| Year |
Citation |
Score |
| 2023 |
DeBoy EA, Tassia MG, Schratz KE, Yan SM, Cosner ZL, McNally EJ, Gable DL, Xiang Z, Lombard DB, Antonarakis ES, Gocke CD, McCoy RC, Armanios M. Familial Clonal Hematopoiesis in a Long Telomere Syndrome. The New England Journal of Medicine. PMID 37140166 DOI: 10.1056/NEJMoa2300503 |
0.333 |
|
| 2022 |
Armanios M. The Role of Telomeres in Human Disease. Annual Review of Genomics and Human Genetics. PMID 35609925 DOI: 10.1146/annurev-genom-010422-091101 |
0.395 |
|
| 2022 |
Alder JK, Armanios M. Telomere-mediated Lung Disease. Physiological Reviews. PMID 35532056 DOI: 10.1152/physrev.00046.2021 |
0.422 |
|
| 2022 |
Taub MA, Conomos MP, Keener R, Iyer KR, Weinstock JS, Yanek LR, Lane J, Miller-Fleming TW, Brody JA, Raffield LM, McHugh CP, Jain D, Gogarten SM, Laurie CA, Keramati A, ... ... Armanios M, et al. Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed. Cell Genomics. 2. PMID 35530816 DOI: 10.1016/j.xgen.2021.100084 |
0.706 |
|
| 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 |
0.333 |
|
| 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 |
0.326 |
|
| 2020 |
Gaysinskaya V, Stanley SE, Adam S, Armanios M. Synonymous mutation in DKC1 causes telomerase RNA insufficiency manifesting as familial pulmonary fibrosis. Chest. PMID 32710892 DOI: 10.1016/J.Chest.2020.07.025 |
0.479 |
|
| 2020 |
Schratz KE, Armanios M. Cancer and myeloid clonal evolution in the short telomere syndromes. Current Opinion in Genetics & Development. 60: 112-118. PMID 32276199 DOI: 10.1016/J.Gde.2020.02.019 |
0.473 |
|
| 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 |
0.466 |
|
| 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 |
0.459 |
|
| 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 |
0.476 |
|
| 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 |
0.462 |
|
| 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 |
0.365 |
|
| 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 |
0.339 |
|
| 2018 |
Popescu I, Mannem H, Winters SA, Hoji A, Silveira F, McNally E, Pipeling MR, Lendermon EA, Morrell MR, Pilewski JM, Hanumanthu VS, Zhang Y, Gulati S, Shah PD, Iasella CJ, ... ... Armanios M, et al. Impaired CMV Immunity in Idiopathic Pulmonary Fibrosis Lung Transplant Recipients with Short Telomeres. American Journal of Respiratory and Critical Care Medicine. PMID 30088779 DOI: 10.1164/Rccm.201805-0825Oc |
0.31 |
|
| 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 |
0.667 |
|
| 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 |
0.349 |
|
| 2017 |
Parry EM, Gable DL, Stanley SE, Khalil SE, Antonescu V, Florea L, Armanios M. Germline mutations in DNA repair genes in lung adenocarcinoma. Journal of Thoracic Oncology : Official Publication of the International Association For the Study of Lung Cancer. PMID 28843361 DOI: 10.1016/J.Jtho.2017.08.011 |
0.371 |
|
| 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 |
0.339 |
|
| 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 |
0.361 |
|
| 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 |
0.539 |
|
| 2016 |
Stanley SE, Merck SJ, Armanios M. Telomerase and the Genetics of Emphysema Susceptibility. Implications for Pathogenesis Paradigms and Patient Care. Annals of the American Thoracic Society. 13: S447-S451. PMID 28005428 DOI: 10.1513/Annalsats.201609-718Aw |
0.468 |
|
| 2016 |
Merck SJ, Armanios M. Shall we call them "telomere-mediated"? Renaming the idiopathic after the cause is found. The European Respiratory Journal. 48: 1556-1558. PMID 27903687 DOI: 10.1183/13993003.02115-2016 |
0.304 |
|
| 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 |
0.364 |
|
| 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 |
0.355 |
|
| 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 |
0.463 |
|
| 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 |
0.319 |
|
| 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 |
0.345 |
|
| 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 |
0.361 |
|
| 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 |
0.452 |
|
| 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 |
0.57 |
|
| 2015 |
Stanley SE, Armanios M. The short and long telomere syndromes: paired paradigms for molecular medicine. Current Opinion in Genetics & Development. 33: 1-9. PMID 26232116 DOI: 10.1016/J.Gde.2015.06.004 |
0.493 |
|
| 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 |
0.503 |
|
| 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 |
0.45 |
|
| 2015 |
Stanley SE, Noth I, Armanios M. What the genetics "RTEL"ing us about telomeres and pulmonary fibrosis. American Journal of Respiratory and Critical Care Medicine. 191: 608-10. PMID 25767920 DOI: 10.1164/Rccm.201501-0119Ed |
0.553 |
|
| 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 |
0.61 |
|
| 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 |
0.465 |
|
| 2015 |
Armanios M. Extrahematopoietic Manifestations of Telomere Syndromes Blood. 126. DOI: 10.1182/Blood.V126.23.Sci-51.Sci-51 |
0.48 |
|
| 2014 |
Stanley SE, Armanios M. Short telomeres: a repeat offender in IPF. The Lancet. Respiratory Medicine. 2: 513-4. PMID 24973280 DOI: 10.1016/S2213-2600(14)70140-7 |
0.391 |
|
| 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 |
0.378 |
|
| 2014 |
Armanios M. Reply: telomerase makes connections between pulmonary fibrosis and emphysema. American Journal of Respiratory and Critical Care Medicine. 189: 754-5. PMID 24628320 DOI: 10.1164/Rccm.201401-0019Le |
0.519 |
|
| 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 |
0.473 |
|
| 2013 |
Armanios M. Telomeres and age-related disease: how telomere biology informs clinical paradigms. The Journal of Clinical Investigation. 123: 996-1002. PMID 23454763 DOI: 10.1172/Jci66370 |
0.447 |
|
| 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 |
0.427 |
|
| 2013 |
Armanios M, Blackburn EH. Erratum: The telomere syndromes Nature Reviews Genetics. 14: 235-235. DOI: 10.1038/Nrg3436 |
0.534 |
|
| 2012 |
Armanios M, Blackburn EH. The telomere syndromes. Nature Reviews. Genetics. 13: 693-704. PMID 22965356 DOI: 10.1038/Nrg3246 |
0.606 |
|
| 2012 |
Armanios M. Telomerase mutations and the pulmonary fibrosis-bone marrow failure syndrome complex. The New England Journal of Medicine. 367: 384; author reply 38. PMID 22830481 DOI: 10.1056/Nejmc1206730 |
0.425 |
|
| 2012 |
Armanios M. An emerging role for the conserved telomere component 1 (CTC1) in human genetic disease. Pediatric Blood & Cancer. 59: 209-10. PMID 22556055 DOI: 10.1002/Pbc.24200 |
0.336 |
|
| 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 |
0.336 |
|
| 2012 |
Armanios M. Telomerase and idiopathic pulmonary fibrosis. Mutation Research. 730: 52-8. PMID 22079513 DOI: 10.1016/J.Mrfmmm.2011.10.013 |
0.504 |
|
| 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 |
0.49 |
|
| 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 |
0.654 |
|
| 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 |
0.613 |
|
| 2011 |
Guo N, Parry EM, Li LS, Kembou F, Lauder N, Hussain MA, Berggren PO, Armanios M. Short telomeres compromise β-cell signaling and survival. Plos One. 6: e17858. PMID 21423765 DOI: 10.1371/Journal.Pone.0017858 |
0.378 |
|
| 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 |
0.616 |
|
| 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 |
0.671 |
|
| 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 |
0.367 |
|
| 2009 |
Armanios M. Syndromes of telomere shortening. Annual Review of Genomics and Human Genetics. 10: 45-61. PMID 19405848 DOI: 10.1146/Annurev-Genom-082908-150046 |
0.477 |
|
| 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 |
0.597 |
|
| 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 |
0.701 |
|
| 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 |
0.603 |
|
| 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 |
0.758 |
|
| 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 |
0.698 |
|
| 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 |
0.646 |
|
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