Daphne A. Haas-Kogan

3.2k total citations
34 papers, 2.5k citations indexed

About

Daphne A. Haas-Kogan is a scholar working on Molecular Biology, Oncology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Daphne A. Haas-Kogan has authored 34 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 12 papers in Oncology and 6 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Daphne A. Haas-Kogan's work include PI3K/AKT/mTOR signaling in cancer (8 papers), Cancer-related Molecular Pathways (5 papers) and Glioma Diagnosis and Treatment (4 papers). Daphne A. Haas-Kogan is often cited by papers focused on PI3K/AKT/mTOR signaling in cancer (8 papers), Cancer-related Molecular Pathways (5 papers) and Glioma Diagnosis and Treatment (4 papers). Daphne A. Haas-Kogan collaborates with scholars based in United States, Israel and France. Daphne A. Haas-Kogan's co-authors include David Stokoe, Mitchel S. Berger, Kathleen R. Lamborn, C. David James, Tarık Tihan, Michael D. Prados, William A. Weiss, Christine Cheng, Nils D. Arvold and Kevan M. Shokat and has published in prestigious journals such as Molecular and Cellular Biology, JNCI Journal of the National Cancer Institute and Cancer Research.

In The Last Decade

Daphne A. Haas-Kogan

34 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Daphne A. Haas-Kogan United States 23 1.4k 731 571 534 378 34 2.5k
Christiane B. Knobbe‐Thomsen Germany 30 2.2k 1.6× 1.1k 1.5× 909 1.6× 605 1.1× 388 1.0× 45 3.5k
Barbara Klink Germany 25 1.0k 0.7× 855 1.2× 775 1.4× 530 1.0× 370 1.0× 73 2.5k
Takashi Sasayama Japan 27 1.8k 1.3× 732 1.0× 785 1.4× 690 1.3× 361 1.0× 152 3.4k
Sridhar Epari India 23 599 0.4× 783 1.1× 293 0.5× 288 0.5× 360 1.0× 198 1.9k
Luca Mologni Italy 32 1.7k 1.2× 784 1.1× 293 0.5× 942 1.8× 596 1.6× 91 3.4k
Andrew M. Donson United States 35 1.7k 1.2× 1.2k 1.7× 536 0.9× 632 1.2× 451 1.2× 112 3.0k
Remco J. Molenaar Netherlands 25 1.1k 0.8× 827 1.1× 733 1.3× 429 0.8× 294 0.8× 63 2.2k
Ruihuan Chen China 13 1.6k 1.1× 1.6k 2.2× 1.1k 1.9× 565 1.1× 296 0.8× 28 3.0k
Lyndon Kim United States 19 756 0.5× 1.6k 2.2× 554 1.0× 412 0.8× 633 1.7× 42 2.4k
W. K. Alfred Yung United States 33 2.3k 1.6× 1.5k 2.0× 1.1k 1.9× 1.2k 2.2× 690 1.8× 80 4.2k

Countries citing papers authored by Daphne A. Haas-Kogan

Since Specialization
Citations

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

Fields of papers citing papers by Daphne A. Haas-Kogan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daphne A. Haas-Kogan. 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 Daphne A. Haas-Kogan. The network helps show where Daphne A. Haas-Kogan may publish in the future.

Co-authorship network of co-authors of Daphne A. Haas-Kogan

This figure shows the co-authorship network connecting the top 25 collaborators of Daphne A. Haas-Kogan. A scholar is included among the top collaborators of Daphne A. Haas-Kogan 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 Daphne A. Haas-Kogan. Daphne A. Haas-Kogan 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.
Tinkle, Christopher L., Charu Singh, Shane Lloyd, et al.. (2020). Stereotactic Body Radiation Therapy for Metastatic and Recurrent Solid Tumors in Children and Young Adults. International Journal of Radiation Oncology*Biology*Physics. 109(5). 1396–1405. 16 indexed citations
2.
Roddy, Erika, Katherine Sear, Erin Felton, et al.. (2016). Presence of cerebral microbleeds is associated with worse executive function in pediatric brain tumor survivors. Neuro-Oncology. 18(11). now163–now163. 42 indexed citations
3.
Hashizume, Rintaro, Ali Zhang, Sabine Mueller, et al.. (2016). Inhibition of DNA damage repair by the CDK4/6 inhibitor palbociclib delays irradiated intracranial atypical teratoid rhabdoid tumor and glioblastoma xenograft regrowth. Neuro-Oncology. 18(11). now106–now106. 100 indexed citations
4.
Braunstein, Steve, Michelle Mourad, I‐Chow Hsu, et al.. (2014). Quality improvement of International Classification of Diseases, 9th revision, diagnosis coding in radiation oncology: Single-institution prospective study at University of California, San Francisco. Practical Radiation Oncology. 5(1). e45–e51. 4 indexed citations
5.
Haas-Kogan, Daphne A. & Christopher L. Tinkle. (2012). Hepatocellular carcinoma: natural history, current management, and emerging tools. Biologics. 6. 207–207. 51 indexed citations
6.
Mueller, Sabine, Xiaodong Yang, Theo Sottero, et al.. (2011). Cooperation of the HDAC inhibitor vorinostat and radiation in metastatic neuroblastoma: Efficacy and underlying mechanisms. Cancer Letters. 306(2). 223–229. 60 indexed citations
7.
Zheng, Shichun, E. Andrés Houseman, Zachary Morrison, et al.. (2011). DNA hypermethylation profiles associated with glioma subtypes and EZH2 and IGFBP2 mRNA expression. Neuro-Oncology. 13(3). 280–289. 58 indexed citations
8.
McBride, Sean M., Daniel Pérez, Mei‐Yin C. Polley, et al.. (2009). Activation of PI3K/mTOR pathway occurs in most adult low-grade gliomas and predicts patient survival. Journal of Neuro-Oncology. 97(1). 33–40. 59 indexed citations
9.
Jabbari, Siavash, David L. Andolino, Vivian Weinberg, et al.. (2009). Successful Treatment of High Risk and Recurrent Pediatric Desmoids Using Radiation as a Component of Multimodality Therapy. International Journal of Radiation Oncology*Biology*Physics. 75(1). 177–182. 18 indexed citations
10.
Wiencke, John K., Shichun Zheng, Tarık Tihan, et al.. (2007). Methylation of the PTEN promoter defines low-grade gliomas and secondary glioblastoma. Neuro-Oncology. 9(3). 271–279. 123 indexed citations
11.
Entin‐Meer, Michal, et al.. (2007). AN-113, a novel prodrug of 4-phenylbutyrate with increased anti-neoplastic activity in glioma cell lines. Cancer Letters. 253(2). 205–214. 11 indexed citations
12.
Haas-Kogan, Daphne A., Michael D. Prados, Tarık Tihan, et al.. (2005). Epidermal Growth Factor Receptor, Protein Kinase B/Akt, and Glioma Response to Erlotinib. JNCI Journal of the National Cancer Institute. 97(12). 880–887. 368 indexed citations
13.
Gottschalk, Alexander, et al.. (2005). Inhibition of phosphatidylinositol-3-kinase causes increased sensitivity to radiation through a PKB-dependent mechanism. International Journal of Radiation Oncology*Biology*Physics. 63(4). 1221–1227. 44 indexed citations
14.
Pore, Nabendu, Shuang Liu, Hui‐Kuo G. Shu, et al.. (2004). Sp1 Is Involved in Akt-mediated Induction of VEGF Expression through an HIF-1–independent Mechanism. Molecular Biology of the Cell. 15(11). 4841–4853. 197 indexed citations
15.
Ermoian, Ralph P., C. Sloane Furniss, Kathleen R. Lamborn, et al.. (2002). Dysregulation of PTEN and protein kinase B is associated with glioma histology and patient survival.. PubMed. 8(5). 1100–6. 142 indexed citations
16.
Wara, William M., Katherine K. Matthay, Arthur R. Ablin, et al.. (2001). Functional and clinical outcomes of limb-sparing therapy for pediatric extremity sarcomas. International Journal of Radiation Oncology*Biology*Physics. 49(3). 763–769. 13 indexed citations
17.
Yount, Garret, et al.. (2001). Transcriptional activation of TRADD mediates p53-independent radiation-induced apoptosis of glioma cells. Oncogene. 20(22). 2826–2835. 24 indexed citations
18.
Shu, Hui‐Kuo G., et al.. (2000). Overexpression of E2F1 in glioma-derived cell lines induces ap53-independent apoptosis that is further enhanced by ionizing radiation. Neuro-Oncology. 2(1). 16–21. 13 indexed citations
19.
20.
Haas-Kogan, Daphne A., Scott C. Kogan, Garret Yount, et al.. (1999). P53 function influences the effect of fractionated radiotherapy on glioblastoma tumors. International Journal of Radiation Oncology*Biology*Physics. 43(2). 399–403. 60 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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