Exome Sequencing Identifies Mutant TINF2 in a Family With Pulmonary Fibrosis

Por Alder, Jonathan K., Stanley, Susan E., Wagner, Christa L., Hamilton, Makenzie, Hanumanthu, Vidya Sagar, Armanios, Mary
Publicado no Chest (2015)

Telomere phenotypes in females with heterozygous mutations in the dyskeratosis congenita 1 (DKC1) gene

Por Alder, Jonathan K., Parry, Erin M., Yegnasubramanian, Srinivasan, Wagner, Christa L., Lieblich, Lawrence M., Auerbach, Robert, Auerbach, Arleen D., Wheelan, Sarah J., Armanios, Mary
Publicado em 2013

Lung transplantation in telomerase mutation carriers with pulmonary fibrosis

Por Silhan, Leann L., Shah, Pali D., Chambers, Daniel C., Snyder, Laurie D., Riise, Gerdt C., Wagner, Christa L., Hellström-Lindberg, Eva, Orens, Jonathan B., Mewton, Juliette F., Danoff, Sonye K., Arcasoy, Murat O., Armanios, Mary
Publicado em 2014

Loss-of-function mutations in the RNA biogenesis factor NAF1 predispose to pulmonary fibrosis–emphysema

Por Stanley, Susan E., Gable, Dustin L., Wagner, Christa L., Carlile, Thomas M., Hanumanthu, Vidya Sagar, Podlevsky, Joshua D., Khalil, Sara E., DeZern, Amy E., Rojas-Duran, Maria F., Applegate, Carolyn D., Alder, Jonathan K., Parry, Erin M., Gilbert, Wendy V., Armanios, Mary
Publicado no Sci Transl Med (2016)