Aplastic anemia and clonal evolution: germ line and somatic genetics von Shimamura, Akiko

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Genetic predisposition to MDS: clinical features and clonal evolution von Kennedy, Alyssa L., Shimamura, Akiko

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Germline Genetic Predisposition to Hematologic Malignancy von Furutani, Elissa, Shimamura, Akiko

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CLONAL HEMATOPOIESIS IN SHWACHMAN DIAMOND SYNDROME: BIOLOGY AND CLINICAL IMPLICATIONS von Shimamura, Akiko

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Genetic predisposition to hematologic malignancies: management and surveillance von Godley, Lucy A., Shimamura, Akiko

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Pathophysiology and management of inherited bone marrow failure syndromes von Shimamura, Akiko, Alter, Blanche P

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Lessons From Pediatric MDS: Approaches to Germline Predisposition to Hematologic Malignancies von Avagyan, Serine, Shimamura, Akiko

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Recent discoveries in the molecular pathogenesis of the inherited bone marrow failure syndrome Fanconi anemia von Mamrak, Nicholas E, Shimamura, Akiko, Howlett, Niall G

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Disease-Specific Induced Pluripotent Stem Cells von Park, In-Hyun, Arora, Natasha, Huo, Hongguang, Maherali, Nimet, Ahfeldt, Tim, Shimamura, Akiko, Lensch, M. William, Cowan, Chad, Hochedlinger, Konrad, Daley, George Q.

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Distinct genetic pathways define pre-malignant versus compensatory clonal hematopoiesis in Shwachman-Diamond syndrome von Kennedy, Alyssa L., Myers, Kasiani C., Bowman, James, Gibson, Christopher J., Camarda, Nicholas D., Furutani, Elissa, Muscato, Gwen M., Klein, Robert H., Ballotti, Kaitlyn, Liu, Shanshan, Harris, Chad E., Galvin, Ashley, Malsch, Maggie, Dale, David, Gansner, John M., Nakano, Taizo A., Bertuch, Alison, Vlachos, Adrianna, Lipton, Jeffrey M., Castillo, Paul, Connelly, James, Churpek, Jane, Edwards, John R., Hijiya, Nobuko, Ho, Richard H., Hofmann, Inga, Huang, James N., Keel, Siobán, Lamble, Adam, Lau, Bonnie W., Norkin, Maxim, Stieglitz, Elliot, Stock, Wendy, Walkovich, Kelly, Boettcher, Steffen, Brendel, Christian, Fleming, Mark D., Davies, Stella M., Weller, Edie A., Bahl, Christopher, Carter, Scott L., Shimamura, Akiko, Lindsley, R. Coleman

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Variable Clinical Presentation of Shwachman–Diamond Syndrome: Update from the North American Shwachman–Diamond Syndrome Registry von Myers, Kasiani C., MD, Bolyard, Audrey Anna, RN, BS, Otto, Barbara, MN, MS, Wong, Trisha E., MD, MS, Jones, Amanda T, Harris, Richard E., MD, Davies, Stella M., MBBS, PhD, Dale, David C., MD, Shimamura, Akiko, MD, PhD

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Germline ETV6 mutations in familial thrombocytopenia and hematologic malignancy von Zhang, Michael Y, Churpek, Jane E, Keel, Siobán B, Walsh, Tom, Lee, Ming K, Loeb, Keith R, Gulsuner, Suleyman, Pritchard, Colin C, Sanchez-Bonilla, Marilyn, Delrow, Jeffrey J, Basom, Ryan S, Forouhar, Melissa, Gyurkocza, Boglarka, Schwartz, Bradford S, Neistadt, Barbara, Marquez, Rafael, Mariani, Christopher J, Coats, Scott A, Hofmann, Inga, Lindsley, R Coleman, Williams, David A, Abkowitz, Janis L, Horwitz, Marshall S, King, Mary-Claire, Godley, Lucy A, Shimamura, Akiko

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Ataxia-Pancytopenia Syndrome Is Caused by Missense Mutations in SAMD9L von Chen, Dong-Hui, Below, Jennifer E., Shimamura, Akiko, Keel, Sioban B., Matsushita, Mark, Wolff, John, Sul, Youngmee, Bonkowski, Emily, Castella, Maria, Taniguchi, Toshiyasu, Nickerson, Deborah, Papayannopoulou, Thalia, Bird, Thomas D., Raskind, Wendy H.

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Genetic features of myelodysplastic syndrome and aplastic anemia in pediatric and young adult patients von Keel, Siobán B, Scott, Angela, Sanchez-Bonilla, Marilyn, Ho, Phoenix A, Gulsuner, Suleyman, Pritchard, Colin C, Abkowitz, Janis L, King, Mary-Claire, Walsh, Tom, Shimamura, Akiko

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Constitutional SAMD9L mutations cause familial myelodysplastic syndrome and transient monosomy 7 von Pastor, Victor B, Sahoo, Sushree S, Boklan, Jessica, Schwabe, Georg C, Saribeyoglu, Ebru, Strahm, Brigitte, Lebrecht, Dirk, Voss, Matthias, Bryceson, Yenan T, Erlacher, Miriam, Ehninger, Gerhard, Niewisch, Marena, Schlegelberger, Brigitte, Baumann, Irith, Achermann, John C, Shimamura, Akiko, Hochrein, Jochen, Tedgård, Ulf, Nilsson, Lars, Hasle, Henrik, Boerries, Melanie, Busch, Hauke, Niemeyer, Charlotte M, Wlodarski, Marcin W

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Clinical approach to marrow failure von Shimamura, Akiko

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The ASPHO 2024 Distinguished Career Award goes to Dr. David A. Williams von Shimamura, Akiko

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Somatic mutations and clonal hematopoiesis in congenital neutropenia von Xia, Jun, Miller, Christopher A., Baty, Jack, Ramesh, Amrita, Jotte, Matthew R.M., Fulton, Robert S., Vogel, Tiphanie P., Cooper, Megan A., Walkovich, Kelly J., Makaryan, Vahagn, Bolyard, Audrey A., Dinauer, Mary C., Wilson, David B., Vlachos, Adrianna, Myers, Kasiani C., Rothbaum, Robert J., Bertuch, Alison A., Dale, David C., Shimamura, Akiko, Boxer, Laurence A., Link, Daniel C.

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On-chip recapitulation of clinical bone marrow toxicities and patient-specific pathophysiology von Chou, David B., Frismantas, Viktoras, Milton, Yuka, David, Rhiannon, Pop-Damkov, Petar, Ferguson, Douglas, MacDonald, Alexander, Vargel Bölükbaşı, Özge, Joyce, Cailin E., Moreira Teixeira, Liliana S., Rech, Arianna, Jiang, Amanda, Calamari, Elizabeth, Jalili-Firoozinezhad, Sasan, Furlong, Brooke A., O’Sullivan, Lucy R., Ng, Carlos F., Choe, Youngjae, Marquez, Susan, Myers, Kasiani C., Weinberg, Olga K., Hasserjian, Robert P., Novak, Richard, Levy, Oren, Prantil-Baun, Rachelle, Novina, Carl D., Shimamura, Akiko, Ewart, Lorna, Ingber, Donald E.

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Pulmonary arteriovenous malformations: an uncharacterised phenotype of dyskeratosis congenita and related telomere biology disorders von Khincha, Payal P, Bertuch, Alison A, Agarwal, Suneet, Townsley, Danielle M, Young, Neal S, Keel, Siobán, Shimamura, Akiko, Boulad, Farid, Simoneau, Tregony, Justino, Henri, Kuo, Christin, Artandi, Steven, McCaslin, Charles, Cox, Des W, Chaffee, Sara, Collins, Bridget F, Giri, Neelam, Alter, Blanche P, Raghu, Ganesh, Savage, Sharon A

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