Gilbert H. Smith

11.0k total citations · 2 hit papers
169 papers, 8.9k citations indexed

About

Gilbert H. Smith is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Gilbert H. Smith has authored 169 papers receiving a total of 8.9k indexed citations (citations by other indexed papers that have themselves been cited), including 81 papers in Molecular Biology, 74 papers in Oncology and 67 papers in Genetics. Recurrent topics in Gilbert H. Smith's work include Cancer Cells and Metastasis (61 papers), Virus-based gene therapy research (35 papers) and Animal Genetics and Reproduction (21 papers). Gilbert H. Smith is often cited by papers focused on Cancer Cells and Metastasis (61 papers), Virus-based gene therapy research (35 papers) and Animal Genetics and Reproduction (21 papers). Gilbert H. Smith collaborates with scholars based in United States, United Kingdom and Switzerland. Gilbert H. Smith's co-authors include Corinne A. Boulanger, Edith C. Kordon, Robert Callahan, Glenn Merlino, Chamelli Jhappan, Lothar Hennighausen, Daniel Medina, Gloria Chepko, Brian W. Booth and Daniel Gallahan and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Gilbert H. Smith

168 papers receiving 8.6k citations

Hit Papers

Notch signaling is essential for vascular morphogenesis i... 1990 2026 2002 2014 2000 1990 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gilbert H. Smith United States 48 5.3k 4.4k 2.1k 1.1k 750 169 8.9k
Nicholas C. Dracopoli United States 37 4.2k 0.8× 2.8k 0.6× 1.9k 0.9× 1.6k 1.5× 812 1.1× 88 7.6k
Robert Bookstein United States 35 4.3k 0.8× 3.8k 0.9× 1.7k 0.8× 1.3k 1.2× 533 0.7× 52 7.9k
Susanne M. Gollin United States 48 4.4k 0.8× 2.0k 0.5× 1.3k 0.6× 1.6k 1.5× 685 0.9× 141 7.2k
Andrea Haegebarth Germany 24 5.4k 1.0× 4.1k 0.9× 1.9k 0.9× 1.1k 1.0× 642 0.9× 47 9.0k
Gordon Peters United Kingdom 48 7.2k 1.4× 4.8k 1.1× 1.1k 0.5× 1.8k 1.7× 912 1.2× 95 10.4k
Gertraud W. Robinson United States 46 4.3k 0.8× 3.8k 0.9× 1.8k 0.8× 1.2k 1.2× 1.8k 2.4× 78 8.4k
Jean Feunteun France 46 5.2k 1.0× 2.2k 0.5× 2.6k 1.2× 1.3k 1.2× 394 0.5× 128 7.6k
Bohdan Wasylyk France 61 9.1k 1.7× 3.3k 0.7× 2.1k 1.0× 1.8k 1.7× 1.6k 2.2× 151 12.5k
Denise Sheer United Kingdom 51 6.0k 1.1× 2.1k 0.5× 1.9k 0.9× 1.3k 1.2× 1.4k 1.8× 178 10.9k
Mark E. Ewen United States 38 7.1k 1.3× 6.7k 1.5× 1.9k 0.9× 1.1k 1.1× 1.1k 1.5× 54 10.4k

Countries citing papers authored by Gilbert H. Smith

Since Specialization
Citations

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

Fields of papers citing papers by Gilbert H. Smith

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gilbert H. Smith. 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 Gilbert H. Smith. The network helps show where Gilbert H. Smith may publish in the future.

Co-authorship network of co-authors of Gilbert H. Smith

This figure shows the co-authorship network connecting the top 25 collaborators of Gilbert H. Smith. A scholar is included among the top collaborators of Gilbert H. Smith 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 Gilbert H. Smith. Gilbert H. Smith 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.
Bruno, Robert D., et al.. (2019). Long-label-retaining mammary epithelial cells are created early in ductal development and distributed throughout the branching ducts. Mechanisms of Development. 159. 103565–103565. 2 indexed citations
2.
Bussard, Karen M. & Gilbert H. Smith. (2012). Human Breast Cancer Cells Are Redirected to Mammary Epithelial Cells upon Interaction with the Regenerating Mammary Gland Microenvironment In-Vivo. PLoS ONE. 7(11). e49221–e49221. 41 indexed citations
3.
Boulanger, Corinne A., Robert D. Bruno, Michael Rosu‐Myles, & Gilbert H. Smith. (2011). The Mouse Mammary Microenvironment Redirects Mesoderm-Derived Bone Marrow Cells to a Mammary Epithelial Progenitor Cell Fate. Stem Cells and Development. 21(6). 948–954. 35 indexed citations
4.
Bruno, Robert D., Corinne A. Boulanger, & Gilbert H. Smith. (2011). Notch-induced mammary tumorigenesis does not involve the lobule-limited epithelial progenitor. Oncogene. 31(1). 60–67. 19 indexed citations
5.
Bussard, Karen M., Corinne A. Boulanger, Brian W. Booth, Robert D. Bruno, & Gilbert H. Smith. (2010). Reprogramming Human Cancer Cells in the Mouse Mammary Gland. Cancer Research. 70(15). 6336–6343. 82 indexed citations
6.
Booth, Brian W., Corinne A. Boulanger, L.H. Anderson, & Gilbert H. Smith. (2010). The normal mammary microenvironment suppresses the tumorigenic phenotype of mouse mammary tumor virus-neu-transformed mammary tumor cells. Oncogene. 30(6). 679–689. 61 indexed citations
7.
Bussard, Karen M., Corinne A. Boulanger, Frances Kittrell, et al.. (2010). Immortalized, premalignant epithelial cell populations contain long-lived, label-retaining cells that asymmetrically divide and retain their template DNA. Breast Cancer Research. 12(5). R86–R86. 15 indexed citations
8.
Booth, Brian W., David L. Mack, Andreas Androutsellis‐Theotokis, et al.. (2008). The mammary microenvironment alters the differentiation repertoire of neural stem cells. Proceedings of the National Academy of Sciences. 105(39). 14891–14896. 110 indexed citations
9.
Callahan, Robert & Gilbert H. Smith. (2008). Common Integration Sites for MMTV in Viral Induced Mouse Mammary Tumors. Journal of Mammary Gland Biology and Neoplasia. 13(3). 309–321. 35 indexed citations
10.
Mack, David L., Corinne A. Boulanger, Robert Callahan, & Gilbert H. Smith. (2007). Expression of truncated Int6/eIF3e in mammary alveolar epithelium leads to persistent hyperplasia and tumorigenesis. Breast Cancer Research. 9(4). R42–R42. 24 indexed citations
11.
Smith, Gilbert H.. (2006). Mammary stem cells come of age, prospectively. Trends in Molecular Medicine. 12(7). 287–289. 11 indexed citations
12.
Booth, Brian W., Chamelli Jhappan, Glenn Merlino, & Gilbert H. Smith. (2006). TGFβ1 and TGFα contrarily affect alveolar survival and tumorigenesis in mouse mammary epithelium. International Journal of Cancer. 120(3). 493–499. 6 indexed citations
13.
Triplett, Aleata A., et al.. (2004). Parity-induced mammary epithelial cells facilitate tumorigenesis in MMTV-neu transgenic mice. Oncogene. 23(41). 6980–6985. 101 indexed citations
14.
Bierie, Brian, Masahiro Nozawa, Gilbert H. Smith, et al.. (2003). Biogenesis and function of mouse mammary epithelium depends on the presence of functional α-catenin. Mechanisms of Development. 121(1). 91–99. 30 indexed citations
15.
Shyamala, G., Yu-Ching Chou, Sharianne G. Louie, et al.. (2002). Cellular expression of estrogen and progesterone receptors in mammary glands: regulation by hormones, development and aging. The Journal of Steroid Biochemistry and Molecular Biology. 80(2). 137–148. 101 indexed citations
16.
Chepko, Gloria & Gilbert H. Smith. (1997). Three division-competent, structurally-distinct cell populations contribute to murine mammary epithelial renewal. Tissue and Cell. 29(2). 239–253. 159 indexed citations
17.
Santis, Marta De, Jean‐Pierre David, Gilbert H. Smith, et al.. (1997). Cripto Enhances the Tyrosine Phosphorylation of Shc and Activates Mitogen-activated Protein Kinase (MAPK) in Mammary Epithelial Cells. Journal of Biological Chemistry. 272(6). 3330–3335. 87 indexed citations
18.
Kordon, Edith C., Robert A. McKnight, Chamelli Jhappan, et al.. (1995). Ectopic TGFβ1 Expression in the Secretory Mammary Epithelium Induces Early Senescence of the Epithelial Stem Cell Population. Developmental Biology. 168(1). 47–61. 153 indexed citations
19.
Callahan, Robert, Daniel Gallahan, Gilbert H. Smith, et al.. (1993). Frequent Mutations in Breast Cancer. Annals of the New York Academy of Sciences. 698(1). 21–30. 7 indexed citations
20.
Smith, Gilbert H., et al.. (1983). Patient Turnover in a new Psychogeriatric Day Hospital: a Pluralistic Evaluation. Ageing and Society. 3(3). 325–356. 6 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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