Natasha Y. Frank

6.3k total citations · 2 hit papers
57 papers, 3.9k citations indexed

About

Natasha Y. Frank is a scholar working on Molecular Biology, Oncology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Natasha Y. Frank has authored 57 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 23 papers in Oncology and 14 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Natasha Y. Frank's work include Cancer Cells and Metastasis (13 papers), Corneal Surgery and Treatments (12 papers) and Immunotherapy and Immune Responses (10 papers). Natasha Y. Frank is often cited by papers focused on Cancer Cells and Metastasis (13 papers), Corneal Surgery and Treatments (12 papers) and Immunotherapy and Immune Responses (10 papers). Natasha Y. Frank collaborates with scholars based in United States, Australia and Germany. Natasha Y. Frank's co-authors include Markus H. Frank, Tobias Schatton, Martin Gasser, Gëorge F. Murphy, Mohamed H. Sayegh, Ana Maria Waaga-Gasser, Qian Zhan, Thomas S. Kupper, K. Yamaura and Brian J. Wilson and has published in prestigious journals such as Nature, New England Journal of Medicine and Journal of Biological Chemistry.

In The Last Decade

Natasha Y. Frank

55 papers receiving 3.9k citations

Hit Papers

Identification of cells initiating human melanomas 2008 2026 2014 2020 2008 2010 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Natasha Y. Frank United States 23 2.6k 2.0k 906 786 356 57 3.9k
Sonja Loges Germany 35 1.9k 0.7× 2.7k 1.3× 926 1.0× 1.4k 1.8× 297 0.8× 98 5.0k
Tobias Schatton United States 27 3.1k 1.2× 2.2k 1.1× 1.4k 1.5× 855 1.1× 344 1.0× 40 4.4k
Karin Vanderkerken Belgium 51 3.2k 1.2× 4.5k 2.2× 1.2k 1.4× 1.4k 1.8× 443 1.2× 227 7.9k
Guillermo Mazzolini Argentina 35 1.5k 0.6× 1.5k 0.7× 1.5k 1.6× 389 0.5× 279 0.8× 115 4.0k
Jérôme Moreaux France 40 1.5k 0.6× 2.9k 1.4× 1.1k 1.2× 690 0.9× 328 0.9× 170 4.9k
Carla Boccaccio Italy 33 1.4k 0.6× 2.1k 1.0× 501 0.6× 809 1.0× 334 0.9× 63 4.2k
Carlos Bais United States 20 1.9k 0.7× 1.9k 1.0× 1.0k 1.1× 967 1.2× 122 0.3× 38 4.1k
Maria Vincenza Carriero Italy 34 1.3k 0.5× 1.5k 0.7× 951 1.0× 1.4k 1.7× 201 0.6× 76 3.8k
Ilaria Malanchi United Kingdom 26 2.5k 1.0× 2.6k 1.3× 1.3k 1.5× 1.0k 1.3× 772 2.2× 44 5.4k
Eline Menu Belgium 41 1.4k 0.6× 2.9k 1.4× 796 0.9× 998 1.3× 268 0.8× 131 4.3k

Countries citing papers authored by Natasha Y. Frank

Since Specialization
Citations

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

Fields of papers citing papers by Natasha Y. Frank

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Natasha Y. Frank. 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 Natasha Y. Frank. The network helps show where Natasha Y. Frank may publish in the future.

Co-authorship network of co-authors of Natasha Y. Frank

This figure shows the co-authorship network connecting the top 25 collaborators of Natasha Y. Frank. A scholar is included among the top collaborators of Natasha Y. Frank 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 Natasha Y. Frank. Natasha Y. Frank 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.
Sasamoto, Yuzuru, Catherine Lee, Yoshiko Fukuda, et al.. (2025). Caveolin 1 and 2 enhance the proliferative capacity of BCAM-positive corneal progenitors. Scientific Reports. 15(1). 6672–6672. 1 indexed citations
2.
Lee, Catherine, Eric Kofman, Megan Riddle, et al.. (2024). Accelerated Aging and Microsatellite Instability in Recessive Dystrophic Epidermolysis Bullosa–Associated Cutaneous Squamous Cell Carcinoma. Journal of Investigative Dermatology. 144(7). 1534–1543.e2. 1 indexed citations
3.
Fieg, Elizabeth L., Natasha Y. Frank, Robert C. Green, et al.. (2024). Processes and outcomes from a clinical genetics e-consultation service managed by a primary care physician champion. SHILAP Revista de lepidopterología. 2. 101831–101831.
4.
Kluth, Mark A., Christoph Ganss, Markus H. Frank, et al.. (2024). Anti-Inflammatory and Anti-(Lymph)angiogenic Properties of an ABCB5+ Limbal Mesenchymal Stem Cell Population. International Journal of Molecular Sciences. 25(17). 9702–9702. 1 indexed citations
5.
Niebergall‐Roth, Elke, Natasha Y. Frank, Christoph Ganss, et al.. (2023). ABCB5+ mesenchymal stromal cells facilitate complete and durable wound closure in recessive dystrophic epidermolysis bullosa. Cytotherapy. 25(7). 782–788. 10 indexed citations
6.
Hou, Yanhong, Mark A. Kluth, Christoph Ganss, et al.. (2023). ABCB5+ Limbal Epithelial Stem Cells Inhibit Developmental but Promote Inflammatory (Lymph) Angiogenesis While Preventing Corneal Inflammation. Cells. 12(13). 1731–1731. 3 indexed citations
7.
Sasamoto, Yuzuru, Catherine Lee, Brian J. Wilson, et al.. (2022). Limbal BCAM expression identifies a proliferative progenitor population capable of holoclone formation and corneal differentiation. Cell Reports. 40(6). 111166–111166. 10 indexed citations
8.
Wang, Diana, Shuyun Xu, Catherine Lee, et al.. (2020). ATF-3 expression inhibits melanoma growth by downregulating ERK and AKT pathways. Laboratory Investigation. 101(5). 636–647. 14 indexed citations
9.
Tóth-Petróczy, Ágnes, Nikkola Carmichael, Elicia Estrella, et al.. (2019). Homozygous TRPV4 mutation causes congenital distal spinal muscular atrophy and arthrogryposis. Neurology Genetics. 5(2). e312–e312. 16 indexed citations
10.
Xu, Shuyun, Catherine Lee, Michael Wells, et al.. (2019). Loss of the Epigenetic Mark 5-hmC in Psoriasis: Implications for Epidermal Stem Cell Dysregulation. Journal of Investigative Dermatology. 140(6). 1266–1275.e3. 22 indexed citations
11.
Sasamoto, Yuzuru, Naoko Sasamoto, Johnathan Tran, et al.. (2019). Investigation of factors associated with ABCB5-positive limbal stem cell isolation yields from human donors. The Ocular Surface. 18(1). 114–120. 10 indexed citations
12.
Ksander, Bruce R., et al.. (2018). In vitro expanded human purified ABCB5-positive limbal stem cells for treatment of limbal stem cell deficiency.. Investigative Ophthalmology & Visual Science. 59(9). 2287–2287. 1 indexed citations
13.
González, Gabriel, Yuzuru Sasamoto, Bruce R. Ksander, Markus H. Frank, & Natasha Y. Frank. (2017). Limbal stem cells: identity, developmental origin, and therapeutic potential. Wiley Interdisciplinary Reviews Developmental Biology. 7(2). 90 indexed citations
14.
Webber, Beau R., Ron McElmurry, Cindy Eide, et al.. (2017). Rapid generation of Col7a1−/− mouse model of recessive dystrophic epidermolysis bullosa and partial rescue via immunosuppressive dermal mesenchymal stem cells. Laboratory Investigation. 97(10). 1218–1224. 29 indexed citations
15.
Frank, Natasha Y., Bertram Illert, Markus H. Frank, et al.. (2017). Clinical Significance of Disseminated Pluripotent Tumor Cell SignatureExpression in the Bone Marrow from Patients with Colorectal Cancer. Journal of Cancer Science & Therapy. 9(10). 669–674. 2 indexed citations
16.
Ksander, Bruce R., et al.. (2016). ABCB5 identifies RPE progenitor cells required for normal retinal development and aging. Investigative Ophthalmology & Visual Science. 57(12). 1 indexed citations
17.
Wilson, Brian J., Karim R. Saab, Jie Ma, et al.. (2014). ABCB5 Maintains Melanoma-Initiating Cells through a Proinflammatory Cytokine Signaling Circuit. Cancer Research. 74(15). 4196–4207. 116 indexed citations
18.
Wilson, Brian J., Tobias Schatton, Qian Zhan, et al.. (2011). ABCB5 Identifies a Therapy-Refractory Tumor Cell Population in Colorectal Cancer Patients. Cancer Research. 71(15). 5307–5316. 113 indexed citations
19.
Frank, Natasha Y., Tobias Schatton, Soo‐Jeong Kim, et al.. (2011). VEGFR-1 Expressed by Malignant Melanoma-Initiating Cells Is Required for Tumor Growth. Cancer Research. 71(4). 1474–1485. 133 indexed citations
20.
Schatton, Tobias, Ute Schütte, Natasha Y. Frank, et al.. (2010). Modulation of T-Cell Activation by Malignant Melanoma Initiating Cells. Cancer Research. 70(2). 697–708. 238 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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