Ian S. Hagemann, Ph.D.

Affiliations: 
2008 Washington University, Saint Louis, St. Louis, MO 
Area:
Cell Biology, Molecular Biology
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"Ian Hagemann"

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Thomas J. Baranski grad student 2008 Washington University
 (Novel determinants of G protein signaling.)
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Publications

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Mullen M, Quinn J, Greenwade M, et al. (2019) AXL in metastatic ovarian cancer tumors is a targetable biomarker associated with chemoresistance and poor prognosis Gynecologic Oncology. 154: 79-80
Zhang X, Kim S, Hundal J, et al. (2017) Breast cancer neoantigens can induce CD8 T cell responses and antitumor immunity. Cancer Immunology Research
Divine LM, Nguyen MR, Meller E, et al. (2016) AXL modulates extracellular matrix protein expression and is essential for invasion and metastasis in endometrial cancer. Oncotarget
Hagemann IS, O'Neill PK, Erill I, et al. (2015) Diagnostic yield of targeted next generation sequencing in various cancer types: An information-theoretic approach. Cancer Genetics
Chernock RD, Hagemann IS. (2015) Molecular pathology of hereditary and sporadic medullary thyroid carcinomas. American Journal of Clinical Pathology. 143: 768-77
Hagemann IS, Devarakonda S, Lockwood CM, et al. (2015) Clinical next-generation sequencing in patients with non-small cell lung cancer. Cancer. 121: 631-9
Sehn JK, Hagemann IS, Pfeifer JD, et al. (2014) Diagnostic utility of targeted next-generation sequencing in problematic cases. The American Journal of Surgical Pathology. 38: 534-41
Hagemann IS, Govindan R, Javidan-Nejad C, et al. (2014) Stabilization of disease after targeted therapy in a thymic carcinoma with KIT mutation detected by clinical next-generation sequencing. Journal of Thoracic Oncology : Official Publication of the International Association For the Study of Lung Cancer. 9: e12-6
Hagemann IS, Al-Kateb H, Cottrell CE, et al. (2013) Abstract 813: Diagnostic yield of targeted next-generation sequencing for personalized cancer therapeutics. Cancer Research. 73: 813-813
Zsiros E, Lee H, Hagemann IS, et al. (2013) Abstract 3968: Ovarian cancer chemokine microenvironment is conducive to homing of CD3/CD28 co-stimulated T cells prepared for adoptive transfer therapy. Cancer Research. 73: 3968-3968
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