Tim Wilson Email and Phone Number
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Group Lead and Translational Medicine Scientist with 13 years of drug development experience. Nineteen years post PhD experience. Within Genentech's Oncology Biomarker Department, our responsibility is to develop and implement both the predictive and phamacodynamic biomarker programs for anti-cancer medicines that are in clinical development. As a Biomarker Sub Team Leader (BMSTL), I lead a multi-disciplined group of individuals from across the organization to implement and deliver the biomarker strategy from pre-IND filings to approvals and beyond. As a group lead, I lead a team of BMSTLs and Scientists that support the development of products within our organization, as well as forward and reverse translation studies that advance the field of oncogene driven cancer research. My lab is focussed on translational research and studying how cancer genomics correlates with response and resistance to anti-cancer agents that are under clinical development.
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Executive Director, Translational MedicineRevolution MedicinesCalifornia, United States -
Senior Principal Scientist | Distinguished ScientistGenentech May 2021 - PresentSouth San Francisco, California, UsOncology Biomarker Development -
Principal ScientistGenentech Oct 2019 - May 2021South San Francisco, California, UsOncology Biomarker Development -
Senior ScientistGenentech Dec 2015 - Sep 2019South San Francisco, California, UsOncology Biomarker Development -
ScientistGenentech Dec 2011 - Dec 2015South San Francisco, California, UsOncology Biomarker DevelopmentPublications:Arthur LM, Turnbull AK, Renshaw L, Keys J, Thomas JS, Wilson TR, Lackner MR, Sims AH, Dixon JM: Changes in PIK3CA mutation status are not associated with recurrence, metastatic disease or progression in endocrine-treated breast cancer. Breast cancer research and treatment 2014, 147(1):211-219.Schleifman EB, Desai R, Spoerke JM, Xiao Y, Wong C, Abbas I, O'Brien C, Patel R, Sumiyoshi T, Fu L et al: Targeted biomarker profiling of matched primary and metastatic estrogen receptor positive breast cancers. PLoS One 2014, 9(2):e88401.Wilson TR, Xiao Y, Spoerke JM, Fridlyand J, Koeppen H, Fuentes E, Huw LY, Abbas I, Gower A, Schleifman EB et al: Development of a robust RNA-based classifier to accurately determine ER, PR, and HER2 status in breast cancer clinical samples. Breast cancer research and treatment 2014, 148(2):315-325.Edgar KA, Crocker L, Cheng E, Wagle MC, Wongchenko M, Yan Y, Wilson TR, Dompe N, Neve RM, Belvin M et al: Amphiregulin and PTEN evoke a multimodal mechanism of acquired resistance to PI3K inhibition. Genes & cancer 2014, 5(3-4):113-126.Wilson TR, Lackner MR: Changing the paradigm: circulating tumor DNA as a ‘liquid biopsy’ for clinical biomarker assessments. Clinical Investigation 2014, 4(12):1083-1093.Shames DS, Carbon J, Walter K, Jubb AM, Kozlowski C, Januario T, Do A, Fu L, Xiao Y, Raja R et al: High heregulin expression is associated with activated HER3 and may define an actionable biomarker in patients with squamous cell carcinomas of the head and neck. PLoS One 2013, 8(2):e56765.Huw LY, O'Brien C, Pandita A, Mohan S, Spoerke JM, Lu S, Wang Y, Hampton GM, Wilson TR, Lackner MR: Acquired PIK3CA amplification causes resistance to selective phosphoinositide 3-kinase inhibitors in breast cancer. Oncogenesis 2013, 2:e83. -
Postdoctoral Research FellowGenentech Sep 2010 - Dec 2011South San Francisco, California, UsMentor: Jeff Settleman.Discovery Oncology/ Kinase Addiction/ Signal TransductionPublications:Timothy R. Wilson, Jane Fridlyand, Yibing Yan, Elicia Penuel, Luciana Burton, Emily Chan, Jing Peng, Eva Lin, Yulei Wang, Jeff Sosman, Antoni Ribas, Jiang Li, John Moffat, Daniel P. Sutherlin, Hartmut Koeppen, Mark Merchant, Richard Neve & Jeff Settleman (2012). Widespread potential for growth-factor-driven resistance to anticancer kinase inhibitors. Nature 487, 505-509.Raha D, Wilson TR, Peng J, Peterson D, Yue P, Evangelista M, Wilson C, Merchant M, Settleman J: The cancer stem cell marker aldehyde dehydrogenase is required to maintain a drug-tolerant tumor cell subpopulation. Cancer Res 2014, 74(13):3579-3590.Wilson, K. J., Mill, C., Lambert, S., Buchman, J., Wilson, T. R., Hernandez-Gordillo, V., Gallo, R. M., Ades, L. M., Settleman, J., and Riese, D. J. (2012). EGFR ligands exhibit functional differences in models of paracrine and autocrine signaling. Growth Factors.Wilson, T. R., Lee, D. Y., Berry, L., Shames, D. S., and Settleman, J. (2011). Neuregulin-1-Mediated Autocrine Signaling Underlies Sensitivity to HER2 Kinase Inhibitors in a Subset of Human Cancers. Cancer Cell 20, 158-172. -
Postdoctoral Research FellowMassachusetts General Hospital / Harvard Medical School Sep 2008 - Aug 2010Boston, Ma, UsMentor: Jeff Settleman.Discovery Oncology/ Signal Transduction/ Kinase Addiction -
Postdoctoral Research FellowQueen'S University Belfast Sep 2005 - Aug 2008Belfast, Antrim, GbPublications:Logan, A. E., Wilson, T. R., Fenning, C., Cummins, R., Kay, E., Johnston, P. G., and Longley, D. B. (2010). In vitro and in vivo characterisation of a novel c-FLIP-targeted antisense phosphorothioate oligonucleotide. Apoptosis 15, 1435-1443.Wilson, T. R., Johnston, P. G., and Longley, D. B. (2009). Anti-apoptotic mechanisms of drug resistance in cancer. Curr Cancer Drug Targets 9, 307-319.Wilson, T. R., McEwan, M., McLaughlin, K., Le Clorennec, C., Allen, W. L., Fennell, D. A., Johnston, P. G., and Longley, D. B. (2009). Combined inhibition of FLIP and XIAP induces Bax-independent apoptosis in type II colorectal cancer cells. Oncogene 28, 63-72.Wilson, T. R., Redmond, K. M., McLaughlin, K. M., Crawford, N., Gately, K., O'Byrne, K., Le-Clorrenec, C., Holohan, C., Fennell, D. A., Johnston, P. G., and Longley, D. B. (2009). Procaspase 8 overexpression in non-small-cell lung cancer promotes apoptosis induced by FLIP silencing. Cell Death Differ 16, 1352-1361.Wilson, C., Wilson, T., Johnston, P. G., Longley, D. B., and Waugh, D. J. (2008). Interleukin-8 signaling attenuates TRAIL- and chemotherapy-induced apoptosis through transcriptional regulation of c-FLIP in prostate cancer cells. Mol Cancer Ther 7, 2649-2661.Redmond, K. M., Wilson, T. R., Johnston, P. G., and Longley, D. B. (2008). Resistance mechanisms to cancer chemotherapy. Front Biosci 13, 5138-5154.Rogers, K. M., Thomas, M., Galligan, L., Wilson, T. R., Allen, W. L., Sakai, H., Johnston, P. G., and Longley, D. B. (2007). Cellular FLICE-inhibitory protein regulates chemotherapy-induced apoptosis in breast cancer cells. Mol Cancer Ther 6, 1544-1551.Wilson, T. R., McLaughlin, K. M., McEwan, M., Sakai, H., Rogers, K. M., Redmond, K. M., Johnston, P. G., and Longley, D. B. (2007). c-FLIP: a key regulator of colorectal cancer cell death. Cancer Res 67, 5754-5762.Wilson, T. R., Longley, D. B., and Johnston, P. G. (2006). Chemoresistance in solid tumours. Ann Oncol 17 Suppl 10, x315-324.
Tim Wilson Skills
Tim Wilson Education Details
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Queen'S University BelfastMolecular Oncology -
Ulster UniversityApplied Biochemical Sciences
Frequently Asked Questions about Tim Wilson
What company does Tim Wilson work for?
Tim Wilson works for Revolution Medicines
What is Tim Wilson's role at the current company?
Tim Wilson's current role is Executive Director, Translational Medicine.
What is Tim Wilson's email address?
Tim Wilson's email address is wi****@****ene.com
What schools did Tim Wilson attend?
Tim Wilson attended Queen's University Belfast, Ulster University.
What skills is Tim Wilson known for?
Tim Wilson has skills like Biomarkers, Molecular Biology, Oncology, Signal Transduction, Cell Biology, Cancer Research, Drug Discovery, Biochemistry, Cell, Life Sciences, Biotechnology, Cancer.
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