Rachel Queen
About
Rachel Queen is a scholar working on Molecular Biology, Ophthalmology and Cellular and Molecular Neuroscience.
According to data from OpenAlex, Rachel Queen has authored 29 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 11 papers in Ophthalmology and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Rachel Queen's work include Retinal Development and Disorders (13 papers), Single-cell and spatial transcriptomics (6 papers) and Retinal Diseases and Treatments (6 papers). Rachel Queen is often cited by papers focused on Retinal Development and Disorders (13 papers), Single-cell and spatial transcriptomics (6 papers) and Retinal Diseases and Treatments (6 papers). Rachel Queen collaborates with scholars based in United Kingdom, Italy and Germany. Rachel Queen's co-authors include Masahiro Yoshida, Fotios Sampaziotis, Ni Huang, Carlos Talavera‐López, Christophe Bécavin, Daniel Reichart, Monika Litviňuková, Waradon Sungnak, Kaylee B. Worlock and Josephine L. Barnes and has published in prestigious journals such as Cell, Nature Medicine and Nature Communications.
In The Last Decade
Rachel Queen
28 papers receiving 2.4k citations
Hit Papers
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late) cites · hero ref
| Name | h | Career | Trend | Papers | Cites | |||||
|---|---|---|---|---|---|---|---|---|---|---|
| Rachel Queen United Kingdom | 17 | 1.2k | 648 | 552 | 365 | 307 | 29 | 2.5k | ||
| Josephine L. Barnes United Kingdom | 9 | 1.2k 1.0× | 506 0.8× | 500 0.9× | 227 0.6× | 103 0.3× | 10 | 2.2k | ||
| Fotios Sampaziotis United Kingdom | 13 | 1.1k 1.0× | 588 0.9× | 501 0.9× | 202 0.6× | 103 0.3× | 26 | 2.6k | ||
| Monika Litviňuková Germany | 7 | 1.1k 1.0× | 281 0.4× | 498 0.9× | 195 0.5× | 103 0.3× | 7 | 1.9k | ||
| Kaylee B. Worlock United Kingdom | 3 | 1.1k 1.0× | 284 0.4× | 500 0.9× | 187 0.5× | 103 0.3× | 5 | 1.8k | ||
| Marijn Berg Netherlands | 6 | 1.1k 1.0× | 255 0.4× | 500 0.9× | 212 0.6× | 103 0.3× | 14 | 1.8k | ||
| Ni Huang China | 3 | 1.1k 1.0× | 237 0.4× | 513 0.9× | 189 0.5× | 103 0.3× | 4 | 1.8k | ||
| Nikolaus Deigendesch Germany | 14 | 781 0.7× | 564 0.9× | 513 0.9× | 482 1.3× | 27 0.1× | 29 | 1.9k | ||
| Astrid Hagelkrüys Austria | 12 | 1.2k 1.0× | 827 1.3× | 417 0.8× | 162 0.4× | 27 0.1× | 21 | 2.1k | ||
| Ryan Conder Canada | 9 | 1.2k 1.0× | 551 0.9× | 416 0.8× | 221 0.6× | 26 0.1× | 11 | 1.9k | ||
| Liang Liang China | 20 | 360 0.3× | 247 0.4× | 417 0.8× | 107 0.3× | 990 3.2× | 60 | 1.8k |
Countries citing papers authored by Rachel Queen
Since
Specialization
Citations
This map shows the geographic impact of Rachel Queen'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 Rachel Queen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rachel Queen more than expected).
Fields of papers citing papers by Rachel Queen
Since
Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences
This network shows the impact of papers produced by Rachel Queen. 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 Rachel Queen. The network helps show where Rachel Queen may publish in the future.
Co-authorship network of co-authors of Rachel Queen
This figure shows the co-authorship network connecting the top 25 collaborators of Rachel Queen. A scholar is included among the top collaborators of Rachel Queen 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 Rachel Queen. Rachel Queen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
1.
Queen, Rachel, Luis Ferrández-Peral, Birthe Dorgau, et al.. (2025). Unravelling genotype-phenotype correlations in Stargardt disease using patient-derived retinal organoids. Cell Death and Disease. 16(1). 108–108.
2.
Dorgau, Birthe, Joseph Collin, Agata Rozanska, et al.. (2024). Single-cell analyses reveal transient retinal progenitor cells in the ciliary margin of developing human retina. Nature Communications. 15(1). 3567–3567.
3.
Alonso‐Pérez, Jorge, A. Nascimento, Giorgio Tasca, et al.. (2024). Single cell RNA sequencing of human FAPs reveals different functional stages in Duchenne muscular dystrophy. Frontiers in Cell and Developmental Biology. 12. 1399319–1399319.
4.
Dorgau, Birthe, Joseph Collin, Agata Rozanska, et al.. (2024). Deciphering the spatiotemporal transcriptional and chromatin accessibility of human retinal organoid development at the single-cell level. iScience. 27(4). 109397–109397.
5.
Chichagova, Valeria, Μαρία Γεωργίου, Birthe Dorgau, et al.. (2023). Incorporating microglia‐like cells in human induced pluripotent stem cell‐derived retinal organoids. Journal of Cellular and Molecular Medicine. 27(3). 435–445.
6.
Collin, Joseph, Darin Zerti, Birthe Dorgau, et al.. (2023). Single-cell RNA sequencing reveals transcriptional changes of human choroidal and retinal pigment epithelium cells during fetal development, in healthy adult and intermediate age-related macular degeneration. Human Molecular Genetics. 32(10). 1698–1710.
7.
Queen, Rachel, Moira Crosier, Lorraine Eley, et al.. (2023). Spatial transcriptomics reveals novel genes during the remodelling of the embryonic human arterial valves. PLoS Genetics. 19(11). e1010777–e1010777.
8.
Zormpas, Eleftherios, Rachel Queen, Alexis Comber, & Simon Cockell. (2023). Mapping the transcriptome: Realizing the full potential of spatial data analysis. Cell. 186(26). 5677–5689.
9.
Walls, Gerard, Mihaela Ghita, Rachel Queen, et al.. (2022). Spatial Gene Expression Changes in the Mouse Heart After Base-Targeted Irradiation. International Journal of Radiation Oncology*Biology*Physics. 115(2). 453–463.
10.
Rozanska, Agata, Rachel Queen, Joseph Collin, et al.. (2022). pRB-Depleted Pluripotent Stem Cell Retinal Organoids Recapitulate Cell State Transitions of Retinoblastoma Development and Suggest an Important Role for pRB in Retinal Cell Differentiation. Stem Cells Translational Medicine. 11(4). 415–433.
11.
Kist, Ralf, Rachel Queen, Rafiqul Hussain, et al.. (2021). Msx1 haploinsufficiency modifies the Pax9-deficient cardiovascular phenotype. BMC Developmental Biology. 21(1). 14–14.
12.
Collin, Joseph, Rachel Queen, Darin Zerti, et al.. (2021). Dissecting the Transcriptional and Chromatin Accessibility Heterogeneity of Proliferating Cone Precursors in Human Retinoblastoma Tumors by Single Cell Sequencing—Opening Pathways to New Therapeutic Strategies?. Investigative Ophthalmology & Visual Science. 62(6). 18–18.
13.
Collin, Joseph, Rachel Queen, Darin Zerti, et al.. (2020). Co-expression of SARS-CoV-2 entry genes in the superficial adult human conjunctival, limbal and corneal epithelium suggests an additional route of entry via the ocular surface. The Ocular Surface. 19. 190–200.
14.
Sungnak, Waradon, Ni Huang, Christophe Bécavin, et al.. (2020). SARS-CoV-2 entry factors are highly expressed in nasal epithelial cells together with innate immune genes. Nature Medicine. 26(5). 681–687.
15.
Cytlak, Urszula, Anastasia Resteu, Sarah Pagan, et al.. (2020). Differential IRF8 Transcription Factor Requirement Defines Two Pathways of Dendritic Cell Development in Humans. Immunity. 53(2). 353–370.e8.
16.
Mellough, Carla, Joseph Collin, Rachel Queen, et al.. (2019). Systematic Comparison of Retinal Organoid Differentiation from Human Pluripotent Stem Cells Reveals Stage Specific, Cell Line, and Methodological Differences. Stem Cells Translational Medicine. 8(7). 694–706.
17.
Collin, Joseph, Rachel Queen, Carla Mellough, & Majlinda Lako. (2018). Using hESC-derived retinal organoids to investigate the transcriptional profile of emerging photoreceptors. Investigative Ophthalmology & Visual Science. 59(9). 570–570.
18.
O’Keefe, Hannah, et al.. (2018). Haplogroup Context is Less Important in the Penetrance of Mitochondrial DNA Complex I Mutations Compared to mt-tRNA Mutations. Journal of Molecular Evolution. 86(6). 395–403.
19.
Bojić, Sanja, Dean Hallam, Rachel Queen, et al.. (2018). CD200 Expression Marks a Population of Quiescent Limbal Epithelial Stem Cells with Holoclone Forming Ability. Stem Cells. 36(11). 1723–1735.
20.
Queen, Rachel, Jannetta S. Steyn, Phillip Lord, & Joanna L. Elson. (2017). Mitochondrial DNA sequence context in the penetrance of mitochondrial t-RNA mutations: A study across multiple lineages with diagnostic implications. PLoS ONE. 12(11). e0187862–e0187862.
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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