Mary Armanios - Publications

Affiliations: 
Sidney Kimmel Comprehensive Cancer Center Johns Hopkins University, Baltimore, MD 
Website:
http://www.jhkcc.net/index.cfm/cID/1686/mpage/expertdata.cfm/expID/473

44 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Schratz KE, Gaysinskaya V, Cosner ZL, DeBoy EA, Xiang Z, Kasch-Semenza L, Florea L, Shah PD, Armanios M. Somatic reversion impacts evolution of myelodysplastic syndromes and acute myeloid leukemia in the short telomere disorders. The Journal of Clinical Investigation. PMID 34343137 DOI: 10.1172/JCI147598  0.317
2021 Oseini AM, Hamilton JP, Hammam MB, Kim A, Oshima K, Woreta T, Rizkalla N, Pustavoitau A, Merlo C, Nguyen MC, King EA, Wesson RN, Garonzik-Wang J, Ottman S, Philosophe B, ... ... Armanios M, et al. 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. PMID 34043865 DOI: 10.1002/lt.26109  0.308
2020 Schratz KE, Haley L, Danoff SK, Blackford A, DeZern A, Gocke CD, Duffield AS, Armanios M. Cancer spectrum and outcomes in the Mendelian short telomere syndromes. Blood. PMID 32076714 DOI: 10.1182/Blood.2019003264  0.448
2019 Gable DL, Gaysinskaya V, Atik CC, Talbot CC, Kang B, Stanley SE, Pugh EW, Amat-Codina N, Schenk KM, Arcasoy MO, Brayton C, Florea L, Armanios M. , the nuclear exosome targeting component, is mutated in familial pulmonary fibrosis and is required for telomerase RNA maturation. Genes & Development. PMID 31488579 DOI: 10.1101/Gad.326785.119  0.44
2019 McNally EJ, Luncsford PJ, Armanios M. Long telomeres and cancer risk: the price of cellular immortality. The Journal of Clinical Investigation. 130. PMID 31380804 DOI: 10.1172/Jci120851  0.431
2019 Lakota K, Hanumanthu VS, Agrawal R, Carns M, Armanios M, Varga J. Short lymphocyte, but not granulocyte, telomere length in a subset of patients with systemic sclerosis. Annals of the Rheumatic Diseases. PMID 30679155 DOI: 10.1136/Annrheumdis-2018-214499  0.436
2018 Wagner CL, Hanumanthu VS, Talbot CC, Abraham RS, Hamm D, Gable DL, Kanakry CG, Applegate CD, Siliciano J, Jackson JB, Desiderio SV, Alder JK, Luznik L, Armanios M. Short telomere syndromes cause a primary T cell immunodeficiency. The Journal of Clinical Investigation. PMID 30179220 DOI: 10.1172/Jci120216  0.368
2018 Higgs C, Crow YJ, Adams DM, Chang E, Hayes D, Herbig U, Huang JN, Himes R, Jajoo K, Johnson FB, Reynolds SD, Yonekawa Y, Armanios M, Boulad F, DiNardo CD, et al. Understanding the evolving phenotype of vascular complications in telomere biology disorders. Angiogenesis. PMID 30168024 DOI: 10.1007/S10456-018-9640-7  0.33
2018 Alder JK, Hanumanthu VS, Strong MA, DeZern AE, Stanley SE, Takemoto CM, Danilova L, Applegate CD, Bolton SG, Mohr DW, Brodsky RA, Casella JF, Greider CW, Jackson JB, Armanios M. Diagnostic utility of telomere length testing in a hospital-based setting. Proceedings of the National Academy of Sciences of the United States of America. PMID 29463756 DOI: 10.1073/Pnas.1720427115  0.657
2017 Alvarez D, Cardenes N, Sellares J, Bueno M, Corey C, Hanumanthu VS, Peng Y, D'Cuhna H, Sembrat J, Nouraie M, Shanker S, Caufield C, Shiva S, Armanios M, Mora AL, et al. IPF lung fibroblasts have a senescent phenotype. American Journal of Physiology. Lung Cellular and Molecular Physiology. ajplung.00220.2017. PMID 28860144 DOI: 10.1152/Ajplung.00220.2017  0.334
2017 Budinger GS, Kohanski RA, Gan W, Kobor MS, Amaral LA, Armanios M, Kelsey KT, Pardo A, Tuder R, Macian F, Chandel N, Vaughan D, Rojas M, Mora AL, Kovacs E, et al. The Intersection Of Aging Biology and The Pathobiology of Lung Diseases: A Joint NHLBI/NIA Workshop. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. PMID 28498894 DOI: 10.1093/Gerona/Glx090  0.318
2017 Lee M, Roos P, Sharma N, Atalar M, Evans TA, Pellicore MJ, Davis E, Lam AN, Stanley SE, Khalil SE, Solomon GM, Walker D, Raraigh KS, Vecchio-Pagan B, Armanios M, et al. Systematic Computational Identification of Variants That Activate Exonic and Intronic Cryptic Splice Sites. American Journal of Human Genetics. 100: 751-765. PMID 28475858 DOI: 10.1016/J.Ajhg.2017.04.001  0.314
2016 Parry EM, Alder JK, Qi X, Chen J, Armanios M. Erratum: Syndrome complex of bone marrow failure and pulmonary fibrosis predicts germline defects in telomerase (Blood (2011) 117:21 (5607-5611)) Blood. 127. PMID 31265491 DOI: 10.1182/Blood-2016-02-700880  0.541
2016 Bhatt N, Ghosh R, Roy S, Gao Y, Armanios M, Cheng L, Franco S. Integration-free erythroblast-derived human induced pluripotent stem cells (iPSCs) from an individual with Ataxia-Telangiectasia (A-T). Stem Cell Research. 17: 205-207. PMID 27879207 DOI: 10.1016/J.Scr.2016.08.003  0.367
2016 Bhatt N, Ghosh R, Roy S, Gao Y, Armanios M, Cheng L, Franco S. Robust reprogramming of Ataxia-Telangiectasia patient and carrier erythroid cells to induced pluripotent stem cells. Stem Cell Research. 17: 296-305. PMID 27596957 DOI: 10.1016/J.Scr.2016.08.006  0.36
2016 Stanley SE, Gable DL, Wagner CL, Carlile TM, Hanumanthu VS, Podlevsky JD, Khalil SE, DeZern AE, Rojas-Duran MF, Applegate CD, Alder JK, Parry EM, Gilbert WV, Armanios M. Loss-of-function mutations in the RNA biogenesis factor NAF1 predispose to pulmonary fibrosis-emphysema. Science Translational Medicine. 8: 351ra107. PMID 27510903 DOI: 10.1126/Scitranslmed.Aaf7837  0.445
2016 DiNardo CD, Bannon SA, Routbort M, Franklin A, Mork M, Armanios M, Mace EM, Orange JS, Jeff-Eke M, Churpek JE, Takahashi K, Jorgensen JL, Garcia-Manero G, Kornblau S, Bertuch A, et al. Evaluation of Patients and Families With Concern for Predispositions to Hematologic Malignancies Within the Hereditary Hematologic Malignancy Clinic (HHMC). Clinical Lymphoma, Myeloma & Leukemia. PMID 27210295 DOI: 10.1016/J.Clml.2016.04.001  0.308
2016 You J, Sobreira NL, Gable DL, Jurgens J, Grange DK, Belnap N, Siniard A, Szelinger S, Schrauwen I, Richholt RF, Vallee SE, Dinulos MB, Valle D, Armanios M, Hoover-Fong J. A Syndromic Intellectual Disability Disorder Caused by Variants in TELO2, a Gene Encoding a Component of the TTT Complex. American Journal of Human Genetics. PMID 27132593 DOI: 10.1016/J.Ajhg.2016.03.014  0.333
2016 Felgentreff K, Baxi SN, Lee YN, Dobbs K, Henderson LA, Csomos K, Tsitsikov EN, Armanios M, Walter JE, Notarangelo LD. Ligase-4 Deficiency Causes Distinctive Immune Abnormalities in Asymptomatic Individuals. Journal of Clinical Immunology. PMID 27063650 DOI: 10.1007/S10875-016-0266-5  0.318
2016 Alvarez D, Cardenes N, Corey C, Hanumanthu V, D'Cunha H, Bueno M, Sembrat J, Armanios M, Mora A, Rojas M. Fibroblasts from IPF explanted lungs have mitochondrial dysfunction and short telomeres leading to an increased senescence phenotype European Respiratory Journal. 48. DOI: 10.1183/13993003.Congress-2016.Pa777  0.346
2015 Stanley SE, Rao AD, Gable DL, McGrath-Morrow S, Armanios M. Radiation Sensitivity and Radiation Necrosis in the Short Telomere Syndromes. International Journal of Radiation Oncology, Biology, Physics. 93: 1115-7. PMID 26581148 DOI: 10.1016/J.Ijrobp.2015.08.048  0.437
2015 Armanios M, Greider CW. Treating Myeloproliferation--On Target or Off? The New England Journal of Medicine. 373: 965-6. PMID 26332552 DOI: 10.1056/Nejme1508740  0.569
2015 Gorgy AI, Jonassaint NL, Stanley SE, Koteish A, DeZern AE, Walter JE, Sopha SC, Hamilton JP, Hoover-Fong J, Chen AR, Anders RA, Kamel IR, Armanios M. Hepatopulmonary syndrome is a frequent cause of dyspnea in the short telomere disorders. Chest. PMID 26158642 DOI: 10.1378/Chest.15-0825  0.487
2015 Alder JK, Barkauskas CE, Limjunyawong N, Stanley SE, Kembou F, Tuder RM, Hogan BL, Mitzner W, Armanios M. Telomere dysfunction causes alveolar stem cell failure. Proceedings of the National Academy of Sciences of the United States of America. 112: 5099-104. PMID 25840590 DOI: 10.1073/Pnas.1504780112  0.437
2015 Stanley SE, Chen JJ, Podlevsky JD, Alder JK, Hansel NN, Mathias RA, Qi X, Rafaels NM, Wise RA, Silverman EK, Barnes KC, Armanios M. Telomerase mutations in smokers with severe emphysema. The Journal of Clinical Investigation. 125: 563-70. PMID 25562321 DOI: 10.1172/Jci78554  0.602
2015 Alder JK, Stanley SE, Wagner CL, Hamilton M, Hanumanthu VS, Armanios M. Exome Sequencing Identifies Mutant TINF2 in a Family With Pulmonary Fibrosis. Chest. 147: 1361-8. PMID 25539146 DOI: 10.1378/Chest.14-1947  0.443
2014 Silhan LL, Shah PD, Chambers DC, Snyder LD, Riise GC, Wagner CL, Hellström-Lindberg E, Orens JB, Mewton JF, Danoff SK, Arcasoy MO, Armanios M. Lung transplantation in telomerase mutation carriers with pulmonary fibrosis. The European Respiratory Journal. 44: 178-87. PMID 24833766 DOI: 10.1183/09031936.00060014  0.372
2013 Alder JK, Parry EM, Yegnasubramanian S, Wagner CL, Lieblich LM, Auerbach R, Auerbach AD, Wheelan SJ, Armanios M. Telomere phenotypes in females with heterozygous mutations in the dyskeratosis congenita 1 (DKC1) gene. Human Mutation. 34: 1481-5. PMID 23946118 DOI: 10.1002/Humu.22397  0.449
2013 Jonassaint NL, Guo N, Califano JA, Montgomery EA, Armanios M. The gastrointestinal manifestations of telomere-mediated disease. Aging Cell. 12: 319-23. PMID 23279657 DOI: 10.1111/Acel.12041  0.415
2013 Armanios M, Blackburn EH. Erratum: The telomere syndromes Nature Reviews Genetics. 14: 235-235. DOI: 10.1038/Nrg3436  0.519
2012 Armanios M, Blackburn EH. The telomere syndromes. Nature Reviews. Genetics. 13: 693-704. PMID 22965356 DOI: 10.1038/Nrg3246  0.587
2012 Armanios M, Price C. Telomeres and disease: an overview. Mutation Research. 730: 1-2. PMID 22100639 DOI: 10.1016/J.Mrfmmm.2011.11.005  0.329
2011 Alder JK, Guo N, Kembou F, Parry EM, Anderson CJ, Gorgy AI, Walsh MF, Sussan T, Biswal S, Mitzner W, Tuder RM, Armanios M. Telomere length is a determinant of emphysema susceptibility. American Journal of Respiratory and Critical Care Medicine. 184: 904-12. PMID 21757622 DOI: 10.1164/Rccm.201103-0520Oc  0.468
2011 Alder JK, Cogan JD, Brown AF, Anderson CJ, Lawson WE, Lansdorp PM, Phillips JA, Loyd JE, Chen JJ, Armanios M. Ancestral mutation in telomerase causes defects in repeat addition processivity and manifests as familial pulmonary fibrosis. Plos Genetics. 7: e1001352. PMID 21483807 DOI: 10.1371/Journal.Pgen.1001352  0.632
2011 Parry EM, Alder JK, Qi X, Chen JJ, Armanios M. Syndrome complex of bone marrow failure and pulmonary fibrosis predicts germline defects in telomerase. Blood. 117: 5607-11. PMID 21436073 DOI: 10.1182/Blood-2010-11-322149  0.603
2011 Parry EM, Alder JK, Lee SS, Phillips JA, Loyd JE, Duggal P, Armanios M. Decreased dyskerin levels as a mechanism of telomere shortening in X-linked dyskeratosis congenita. Journal of Medical Genetics. 48: 327-33. PMID 21415081 DOI: 10.1136/Jmg.2010.085100  0.409
2009 Armanios M, Alder JK, Parry EM, Karim B, Strong MA, Greider CW. Short telomeres are sufficient to cause the degenerative defects associated with aging. American Journal of Human Genetics. 85: 823-32. PMID 19944403 DOI: 10.1016/J.Ajhg.2009.10.028  0.662
2009 Savage SA, Dokal I, Armanios M, Aubert G, Cowen EW, Domingo DL, Giri N, Greene MH, Orchard PJ, Tolar J, Tsilou E, Van Waes C, Wong JM, Young NS, Alter BP. Dyskeratosis congenita: the first NIH clinical research workshop. Pediatric Blood & Cancer. 53: 520-3. PMID 19415736 DOI: 10.1002/Pbc.22061  0.356
2008 Alder JK, Chen JJ, Lancaster L, Danoff S, Su SC, Cogan JD, Vulto I, Xie M, Qi X, Tuder RM, Phillips JA, Lansdorp PM, Loyd JE, Armanios MY. Short telomeres are a risk factor for idiopathic pulmonary fibrosis. Proceedings of the National Academy of Sciences of the United States of America. 105: 13051-6. PMID 18753630 DOI: 10.1073/Pnas.0804280105  0.575
2007 Armanios MY, Chen JJ, Cogan JD, Alder JK, Ingersoll RG, Markin C, Lawson WE, Xie M, Vulto I, Phillips JA, Lansdorp PM, Greider CW, Loyd JE. Telomerase mutations in families with idiopathic pulmonary fibrosis. The New England Journal of Medicine. 356: 1317-26. PMID 17392301 DOI: 10.1056/Nejmoa066157  0.688
2005 Armanios M, Greider CW. Telomerase and cancer stem cells. Cold Spring Harbor Symposia On Quantitative Biology. 70: 205-8. PMID 16869755 DOI: 10.1101/Sqb.2005.70.030  0.597
2005 Hao LY, Armanios M, Strong MA, Karim B, Feldser DM, Huso D, Greider CW. Short telomeres, even in the presence of telomerase, limit tissue renewal capacity. Cell. 123: 1121-31. PMID 16360040 DOI: 10.1016/J.Cell.2005.11.020  0.738
2005 Armanios M, Chen JL, Chang YP, Brodsky RA, Hawkins A, Griffin CA, Eshleman JR, Cohen AR, Chakravarti A, Hamosh A, Greider CW. Haploinsufficiency of telomerase reverse transcriptase leads to anticipation in autosomal dominant dyskeratosis congenita. Proceedings of the National Academy of Sciences of the United States of America. 102: 15960-4. PMID 16247010 DOI: 10.1073/Pnas.0508124102  0.683
2003 Qi L, Strong MA, Karim BO, Armanios M, Huso DL, Greider CW. Short telomeres and ataxia-telangiectasia mutated deficiency cooperatively increase telomere dysfunction and suppress tumorigenesis. Cancer Research. 63: 8188-96. PMID 14678974  0.652
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