Mary Armanios

10.7k total citations · 4 hit papers
67 papers, 7.1k citations indexed

About

Mary Armanios is a scholar working on Physiology, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Mary Armanios has authored 67 papers receiving a total of 7.1k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Physiology, 26 papers in Molecular Biology and 19 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Mary Armanios's work include Telomeres, Telomerase, and Senescence (39 papers), Occupational and environmental lung diseases (9 papers) and Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis (8 papers). Mary Armanios is often cited by papers focused on Telomeres, Telomerase, and Senescence (39 papers), Occupational and environmental lung diseases (9 papers) and Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis (8 papers). Mary Armanios collaborates with scholars based in United States, United Kingdom and Canada. Mary Armanios's co-authors include Elizabeth H. Blackburn, Jonathan K. Alder, Carol W. Greider, Julian J.‐L. Chen, Susan E. Stanley, John A. Phillips, James E. Loyd, Joy D. Cogan, Peter M. Lansdorp and Erin M. Parry and has published in prestigious journals such as New England Journal of Medicine, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Mary Armanios

65 papers receiving 7.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Telomerase Mutations in Families with Idiopathic Pulmonary Fibrosis

2007 920 citations Mary Armanios, Julian J.‐L. Chen et al. New England Journal of Medicine profile →
The telomere syndromes

2012 700 citations Mary Armanios et al. profile →
Short telomeres are a risk factor for idiopathic pulmonary fibrosis

2008 553 citations Jonathan K. Alder, Julian J.‐L. Chen et al. Proceedings of the National Academy of Sciences profile →
Haploinsufficiency of t e lomerase reverse transcriptase leads to anticipation in autosomal dominant dyskeratosis congenita

2005 324 citations Mary Armanios, Julian J.‐L. Chen et al. Proceedings of the National Academy of Sciences profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Mary Armanios United States	42	3.9k	2.6k	2.4k	845	620	67	7.1k
Tom Vulliamy United Kingdom	48	4.2k 1.1×	982 0.4×	3.9k 1.6×	383 0.5×	350 0.6×	111	8.2k
Kaiyo Takubo Japan	39	1.3k 0.3×	1.4k 0.5×	1.2k 0.5×	2.2k 2.6×	318 0.5×	249	5.3k
Joy D. Cogan United States	37	1.0k 0.3×	2.4k 0.9×	1.4k 0.6×	561 0.7×	90 0.1×	84	5.0k
Gabriela M. Baerlocher Switzerland	31	2.4k 0.6×	228 0.1×	2.3k 1.0×	230 0.3×	338 0.5×	104	4.8k
Utz Herbig United States	23	3.1k 0.8×	157 0.1×	2.7k 1.1×	157 0.2×	867 1.4×	37	4.8k
Thomas H. Norwood United States	34	759 0.2×	493 0.2×	1.7k 0.7×	370 0.4×	185 0.3×	79	3.4k
Jaroslav Jelı́nek United States	49	484 0.1×	715 0.3×	5.8k 2.4×	427 0.5×	86 0.1×	159	8.3k
John T. Cunningham United States	28	529 0.1×	1.5k 0.6×	1.4k 0.6×	2.1k 2.5×	105 0.2×	88	4.2k
Riitta Herva Finland	39	542 0.1×	1.3k 0.5×	3.4k 1.4×	872 1.0×	23 0.0×	124	6.6k
Jun Araya Japan	33	608 0.2×	1.8k 0.7×	1.8k 0.7×	311 0.4×	27 0.0×	102	3.8k

Countries citing papers authored by Mary Armanios

Since Specialization

Citations

This map shows the geographic impact of Mary Armanios's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Mary Armanios with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mary Armanios more than expected).

Fields of papers citing papers by Mary Armanios

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mary Armanios. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Mary Armanios. The network helps show where Mary Armanios may publish in the future.

Co-authorship network of co-authors of Mary Armanios

This figure shows the co-authorship network connecting the top 25 collaborators of Mary Armanios. A scholar is included among the top collaborators of Mary Armanios based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Mary Armanios. Mary Armanios is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Schratz, Kristen E., et al.. (2025). Adult-Onset Presentations of Retinopathy Associated With Short Telomere Syndromes. Journal of VitreoRetinal Diseases. 9(3). 357–361.

Liyanarachchi, Sandya, et al.. (2024). Telomere-lengthening germline variants predispose to a syndromic papillary thyroid cancer subtype. The American Journal of Human Genetics. 111(6). 1114–1124. 5 indexed citations

Tassia, Michael G., Kristen E. Schratz, Stephanie M. Yan, et al.. (2023). Familial Clonal Hematopoiesis in a Long Telomere Syndrome. New England Journal of Medicine. 388(26). 2422–2433. 64 indexed citations

Schratz, Kristen E. & Mary Armanios. (2020). Cancer and myeloid clonal evolution in the short telomere syndromes. Current Opinion in Genetics & Development. 60. 112–118. 24 indexed citations

Schratz, Kristen E., Lisa Haley, Sonye K. Danoff, et al.. (2020). Cancer spectrum and outcomes in the Mendelian short telomere syndromes. Blood. 135(22). 1946–1956. 79 indexed citations

Alder, Jonathan K., Vidya Sagar Hanumanthu, Margaret A. Strong, et al.. (2018). Diagnostic utility of telomere length testing in a hospital-based setting. Proceedings of the National Academy of Sciences. 115(10). E2358–E2365. 144 indexed citations

Popescu, Iulia, H. Mannem, Spencer Winters, et al.. (2018). Impaired Cytomegalovirus Immunity in Idiopathic Pulmonary Fibrosis Lung Transplant Recipients with Short Telomeres. American Journal of Respiratory and Critical Care Medicine. 199(3). 362–376. 68 indexed citations

Lee, Melissa, Patrick Roos, Neeraj Sharma, et al.. (2017). Systematic Computational Identification of Variants That Activate Exonic and Intronic Cryptic Splice Sites. The American Journal of Human Genetics. 100(5). 751–765. 51 indexed citations

DiNardo, Courtney D., Sarah A. Bannon, Mark J. Routbort, et al.. (2016). Evaluation of Patients and Families With Concern for Predispositions to Hematologic Malignancies Within the Hereditary Hematologic Malignancy Clinic (HHMC). Clinical Lymphoma Myeloma & Leukemia. 16(7). 417–428.e2. 66 indexed citations

10.

Stanley, Susan E., Dustin L. Gable, Christa L. Wagner, et al.. (2016). Loss-of-function mutations in the RNA biogenesis factor NAF1 predispose to pulmonary fibrosis–emphysema. Science Translational Medicine. 8(351). 351ra107–351ra107. 129 indexed citations

11.

You, Jing, Nara Sobreira, Dustin L. Gable, et al.. (2016). A Syndromic Intellectual Disability Disorder Caused by Variants in TELO2 , a Gene Encoding a Component of the TTT Complex. The American Journal of Human Genetics. 98(5). 909–918. 26 indexed citations

12.

Bhatt, Niraj, Rajib Ghosh, Sanchita Roy, et al.. (2016). Robust reprogramming of Ataxia-Telangiectasia patient and carrier erythroid cells to induced pluripotent stem cells. Stem Cell Research. 17(2). 296–305. 5 indexed citations

13.

Gorgy, Amany, Naudia Jonassaint, Susan E. Stanley, et al.. (2015). Hepatopulmonary Syndrome Is a Frequent Cause of Dyspnea in the Short Telomere Disorders. CHEST Journal. 148(4). 1019–1026. 74 indexed citations

14.

Alder, Jonathan K., Erin M. Parry, Srinivasan Yegnasubramanian, et al.. (2013). Telomere Phenotypes in Females with Heterozygous Mutations in the Dyskeratosis Congenita 1 (DKC1) Gene. Human Mutation. 34(11). 1481–1485. 69 indexed citations

15.

Jonassaint, Naudia, Nini Guo, Joseph A. Califano, Elizabeth A. Montgomery, & Mary Armanios. (2012). The gastrointestinal manifestations of telomere‐mediated disease. Aging Cell. 12(2). 319–323. 68 indexed citations

16.

Alder, Jonathan K., Nini Guo, Erin M. Parry, et al.. (2011). Telomere Length Is a Determinant of Emphysema Susceptibility. American Journal of Respiratory and Critical Care Medicine. 184(8). 904–912. 178 indexed citations

17.

Parry, Erin M., Jonathan K. Alder, Stella S. Lee, et al.. (2011). Decreased dyskerin levels as a mechanism of telomere shortening in X-linked dyskeratosis congenita. Journal of Medical Genetics. 48(5). 327–333. 45 indexed citations

18.

Armanios, Mary. (2011). Telomerase and idiopathic pulmonary fibrosis. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 730(1-2). 52–58. 165 indexed citations

19.

Alder, Jonathan K., Julian J.‐L. Chen, Lisa Lancaster, et al.. (2008). Short telomeres are a risk factor for idiopathic pulmonary fibrosis. Proceedings of the National Academy of Sciences. 105(35). 13051–13056. 553 indexed citations breakdown →

20.

Armanios, Mary, Julian J.‐L. Chen, Yen-Pei C. Chang, et al.. (2005). Haploinsufficiency of t e lomerase reverse transcriptase leads to anticipation in autosomal dominant dyskeratosis congenita. Proceedings of the National Academy of Sciences. 102(44). 15960–15964. 324 indexed citations breakdown →

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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