A Phase II Trial of Dovitinib in BCG-Unresponsive Urothelial Carcinoma with FGFR3 Mutations or Overexpression: Hoosier Cancer Research Network Trial HCRN 12-157 von Hahn, Noah M, Bivalacqua, Trinity J, Ross, Ashley E, Netto, George J, Baras, Alex, Park, Jong Chul, Chapman, Carolyn, Masterson, Timothy A, Koch, Michael O, Bihrle, Richard, Foster, Richard S, Gardner, Thomas A, Cheng, Liang, Jones, David R, McElyea, Kyle, Sandusky, George E, Breen, Timothy, Liu, Ziyue, Albany, Costantine, Moore, Marietta L, Loman, Rhoda L, Reed, Angela, Turner, Scott A, De Abreu, Francine B, Gallagher, Torrey, Tsongalis, Gregory J, Plimack, Elizabeth R, Greenberg, Richard E, Geynisman, Daniel M

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Implementation of a Molecular Tumor Board: The Impact on Treatment Decisions for 35 Patients Evaluated at Dartmouth‐Hitchcock Medical Center von Tafe, Laura J., Gorlov, Ivan P., Abreu, Francine B., Lefferts, Joel A., Liu, Xiaoying, Pettus, Jason R., Marotti, Jonathan D., Bloch, Kasia J., Memoli, Vincent A., Suriawinata, Arief A., Dragnev, Konstantin H., Fadul, Camilo E., Schwartz, Gary N., Morgan, Clinton R., Holderness, Britt M., Peterson, Jason D., Tsongalis, Gregory J., Miller, Todd W., Chamberlin, Mary D.

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Synchronous Pulmonary Adenofibroma and Solitary Fibrous Tumor: Case Report and Review of the Literature von Olson, Nicholas J., Czum, Julianna M., de Abreu, Francine B., Linos, Konstantinos, Black, Candice C.

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Molecular profiling of appendiceal epithelial tumors using massively parallel sequencing to identify somatic mutations von Liu, Xiaoying, Mody, Kabir, de Abreu, Francine B, Pipas, J Marc, Peterson, Jason D, Gallagher, Torrey L, Suriawinata, Arief A, Ripple, Gregory H, Hourdequin, Kathryn C, Smith, Kerrington D, Barth, Jr, Richard J, Colacchio, Thomas A, Tsapakos, Michael J, Zaki, Bassem I, Gardner, Timothy B, Gordon, Stuart R, Amos, Christopher I, Wells, Wendy A, Tsongalis, Gregory J

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The Emerging Role of the Molecular Diagnostics Laboratory in Breast Cancer Personalized Medicine von De Abreu, Francine B, Wells, Wendy A, Tsongalis, Gregory J

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Central xanthoma of the jaw in association with Noonan syndrome von Olson, Nicholas J., Addante, Rocco R., de Abreu, Francine B., Memoli, Vincent A.

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Improving Adequacy of Small Biopsy and Fine-Needle Aspiration Specimens for Molecular Testing by Next-Generation Sequencing in Patients With Lung Cancer: A Quality Improvement Stud... von Padmanabhan, Vijayalakshmi, Steinmetz, Heather B, Rizzo, Elizabeth J, Erskine, Amber J, Fairbank, Tamara L, de Abreu, Francine B, Tsongalis, Gregory J, Tafe, Laura J

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Impact of Molecular Sequencing Information as Related to 2008 and 2016 World Health Organization Classification of Acute Myeloid Leukemia and Myelodysplasia von Toth, Laura N, de Abreu, Francine B, Peterson, Jason D, Loo, Eric Y

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Effective quality management practices in routine clinical next-generation sequencing von de Abreu, Francine B., Peterson, Jason D., Amos, Christopher I., Wells, Wendy A., Tsongalis, Gregory J.

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Somatic mutation analysis in melanoma using targeted next generation sequencing von Miraflor, Allen P., de Abreu, Francine B., Peterson, Jason D., Turner, Scott A., Amos, Christopher I., Tsongalis, Gregory J., Yan, Shaofeng

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Identification of Somatic Mutations in Acute Myeloid Leukemia Patients Using the TruSight Myeloid Sequencing Panel von Gardner, Juli-Anne, Abreu, Francine de, Peterson, Jason, Tsongalis, Gregory, Kaur, Prabhjot

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Rat-bite fever: An uncommon cause of fever and rash in a 9-year-old patient von Miraflor, Allen P., Davallow Ghajar, Ladan, Subramaniam, Sathyaseelan, de Abreu, Francine B., Castanedo-Tardan, Mari Paz, Samie, Faramarz H., Mann, Julianne Anderson, Holmes, Alison Volpe, Tsongalis, Gregory J., Yan, Shaofeng

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Detection of CALR Mutation in Clonal and Nonclonal Hematologic Diseases Using Fragment Analysis and Next-Generation Sequencing von Gardner, Juli-Anne, Peterson, Jason D., Turner, Scott A., Soares, Barbara L., Lancor, Courtney R., dos Santos, Luciana L., Kaur, Prabhjot, Ornstein, Deborah L., Tsongalis, Gregory J., de Abreu, Francine B.

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Targeted next-generation sequencing detects a high frequency of potentially actionable mutations in metastatic breast cancers von Muller, Kristen E., Marotti, Jonathan D., de Abreu, Francine B., Peterson, Jason D., Miller, Todd W., Chamberlin, Mary D., Tsongalis, Gregory J., Tafe, Laura J.

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Clinical Genotyping of Non–Small Cell Lung Cancers Using Targeted Next-Generation Sequencing: Utility of Identifying Rare and Co-mutations in Oncogenic Driver Genes von Tafe, Laura J, Pierce, Kirsten J, Peterson, Jason D, de Abreu, Francine, Memoli, Vincent A, Black, Candice C, Pettus, Jason R, Marotti, Jonathan D, Gutmann, Edward J, Liu, Xiaoying, Shirai, Keisuke, Dragnev, Konstantin H, Amos, Christopher I, Tsongalis, Gregory J

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The first pancreatic neuroendocrine tumor in Li-Fraumeni syndrome: a case report von Aversa, John G., De Abreu, Francine Blumental, Yano, Sho, Xi, Liqiang, Hadley, Donald W., Manoli, Irini, Raffeld, Mark, Sadowski, Samira M., Nilubol, Naris

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The Pitfalls of Companion Diagnostics: Evaluation of Discordant EGFR Mutation Results from a Clinical Laboratory and a Central Laboratory von Turner, Scott A, Peterson, Jason D, Pettus, Jason R, de Abreu, Francine B, Amos, Christopher I, Dragnev, Konstantin H, Tsongalis, Gregory J

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Recurrent copy number gains of ACVR1 and corresponding transcript overexpression are associated with survival in head and neck squamous cell carcinomas von Ambrosio, Eliane P, Drigo, Sandra A, Bérgamo, Nádia A, Rosa, Fabíola E, Bertonha, Fernanda B, de Abreu, Francine B, Kowalski, Luis P, Rogatto, Silvia R

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Frequency of Somatic TP53 Mutations in Combination With Known Pathogenic Mutations as Identified by Next-Generation Sequencing von Shajani-Yi, Zahra, De Abreu, Francine, Peterson, Jason, Tsongalis, Gregory

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Triple-Negative Breast Cancer von Marotti, Jonathan D., de Abreu, Francine B., Wells, Wendy A., Tsongalis, Gregory J.

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