Maeve A. Caldwell

6.5k total citations
86 papers, 5.1k citations indexed

About

Maeve A. Caldwell is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Developmental Neuroscience. According to data from OpenAlex, Maeve A. Caldwell has authored 86 papers receiving a total of 5.1k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Molecular Biology, 48 papers in Cellular and Molecular Neuroscience and 40 papers in Developmental Neuroscience. Recurrent topics in Maeve A. Caldwell's work include Neurogenesis and neuroplasticity mechanisms (39 papers), Pluripotent Stem Cells Research (32 papers) and Nerve injury and regeneration (23 papers). Maeve A. Caldwell is often cited by papers focused on Neurogenesis and neuroplasticity mechanisms (39 papers), Pluripotent Stem Cells Research (32 papers) and Nerve injury and regeneration (23 papers). Maeve A. Caldwell collaborates with scholars based in United Kingdom, Ireland and United States. Maeve A. Caldwell's co-authors include Clive N. Svendsen, Thor Ostenfeld, Anne Rosser, Siddharthan Chandran, Eric Jauniaux, Xiaoling He, Pam Tyers, Richard Armstrong, Roger A. Barker and James B. Uney and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Nucleic Acids Research.

In The Last Decade

Maeve A. Caldwell

86 papers receiving 5.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Maeve A. Caldwell United Kingdom 38 2.9k 2.1k 1.9k 700 595 86 5.1k
Dies Meijer Netherlands 43 3.1k 1.1× 1.7k 0.8× 2.6k 1.4× 553 0.8× 703 1.2× 74 6.7k
Philip J. Horner United States 41 2.9k 1.0× 1.4k 0.7× 2.0k 1.0× 556 0.8× 384 0.6× 96 6.4k
Cynthia Wetmore United States 37 2.5k 0.9× 1.6k 0.8× 2.6k 1.4× 1.1k 1.5× 522 0.9× 86 5.6k
Jean‐Léon Thomas France 39 2.6k 0.9× 1.1k 0.6× 1.8k 0.9× 533 0.8× 439 0.7× 87 5.3k
Luciano Conti Italy 35 4.2k 1.5× 1.3k 0.6× 2.7k 1.4× 434 0.6× 690 1.2× 122 6.2k
Jun Takahashi Japan 38 6.1k 2.1× 1.7k 0.8× 2.5k 1.3× 598 0.9× 527 0.9× 112 8.2k
Alberto Martínez‐Serrano Spain 37 2.6k 0.9× 1.8k 0.9× 2.5k 1.3× 515 0.7× 434 0.7× 92 4.9k
David Prevette United States 42 2.8k 1.0× 1.8k 0.9× 3.4k 1.8× 837 1.2× 1000 1.7× 61 5.9k
Yang D. Teng United States 37 2.1k 0.7× 2.1k 1.0× 2.3k 1.2× 1.3k 1.8× 561 0.9× 102 6.1k
Alison C. Lloyd United Kingdom 30 2.7k 0.9× 1.0k 0.5× 2.6k 1.3× 492 0.7× 549 0.9× 52 5.9k

Countries citing papers authored by Maeve A. Caldwell

Since Specialization
Citations

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

Fields of papers citing papers by Maeve A. Caldwell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maeve A. Caldwell. 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 Maeve A. Caldwell. The network helps show where Maeve A. Caldwell may publish in the future.

Co-authorship network of co-authors of Maeve A. Caldwell

This figure shows the co-authorship network connecting the top 25 collaborators of Maeve A. Caldwell. A scholar is included among the top collaborators of Maeve A. Caldwell 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 Maeve A. Caldwell. Maeve A. Caldwell 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.
McComish, Sarah F., Julia O’Sullivan, Noreen T. Boyle, et al.. (2024). Reactive astrocytes generated from human iPSC are pro-inflammatory and display altered metabolism. Experimental Neurology. 382. 114979–114979. 1 indexed citations
2.
Borah, Rajiv, et al.. (2024). Electrically Conductive Injectable Silk/PEDOT: PSS Hydrogel for Enhanced Neural Network Formation. Journal of Biomedical Materials Research Part A. 113(1). e37859–e37859. 8 indexed citations
4.
McComish, Sarah F., Julia O’Sullivan, Ian Woods, et al.. (2024). Neurotrophic extracellular matrix proteins promote neuronal and iPSC astrocyte progenitor cell‐ and nano‐scale process extension for neural repair applications. Journal of Anatomy. 246(4). 585–601. 3 indexed citations
5.
Crompton, Lucy, et al.. (2023). Human stem cell-derived ventral midbrain astrocytes exhibit a region-specific secretory profile. Brain Communications. 5(2). fcad114–fcad114. 1 indexed citations
6.
Jiménez-Moreno, Natalia, Madhu Kollareddy, Zuriñe Antón, et al.. (2023). ATG8-dependent LMX1B-autophagy crosstalk shapes human midbrain dopaminergic neuronal resilience. The Journal of Cell Biology. 222(5). 9 indexed citations
7.
Crompton, Lucy, et al.. (2021). Efficient and Scalable Generation of Human Ventral Midbrain Astrocytes from Human-Induced Pluripotent Stem Cells. Journal of Visualized Experiments. 7 indexed citations
8.
McComish, Sarah F., et al.. (2021). The Pathogenesis of Parkinson's Disease: A Complex Interplay Between Astrocytes, Microglia, and T Lymphocytes?. Frontiers in Neurology. 12. 666737–666737. 123 indexed citations
9.
Jiménez-Moreno, Natalia, Lucy Crompton, Jennifer L. Badger, et al.. (2020). A monolayer hiPSC culture system for autophagy/mitophagy studies in human dopaminergic neurons. Autophagy. 17(4). 855–871. 21 indexed citations
10.
McComish, Sarah F. & Maeve A. Caldwell. (2018). Generation of defined neural populations from pluripotent stem cells. Philosophical Transactions of the Royal Society B Biological Sciences. 373(1750). 20170214–20170214. 22 indexed citations
11.
Crompton, Lucy, Aman Sood, Margaret Saunders, et al.. (2018). Nanoparticle-induced neuronal toxicity across placental barriers is mediated by autophagy and dependent on astrocytes. Nature Nanotechnology. 13(5). 427–433. 112 indexed citations
12.
Wang, Wenzhang, Xinglong Wang, Hisashi Fujioka, et al.. (2015). Parkinson's disease–associated mutant VPS35 causes mitochondrial dysfunction by recycling DLP1 complexes. Nature Medicine. 22(1). 54–63. 259 indexed citations
13.
Rinaldi, Federica & Maeve A. Caldwell. (2013). Modeling astrocytic contribution toward neurodegeneration with pluripotent stem cells. Neuroreport. 24(18). 1053–1057. 4 indexed citations
14.
O’Keeffe, Gráinne C., Pam Tyers, Dag Aarsland, et al.. (2009). Dopamine-induced proliferation of adult neural precursor cells in the mammalian subventricular zone is mediated through EGF. Proceedings of the National Academy of Sciences. 106(21). 8754–8759. 162 indexed citations
15.
Crompton, Lucy, et al.. (2009). The Generation of Photoreceptors from Embryonic Stem Cells: Towards a Transplant Model. Investigative Ophthalmology & Visual Science. 50(13). 5141–5141. 1 indexed citations
16.
Scott, Sarah, Pam Tyers, Gerard W. O’Keeffe, et al.. (2008). Induction of A9 dopaminergic neurons from neural stem cells improves motor function in an animal model of Parkinson's disease. Brain. 131(3). 630–641. 71 indexed citations
17.
Burnstein, Rowan, Xiaoling He, Richard Luce, et al.. (2007). Gene expression changes in long term expanded human neural progenitor cells passaged by chopping lead to loss of neurogenic potential in vivo. Experimental Neurology. 204(2). 512–524. 49 indexed citations
19.
Ostenfeld, Thor, Etienne Joly, Yu‐Tzu Tai, et al.. (2002). Regional specification of rodent and human neurospheres. Developmental Brain Research. 134(1-2). 43–55. 163 indexed citations
20.
Svendsen, Clive N. & Maeve A. Caldwell. (2000). Chapter 2 Neural stem cells in the developing central nervous system: implications for cell therapy through transplantation. Progress in brain research. 127. 13–34. 73 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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