Martha R. Stampfer

12.2k total citations
132 papers, 9.4k citations indexed

About

Martha R. Stampfer is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, Martha R. Stampfer has authored 132 papers receiving a total of 9.4k indexed citations (citations by other indexed papers that have themselves been cited), including 76 papers in Molecular Biology, 64 papers in Oncology and 30 papers in Cancer Research. Recurrent topics in Martha R. Stampfer's work include Cancer Cells and Metastasis (37 papers), Telomeres, Telomerase, and Senescence (27 papers) and Cancer-related Molecular Pathways (23 papers). Martha R. Stampfer is often cited by papers focused on Cancer Cells and Metastasis (37 papers), Telomeres, Telomerase, and Senescence (27 papers) and Cancer-related Molecular Pathways (23 papers). Martha R. Stampfer collaborates with scholars based in United States, United Kingdom and Norway. Martha R. Stampfer's co-authors include Paul Yaswen, James C. Garbe, J. C. Bartley, Joyce Taylor‐Papadimitriou, R G Ham, A. J. Hackett, Keith R. Yamamoto, R. C. Hallowes, Mark A. LaBarge and Bernard W. Futscher and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Martha R. Stampfer

130 papers receiving 9.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Martha R. Stampfer United States 54 6.0k 3.7k 1.8k 1.5k 1.3k 132 9.4k
Samuel Benchimol Canada 46 5.7k 0.9× 4.6k 1.2× 1.4k 0.8× 971 0.6× 1.3k 1.0× 94 8.8k
Michael A. Tainsky United States 47 7.8k 1.3× 5.2k 1.4× 2.5k 1.4× 1.9k 1.2× 727 0.5× 156 12.5k
Asha S. Multani United States 40 5.0k 0.8× 3.3k 0.9× 1.9k 1.1× 691 0.5× 1.4k 1.0× 126 8.2k
Onno Kranenburg Netherlands 52 5.4k 0.9× 3.0k 0.8× 1.5k 0.9× 1.0k 0.7× 596 0.4× 188 9.8k
Per Guldberg Denmark 53 7.3k 1.2× 3.2k 0.9× 1.5k 0.8× 1.1k 0.7× 802 0.6× 195 10.9k
Douglas C. Dean United States 54 8.4k 1.4× 4.6k 1.2× 1.9k 1.1× 1.2k 0.8× 603 0.5× 107 11.9k
Wilhelm Krek Switzerland 52 7.6k 1.3× 3.7k 1.0× 2.3k 1.3× 1.4k 0.9× 685 0.5× 93 10.8k
Shinichi Saito Japan 42 6.1k 1.0× 4.0k 1.1× 1.2k 0.7× 497 0.3× 882 0.7× 115 9.4k
Roger A. Greenberg United States 51 7.9k 1.3× 2.6k 0.7× 1.3k 0.7× 1.2k 0.8× 2.0k 1.5× 98 10.3k
David T. Weaver United States 49 6.5k 1.1× 2.6k 0.7× 1.3k 0.8× 865 0.6× 459 0.3× 150 9.0k

Countries citing papers authored by Martha R. Stampfer

Since Specialization
Citations

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

Fields of papers citing papers by Martha R. Stampfer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Martha R. Stampfer. 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 Martha R. Stampfer. The network helps show where Martha R. Stampfer may publish in the future.

Co-authorship network of co-authors of Martha R. Stampfer

This figure shows the co-authorship network connecting the top 25 collaborators of Martha R. Stampfer. A scholar is included among the top collaborators of Martha R. Stampfer 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 Martha R. Stampfer. Martha R. Stampfer 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.
Sayaman, Rosalyn W., Masaru Miyano, Parijat Senapati, et al.. (2024). Luminal epithelial cells integrate variable responses to aging into stereotypical changes that underlie breast cancer susceptibility. eLife. 13. 5 indexed citations
2.
Tyler, Eleanor J., Ana Gutierrez del Arroyo, James C. Garbe, et al.. (2021). Early growth response 2 (EGR2) is a novel regulator of the senescence programme. Aging Cell. 20(3). e13318–e13318. 22 indexed citations
3.
Miyano, Masaru, Rosalyn W. Sayaman, Parijat Senapati, et al.. (2021). Breast-Specific Molecular Clocks Comprised ofELF5Expression and Promoter Methylation Identify Individuals Susceptible to Cancer Initiation. Cancer Prevention Research. 14(8). 779–794. 14 indexed citations
4.
Severson, Paul, Lukáš Vrba, Martha R. Stampfer, & Bernard W. Futscher. (2014). Exome-wide mutation profile in benzo[a]pyrene-derived post-stasis and immortal human mammary epithelial cells. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 775-776. 48–54. 28 indexed citations
5.
Garbe, James C., François Pépin, Agla J. Fridriksdottir, et al.. (2012). Accumulation of Multipotent Progenitors with a Basal Differentiation Bias during Aging of Human Mammary Epithelia. Cancer Research. 72(14). 3687–3701. 80 indexed citations
6.
Sherman, Michael Y., Le Meng, Martha R. Stampfer, Vladimir L. Gabai, & Julia A. Yaglom. (2011). Oncogenes induce senescence with incomplete growth arrest and suppress the DNA damage response in immortalized cells. Aging Cell. 10(6). 949–961. 25 indexed citations
7.
Bishop, Cleo L., Delphine Fessart, Viola Borgdorff, et al.. (2010). Primary Cilium-Dependent and -Independent Hedgehog Signaling Inhibits p16INK4A. Molecular Cell. 40(4). 533–547. 43 indexed citations
8.
Novák, Petr, Taylor J. Jensen, James C. Garbe, Martha R. Stampfer, & Bernard W. Futscher. (2009). Stepwise DNA Methylation Changes Are Linked to Escape from Defined Proliferation Barriers and Mammary Epithelial Cell Immortalization. Cancer Research. 69(12). 5251–5258. 94 indexed citations
9.
Garbe, James C., Sanchita Bhattacharya, Ekaterina Bassett, et al.. (2009). Molecular Distinctions between Stasis and Telomere Attrition Senescence Barriers Shown by Long-term Culture of Normal Human Mammary Epithelial Cells. Cancer Research. 69(19). 7557–7568. 127 indexed citations
10.
Annab, Lois A., Lori Terry, P. LouAnn Cable, et al.. (2000). Establishment and Characterization of a Breast Cell Strain Containing a BRCA1 185delAG Mutation. Gynecologic Oncology. 77(1). 121–128. 9 indexed citations
11.
Sandhu, Charanjit, Jeffrey Donovan, Nandita Bhattacharya, et al.. (2000). Reduction of Cdc25A contributes to cyclin E1-Cdk2 inhibition at senescence in human mammary epithelial cells. Oncogene. 19(47). 5314–5323. 45 indexed citations
12.
Brenner, Andrew, Martha R. Stampfer, & C. Marcelo Aldaz. (1998). Increased p16 expression with first senescence arrest in human mammary epithelial cells and extended growth capacity with p16 inactivation. Oncogene. 17(2). 199–205. 236 indexed citations
13.
Slingerland, Joyce M., et al.. (1994). A Novel Inhibitor of Cyclin-Cdk Activity Detected in Transforming Growth Factor β-Arrested Epithelial Cells. Molecular and Cellular Biology. 14(6). 3683–3694. 60 indexed citations
14.
Lehman, Teresa A., Ramakrishna Modali, Petra Boukamp, et al.. (1993). Errata: p53 Mutations in human immortalized epithelial cell lines (Carcinogenesis (1993) 14 (833-839)). Carcinogenesis. 14(7). 40 indexed citations
15.
16.
Stampfer, Martha R. & J. C. Bartley. (1988). Human mammary epithelial cells in culture: differentiation and transformation. Cancer treatment and research. 40. 1–24. 66 indexed citations
17.
Leadon, Steven A., Martha R. Stampfer, & J. C. Bartley. (1988). Production of oxidative DNA damage during the metabolic activation of benzo[a]pyrene in human mammary epithelial cells correlates with cell killing.. Proceedings of the National Academy of Sciences. 85(12). 4365–4368. 63 indexed citations
18.
Stampfer, Martha R.. (1985). Isolation and growth of human mammary epithelial cells. Methods in Cell Science. 9(2). 107–115. 157 indexed citations
19.
Ham, R G, et al.. (1984). Serum-free growth of human mammary epithelial cells: rapid clonal growth in defined medium and extended serial passage with pituitary extract.. Proceedings of the National Academy of Sciences. 81(17). 5435–5439. 373 indexed citations
20.
Stampfer, Martha R., R. C. Hallowes, & A. J. Hackett. (1980). Growth of normal human mammary cells in culture. In Vitro Cellular & Developmental Biology - Plant. 16(5). 415–425. 263 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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