H. Elizabeth Shick

2.4k total citations
14 papers, 1.7k citations indexed

About

H. Elizabeth Shick is a scholar working on Molecular Biology, Developmental Neuroscience and Neurology. According to data from OpenAlex, H. Elizabeth Shick has authored 14 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Developmental Neuroscience and 4 papers in Neurology. Recurrent topics in H. Elizabeth Shick's work include Neurogenesis and neuroplasticity mechanisms (6 papers), Neuroinflammation and Neurodegeneration Mechanisms (4 papers) and MicroRNA in disease regulation (3 papers). H. Elizabeth Shick is often cited by papers focused on Neurogenesis and neuroplasticity mechanisms (6 papers), Neuroinflammation and Neurodegeneration Mechanisms (4 papers) and MicroRNA in disease regulation (3 papers). H. Elizabeth Shick collaborates with scholars based in United States and Japan. H. Elizabeth Shick's co-authors include Wendy B. Macklin, Grahame J. Kidd, Richard M. Ransohoff, Barbara S. Mallon, Mark H. Stoler, Dawn Thomas, Marie Tani, Jennifer Major, Thomas A. Hamilton and Melinda L. Estes and has published in prestigious journals such as Nature Communications, Journal of Neuroscience and Nature Neuroscience.

In The Last Decade

H. Elizabeth Shick

14 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
H. Elizabeth Shick United States	12	763	525	426	417	331	14	1.7k
Chay T. Kuo United States	23	1.5k 2.0×	693 1.3×	536 1.3×	273 0.7×	731 2.2×	32	2.7k
Julie A. Siegenthaler United States	28	1.2k 1.6×	577 1.1×	157 0.4×	469 1.1×	515 1.6×	50	2.4k
Emma E. Frost United States	22	658 0.9×	782 1.5×	198 0.5×	328 0.8×	449 1.4×	41	1.8k
Sarah E. Lutz United States	19	914 1.2×	139 0.3×	222 0.5×	824 2.0×	346 1.0×	30	1.9k
Tobias Goldmann Germany	21	1.1k 1.4×	102 0.2×	658 1.5×	798 1.9×	333 1.0×	31	2.1k
Wael M. ElShamy United States	21	781 1.0×	353 0.7×	147 0.3×	74 0.2×	632 1.9×	41	1.7k
Dejan Lazarević Italy	26	1.9k 2.5×	216 0.4×	324 0.8×	84 0.2×	466 1.4×	65	2.8k
Mary C. Whitman United States	17	477 0.6×	721 1.4×	296 0.7×	297 0.7×	518 1.6×	48	1.8k
Benjamin K. August United States	19	717 0.9×	194 0.4×	108 0.3×	232 0.6×	153 0.5×	40	1.5k
Anne L. Prieto United States	23	684 0.9×	169 0.3×	708 1.7×	188 0.5×	389 1.2×	30	2.1k

Countries citing papers authored by H. Elizabeth Shick

Since Specialization

Citations

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

Fields of papers citing papers by H. Elizabeth Shick

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by H. Elizabeth Shick. 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 H. Elizabeth Shick. The network helps show where H. Elizabeth Shick may publish in the future.

Co-authorship network of co-authors of H. Elizabeth Shick

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

All Works

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14 of 14 papers shown

Clayton, Benjamin L.L., Kevin Allan, Molly Karl, et al.. (2024). A phenotypic screening platform for identifying chemical modulators of astrocyte reactivity. Nature Neuroscience. 27(4). 656–665. 13 indexed citations

Hubler, Zita, David Yan, Ilya Bederman, et al.. (2021). Inhibition of SC4MOL and HSD17B7 shifts cellular sterol composition and promotes oligodendrocyte formation. RSC Chemical Biology. 3(1). 56–68. 9 indexed citations

Madhavan, Mayur, Zachary S. Nevin, H. Elizabeth Shick, et al.. (2018). Induction of myelinating oligodendrocytes in human cortical spheroids. Nature Methods. 15(9). 700–706. 240 indexed citations

Lager, Angela M., Olivia Corradin, Jared M. Cregg, et al.. (2018). Rapid functional genetics of the oligodendrocyte lineage using pluripotent stem cells. Nature Communications. 9(1). 3708–3708. 17 indexed citations

Elitt, Matthew S., H. Elizabeth Shick, Mayur Madhavan, et al.. (2018). Chemical Screening Identifies Enhancers of Mutant Oligodendrocyte Survival and Unmasks a Distinct Pathological Phase in Pelizaeus-Merzbacher Disease. Stem Cell Reports. 11(3). 711–726. 27 indexed citations

Zhao, Lihong, Stefka D. Spassieva, Leonard D. Shultz, et al.. (2011). A Deficiency of Ceramide Biosynthesis Causes Cerebellar Purkinje Cell Neurodegeneration and Lipofuscin Accumulation. PLoS Genetics. 7(5). e1002063–e1002063. 138 indexed citations

Sato, Eisuke, H. Elizabeth Shick, Richard M. Ransohoff, & Keiko Hirose. (2009). Expression of Fractalkine Receptor CX3CR1 on Cochlear Macrophages Influences Survival of Hair Cells Following Ototoxic Injury. Journal of the Association for Research in Otolaryngology. 11(2). 223–234. 86 indexed citations

Flores, Ana I., S. Priya Narayanan, H. Elizabeth Shick, et al.. (2008). Constitutively Active Akt Induces Enhanced Myelination in the CNS. Journal of Neuroscience. 28(28). 7174–7183. 298 indexed citations

Sato, Eisuke, H. Elizabeth Shick, Richard M. Ransohoff, & Keiko Hirose. (2007). Repopulation of cochlear macrophages in murine hematopoietic progenitor cell chimeras: The role of CX3CR1. The Journal of Comparative Neurology. 506(6). 930–942. 59 indexed citations

10.

Wight, P.A.L., Cynthia S. Duchala, H. Elizabeth Shick, Tatyana I. Gudz, & Wendy B. Macklin. (2006). Expression of a Myelin Proteolipid Protein (Plp)-lacZ Transgene is Reduced in both the CNS and PNS of Plp jp Mice. Neurochemical Research. 32(2). 343–351. 7 indexed citations

11.

Duchala, Cynthia S., et al.. (2004). The toppler mouse: A novel mutant exhibiting loss of Purkinje cells. The Journal of Comparative Neurology. 476(2). 113–129. 29 indexed citations

12.

Mallon, Barbara S., H. Elizabeth Shick, Grahame J. Kidd, & Wendy B. Macklin. (2002). Proteolipid Promoter Activity Distinguishes Two Populations of NG2-Positive Cells throughout Neonatal Cortical Development. Journal of Neuroscience. 22(3). 876–885. 314 indexed citations

13.

Kalayjian, Robert C., et al.. (1997). Polymerase Chain Reaction Detection and Clinical Significance of Varicella‐Zoster Virus in Cerebrospinal Fluid from Human Immunodeficiency Virus‐Infected Patients. The Journal of Infectious Diseases. 176(4). 1080–1084. 32 indexed citations

14.

Ransohoff, Richard M., Thomas A. Hamilton, Marie Tani, et al.. (1993). Astrocyte expression of mRNA encoding cytokines IP‐10 and JE/MCP‐1 in experimental autoimmune encephalomyelitis. The FASEB Journal. 7(6). 592–600. 436 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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