neurotrophin signaling and neuronal extension and branching. Cell Death and Disease. 4(4). e602–e602. 24 indexed citations
15.
Torre, Anna La, et al.. (2012). Production and Transplantation of Retinal Cells from Human and Mouse Embryonic Stem Cells. Methods in molecular biology. 884. 229–246. 30 indexed citations
16.
Quintana, Albert, Elisenda Sanz, Wengang Wang, et al.. (2012). Lack of GPR88 enhances medium spiny neuron activity and alters motor- and cue-dependent behaviors. Nature Neuroscience. 15(11). 1547–1555. 90 indexed citations
17.
Simó, Sergi, Lluı́s Pujadas, Miguel F. Segura, et al.. (2006). Reelin Induces the Detachment of Postnatal Subventricular Zone Cells and the Expression of the Egr-1 through Erk1/2 Activation. Cerebral Cortex. 17(2). 294–303. 56 indexed citations
18.
Torre, Anna La, José Antonio del Rı́o, Eduardo Soriano, & Jesús M. Ureña. (2006). Expression pattern of ACK1 tyrosine kinase during brain development in the mouse. Gene Expression Patterns. 6(8). 886–892. 6 indexed citations
19.
Ureña, Jesús M., Anna La Torre, Albert Martı́nez, et al.. (2005). Expression, synaptic localization, and developmental regulation of Ack1/Pyk1, a cytoplasmic tyrosine kinase highly expressed in the developing and adult brain. The Journal of Comparative Neurology. 490(2). 119–132. 20 indexed citations
20.
Rı́o, José Antonio del, Christian González‐Billault, Jesús M. Ureña, et al.. (2004). MAP1B Is Required for Netrin 1 Signaling in Neuronal Migration and Axonal Guidance. Current Biology. 14(10). 840–850. 100 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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