Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort

por Altintas, Burak, Giri, Neelam, McReynolds, Lisa J., Best, Ana, Alter, Blanche P.
Publicado 2022

Gata2 deficiency delays leukemogenesis while contributing to aggressive leukemia phenotype in Cbfb-MYH11 knockin mice

por Saida, Satoshi, Zhen, Tao, Kim, Erika, Yu, Kai, Lopez, Guadalupe, McReynolds, Lisa J, Liu, Paul P
Publicado 2019

Shwachman Diamond Syndrome: Narrow Genotypic Spectrum and Variable Clinical Features

por Thompson, Ashley S., Giri, Neelam, Gianferante, D. Matthew, Jones, Kristine, Savage, Sharon A., Alter, Blanche P., McReynolds, Lisa J.
Publicado 2022

Dyskeratosis congenita with a novel genetic variant in the DKC1 gene: a case report

por Ratnasamy, Vithiya, Navaneethakrishnan, Suganthan, Sirisena, Nirmala Dushyanthi, Grüning, Nana-Maria, Brandau, Oliver, Thirunavukarasu, Kumanan, Dagnall, Casey L., McReynolds, Lisa J., Savage, Sharon A., Dissanayake, Vajira H. W.
Publicado 2018

The causes of Fanconi anemia in South Asia and the Middle East: A case series and review of the literature

por Thompson, Ashley S., Saba, Nusrat, McReynolds, Lisa J., Munir, Saeeda, Ahmed, Parvez, Sajjad, Sumaira, Jones, Kristine, Yeager, Meredith, Donovan, Frank X., Chandrasekharappa, Settara C., Alter, Blanche P., Savage, Sharon A., Rehman, Sadia
Publicado 2021

Rapid progression to AML in a patient with germline GATA2 mutation and acquired NRAS Q61K mutation

por McReynolds, Lisa J., Zhang, Yubo, Yang, Yanqin, Tang, Jingrong, Mulé, Matthew, Hsu, Amy P., Townsley, Danielle M., West, Robert R., Zhu, Jun, Hickstein, Dennis D., Holland, Steven M., Calvo, Katherine R., Hourigan, Christopher S.
Publicado 2019

Prognostic impact of pre-transplant chromosomal aberrations in peripheral blood of patients undergoing unrelated donor hematopoietic cell transplant for acute myeloid leukemia

por Wang, Youjin, Zhou, Weiyin, McReynolds, Lisa J., Katki, Hormuzd A., Griffiths, Elizabeth A., Thota, Swapna, Machiela, Mitchell J., Yeager, Meredith, McCarthy, Philip, Pasquini, Marcelo, Wang, Junke, Karaesmen, Ezgi, Rizvi, Abbas, Preus, Leah, Tang, Hancong, Wang, Yiwen, Pooler, Loreall, Sheng, Xin, Haiman, Christopher A., Van Den Berg, David, Spellman, Stephen R., Wang, Tao, Kuxhausen, Michelle, Chanock, Stephen J., Lee, Stephanie J., Hahn, Theresa E., Sucheston-Campbell, Lara E., Gadalla, Shahinaz M.
Publicado 2021

Prevalence of pathogenic/likely pathogenic variants in the 24 cancer genes of the ACMG Secondary Findings v2.0 list in a large cancer cohort and ethnicity-matched controls

por Kim, Jung, Luo, Wen, Wang, Mingyi, Wegman-Ostrosky, Talia, Frone, Megan N., Johnston, Jennifer J., Nickerson, Michael L., Rotunno, Melissa, Li, Shengchao A., Achatz, Maria I., Brodie, Seth A., Dean, Michael, de Andrade, Kelvin C., Fortes, Fernanda P., Gianferante, Matthew, Khincha, Payal, McMaster, Mary L., McReynolds, Lisa J., Pemov, Alexander, Pinheiro, Maisa, Santiago, Karina M., Alter, Blanche P., Caporaso, Neil E., Gadalla, Shahinaz M., Goldin, Lynn R., Greene, Mark H., Loud, Jennifer, Yang, Xiaohong R., Freedman, Neal D., Gapstur, Susan M., Gaudet, Mia M., Calista, Donato, Ghiorzo, Paola, Fargnoli, Maria Concetta, Nagore, Eduardo, Peris, Ketty, Puig, Susana, Landi, Maria Teresa, Hicks, Belynda, Zhu, Bin, Liu, Jia, Sampson, Joshua N., Chanock, Stephen J., Mirabello, Lisa J., Morton, Lindsay M., Biesecker, Leslie G., Tucker, Margaret A., Savage, Sharon A., Goldstein, Alisa M., Stewart, Douglas R.
Publicado 2018