Vanda S. Lopes

2.4k total citations · 1 hit paper
27 papers, 1.5k citations indexed

About

Vanda S. Lopes is a scholar working on Molecular Biology, Cell Biology and Ophthalmology. According to data from OpenAlex, Vanda S. Lopes has authored 27 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 11 papers in Cell Biology and 8 papers in Ophthalmology. Recurrent topics in Vanda S. Lopes's work include Retinal Development and Disorders (20 papers), Retinal Diseases and Treatments (8 papers) and Photoreceptor and optogenetics research (6 papers). Vanda S. Lopes is often cited by papers focused on Retinal Development and Disorders (20 papers), Retinal Diseases and Treatments (8 papers) and Photoreceptor and optogenetics research (6 papers). Vanda S. Lopes collaborates with scholars based in United States, Portugal and United Kingdom. Vanda S. Lopes's co-authors include David S. Williams, Gabriel Manske, Roli K. Hirata, David W. Russell, Laïla‐Aïcha Hanafi, Donna Prunkard, Laura Riolobos, Germán G. Gornalusse, Sarah E. Funk and Dennis Clegg and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Neuroscience and The Journal of Cell Biology.

In The Last Decade

Vanda S. Lopes

27 papers receiving 1.4k citations

Hit Papers

HLA-E-expressing pluripotent stem cells escape allogeneic... 2017 2026 2020 2023 2017 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vanda S. Lopes United States 19 1.1k 265 255 235 208 27 1.5k
Heinrich Schrewe Germany 28 1.5k 1.4× 182 0.7× 217 0.9× 373 1.6× 254 1.2× 46 2.2k
Xianjun Zhu China 22 1.2k 1.1× 211 0.8× 398 1.6× 175 0.7× 90 0.4× 106 1.7k
Heide Hellebrand Germany 16 1.2k 1.2× 239 0.9× 201 0.8× 427 1.8× 100 0.5× 21 1.7k
Yumei Li United States 29 1.9k 1.7× 556 2.1× 503 2.0× 439 1.9× 84 0.4× 72 2.4k
R.L. Eddy United States 14 873 0.8× 177 0.7× 85 0.3× 202 0.9× 230 1.1× 18 1.4k
Kerstin Nagel‐Wolfrum Germany 20 1.3k 1.2× 257 1.0× 180 0.7× 349 1.5× 102 0.5× 42 1.6k
Raymond C.B. Wong Australia 27 1.5k 1.4× 144 0.5× 200 0.8× 123 0.5× 83 0.4× 79 1.9k
Marion A. Maw New Zealand 19 2.1k 2.0× 204 0.8× 279 1.1× 616 2.6× 121 0.6× 23 2.5k
Frauke Coppieters Belgium 20 1.3k 1.2× 143 0.5× 421 1.7× 491 2.1× 132 0.6× 46 1.7k
Dorothea Schulte Germany 24 1.5k 1.4× 262 1.0× 74 0.3× 220 0.9× 141 0.7× 53 1.7k

Countries citing papers authored by Vanda S. Lopes

Since Specialization
Citations

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

Fields of papers citing papers by Vanda S. Lopes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Vanda S. Lopes. 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 Vanda S. Lopes. The network helps show where Vanda S. Lopes may publish in the future.

Co-authorship network of co-authors of Vanda S. Lopes

This figure shows the co-authorship network connecting the top 25 collaborators of Vanda S. Lopes. A scholar is included among the top collaborators of Vanda S. Lopes 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 Vanda S. Lopes. Vanda S. Lopes 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.
Karumbayaram, Saravanan, Mei Jiang, Vanda S. Lopes, et al.. (2017). Differentiation of RPE cells from integration-free iPS cells and their cell biological characterization. Stem Cell Research & Therapy. 8(1). 217–217. 50 indexed citations
2.
Gornalusse, Germán G., Roli K. Hirata, Sarah E. Funk, et al.. (2017). HLA-E-expressing pluripotent stem cells escape allogeneic responses and lysis by NK cells. Nature Biotechnology. 35(8). 765–772. 446 indexed citations breakdown →
3.
Jiang, Mei, et al.. (2015). Live-Cell Imaging of Phagosome Motility in Primary Mouse RPE Cells. Advances in experimental medicine and biology. 854. 751–755. 4 indexed citations
4.
Lopes, Vanda S. & David S. Williams. (2015). Gene Therapy for the Retinal Degeneration of Usher Syndrome Caused by Mutations in MYO7A. Cold Spring Harbor Perspectives in Medicine. 5(6). a017319–a017319. 18 indexed citations
5.
Frost, Laura, Vanda S. Lopes, Alvina Bragin, et al.. (2014). The Contribution of Melanoregulin to Microtubule-Associated Protein 1 Light Chain 3 (LC3) Associated Phagocytosis in Retinal Pigment Epithelium. Molecular Neurobiology. 52(3). 1135–1151. 46 indexed citations
6.
Lopes, Vanda S., Tanja Diemer, & David S. Williams. (2014). Assessment of Different Virus-Mediated Approaches for Retinal Gene Therapy of Usher 1B. Advances in experimental medicine and biology. 801. 725–731. 2 indexed citations
7.
Mei, Hua, Sheyla González, Martin N. Nakatsu, et al.. (2013). A Three-Dimensional Culture Method to Expand Limbal Stem/Progenitor Cells. Tissue Engineering Part C Methods. 20(5). 393–400. 1 indexed citations
8.
Engelhardt, Maren, et al.. (2012). Functional and morphological analysis of the subretinal injection of retinal pigment epithelium cells. Visual Neuroscience. 29(2). 83–93. 15 indexed citations
9.
Cruz, Sandrine Da, Philippe A. Parone, Vanda S. Lopes, et al.. (2012). Elevated PGC-1α Activity Sustains Mitochondrial Biogenesis and Muscle Function without Extending Survival in a Mouse Model of Inherited ALS. Cell Metabolism. 15(5). 778–786. 144 indexed citations
10.
Lopes, Vanda S., Daniel Gibbs, Richard T. Libby, et al.. (2011). The Usher 1B protein, MYO7A, is required for normal localization and function of the visual retinoid cycle enzyme, RPE65. Human Molecular Genetics. 20(13). 2560–2570. 51 indexed citations
11.
Harkewicz, Richard, Hongjun Du, Zongzhong Tong, et al.. (2011). Essential Role of ELOVL4 Protein in Very Long Chain Fatty Acid Synthesis and Retinal Function. Journal of Biological Chemistry. 287(14). 11469–11480. 78 indexed citations
12.
Williams, David S. & Vanda S. Lopes. (2011). Gene Therapy Strategies for Usher Syndrome Type 1B. Advances in experimental medicine and biology. 723. 235–242. 3 indexed citations
13.
Lopes, Vanda S., David Jimeno, Kornnika Khanobdee, et al.. (2010). Rapid Rod Photoreceptor Cell Death Due to Kinesin-2 Dysfunction is Dependent on Apoptosis Triggered by Mislocalized Opsin. Investigative Ophthalmology & Visual Science. 51(13). 5809–5809. 1 indexed citations
14.
Lopes, Vanda S., David Jimeno, Kornnika Khanobdee, et al.. (2010). Dysfunction of Heterotrimeric Kinesin-2 in Rod Photoreceptor Cells and the Role of Opsin Mislocalization in Rapid Cell Death. Molecular Biology of the Cell. 21(23). 4076–4088. 43 indexed citations
15.
Damek-Poprawa, Monika, Tanja Diemer, Vanda S. Lopes, et al.. (2009). Melanoregulin (MREG) Modulates Lysosome Function in Pigment Epithelial Cells. Journal of Biological Chemistry. 284(16). 10877–10889. 39 indexed citations
16.
Ramalho, José S., Vanda S. Lopes, Abul K. Tarafder, Miguel C. Seabra, & Alistair N. Hume. (2009). Myrip uses distinct domains in the cellular activation of myosin VA and myosin VIIA in melanosome transport. Pigment Cell & Melanoma Research. 22(4). 461–473. 19 indexed citations
17.
Schwander, Martin, Vanda S. Lopes, Anna Sczaniecka, et al.. (2009). A Novel Allele of Myosin VIIa Reveals a Critical Function for the C-Terminal FERM Domain for Melanosome Transport in Retinal Pigment Epithelial Cells. Journal of Neuroscience. 29(50). 15810–15818. 32 indexed citations
18.
Williams, David S., Tomás S. Alemán, Concepción Lillo, et al.. (2009). Harmonin in the Murine Retina and the Retinal Phenotypes ofUsh1c-Mutant Mice and Human USH1C. Investigative Ophthalmology & Visual Science. 50(8). 3881–3881. 29 indexed citations
19.
Lopes, Vanda S., José S. Ramalho, Dylan M. Owen, et al.. (2007). The Ternary Rab27a–Myrip–Myosin VIIa Complex Regulates Melanosome Motility in the Retinal Pigment Epithelium. Traffic. 8(5). 486–499. 77 indexed citations
20.
Lopes, Vanda S., Christina Wasmeier, Miguel C. Seabra, & Clare E. Futter. (2007). Melanosome Maturation Defect in Rab38-deficient Retinal Pigment Epithelium Results in Instability of Immature Melanosomes during Transient Melanogenesis. Molecular Biology of the Cell. 18(10). 3914–3927. 75 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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