Michelle Reed

629 total citations
17 papers, 494 citations indexed

About

Michelle Reed is a scholar working on Molecular Biology, Epidemiology and Cell Biology. According to data from OpenAlex, Michelle Reed has authored 17 papers receiving a total of 494 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Epidemiology and 4 papers in Cell Biology. Recurrent topics in Michelle Reed's work include Microtubule and mitosis dynamics (4 papers), Retinal Development and Disorders (4 papers) and Respiratory viral infections research (3 papers). Michelle Reed is often cited by papers focused on Microtubule and mitosis dynamics (4 papers), Retinal Development and Disorders (4 papers) and Respiratory viral infections research (3 papers). Michelle Reed collaborates with scholars based in United States. Michelle Reed's co-authors include Nicholas W. Lukacs, Zhenyu Yue, Sarah E. Bush, Sihyug Jang, Sumanta Mukherjee, Matthew Schaller, Wolfgang Baehr, Dennis M. Lindell, Sean P. Maher and Guoxin Ying and has published in prestigious journals such as Nature Communications, The Journal of Immunology and PLoS ONE.

In The Last Decade

Michelle Reed

16 papers receiving 493 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michelle Reed United States 12 191 190 135 63 57 17 494
E. Dahme Germany 15 246 1.3× 179 0.9× 114 0.8× 89 1.4× 51 0.9× 78 714
Sophie Dhorne‐Pollet France 17 98 0.5× 330 1.7× 97 0.7× 139 2.2× 27 0.5× 33 763
Ronald C. Riis United States 18 132 0.7× 190 1.0× 84 0.6× 76 1.2× 79 1.4× 45 774
Céline Van den Broeke Belgium 13 281 1.5× 151 0.8× 137 1.0× 69 1.1× 42 0.7× 16 524
Bernhard Steiner Switzerland 17 92 0.5× 426 2.2× 232 1.7× 143 2.3× 22 0.4× 28 846
Kevin Galles United States 12 228 1.2× 256 1.3× 194 1.4× 38 0.6× 20 0.4× 16 689
Alexandra Brower United States 10 99 0.5× 90 0.5× 29 0.2× 30 0.5× 35 0.6× 24 475
Brett J. Hilton United States 7 160 0.8× 227 1.2× 93 0.7× 43 0.7× 30 0.5× 9 556
Susumu TATEYAMA Japan 15 119 0.6× 162 0.9× 47 0.3× 144 2.3× 38 0.7× 70 657
Chunhua Xu China 11 41 0.2× 272 1.4× 133 1.0× 84 1.3× 26 0.5× 20 495

Countries citing papers authored by Michelle Reed

Since Specialization
Citations

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

Fields of papers citing papers by Michelle Reed

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michelle Reed. 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 Michelle Reed. The network helps show where Michelle Reed may publish in the future.

Co-authorship network of co-authors of Michelle Reed

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

All Works

17 of 17 papers shown
1.
Gerstner, Cecilia D., et al.. (2022). Arf-like Protein 2 (ARL2) Controls Microtubule Neogenesis during Early Postnatal Photoreceptor Development. Cells. 12(1). 147–147. 2 indexed citations
2.
Reed, Michelle, Ken‐Ichi Takemaru, Guoxin Ying, Jeanne M. Frederick, & Wolfgang Baehr. (2022). Deletion of CEP164 in mouse photoreceptors post-ciliogenesis interrupts ciliary intraflagellar transport (IFT). PLoS Genetics. 18(9). e1010154–e1010154. 13 indexed citations
3.
Reed, Michelle, et al.. (2021). Conditional Deletion of Cytoplasmic Dynein Heavy Chain in Postnatal Photoreceptors. Investigative Ophthalmology & Visual Science. 62(14). 23–23. 7 indexed citations
4.
Reed, Michelle, et al.. (2021). Effect of conditional deletion of cytoplasmic dynein heavy chain DYNC1H1 on postnatal photoreceptors. PLoS ONE. 16(3). e0248354–e0248354. 11 indexed citations
5.
Reed, Michelle, Anny‐Claude Luissint, Verónica Azcutia, et al.. (2019). Epithelial CD47 is critical for mucosal repair in the murine intestine in vivo. Nature Communications. 10(1). 5004–5004. 36 indexed citations
6.
O’Leary, Monique N., Miguel Quirós, Verónica Azcutia, et al.. (2019). Formyl peptide receptor 2 regulates monocyte recruitment to promote intestinal mucosal wound repair. The FASEB Journal. 33(12). 13632–13643. 43 indexed citations
7.
Baehr, Wolfgang, et al.. (2018). Insights into photoreceptor ciliogenesis revealed by animal models. Progress in Retinal and Eye Research. 71. 26–56. 40 indexed citations
8.
Schaller, Matthew, et al.. (2015). Sirtuin 1 Regulates Dendritic Cell Activation and Autophagy during Respiratory Syncytial Virus–Induced Immune Responses. The Journal of Immunology. 195(4). 1637–1646. 55 indexed citations
9.
Nagata, Denise E. de Almeida, Tine Demoor, Catherine Ptaschinski, et al.. (2014). IL-27R–Mediated Regulation of IL-17 Controls the Development of Respiratory Syncytial Virus–Associated Pathogenesis. American Journal Of Pathology. 184(6). 1807–1818. 43 indexed citations
10.
Reed, Michelle, et al.. (2013). Autophagy-Inducing Protein Beclin-1 in Dendritic Cells Regulates CD4 T Cell Responses and Disease Severity during Respiratory Syncytial Virus Infection. The Journal of Immunology. 191(5). 2526–2537. 64 indexed citations
11.
Bush, Sarah E., Michelle Reed, & Sean P. Maher. (2013). Impact of forest size on parasite biodiversity: implications for conservation of hosts and parasites. Biodiversity and Conservation. 22(6-7). 1391–1404. 34 indexed citations
12.
Petersen, Bryan, Matthew Schaller, Michelle Reed, et al.. (2012). The role of SIRT1 in the activation of innate immune responses during RSV infection (68.6). The Journal of Immunology. 188(1_Supplement). 68.6–68.6.
13.
Morris, Susan B., Michele S. Swanson, Andrew P. Lieberman, et al.. (2011). Autophagy-Mediated Dendritic Cell Activation Is Essential for Innate Cytokine Production and APC Function with Respiratory Syncytial Virus Responses. The Journal of Immunology. 187(8). 3953–3961. 80 indexed citations
14.
Bush, Sarah E., et al.. (2010). Evolution of Cryptic Coloration in Ectoparasites. The American Naturalist. 176(4). 529–535. 28 indexed citations
15.
Gahring, Lorise C., et al.. (2010). Neuronal nicotinic alpha7 receptors modulate early neutrophil infiltration to sites of skin inflammation. Journal of Neuroinflammation. 7(1). 38–38. 18 indexed citations
16.
Bungard, David, Michelle Reed, & Edward Winter. (2004). RSC1 and RSC2 Are Required for Expression of Mid-Late Sporulation-Specific Genes in Saccharomyces cerevisiae. Eukaryotic Cell. 3(4). 910–918. 18 indexed citations
17.
Reed, Michelle, et al.. (1978). The quantitative relationships among the induction of gene mutations, sister chromatid exchanges and chromosomal aberrations in L5178Y mouse lymphoma cells by TEM. Mutation Research/Environmental Mutagenesis and Related Subjects. 53(1). 77–78. 2 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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