Judith B. Grinspan

4.4k total citations
77 papers, 3.7k citations indexed

About

Judith B. Grinspan is a scholar working on Molecular Biology, Developmental Neuroscience and Neurology. According to data from OpenAlex, Judith B. Grinspan has authored 77 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 35 papers in Developmental Neuroscience and 19 papers in Neurology. Recurrent topics in Judith B. Grinspan's work include Neurogenesis and neuroplasticity mechanisms (35 papers), Neuroinflammation and Neurodegeneration Mechanisms (18 papers) and Epigenetics and DNA Methylation (10 papers). Judith B. Grinspan is often cited by papers focused on Neurogenesis and neuroplasticity mechanisms (35 papers), Neuroinflammation and Neurodegeneration Mechanisms (18 papers) and Epigenetics and DNA Methylation (10 papers). Judith B. Grinspan collaborates with scholars based in United States, United Kingdom and Australia. Judith B. Grinspan's co-authors include Steven S. Scherer, Jacqueline Beesley, David Pleasure, Jill See, Barbara Franceschini, Jeffrey A. Golden, Matthew F. Reeves, John Kamholz, Mark A. Marchionni and Rebecca A. Simmons and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Neuron.

In The Last Decade

Judith B. Grinspan

75 papers receiving 3.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Judith B. Grinspan United States 34 1.7k 1.3k 1.2k 653 330 77 3.7k
Robert P. Skoff United States 42 2.3k 1.3× 2.3k 1.8× 1.5k 1.2× 1.2k 1.9× 445 1.3× 96 5.0k
Jeffrey K. Huang United States 25 1.3k 0.7× 1.1k 0.9× 949 0.8× 659 1.0× 204 0.6× 58 3.0k
Danielle Pham-Dinh France 27 1.4k 0.8× 970 0.7× 833 0.7× 631 1.0× 220 0.7× 40 3.3k
Hiroaki Asou Japan 34 1.6k 0.9× 760 0.6× 988 0.8× 435 0.7× 205 0.6× 126 3.4k
Maria K. Lehtinen United States 30 2.5k 1.4× 782 0.6× 1.2k 1.0× 422 0.6× 260 0.8× 63 4.5k
Julia M. Edgar United Kingdom 30 1.7k 1.0× 1.6k 1.3× 1.4k 1.2× 1.2k 1.8× 356 1.1× 69 4.2k
John Kamholz United States 45 2.8k 1.6× 909 0.7× 2.1k 1.8× 774 1.2× 238 0.7× 138 5.5k
Peter Bannerman United States 33 1.3k 0.7× 719 0.6× 1.1k 0.9× 530 0.8× 261 0.8× 67 2.8k
I. K. Hart United Kingdom 21 1.2k 0.7× 797 0.6× 801 0.7× 337 0.5× 248 0.8× 38 3.5k
Ulrika Wilhelmsson Sweden 30 1.5k 0.9× 963 0.7× 1.2k 1.0× 1.8k 2.7× 169 0.5× 47 4.1k

Countries citing papers authored by Judith B. Grinspan

Since Specialization
Citations

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

Fields of papers citing papers by Judith B. Grinspan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Judith B. Grinspan. 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 Judith B. Grinspan. The network helps show where Judith B. Grinspan may publish in the future.

Co-authorship network of co-authors of Judith B. Grinspan

This figure shows the co-authorship network connecting the top 25 collaborators of Judith B. Grinspan. A scholar is included among the top collaborators of Judith B. Grinspan 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 Judith B. Grinspan. Judith B. Grinspan 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
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Grinspan, Judith B., et al.. (2023). Antiretroviral treatment reveals a novel role for lysosomes in oligodendrocyte maturation. Journal of Neurochemistry. 165(5). 722–740. 4 indexed citations
3.
Monnerie, Hubert, et al.. (2023). Inhibition of lipid synthesis by the HIV integrase strand transfer inhibitor elvitegravir in primary rat oligodendrocyte cultures. Frontiers in Molecular Neuroscience. 16. 1323431–1323431. 1 indexed citations
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Helman, Guy, Ayelet Zerem, Sarah Woidill, et al.. (2021). Further Delineation of the Clinical and Pathologic Features of HIKESHI-Related Hypomyelinating Leukodystrophy. Pediatric Neurology. 121. 11–19. 4 indexed citations
6.
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Jensen, Brigid K., et al.. (2019). Protease Inhibitors, Saquinavir and Darunavir, Inhibit Oligodendrocyte Maturation: Implications for Lysosomal Stress. Journal of Neuroimmune Pharmacology. 16(1). 169–180. 16 indexed citations
8.
Lawrence, Kendall M., Patrick E. McGovern, Ali Y. Mejaddam, et al.. (2019). Chronic intrauterine hypoxia alters neurodevelopment in fetal sheep. Journal of Thoracic and Cardiovascular Surgery. 157(5). 1982–1991. 35 indexed citations
9.
Lim, Youngshin, Il‐Taeg Cho, Xiuyu Shi, et al.. (2019). Arx Expression Suppresses Ventralization of the Developing Dorsal Forebrain. Scientific Reports. 9(1). 226–226. 10 indexed citations
10.
Jensen, Brigid K., Hubert Monnerie, Maggie V. Mannell, et al.. (2015). Altered Oligodendrocyte Maturation and Myelin Maintenance: The Role of Antiretrovirals in HIV-Associated Neurocognitive Disorders. Journal of Neuropathology & Experimental Neurology. 74(11). 1093–1118. 46 indexed citations
11.
Simmons, Rebecca A., et al.. (2009). Oxidative stress disrupts oligodendrocyte maturation. Journal of Neuroscience Research. 87(14). 3076–3087. 183 indexed citations
12.
Ara, Jahan, Jill See, Ashleigh Hahn, et al.. (2007). Bone morphogenetic proteins 4, 6, and 7 are up‐regulated in mouse spinal cord during experimental autoimmune encephalomyelitis. Journal of Neuroscience Research. 86(1). 125–135. 69 indexed citations
13.
Guo, Changjiang, Steven D. Douglas, Zhiyong Gao, et al.. (2004). Interleukin‐1β upregulates functional expression of neurokinin‐1 receptor (NK‐1R) via NF‐κB in astrocytes. Glia. 48(3). 259–266. 57 indexed citations
14.
Grinspan, Judith B.. (2002). Cells and Signaling in Oligodendrocyte Development. Journal of Neuropathology & Experimental Neurology. 61(4). 297–306. 53 indexed citations
15.
Beesley, Jacqueline, et al.. (2001). ST8Sia IV mRNA corresponds with the biosynthesis of α2,8sialyl polymers but not oligomers in rat oligodendrocytes. Journal of Neuroscience Research. 66(3). 497–505. 8 indexed citations
16.
Beesley, Jacqueline, et al.. (2000). Neurotrophin-3 (NT-3) diminishes susceptibility of the oligodendroglial lineage to AMPA glutamate receptor-mediated excitotoxicity. Journal of Neuroscience Research. 60(6). 725–732. 41 indexed citations
17.
Grinspan, Judith B., et al.. (1996). Axonal Interactions Regulate Schwann Cell Apoptosis in Developing Peripheral Nerve: Neuregulin Receptors and the Role of Neuregulins. Journal of Neuroscience. 16(19). 6107–6118. 273 indexed citations
18.
Sinor, Amy D., et al.. (1995). Pharmacology of Sodium‐Dependent High‐Affinity l‐[3H]Glutamate Transport in Glial Cultures. Journal of Neurochemistry. 64(6). 2572–2580. 77 indexed citations
19.
Grinspan, Judith B., Jeffrey Stern, Barbara Franceschini, Tadashi Yasuda, & David Pleasure. (1994). Protein growth factors as potential therapies for central nervous system demyelinative disorders. Annals of Neurology. 36(S1). S140–S142. 25 indexed citations
20.
Grinspan, Judith B., et al.. (1993). Trophic effects of basic fibroblast growth factor (bFGF) on differentiated oligodendroglia: A mechanism for regeneration of the oligodendroglial lineage. Journal of Neuroscience Research. 36(6). 672–680. 91 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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