Patrick N. Anderson

4.6k total citations
84 papers, 3.8k citations indexed

About

Patrick N. Anderson is a scholar working on Cellular and Molecular Neuroscience, Developmental Neuroscience and Molecular Biology. According to data from OpenAlex, Patrick N. Anderson has authored 84 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 63 papers in Cellular and Molecular Neuroscience, 38 papers in Developmental Neuroscience and 19 papers in Molecular Biology. Recurrent topics in Patrick N. Anderson's work include Nerve injury and regeneration (57 papers), Neurogenesis and neuroplasticity mechanisms (38 papers) and Axon Guidance and Neuronal Signaling (25 papers). Patrick N. Anderson is often cited by papers focused on Nerve injury and regeneration (57 papers), Neurogenesis and neuroplasticity mechanisms (38 papers) and Axon Guidance and Neuronal Signaling (25 papers). Patrick N. Anderson collaborates with scholars based in United Kingdom, United States and Switzerland. Patrick N. Anderson's co-authors include A. R. Lieberman, Mark Turmaine, G. Campbell, Melitta Schachner, Joost Verhaagen, David Hunt, Yonghui Zhang, Gennadij Raivich, Matthew R. J. Mason and Stephen R. Bolsover and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Medicine and Journal of Neuroscience.

In The Last Decade

Patrick N. Anderson

82 papers receiving 3.7k citations

Peers

Patrick N. Anderson
Cynthia Wetmore United States
Lucien J. Houenou United States
Pantelis Tsoulfas United States
Shuqian Jing United States
Judith B. Grinspan United States
Patrick N. Anderson
Citations per year, relative to Patrick N. Anderson Patrick N. Anderson (= 1×) peers Clas B. Johansson

Countries citing papers authored by Patrick N. Anderson

Since Specialization
Citations

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

Fields of papers citing papers by Patrick N. Anderson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Patrick N. Anderson. 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 Patrick N. Anderson. The network helps show where Patrick N. Anderson may publish in the future.

Co-authorship network of co-authors of Patrick N. Anderson

This figure shows the co-authorship network connecting the top 25 collaborators of Patrick N. Anderson. A scholar is included among the top collaborators of Patrick N. Anderson 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 Patrick N. Anderson. Patrick N. Anderson 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.
Wiegandt, Florian, Patrick N. Anderson, Fei Yu, et al.. (2019). Quasi-phase-matched high-harmonic generation in gas-filled hollow-core photonic crystal fiber. Optica. 6(4). 442–442. 13 indexed citations
2.
Hunt, David, Gennadij Raivich, & Patrick N. Anderson. (2012). Activating Transcription Factor 3 and the Nervous System. Frontiers in Molecular Neuroscience. 5. 7–7. 126 indexed citations
3.
Lieberman, A. R., et al.. (2010). Microglial responses around intrinsic CNS neurons are correlated with axonal regeneration. BMC Neuroscience. 11(1). 13–13. 30 indexed citations
4.
Burnet, Philip W. J., et al.. (2010). d-Amino acid oxidase knockdown in the mouse cerebellum reduces NR2A mRNA. Molecular and Cellular Neuroscience. 46(1). 167–175. 17 indexed citations
5.
Makwana, Milan, Alexander Werner, Crystal A. Ruff, et al.. (2009). Peripheral facial nerve axotomy in mice causes sprouting of motor axons into perineuronal central white matter: Time course and molecular characterization. The Journal of Comparative Neurology. 518(5). 699–721. 23 indexed citations
6.
Anderson, Patrick N., et al.. (2007). Regeneration‐enhancing effects of EphA4 blocking peptide following corticospinal tract injury in adult rat spinal cord. European Journal of Neuroscience. 26(9). 2496–2505. 89 indexed citations
7.
Rezajooi, Kia, et al.. (2007). Analysis of axonal regeneration in the central and peripheral nervous systems of the NG2-deficient mouse. BMC Neuroscience. 8(1). 80–80. 37 indexed citations
8.
Zhang, Xinyu, Xuenong Bo, Patrick N. Anderson, A. R. Lieberman, & Yi Zhang. (2006). Distribution and expression of tissue inhibitors of metalloproteinase in dorsal root entry zone and dorsal column after dorsal root injury. Journal of Neuroscience Research. 84(2). 278–290. 3 indexed citations
9.
Zhang, Yi, Xuenong Bo, Ralf Schoepfer, et al.. (2005). Growth-associated protein GAP-43 and L1 act synergistically to promote regenerative growth of Purkinje cell axons in vivo. Proceedings of the National Academy of Sciences. 102(41). 14883–14888. 72 indexed citations
10.
Campbell, G., et al.. (2005). Upregulation of activating transcription factor 3 (ATF3) by intrinsic CNS neurons regenerating axons into peripheral nerve grafts. Experimental Neurology. 192(2). 340–347. 29 indexed citations
11.
Ahmed, Bushra, Sridhara Chakravarthy, Ruben Eggers, et al.. (2004). Efficient delivery of Cre-recombinase to neurons in vivo and stable transduction of neurons using adeno-associated and lentiviral vectors. BMC Neuroscience. 5(1). 4–4. 82 indexed citations
12.
Campbell, Gregor, et al.. (2003). Different effects of astrocytes and Schwann cells on regenerating retinal axons. Neuroreport. 14(16). 2085–2088. 6 indexed citations
13.
Hunt, David, R. S. Coffin, Rabinder Prinjha, G. Campbell, & Patrick N. Anderson. (2003). Nogo-A expression in the intact and injured nervous system. Molecular and Cellular Neuroscience. 24(4). 1083–1102. 97 indexed citations
14.
Campbell, G., et al.. (2003). Expression of regeneration-related molecules in injured and regenerating striatal and nigral neurons. Journal of Neurocytology. 32(2). 161–183. 15 indexed citations
15.
Smith, Martin D., Lisa Melton, Elizabeth Ensor, et al.. (2001). Brn-3a Activates the Expression of Bcl-xL and Promotes Neuronal Survival in Vivo as Well as in Vitro. Molecular and Cellular Neuroscience. 17(3). 460–470. 45 indexed citations
17.
Saffrey, M. Jill, et al.. (1996). NADPH-diaphorase-containing enteric neurones survive for a year in the adult rat striatum. Neuroreport. 7(4). 958–960. 6 indexed citations
18.
Saffrey, M. Jill, et al.. (1993). Postnatal Rat NADPH-Diaphorase-Containing Myenteric Neurons Extend Processes When Transplanted into Adult Rat Corpus Striatum. Experimental Neurology. 124(2). 265–273. 10 indexed citations
19.
Anderson, Patrick N., et al.. (1990). The role of Schwann cells and basal lamina tubes in the regeneration of axons through long lengths of freeze‐killed nerve grafts. Neuropathology and Applied Neurobiology. 16(5). 411–421. 77 indexed citations
20.
Anderson, Patrick N., et al.. (1989). Peripheral nerve regeneration through optic nerve grafts. Acta Neuropathologica. 77(5). 525–534. 11 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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