Stephen P. Malkoski

2.1k total citations
35 papers, 1.4k citations indexed

About

Stephen P. Malkoski is a scholar working on Pulmonary and Respiratory Medicine, Molecular Biology and Oncology. According to data from OpenAlex, Stephen P. Malkoski has authored 35 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Pulmonary and Respiratory Medicine, 13 papers in Molecular Biology and 13 papers in Oncology. Recurrent topics in Stephen P. Malkoski's work include Lung Cancer Diagnosis and Treatment (7 papers), TGF-β signaling in diseases (6 papers) and Lung Cancer Treatments and Mutations (6 papers). Stephen P. Malkoski is often cited by papers focused on Lung Cancer Diagnosis and Treatment (7 papers), TGF-β signaling in diseases (6 papers) and Lung Cancer Treatments and Mutations (6 papers). Stephen P. Malkoski collaborates with scholars based in United States, India and China. Stephen P. Malkoski's co-authors include Richard I. Dorin, Xiao‐Jing Wang, Timothy G. Cleaver, X‐J Wang, R. A. White, Gangwen Han, Shi‐Long Lu, Chu‐Xia Deng, Neil D. Gross and Sophia Bornstein and has published in prestigious journals such as Journal of Clinical Investigation, Journal of Clinical Oncology and PLoS ONE.

In The Last Decade

Stephen P. Malkoski

34 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stephen P. Malkoski United States 18 544 399 390 190 177 35 1.4k
Yuko Nakayama Japan 20 241 0.4× 311 0.8× 429 1.1× 163 0.9× 171 1.0× 98 1.4k
Eduardo Cortes Gomez United States 15 706 1.3× 648 1.6× 487 1.2× 351 1.8× 214 1.2× 43 1.6k
Yoshiro Otsuki Japan 23 834 1.5× 276 0.7× 303 0.8× 284 1.5× 101 0.6× 130 1.7k
Christina Heppner Germany 17 361 0.7× 91 0.2× 521 1.3× 100 0.5× 91 0.5× 29 1.4k
Valentina Salvestrini Italy 22 527 1.0× 76 0.2× 338 0.9× 137 0.7× 721 4.1× 41 1.9k
Jan Bruder United States 20 411 0.8× 187 0.5× 512 1.3× 118 0.6× 46 0.3× 51 1.4k
Caterina Pellegrini Italy 24 616 1.1× 451 1.1× 479 1.2× 155 0.8× 91 0.5× 34 1.5k
Mats Sjöquist Sweden 14 397 0.7× 151 0.4× 211 0.5× 129 0.7× 46 0.3× 27 976
Francesco Boin United States 28 364 0.7× 383 1.0× 122 0.3× 26 0.1× 522 2.9× 59 2.0k

Countries citing papers authored by Stephen P. Malkoski

Since Specialization
Citations

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

Fields of papers citing papers by Stephen P. Malkoski

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephen P. Malkoski. 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 Stephen P. Malkoski. The network helps show where Stephen P. Malkoski may publish in the future.

Co-authorship network of co-authors of Stephen P. Malkoski

This figure shows the co-authorship network connecting the top 25 collaborators of Stephen P. Malkoski. A scholar is included among the top collaborators of Stephen P. Malkoski 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 Stephen P. Malkoski. Stephen P. Malkoski 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.
2.
Barón, Anna E., et al.. (2021). Determinants Associated With Longitudinal Adherence to Annual Lung Cancer Screening: A Retrospective Analysis of Claims Data. Journal of the American College of Radiology. 18(8). 1084–1094. 13 indexed citations
3.
Xing, Fuyong, Anna E. Barón, William J. Feser, et al.. (2020). Quantifying the incremental value of deep learning: Application to lung nodule detection. PLoS ONE. 15(4). e0231468–e0231468. 2 indexed citations
4.
Wang, Xiao‐Jing, Christian D. Young, Anh T. Le, et al.. (2020). Development of syngeneic murine cell lines for use in immunocompetent orthotopic lung cancer models. Cancer Cell International. 20(1). 417–417. 15 indexed citations
5.
Rivera, M. Patricia, Nichole T. Tanner, Gerard A. Silvestri, et al.. (2018). Incorporating Coexisting Chronic Illness into Decisions about Patient Selection for Lung Cancer Screening. An Official American Thoracic Society Research Statement. American Journal of Respiratory and Critical Care Medicine. 198(2). e3–e13. 66 indexed citations
6.
Poczobutt, Joanna M., Howard Li, Jing Huang, et al.. (2018). Adenoviral vectors transduce alveolar macrophages in lung cancer models. OncoImmunology. 7(6). e1438105–e1438105. 13 indexed citations
7.
Kwak, Jeff, Jennifer Laskowski, Howard Li, et al.. (2017). Complement Activation via a C3a Receptor Pathway Alters CD4+ T Lymphocytes and Mediates Lung Cancer Progression. Cancer Research. 78(1). 143–156. 103 indexed citations
8.
Barón, Anna E., Severine Kako, William J. Feser, et al.. (2017). Clinical Utility of Chromosomal Aneusomy in Individuals at High Risk of Lung Cancer. Journal of Thoracic Oncology. 12(10). 1512–1523. 6 indexed citations
9.
Nolan, Kathleen F., et al.. (2017). Reduced TGFBR2 Expression in NSCLC Drives IL-17A Dependent Inflammation via γδT Cells. Journal of Thoracic Oncology. 12(8). S1537–S1537. 1 indexed citations
10.
Haeger, Sarah M., Joshua J. Thompson, Timothy G. Cleaver, et al.. (2015). Smad4 loss promotes lung cancer formation but increases sensitivity to DNA topoisomerase inhibitors. Oncogene. 35(5). 577–586. 35 indexed citations
11.
MacLaren, Robert, Candice Preslaski, Scott W. Mueller, et al.. (2013). A Randomized, Double-Blind Pilot Study of Dexmedetomidine Versus Midazolam for Intensive Care Unit Sedation. Journal of Intensive Care Medicine. 30(3). 167–175. 26 indexed citations
12.
Malkoski, Stephen P., Sarah M. Haeger, Timothy G. Cleaver, et al.. (2012). Loss of Transforming Growth Factor Beta Type II Receptor Increases Aggressive Tumor Behavior and Reduces Survival in Lung Adenocarcinoma and Squamous Cell Carcinoma. Clinical Cancer Research. 18(8). 2173–2183. 52 indexed citations
13.
Malkoski, Stephen P. & Xiao‐Jing Wang. (2012). Two sides of the story? Smad4 loss in pancreatic cancer versus head‐and‐neck cancer. FEBS Letters. 586(14). 1984–1992. 54 indexed citations
14.
Hudish, Tyler M., Anthony B. Mozer, M. S. Johnson, et al.. (2011). N-nitroso-tris-chloroethylurea Induces Premalignant Squamous Dysplasia in Mice. Cancer Prevention Research. 5(2). 283–289. 21 indexed citations
15.
Mitra, Doyel, Stephen P. Malkoski, & Xiao‐Jing Wang. (2011). Cancer Stem Cells in Head and Neck Cancer. Cancers. 3(1). 415–427. 13 indexed citations
16.
Malkoski, Stephen P., Timothy G. Cleaver, Shi‐Long Lu, Jessyka G. Lighthall, & Xiao‐Jing Wang. (2010). Keratin promoter based gene manipulation in the murine conducting airway. International Journal of Biological Sciences. 6(1). 68–79. 9 indexed citations
17.
Deng, Yu, Jing Liu, Gangwen Han, et al.. (2010). Redox-dependent Brca1 transcriptional regulation by an NADH-sensor CtBP1. Oncogene. 29(50). 6603–6608. 33 indexed citations
18.
White, R. A., Stephen P. Malkoski, & X‐J Wang. (2010). TGFβ signaling in head and neck squamous cell carcinoma. Oncogene. 29(40). 5437–5446. 76 indexed citations
19.
Bredow, Sebastian, Thomas H. March, Christin M. Yingling, et al.. (2007). Subchronic inhalation of soluble manganese induces expression of hypoxia-associated angiogenic genes in adult mouse lungs. Toxicology and Applied Pharmacology. 221(2). 148–157. 18 indexed citations
20.
Malkoski, Stephen P. & Richard I. Dorin. (1999). Composite Glucocorticoid Regulation at a Functionally Defined Negative Glucocorticoid Response Element of the Human Corticotropin-Releasing Hormone Gene. Molecular Endocrinology. 13(10). 1629–1644. 165 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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