Ameloblastoma: A Review of Recent Molecular Pathogenetic Discoveries

由 Brown, Noah A., Betz, Bryan L.
發表在 Biomark Cancer (2015)

In Vivo Imatinib Sensitivity in a Patient With GI Stromal Tumor Bearing a PDGFRA Deletion DIM842-844

由 Fanta, Paul T., Sicklick, Jason K., Betz, Bryan L., Peterson, Michael R.
發表在 J Clin Oncol (2015)

Cutaneous Syncytial Myoepithelioma: A Recently Described Neoplasm Which May Mimic Nevoid Melanoma and Epithelioid Sarcoma

由 Alomari, Ahmed K., Brown, Noah, Andea, Aleodor, Betz, Bryan L., Patel, Rajiv M.
發表在 J Cutan Pathol (2017)

The EGFR T790M mutation is acquired through AICDA-mediated deamination of 5-methylcytosine following TKI treatment in lung cancer.

由 Kadi, Najwa El, Wang, Luo, Davis, April, Korkaya, Hasan, Cooke, Alexander, Vadnala, Varun, Brown, Noah A., Betz, Bryan L., Cascalho, Marilia, Kalemkerian, Gregory P., Hassan, Khaled A.
發表在 Cancer Res (2018)

TP53 Mutations and CDKN2A Mutations/Deletions are Highly Recurrent Molecular Alterations in the Malignant Progression of Sinonasal Papillomas

由 Brown, Noah A., Plouffe, Komal R., Yilmaz, Osman, Weindorf, Steven C., Betz, Bryan L., Carey, Thomas E., Seethala, Raja R., McHugh, Jonathan B., Tomlins, Scott A., Udager, Aaron M.
發表在 Mod Pathol (2020)

Molecular Characterization of a Rare Case of Bilateral Vitreoretinal T Cell Lymphoma through Vitreous Liquid Biopsy

由 Cani, Andi K., Toral, Marcus A., Balikov, Daniel A., Betz, Bryan L., Hu, Kevin, Liu, Chia-Jen, Prifti, Matthew V., Chinnaiyan, Arul M., Tomlins, Scott A., Mahajan, Vinit B., Rao, Rajesh C.
發表在 Int J Mol Sci (2021)

Gemcitabine Plus Radiation Therapy for High Grade Glioma: Long-term Results of a Phase I Dose-Escalation Study

由 Kim, Michelle M., Camelo-Piragua, Sandra, Schipper, Matthew, Tao, Yebin, Normolle, Daniel, Junck, Larry, Mammoser, Aaron, Betz, Bryan L., Cao, Yue, Kim, Christopher J, Heth, Jason, Sagher, Oren, Lawrence, Theodore S, Tsien, Christina I
發表在 Int J Radiat Oncol Biol Phys (2015)

Brainstem Low-Grade Gliomas in Children—Excellent Outcomes With Multimodality Therapy

由 Upadhyaya, Santhosh A., Koschmann, Carl, Muraszko, Karin, Venneti, Sriram, Garton, Hugh J., Hamstra, Daniel A., Maher, Cormac O., Betz, Bryan L., Brown, Noah A., Wahl, Daniel, Weigelin, Helmut C., DuRoss, Kathleen E., Leonard, Annette S., Robertson, Patricia L.
發表在 J Child Neurol (2016)

High frequency targetable EGFR mutations in sinonasal squamous cell carcinomas arising from inverted sinonasal papilloma

由 Udager, Aaron M., Rolland, Delphine C.M., McHugh, Jonathan B., Betz, Bryan L., Murga-Zamalloa, Carlos, Carey, Thomas E., Marentette, Lawrence J., Hermsen, Mario A., DuRoss, Kathleen E., Lim, Megan S., Elenitoba-Johnson, Kojo S. J., Brown, Noah A.
發表在 Cancer Res (2015)

Whole-genome sequencing identifies recurrent somatic NOTCH2 mutations in splenic marginal zone lymphoma

由 Kiel, Mark J., Velusamy, Thirunavukkarasu, Betz, Bryan L., Zhao, Lili, Weigelin, Helmut G., Chiang, Mark Y., Huebner-Chan, David R., Bailey, Nathanael G., Yang, David T., Bhagat, Govind, Miranda, Roberto N., Bahler, David W., Medeiros, L. Jeffrey, Lim, Megan S., Elenitoba-Johnson, Kojo S.J.
出版 2012

Integrated genomic sequencing reveals mutational landscape of T-cell prolymphocytic leukemia

由 Kiel, Mark J., Velusamy, Thirunavukkarasu, Rolland, Delphine, Sahasrabuddhe, Anagh A., Chung, Fuzon, Bailey, Nathanael G., Schrader, Alexandra, Li, Bo, Li, Jun Z., Ozel, Ayse B., Betz, Bryan L., Miranda, Roberto N., Medeiros, L. Jeffrey, Zhao, Lili, Herling, Marco, Lim, Megan S., Elenitoba-Johnson, Kojo S. J.
出版 2014

Genomic analyses reveal recurrent mutations in epigenetic modifiers and the JAK–STAT pathway in Sézary syndrome

由 Kiel, Mark J., Sahasrabuddhe, Anagh A., Rolland, Delphine C. M., Velusamy, Thirunavukkarasu, Chung, Fuzon, Schaller, Matthew, Bailey, Nathanael G., Betz, Bryan L., Miranda, Roberto N., Porcu, Pierluigi, Byrd, John C., Jeffrey Medeiros, L., Kunkel, Steven L., Bahler, David W., Lim, Megan S., Elenitoba-Johnson, Kojo S. J.
發表在 Nat Commun (2015)

TRIM63 is a sensitive and specific biomarker for MiT family aberration-associated renal cell carcinoma

由 Wang, Xiao-Ming, Zhang, Yuping, Mannan, Rahul, Skala, Stephanie L., Rangaswamy, Roshni, Chinnaiyan, Anya, Su, Fengyun, Cao, Xuhong, Zelenka-Wang, Sylvia, McMurry, Lisa, Xiao, Hong, Spratt, Daniel E., Sangoi, Ankur, Shao, Lina, Betz, Bryan L., Brown, Noah, Tickoo, Satish K., McKenney, Jesse K., Argani, Pedram, Gupta, Sounak, Reuter, Victor E., Chinnaiyan, Arul M., Dhanasekaran, Saravana M., Mehra, Rohit
發表在 Mod Pathol (2021)

Development and Validation of a Scalable Next-Generation Sequencing System for Assessing Relevant Somatic Variants in Solid Tumors()()

由 Hovelson, Daniel H., McDaniel, Andrew S., Cani, Andi K., Johnson, Bryan, Rhodes, Kate, Williams, Paul D., Bandla, Santhoshi, Bien, Geoffrey, Choppa, Paul, Hyland, Fiona, Gottimukkala, Rajesh, Liu, Guoying, Manivannan, Manimozhi, Schageman, Jeoffrey, Ballesteros-Villagrana, Efren, Grasso, Catherine S., Quist, Michael J., Yadati, Venkata, Amin, Anmol, Siddiqui, Javed, Betz, Bryan L., Knudsen, Karen E., Cooney, Kathleen A., Feng, Felix Y., Roh, Michael H., Nelson, Peter S., Liu, Chia-Jen, Beer, David G., Wyngaard, Peter, Chinnaiyan, Arul M., Sadis, Seth, Rhodes, Daniel R., Tomlins, Scott A.
發表在 Neoplasia (2015)