Telomerase Mutations in Families with Idiopathic Pulmonary FibrosisMary Armanios, James E. Loyd, William E. Lawson et al.|New England Journal of Medicine|2007Cited by 1.4k
<i>ZCCHC8</i>, the nuclear exosome targeting component, is mutated in familial pulmonary fibrosis and is required for telomerase RNA maturationDustin L. Gable, Mary Armanios|Genes & Development|2019Cited by 121
Ancestral Mutation in Telomerase Causes Defects in Repeat Addition Processivity and Manifests As Familial Pulmonary FibrosisJonathan K. Alder, Mary Armanios, Joy D. Cogan et al.|PLoS Genetics|2011Cited by 119
Detection of paroxysmal nocturnal hemoglobinuria clones to exclude inherited bone marrow failure syndromesAmy E. DeZern, Robert A. Brodsky, Mary Armanios et al.|European Journal Of Haematology|2014Cited by 70
Somatic reversion impacts myelodysplastic syndromes and acute myeloid leukemia evolution in the short telomere disordersKristen E. Schratz, Mary Armanios|Journal of Clinical Investigation|2021Cited by 70