Lewis A. Chodosh

18.9k total citations · 6 hit papers
153 papers, 14.4k citations indexed

About

Lewis A. Chodosh is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Lewis A. Chodosh has authored 153 papers receiving a total of 14.4k indexed citations (citations by other indexed papers that have themselves been cited), including 102 papers in Molecular Biology, 70 papers in Oncology and 37 papers in Genetics. Recurrent topics in Lewis A. Chodosh's work include Cancer Cells and Metastasis (37 papers), Cancer-related Molecular Pathways (25 papers) and Genomics and Chromatin Dynamics (17 papers). Lewis A. Chodosh is often cited by papers focused on Cancer Cells and Metastasis (37 papers), Cancer-related Molecular Pathways (25 papers) and Genomics and Chromatin Dynamics (17 papers). Lewis A. Chodosh collaborates with scholars based in United States, Canada and Slovakia. Lewis A. Chodosh's co-authors include Phillip A. Sharp, Richard W. Carthew, M. Celeste Simon, Susan E. Moody, Cheng‐Jun Hu, Brian Keith, Albert S. Baldwin, Robert Boxer, George K. Belka and Christopher J. Sarkisian and has published in prestigious journals such as Science, New England Journal of Medicine and Cell.

In The Last Decade

Lewis A. Chodosh

150 papers receiving 14.2k citations

Hit Papers

Differential Roles of Hyp... 1985 2026 1998 2012 2003 1985 1988 2005 1998 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
Lewis A. Chodosh United States 61 9.6k 4.4k 3.1k 2.8k 1.5k 153 14.4k
Hartmut Land United States 43 10.9k 1.1× 5.3k 1.2× 2.1k 0.7× 2.7k 1.0× 1.9k 1.3× 75 16.0k
Michael A. Tainsky United States 47 7.8k 0.8× 5.2k 1.2× 2.5k 0.8× 1.9k 0.7× 944 0.6× 156 12.5k
David D.L. Bowtell Australia 71 11.6k 1.2× 5.4k 1.2× 3.5k 1.1× 2.1k 0.8× 2.2k 1.5× 221 18.4k
Jacqueline A. Lees United States 53 9.2k 1.0× 5.7k 1.3× 1.7k 0.5× 2.5k 0.9× 902 0.6× 101 12.3k
James DeGregori United States 59 8.2k 0.9× 5.1k 1.1× 2.2k 0.7× 1.4k 0.5× 1.3k 0.9× 172 12.0k
Akira Nakagawara Japan 69 11.4k 1.2× 5.3k 1.2× 4.4k 1.4× 1.5k 0.5× 1.4k 1.0× 347 18.0k
Jiřina Bártková Denmark 62 10.5k 1.1× 7.8k 1.8× 2.8k 0.9× 1.8k 0.6× 1.0k 0.7× 136 15.4k
Robert B. Dickson United States 73 8.9k 0.9× 5.9k 1.3× 3.6k 1.2× 4.3k 1.5× 1.2k 0.8× 221 16.1k
Lawrence A. Donehower United States 59 12.1k 1.3× 9.0k 2.0× 3.4k 1.1× 1.7k 0.6× 1.4k 0.9× 148 17.7k
Douglas C. Dean United States 54 8.4k 0.9× 4.6k 1.0× 1.9k 0.6× 1.2k 0.4× 1.4k 0.9× 107 11.9k

Countries citing papers authored by Lewis A. Chodosh

Since Specialization
Citations

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

Fields of papers citing papers by Lewis A. Chodosh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lewis A. Chodosh. 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 Lewis A. Chodosh. The network helps show where Lewis A. Chodosh may publish in the future.

Co-authorship network of co-authors of Lewis A. Chodosh

This figure shows the co-authorship network connecting the top 25 collaborators of Lewis A. Chodosh. A scholar is included among the top collaborators of Lewis A. Chodosh 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 Lewis A. Chodosh. Lewis A. Chodosh 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.
McDonald, Elizabeth S., Eric A. Cohen, Lauren Pantalone, et al.. (2024). Evaluating the association between radiomic features on breast MRI and dormant tumor cell presence in the SURMOUNT trial.. Journal of Clinical Oncology. 42(16_suppl). 561–561. 1 indexed citations
2.
Ruth, Jason R., et al.. (2024). Autophagy is required for mammary tumor recurrence by promoting dormant tumor cell survival following therapy. Breast Cancer Research. 26(1). 143–143. 10 indexed citations
3.
Schere‐Levy, Carolina, Roberto P. Meiss, Gladys N. Hermida, et al.. (2022). Aberrant RET expression affects normal mammary gland post-lactation transition, enhancing cancer potential. Disease Models & Mechanisms. 15(3). 2 indexed citations
4.
Ruth, Jason R., Dhruv K. Pant, Tien-Chi Pan, et al.. (2021). Cellular dormancy in minimal residual disease following targeted therapy. Breast Cancer Research. 23(1). 63–63. 27 indexed citations
5.
Tsao, Li-Chung, Erika J. Crosby, Timothy N. Trotter, et al.. (2019). CD47 blockade augmentation of trastuzumab antitumor efficacy dependent on antibody-dependent cellular phagocytosis. JCI Insight. 4(24). 83 indexed citations
7.
Alvarez, James V., George K. Belka, Tien-Chi Pan, et al.. (2014). Oncogene Pathway Activation in Mammary Tumors Dictates FDG-PET Uptake. Cancer Research. 74(24). 7583–7598. 55 indexed citations
8.
Pant, Dhruv K., et al.. (2014). Ceramide Kinase Promotes Tumor Cell Survival and Mammary Tumor Recurrence. Cancer Research. 74(21). 6352–6363. 56 indexed citations
9.
Feng, Yi, Tien-Chi Pan, Dhruv K. Pant, et al.. (2014). SPSB1 Promotes Breast Cancer Recurrence by Potentiating c-MET Signaling. Cancer Discovery. 4(7). 790–803. 33 indexed citations
10.
Abate‐Shen, Cory, Katerina Politi, Lewis A. Chodosh, & Kenneth P. Olive. (2014). Mouse models of cancer : a laboratory manual. 4 indexed citations
11.
Searleman, Adam C., Anton Iliuk, Timothy S. Collier, et al.. (2014). Tissue phosphoproteomics with PolyMAC identifies potential therapeutic targets in a transgenic mouse model of HER2 positive breast cancer. Electrophoresis. 35(24). 3463–3469. 12 indexed citations
12.
Alvarez, James V., Tien-Chi Pan, Jason R. Ruth, et al.. (2013). Par-4 Downregulation Promotes Breast Cancer Recurrence by Preventing Multinucleation following Targeted Therapy. Cancer Cell. 24(1). 30–44. 68 indexed citations
13.
Bean, Gregory R., Yogesh Tengarai Ganesan, Yiyu Dong, et al.. (2013). PUMA and BIM Are Required for Oncogene Inactivation–Induced Apoptosis. Science Signaling. 6(268). ra20–ra20. 97 indexed citations
14.
Pitteri, Sharon J., Karen S. Kelly‐Spratt, Kay E. Gurley, et al.. (2011). Tumor Microenvironment–Derived Proteins Dominate the Plasma Proteome Response during Breast Cancer Induction and Progression. Cancer Research. 71(15). 5090–5100. 69 indexed citations
15.
Brown, Rhonda L., Lauren M. Reinke, Denise Perez, et al.. (2011). CD44 splice isoform switching in human and mouse epithelium is essential for epithelial-mesenchymal transition and breast cancer progression. Journal of Clinical Investigation. 121(3). 1064–1074. 502 indexed citations breakdown →
16.
Muraoka-Cook, Rebecca S., Melissa Sandahl, Karen E. Strunk, et al.. (2009). ErbB4 Splice Variants Cyt1 and Cyt2 Differ by 16 Amino Acids and Exert Opposing Effects on the Mammary Epithelium In Vivo. Molecular and Cellular Biology. 29(18). 4935–4948. 63 indexed citations
17.
Blakely, Collin M., Alexander J. Stoddard, George K. Belka, et al.. (2006). Hormone-Induced Protection against Mammary Tumorigenesis Is Conserved in Multiple Rat Strains and Identifies a Core Gene Expression Signature Induced by Pregnancy. Cancer Research. 66(12). 6421–6431. 80 indexed citations
18.
Hu, Cheng‐Jun, et al.. (2003). Differential Roles of Hypoxia-Inducible Factor 1α (HIF-1α) and HIF-2α in Hypoxic Gene Regulation. Molecular and Cellular Biology. 23(24). 9361–9374. 1128 indexed citations breakdown →
19.
Fox, Casey, Peter S. Hammerman, Ryan M. Cinalli, et al.. (2003). The serine/threonine kinase Pim-2 is a transcriptionally regulated apoptotic inhibitor. Genes & Development. 17(15). 1841–1854. 271 indexed citations
20.
Chodosh, Lewis A., Stephen Buratowski, & Phillip A. Sharp. (1989). A Yeast Protein Possesses the DNA-Binding Properties of the Adenovirus Major Late Transcription Factor. Molecular and Cellular Biology. 9(2). 820–822. 18 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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