Mailis C. McCulloch

1.1k total citations
13 papers, 881 citations indexed

About

Mailis C. McCulloch is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Developmental Neuroscience. According to data from OpenAlex, Mailis C. McCulloch has authored 13 papers receiving a total of 881 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Cellular and Molecular Neuroscience, 7 papers in Molecular Biology and 6 papers in Developmental Neuroscience. Recurrent topics in Mailis C. McCulloch's work include Neurogenesis and neuroplasticity mechanisms (6 papers), Neuroscience and Neuropharmacology Research (3 papers) and Nerve injury and regeneration (3 papers). Mailis C. McCulloch is often cited by papers focused on Neurogenesis and neuroplasticity mechanisms (6 papers), Neuroscience and Neuropharmacology Research (3 papers) and Nerve injury and regeneration (3 papers). Mailis C. McCulloch collaborates with scholars based in United Kingdom, Germany and United States. Mailis C. McCulloch's co-authors include Julia M. Edgar, Ian R. Griffiths, James McCulloch, Louis Sokoloff, Jennifer A. Barrie, Marκ McLaughlin, Helen E. Savaki, Paul Montague, Klaus Armin Nave and Klaus‐Armin Nave and has published in prestigious journals such as Nature, Science and The Journal of Cell Biology.

In The Last Decade

Mailis C. McCulloch

13 papers receiving 868 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mailis C. McCulloch United Kingdom	13	385	379	309	205	112	13	881
Sara Kirvell United Kingdom	15	380 1.0×	389 1.0×	305 1.0×	193 0.9×	59 0.5×	24	936
Yangzhou Du United States	8	223 0.6×	338 0.9×	387 1.3×	167 0.8×	70 0.6×	9	734
Inmaculada Rite Spain	8	378 1.0×	396 1.0×	424 1.4×	437 2.1×	216 1.9×	8	1.0k
Carmen Sato‐Bigbee United States	20	540 1.4×	289 0.8×	357 1.2×	196 1.0×	52 0.5×	29	1.1k
Sumiko Mikawa Japan	18	717 1.9×	681 1.8×	208 0.7×	204 1.0×	75 0.7×	37	1.2k
Kathryn K. Bercury United States	13	616 1.6×	362 1.0×	461 1.5×	217 1.1×	174 1.6×	15	1.3k
Li‐Jin Chew United States	16	469 1.2×	153 0.4×	292 0.9×	283 1.4×	51 0.5×	24	1.2k
Haviryaji S. G. Kalluri United States	14	308 0.8×	322 0.8×	144 0.5×	180 0.9×	88 0.8×	21	777
Catherine L. Delaney United States	6	393 1.0×	316 0.8×	217 0.7×	151 0.7×	61 0.5×	7	888
Anne Desmazières France	14	273 0.7×	374 1.0×	265 0.9×	251 1.2×	99 0.9×	21	792

Countries citing papers authored by Mailis C. McCulloch

Since Specialization

Citations

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

Fields of papers citing papers by Mailis C. McCulloch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mailis C. McCulloch. 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 Mailis C. McCulloch. The network helps show where Mailis C. McCulloch may publish in the future.

Co-authorship network of co-authors of Mailis C. McCulloch

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

All Works

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13 of 13 papers shown

Deighton, Ruth F., Thierry Le Bihan, Sarah F. Martin, et al.. (2014). Interactions among mitochondrial proteins altered in glioblastoma. Journal of Neuro-Oncology. 118(2). 247–256. 60 indexed citations

Herrmann, Abigail G., Ruth F. Deighton, Thierry Le Bihan, et al.. (2013). Adaptive Changes in the Neuronal Proteome: Mitochondrial Energy Production, Endoplasmic Reticulum Stress, and Ribosomal Dysfunction in the Cellular Response to Metabolic Stress. Journal of Cerebral Blood Flow & Metabolism. 33(5). 673–683. 37 indexed citations

Karim, Saadia A., Jennifer A. Barrie, Mailis C. McCulloch, et al.. (2010). PLP/DM20 Expression and turnover in a transgenic mouse model of pelizaeus‐merzbacher disease. Glia. 58(14). 1727–1738. 28 indexed citations

Edgar, Julia M., Mailis C. McCulloch, Paul Montague, et al.. (2010). Demyelination and axonal preservation in a transgenic mouse model of Pelizaeus‐Merzbacher disease. EMBO Molecular Medicine. 2(2). 42–50. 55 indexed citations

Edgar, Julia M., Marκ McLaughlin, Hauke Werner, et al.. (2009). Early ultrastructural defects of axons and axon–glia junctions in mice lacking expression of Cnp1. Glia. 57(16). 1815–1824. 122 indexed citations

Edgar, Julia M., Mailis C. McCulloch, Christine E. Thomson, & Ian R. Griffiths. (2008). Distribution of mitochondria along small‐diameter myelinated central nervous system axons. Journal of Neuroscience Research. 86(10). 2250–2257. 33 indexed citations

Wang, Erming, Neviana Dimova, Karen Sperle, et al.. (2008). Deletion of a splicing enhancer disrupts PLP1/DM20 ratio and myelin stability. Experimental Neurology. 214(2). 322–330. 26 indexed citations

Thomson, Christine E., et al.. (2006). Murine spinal cord explants: A model for evaluating axonal growth and myelination in vitro. Journal of Neuroscience Research. 84(8). 1703–1715. 39 indexed citations

Karim, Saadia A., Jennifer A. Barrie, Mailis C. McCulloch, et al.. (2006). PLP overexpression perturbs myelin protein composition and myelination in a mouse model of Pelizaeus‐Merzbacher disease. Glia. 55(4). 341–351. 54 indexed citations

10.

Edgar, Julia M., Marκ McLaughlin, D. A. Yool, et al.. (2004). Oligodendroglial modulation of fast axonal transport in a mouse model of hereditary spastic paraplegia. The Journal of Cell Biology. 166(1). 121–131. 244 indexed citations

11.

McCulloch, James, Helen E. Savaki, Mailis C. McCulloch, Jane Jehle, & Louis Sokoloff. (1982). The distribution of alterations in energy metabolism in the rat brain produced by apomorphine. Brain Research. 243(1). 67–80. 104 indexed citations

12.

McCulloch, James, Helen E. Savaki, Mailis C. McCulloch, & Louis Sokoloff. (1980). Retina-Dependent Activation by Apomorphine of Metabolic Activity in the Superficial Layer of the Superior Colliculus. Science. 207(4428). 313–315. 33 indexed citations

13.

McCulloch, James, Helen E. Savaki, Mailis C. McCulloch, & Louis Sokoloff. (1979). Specific distribution of metabolic alterations in cerebral cortex following apomorphine administration. Nature. 282(5736). 303–305. 46 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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