Louise Chappell‐Maor

3.2k total citations · 1 hit paper
21 papers, 2.3k citations indexed

About

Louise Chappell‐Maor is a scholar working on Molecular Biology, Immunology and Neurology. According to data from OpenAlex, Louise Chappell‐Maor has authored 21 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 10 papers in Immunology and 8 papers in Neurology. Recurrent topics in Louise Chappell‐Maor's work include Neuroinflammation and Neurodegeneration Mechanisms (8 papers), Immune cells in cancer (7 papers) and Single-cell and spatial transcriptomics (3 papers). Louise Chappell‐Maor is often cited by papers focused on Neuroinflammation and Neurodegeneration Mechanisms (8 papers), Immune cells in cancer (7 papers) and Single-cell and spatial transcriptomics (3 papers). Louise Chappell‐Maor collaborates with scholars based in Israel, United Kingdom and Germany. Louise Chappell‐Maor's co-authors include Steffen Jung, Eyal David, Anat Shemer, Jung‐Seok Kim, Jonathan Grozovski, Marco Prinz, Mor Gross-Vered, Alberto Ardura-Fabregat, Tuan Leng Tay and Jenhan Tao and has published in prestigious journals such as Nature Communications, Immunity and Nature Immunology.

In The Last Decade

Louise Chappell‐Maor

19 papers receiving 2.3k citations

Hit Papers

Engrafted parenchymal brain macrophages differ from micro... 2018 2026 2020 2023 2018 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Louise Chappell‐Maor Israel 16 802 677 663 272 199 21 2.3k
Hiromi Suzuki Japan 28 310 0.4× 840 1.2× 560 0.8× 69 0.3× 372 1.9× 98 2.5k
Shigeru Sato Japan 31 327 0.4× 1.6k 2.3× 290 0.4× 127 0.5× 158 0.8× 158 3.9k
Alan G. Cheng United States 27 244 0.3× 1.2k 1.8× 481 0.7× 116 0.4× 93 0.5× 87 3.5k
Shohei Watanabe Japan 31 396 0.5× 669 1.0× 275 0.4× 103 0.4× 247 1.2× 157 3.9k
Kristian Pfaller Austria 31 358 0.4× 851 1.3× 138 0.2× 148 0.5× 102 0.5× 79 3.3k
Anat Shemer Israel 13 655 0.8× 439 0.6× 767 1.2× 29 0.1× 122 0.6× 17 1.8k
Lisa L. Cunningham United States 33 321 0.4× 1.3k 1.9× 679 1.0× 92 0.3× 93 0.5× 60 3.6k
Tuan Leng Tay Germany 15 1.1k 1.3× 875 1.3× 1.7k 2.6× 44 0.2× 323 1.6× 20 3.4k
Katsumi Doi Japan 37 271 0.3× 2.1k 3.1× 903 1.4× 213 0.8× 198 1.0× 217 4.8k
Clemens Grabher Germany 25 930 1.2× 2.9k 4.3× 206 0.3× 137 0.5× 283 1.4× 34 4.9k

Countries citing papers authored by Louise Chappell‐Maor

Since Specialization
Citations

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

Fields of papers citing papers by Louise Chappell‐Maor

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Louise Chappell‐Maor. 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 Louise Chappell‐Maor. The network helps show where Louise Chappell‐Maor may publish in the future.

Co-authorship network of co-authors of Louise Chappell‐Maor

This figure shows the co-authorship network connecting the top 25 collaborators of Louise Chappell‐Maor. A scholar is included among the top collaborators of Louise Chappell‐Maor 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 Louise Chappell‐Maor. Louise Chappell‐Maor 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.
Chappell‐Maor, Louise, Sarah M. Russell, Isabel Iglesias‐Platas, et al.. (2025). PIK3R1 and G0S2 are human placenta-specific imprinted genes associated with germline-inherited maternal DNA methylation. Epigenetics. 20(1). 2523191–2523191. 1 indexed citations
2.
Chappell‐Maor, Louise, Philippe Arnaúd, Isabel Iglesias‐Platas, et al.. (2025). Non-canonical imprinting, manifesting as post-fertilization placenta-specific parent-of-origin dependent methylation, is not conserved in humans. Human Molecular Genetics. 34(7). 626–638. 3 indexed citations
3.
Panda, Sayantan, Louise Chappell‐Maor, Luis Alejandro de Haro, et al.. (2025). Molecular mechanisms driving the unusual pigmentation shift during eggplant fruit development. Plant Communications. 6(5). 101321–101321.
5.
Haimon, Zhana, Jung‐Seok Kim, Sébastien Trzebanski, et al.. (2022). Cognate microglia–T cell interactions shape the functional regulatory T cell pool in experimental autoimmune encephalomyelitis pathology. Nature Immunology. 23(12). 1749–1762. 35 indexed citations
6.
Kim, Jung‐Seok, Masha Kolesnikov, Isabelle Scheyltjens, et al.. (2020). A Binary Cre Transgenic Approach Dissects Microglia and CNS Border-Associated Macrophages. Immunity. 54(1). 176–190.e7. 119 indexed citations
7.
Shemer, Anat, Isabelle Scheyltjens, Jung‐Seok Kim, et al.. (2020). Interleukin-10 Prevents Pathological Microglia Hyperactivation following Peripheral Endotoxin Challenge. Immunity. 53(5). 1033–1049.e7. 114 indexed citations
8.
Curato, Caterina, Biana Bernshtein, Eva Zupančič, et al.. (2019). DC Respond to Cognate T Cell Interaction in the Antigen-Challenged Lymph Node. Frontiers in Immunology. 10. 863–863. 17 indexed citations
9.
Chappell‐Maor, Louise, Masha Kolesnikov, Jung‐Seok Kim, et al.. (2019). Comparative analysis of CreER transgenic mice for the study of brain macrophages: A case study. European Journal of Immunology. 50(3). 353–362. 45 indexed citations
10.
Bernshtein, Biana, Caterina Curato, Μαριάννα Ιωάννου, et al.. (2019). IL-23–producing IL-10Rα–deficient gut macrophages elicit an IL-22–driven proinflammatory epithelial cell response. Science Immunology. 4(36). 81 indexed citations
11.
Gross-Vered, Mor, Liraz Shmuel-Galia, Fiachra Humphries, et al.. (2019). TLR2 Dimerization Blockade Allows Generation of Homeostatic Intestinal Macrophages under Acute Colitis Challenge. The Journal of Immunology. 204(3). 707–717. 5 indexed citations
12.
Haimon, Zhana, Johannes Orthgieß, Sigalit Boura‐Halfon, et al.. (2018). Re-evaluating microglia expression profiles using RiboTag and cell isolation strategies. Nature Immunology. 19(6). 636–644. 141 indexed citations
13.
Shemer, Anat, Jonathan Grozovski, Tuan Leng Tay, et al.. (2018). Engrafted parenchymal brain macrophages differ from microglia in transcriptome, chromatin landscape and response to challenge. Nature Communications. 9(1). 5206–5206. 877 indexed citations breakdown →
14.
Wolf, Yochai, Anat Shemer, Mor Gross, et al.. (2018). Microglial MHC class II is dispensable for experimental autoimmune encephalomyelitis and cuprizone‐induced demyelination. European Journal of Immunology. 48(8). 1308–1318. 86 indexed citations
15.
Varol, Diana, Alexander Mildner, Thomas Blank, et al.. (2017). Dicer Deficiency Differentially Impacts Microglia of the Developing and Adult Brain. Immunity. 46(6). 1030–1044.e8. 68 indexed citations
16.
Mildner, Alexander, Jörg Schönheit, Amir Giladi, et al.. (2017). Genomic Characterization of Murine Monocytes Reveals C/EBPβ Transcription Factor Dependence of Ly6C − Cells. Immunity. 46(5). 849–862.e7. 204 indexed citations
17.
Wolf, Yochai, Sigalit Boura‐Halfon, Nina Cortese, et al.. (2017). Brown-adipose-tissue macrophages control tissue innervation and homeostatic energy expenditure. Nature Immunology. 18(6). 665–674. 194 indexed citations
18.
Szymański, Jędrzej, Yishai Levin, Alon Savidor, et al.. (2017). Label‐free deep shotgun proteomics reveals protein dynamics during tomato fruit tissues development. The Plant Journal. 90(2). 396–417. 66 indexed citations
19.
Breitel, Dario, Louise Chappell‐Maor, Sagit Meir, et al.. (2016). AUXIN RESPONSE FACTOR 2 Intersects Hormonal Signals in the Regulation of Tomato Fruit Ripening. PLoS Genetics. 12(3). e1005903–e1005903. 129 indexed citations
20.
Shalit-Kaneh, Akiva, et al.. (2013). A Cytokinin-Activating Enzyme Promotes Tuber Formation in Tomato. Current Biology. 23(12). 1057–1064. 96 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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