Mary Armanios
Affiliations: | Sidney Kimmel Comprehensive Cancer Center | Johns Hopkins University, Baltimore, MD |
Website:
http://www.jhkcc.net/index.cfm/cID/1686/mpage/expertdata.cfm/expID/473Google:
"Mary Armanios"
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Publications
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| DeBoy EA, Tassia MG, Schratz KE, et al. (2023) Familial Clonal Hematopoiesis in a Long Telomere Syndrome. The New England Journal of Medicine |
| Armanios M. (2022) The Role of Telomeres in Human Disease. Annual Review of Genomics and Human Genetics |
| Alder JK, Armanios M. (2022) Telomere-mediated Lung Disease. Physiological Reviews |
| Taub MA, Conomos MP, Keener R, et al. (2022) Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed. Cell Genomics. 2 |
| Schratz KE, Gaysinskaya V, Cosner ZL, et al. (2021) Somatic reversion impacts evolution of myelodysplastic syndromes and acute myeloid leukemia in the short telomere disorders. The Journal of Clinical Investigation |
| Oseini AM, Hamilton JP, Hammam MB, et al. (2021) Liver transplantation in short-telomere-mediated hepatopulmonary syndrome following bone marrow transplantion, using HCV positive allografts: a case series. Liver Transplantation : Official Publication of the American Association For the Study of Liver Diseases and the International Liver Transplantation Society |
| Gaysinskaya V, Stanley SE, Adam S, et al. (2020) Synonymous mutation in DKC1 causes telomerase RNA insufficiency manifesting as familial pulmonary fibrosis. Chest |
| Schratz KE, Armanios M. (2020) Cancer and myeloid clonal evolution in the short telomere syndromes. Current Opinion in Genetics & Development. 60: 112-118 |
| Schratz KE, Haley L, Danoff SK, et al. (2020) Cancer spectrum and outcomes in the Mendelian short telomere syndromes. Blood |
| Gable DL, Gaysinskaya V, Atik CC, et al. (2019) , the nuclear exosome targeting component, is mutated in familial pulmonary fibrosis and is required for telomerase RNA maturation. Genes & Development |