Hereditary Predispositions to Myelodysplastic Syndrome von Bannon, Sarah A, DiNardo, Courtney D

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Next-Generation Sequencing of DDX41 in Myeloid Neoplasms Leads to Increased Detection of Germline Alterations von Bannon, Sarah A., Routbort, Mark J., Montalban-Bravo, Guillermo, Mehta, Rohtesh S., Jelloul, Fatima Zahra, Takahashi, Koichi, Daver, Naval, Oran, Betul, Pemmaraju, Naveen, Borthakur, Gautam, Naqvi, Kiran, Issa, Ghayas, Sasaki, Koji, Alvarado, Yesid, Kadia, Tapan M., Konopleva, Marina, Shamanna, Rashmi Kanagal, Khoury, Joseph D., Ravandi, Farhad, Champlin, Richard, Kantarjian, Hagop M., Bhalla, Kapil, Garcia-Manero, Guillermo, Patel, Keyur P., DiNardo, Courtney D.

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Germline DNMT3A mutation in familial acute myeloid leukaemia von DiNardo, Courtney D., Beird, Hannah C., Estecio, Marcos, Hardikar, Swanand, Takahashi, Koichi, Bannon, Sarah A., Borthakur, Gautam, Jabbour, Elias, Gumbs, Curtis, Khoury, Joseph D., Routbort, Mark, Gong, Ting, Kondo, Kimie, Kantarjian, Hagop, Garcia-Manero, Guillermo, Chen, Taiping, Futreal, P. Andrew

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High Prevalence of Hereditary Cancer Syndromes in Adolescents and Young Adults With Colorectal Cancer von Mork, Maureen E, You, Y Nancy, Ying, Jun, Bannon, Sarah A, Lynch, Patrick M, Rodriguez-Bigas, Miguel A, Vilar, Eduardo

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DDX41 mutations in myeloid neoplasms are associated with male gender, TP53 mutations and high‐risk disease von Quesada, Andrés E., Routbort, Mark J., DiNardo, Courtney D., Bueso‐Ramos, Carlos E., Kanagal‐Shamanna, Rashmi, Khoury, Joseph D., Thakral, Beenu, Zuo, Zhuang, Yin, C. Cameron, Loghavi, Sanam, Ok, Chi Y., Wang, Sa A., Tang, Zhenya, Bannon, Sarah A., Benton, Christopher B., Garcia‐Manero, Guillermo, Kantarjian, Hagop, Luthra, Rajyalakshmi, Medeiros, L. Jeffrey, Patel, Keyur P.

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Frequency of Germline BRCA1/2 Mutations in Unselected Patients With Colorectal Cancer von Daniels, Molly S, Bannon, Sarah A, Mork, Maureen E

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Successful lenalidomide treatment in high risk myelodysplastic syndrome with germline DDX41 mutation von Abou Dalle, Iman, Kantarjian, Hagop, Bannon, Sarah A., Kanagal‐Shamanna, Rashmi, Routbort, Mark, Patel, Keyur P., Hu, Shimin, Bhalla, Kapil, Garcia‐Manero, Guillermo, DiNardo, Courtney D.

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Risk assessment and genetic counseling for hematologic malignancies-Practice resource of the National Society of Genetic Counselors von Stewart, Brittany L, Helber, Hannah, Bannon, Sarah A, Deuitch, Natalie T, Ferguson, Meghan, Fiala, Elise, Hamilton, Kayla V, Malcolmson, Janet, Pencheva, Bojana, Smith-Simmer, Kelcy

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Assessing patient attitudes toward genetic testing for hereditary hematologic malignancy von Johnson, Addison Q., Bannon, Sarah A., Farach, Laura S., Hyde, Samuel M., Hashmi, S. Shahrukh, Wagner, Chelsea, DiNardo, Courtney D.

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Improving the detection of patients with inherited predispositions to hematologic malignancies using next‐generation sequencing‐based leukemia prognostication panels von DiNardo, Courtney D., Routbort, Mark J., Bannon, Sarah A., Benton, Christopher B., Takahashi, Koichi, Kornblau, Steve M., Luthra, Rajyalakshmi, Kanagal‐Shamanna, Rashmi, Medeiros, L. Jeffrey, Garcia‐Manero, Guillermo, M. Kantarjian, Hagop, Futreal, P. Andrew, Meric‐Bernstam, Funda, Patel, Keyur P.

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Can Microsatellite Status of Colorectal Cancer Be Reliably Assessed after Neoadjuvant Therapy? von Goldstein, Jennifer B, Wu, William, Borras, Ester, Masand, Gita, Cuddy, Amanda, Mork, Maureen E, Bannon, Sarah A, Lynch, Patrick M, Rodriguez-Bigas, Miguel, Taggart, Melissa W, Wu, Ji, Scheet, Paul, Kopetz, Scott, You, Y Nancy, Vilar, Eduardo

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High Prevalence of Hereditary Cancer Syndromes and Outcomes in Adults with Early-Onset Pancreatic Cancer von Bannon, Sarah A, Montiel, Maria F, Goldstein, Jennifer B, Dong, Wenli, Mork, Maureen E, Borras, Ester, Hasanov, Merve, Varadhachary, Gauri R, Maitra, Anirban, Katz, Matthew H, Feng, Lei, Futreal, Andrew, Fogelman, David R, Vilar, Eduardo, McAllister, Florencia

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Evaluation of patients and families with concern for predispositions to hematologic malignancies within the Hereditary Hematologic Malignancy Clinic (HHMC) von DiNardo, Courtney D, Bannon, Sarah A, Routbort, Mark, Franklin, Anna, Mork, Maureen, Armanios, Mary, Mace, Emily M, Orange, Jordan S, Jeff-Eke, Meselle, Churpek, Jane E, Takahashi, Koichi, Jorgensen, Jeffrey L, Garcia-Manero, Guillermo, Kornblau, Steve, Bertuch, Alison, Cheung, Hannah, Bhalla, Kapil, Futreal, Andrew, Godley, Lucy A, Patel, Keyur P

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Hematologic malignancies and Li-Fraumeni syndrome von Swaminathan, Mahesh, Bannon, Sarah A, Routbort, Mark, Naqvi, Kiran, Kadia, Tapan M, Takahashi, Koichi, Alvarado, Yesid, Ravandi-Kashani, Farhad, Patel, Keyur P, Champlin, Richard, Kantarjian, Hagop, Strong, Louise, DiNardo, Courtney D

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Outcomes of disease-specific next-generation sequencing gene panel testing in adolescents and young adults with colorectal cancer von Mork, Maureen E., Rodriguez, Andrea, Bannon, Sarah A., Lynch, Patrick M., Rodriguez-Bigas, Miguel A., Thirumurthi, Selvi, You, Y. Nancy, Vilar, Eduardo

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In Silico Systems Biology Analysis of Variants of Uncertain Significance in Lynch Syndrome Supports the Prioritization of Functional Molecular Validation von Borras, Ester, Chang, Kyle, Pande, Mala, Cuddy, Amanda, Bosch, Jennifer L, Bannon, Sarah A, Mork, Maureen E, Rodriguez-Bigas, Miguel A, Taggart, Melissa W, Lynch, Patrick M, You, Y Nancy, Vilar, Eduardo

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Comparison of attitudes regarding preimplantation genetic diagnosis among patients with hereditary cancer syndromes von Rich, Thereasa A., Liu, Mei, Etzel, Carol J., Bannon, Sarah A., Mork, Maureen E., Ready, Kaylene, Saraiya, Devki S., Grubbs, Elizabeth G., Perrier, Nancy D., Lu, Karen H., Arun, Banu K., Woodard, Terri L., Schover, Leslie R., Litton, Jennifer K.

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Identification of MSH2 inversion of exons 1–7 in clinical evaluation of families with suspected Lynch syndrome von Mork, Maureen E., Rodriguez, Andrea, Taggart, Melissa W., Rodriguez-Bigas, Miguel A., Lynch, Patrick M., Bannon, Sarah A., You, Y. Nancy, Vilar, Eduardo

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Cancer spectrum in DNA mismatch repair gene mutation carriers: results from a hospital based Lynch syndrome registry von Pande, Mala, Wei, Chongjuan, Chen, Jinyun, Amos, Christopher I., Lynch, Patrick M., Lu, Karen H., Lucio, Laura A., Boyd-Rogers, Stephanie G., Bannon, Sarah A., Mork, Maureen E., Frazier, Marsha L.

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Mo1111 Completion of Follow-up After Abnormal Screening Test for Lynch Syndrome: A Framework for Multi-Level Cancer Care Delivery von You, Y. Nancy, Vilar, Eduardo, Mork, Maureen E, Bannon, Sarah A, Patel, Sameer H, Egger, Michael E, Holder, Ashley, Chang, George J, Bednarski, Brian K, Messick, Craig A, Feig, Barry W, Skibber, John M, Lynch, Patrick M, Rodriguez-Bigas, Miguel A

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