A citation-based method for searching scientific literature

Jonathan K Alder, Vidya Sagar Hanumanthu, Margaret A Strong, Amy E DeZern, Susan E Stanley, Clifford M Takemoto, Ludmila Danilova, Carolyn D Applegate, Stephen G Bolton, David W Mohr, Robert A Brodsky, James F Casella, Carol W Greider, J Brooks Jackson, Mary Armanios. Proc Natl Acad Sci U S A 2018
Times Cited: 67







List of co-cited articles
536 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Telomerase mutations in families with idiopathic pulmonary fibrosis.
Mary Y Armanios, Julian J-L Chen, Joy D Cogan, Jonathan K Alder, Roxann G Ingersoll, Cheryl Markin, William E Lawson, Mingyi Xie, Irma Vulto, John A Phillips,[...]. N Engl J Med 2007
776
40

The telomere syndromes.
Mary Armanios, Elizabeth H Blackburn. Nat Rev Genet 2012
536
38

Loss-of-function mutations in the RNA biogenesis factor NAF1 predispose to pulmonary fibrosis-emphysema.
Susan E Stanley, Dustin L Gable, Christa L Wagner, Thomas M Carlile, Vidya Sagar Hanumanthu, Joshua D Podlevsky, Sara E Khalil, Amy E DeZern, Maria F Rojas-Duran, Carolyn D Applegate,[...]. Sci Transl Med 2016
92
35

Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening.
Bridget D Stuart, Jungmin Choi, Samir Zaidi, Chao Xing, Brody Holohan, Rui Chen, Mihwa Choi, Pooja Dharwadkar, Fernando Torres, Carlos E Girod,[...]. Nat Genet 2015
230
28

Short telomeres are a risk factor for idiopathic pulmonary fibrosis.
Jonathan K Alder, Julian J-L Chen, Lisa Lancaster, Sonye Danoff, Shu-chih Su, Joy D Cogan, Irma Vulto, Mingyi Xie, Xiaodong Qi, Rubin M Tuder,[...]. Proc Natl Acad Sci U S A 2008
452
26

Flow cytometry and FISH to measure the average length of telomeres (flow FISH).
Gabriela M Baerlocher, Irma Vulto, Gary de Jong, Peter M Lansdorp. Nat Protoc 2006
274
23

Adult-onset pulmonary fibrosis caused by mutations in telomerase.
Kalliopi D Tsakiri, Jennifer T Cronkhite, Phillip J Kuan, Chao Xing, Ganesh Raghu, Jonathan C Weissler, Randall L Rosenblatt, Jerry W Shay, Christine Kim Garcia. Proc Natl Acad Sci U S A 2007
543
23

The gastrointestinal manifestations of telomere-mediated disease.
Naudia L Jonassaint, Nini Guo, Joseph A Califano, Elizabeth A Montgomery, Mary Armanios. Aging Cell 2013
54
27

Lung transplantation in telomerase mutation carriers with pulmonary fibrosis.
Leann L Silhan, Pali D Shah, Daniel C Chambers, Laurie D Snyder, Gerdt C Riise, Christa L Wagner, Eva Hellström-Lindberg, Jonathan B Orens, Juliette F Mewton, Sonye K Danoff,[...]. Eur Respir J 2014
95
22

Direct comparison of flow-FISH and qPCR as diagnostic tests for telomere length measurement in humans.
Fernanda Gutierrez-Rodrigues, Bárbara A Santana-Lemos, Priscila S Scheucher, Raquel M Alves-Paiva, Rodrigo T Calado. PLoS One 2014
81
20

Syndrome complex of bone marrow failure and pulmonary fibrosis predicts germline defects in telomerase.
Erin M Parry, Jonathan K Alder, Xiaodong Qi, Julian J-L Chen, Mary Armanios. Blood 2011
95
20

Exome sequencing identifies mutant TINF2 in a family with pulmonary fibrosis.
Jonathan K Alder, Susan E Stanley, Christa L Wagner, Makenzie Hamilton, Vidya Sagar Hanumanthu, Mary Armanios. Chest 2015
83
20

X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions.
N S Heiss, S W Knight, T J Vulliamy, S M Klauck, S Wiemann, P J Mason, A Poustka, I Dokal. Nat Genet 1998
626
19

The short and long telomere syndromes: paired paradigms for molecular medicine.
Susan E Stanley, Mary Armanios. Curr Opin Genet Dev 2015
67
19

Telomere-related lung fibrosis is diagnostically heterogeneous but uniformly progressive.
Chad A Newton, Kiran Batra, Jose Torrealba, Julia Kozlitina, Craig S Glazer, Carlos Aravena, Keith Meyer, Ganesh Raghu, Harold R Collard, Christine Kim Garcia. Eur Respir J 2016
115
19


An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary Fibrosis.
Slavé Petrovski, Jamie L Todd, Michael T Durheim, Quanli Wang, Jason W Chien, Fran L Kelly, Courtney Frankel, Caroline M Mebane, Zhong Ren, Joshua Bridgers,[...]. Am J Respir Crit Care Med 2017
92
19

Telomerase mutations in smokers with severe emphysema.
Susan E Stanley, Julian J L Chen, Joshua D Podlevsky, Jonathan K Alder, Nadia N Hansel, Rasika A Mathias, Xiaodong Qi, Nicholas M Rafaels, Robert A Wise, Edwin K Silverman,[...]. J Clin Invest 2015
95
17

Danazol Treatment for Telomere Diseases.
Danielle M Townsley, Bogdan Dumitriu, Delong Liu, Angélique Biancotto, Barbara Weinstein, Christina Chen, Nathan Hardy, Andrew D Mihalek, Shilpa Lingala, Yun Ju Kim,[...]. N Engl J Med 2016
159
17

Hepatopulmonary syndrome is a frequent cause of dyspnea in the short telomere disorders.
Amany I Gorgy, Naudia L Jonassaint, Susan E Stanley, Ayman Koteish, Amy E DeZern, Jolan E Walter, Sabrina C Sopha, James P Hamilton, Julie Hoover-Fong, Allen R Chen,[...]. Chest 2015
47
25

Telomeres shorten during ageing of human fibroblasts.
C B Harley, A B Futcher, C W Greider. Nature 1990
17

Heterozygous RTEL1 mutations are associated with familial pulmonary fibrosis.
Caroline Kannengiesser, Raphael Borie, Christelle Ménard, Marion Réocreux, Patrick Nitschké, Steven Gazal, Hervé Mal, Camille Taillé, Jacques Cadranel, Hilario Nunes,[...]. Eur Respir J 2015
85
17


Telomere lengths, pulmonary fibrosis and telomerase (TERT) mutations.
Alberto Diaz de Leon, Jennifer T Cronkhite, Anna-Luise A Katzenstein, J David Godwin, Ganesh Raghu, Craig S Glazer, Randall L Rosenblatt, Carlos E Girod, Edward R Garrity, Chao Xing,[...]. PLoS One 2010
204
16

Haploinsufficiency of telomerase reverse transcriptase leads to anticipation in autosomal dominant dyskeratosis congenita.
Mary Armanios, Jiunn-Liang Chen, Yen-Pei Christy Chang, Robert A Brodsky, Anita Hawkins, Constance A Griffin, James R Eshleman, Alan R Cohen, Aravinda Chakravarti, Ada Hamosh,[...]. Proc Natl Acad Sci U S A 2005
291
16

Telomere phenotypes in females with heterozygous mutations in the dyskeratosis congenita 1 (DKC1) gene.
Jonathan K Alder, Erin M Parry, Srinivasan Yegnasubramanian, Christa L Wagner, Lawrence M Lieblich, Robert Auerbach, Arleen D Auerbach, Sarah J Wheelan, Mary Armanios. Hum Mutat 2013
57
19

Rare variants in RTEL1 are associated with familial interstitial pneumonia.
Joy D Cogan, Jonathan A Kropski, Min Zhao, Daphne B Mitchell, Lynette Rives, Cheryl Markin, Errine T Garnett, Keri H Montgomery, Wendi R Mason, David F McKean,[...]. Am J Respir Crit Care Med 2015
104
16

Short Telomere Syndromes in Clinical Practice: Bridging Bench and Bedside.
Abhishek A Mangaonkar, Mrinal M Patnaik. Mayo Clin Proc 2018
27
37


Mutations in TERT, the gene for telomerase reverse transcriptase, in aplastic anemia.
Hiroki Yamaguchi, Rodrigo T Calado, Hinh Ly, Sachiko Kajigaya, Gabriela M Baerlocher, Stephen J Chanock, Peter M Lansdorp, Neal S Young. N Engl J Med 2005
479
14

Short telomere syndromes cause a primary T cell immunodeficiency.
Christa L Wagner, Vidya Sagar Hanumanthu, C Conover Talbot, Roshini S Abraham, David Hamm, Dustin L Gable, Christopher G Kanakry, Carolyn D Applegate, Janet Siliciano, J Brooks Jackson,[...]. J Clin Invest 2018
34
29

Telomere measurement by quantitative PCR.
Richard M Cawthon. Nucleic Acids Res 2002
14

ZCCHC8, the nuclear exosome targeting component, is mutated in familial pulmonary fibrosis and is required for telomerase RNA maturation.
Dustin L Gable, Valeriya Gaysinskaya, Christine C Atik, C Conover Talbot, Byunghak Kang, Susan E Stanley, Elizabeth W Pugh, Nuria Amat-Codina, Kara M Schenk, Murat O Arcasoy,[...]. Genes Dev 2019
27
37

Poly(A)-specific ribonuclease (PARN) mediates 3'-end maturation of the telomerase RNA component.
Diane H Moon, Matthew Segal, Baris Boyraz, Eva Guinan, Inga Hofmann, Patrick Cahan, Albert K Tai, Suneet Agarwal. Nat Genet 2015
98
13

Cancer in the National Cancer Institute inherited bone marrow failure syndrome cohort after fifteen years of follow-up.
Blanche P Alter, Neelam Giri, Sharon A Savage, Philip S Rosenberg. Haematologica 2018
86
13

Dyskeratosis congenita in all its forms.
I Dokal. Br J Haematol 2000
350
13

Correlation of Leukocyte Telomere Length Measurement Methods in Patients with Dyskeratosis Congenita and in Their Unaffected Relatives.
Payal P Khincha, Casey L Dagnall, Belynda Hicks, Kristine Jones, Abraham Aviv, Masayuki Kimura, Hormuzd Katki, Geraldine Aubert, Neelam Giri, Blanche P Alter,[...]. Int J Mol Sci 2017
18
50

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
13

Disease-specific hematopoietic cell transplantation: nonmyeloablative conditioning regimen for dyskeratosis congenita.
A C Dietz, P J Orchard, K S Baker, R H Giller, S A Savage, B P Alter, J Tolar. Bone Marrow Transplant 2011
92
11

The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita.
T Vulliamy, A Marrone, F Goldman, A Dearlove, M Bessler, P J Mason, I Dokal. Nature 2001
679
11

Unraveling the pathogenesis of Hoyeraal-Hreidarsson syndrome, a complex telomere biology disorder.
Galina Glousker, Fabien Touzot, Patrick Revy, Yehuda Tzfati, Sharon A Savage. Br J Haematol 2015
57
14

Response to androgen therapy in patients with dyskeratosis congenita.
Payal P Khincha, Ingrid M Wentzensen, Neelam Giri, Blanche P Alter, Sharon A Savage. Br J Haematol 2014
53
15

Bone marrow failure and the telomeropathies.
Danielle M Townsley, Bogdan Dumitriu, Neal S Young. Blood 2014
137
11

A spectrum of severe familial liver disorders associate with telomerase mutations.
Rodrigo T Calado, Joshua A Regal, David E Kleiner, David S Schrump, Nathan R Peterson, Veronica Pons, Stephen J Chanock, Peter M Lansdorp, Neal S Young. PLoS One 2009
120
11

Short telomeres, even in the presence of telomerase, limit tissue renewal capacity.
Ling-Yang Hao, Mary Armanios, Margaret A Strong, Baktiar Karim, David M Feldser, David Huso, Carol W Greider. Cell 2005
199
11

Short telomeres are sufficient to cause the degenerative defects associated with aging.
Mary Armanios, Jonathan K Alder, Erin M Parry, Baktiar Karim, Margaret A Strong, Carol W Greider. Am J Hum Genet 2009
147
11

Triallelic and epigenetic-like inheritance in human disorders of telomerase.
Laura C Collopy, Amanda J Walne, Shirleny Cardoso, Josu de la Fuente, Mahfuzah Mohamed, Helga Toriello, Hannah Tamary, Adam J Y V Ling, Timothy Lloyd, Rebecca Kassam,[...]. Blood 2015
27
29

Severe hematologic complications after lung transplantation in patients with telomerase complex mutations.
Raphael Borie, Caroline Kannengiesser, Sandrine Hirschi, Jérôme Le Pavec, Hervé Mal, Emmanuel Bergot, Stéphane Jouneau, Jean-Marc Naccache, Patrick Revy, David Boutboul,[...]. J Heart Lung Transplant 2015
57
14


Prevalence and characteristics of TERT and TERC mutations in suspected genetic pulmonary fibrosis.
Raphael Borie, Laure Tabèze, Gabriel Thabut, Hilario Nunes, Vincent Cottin, Sylvain Marchand-Adam, Grégoire Prevot, Abdellatif Tazi, Jacques Cadranel, Herve Mal,[...]. Eur Respir J 2016
57
14


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.